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SYSTEMATIC REVIEW article

Front. Physiol., 24 August 2021
Sec. Exercise Physiology
This article is part of the Research Topic Exercise as a Countermeasure to Human Aging, Volume II View all 11 articles

High Intensity Interval Training (HIIT) as a Potential Countermeasure for Phenotypic Characteristics of Sarcopenia: A Scoping Review

  • 1School of Health and Life Sciences, University of the West of Scotland, Hamilton, United Kingdom
  • 2Translational Physiology Research Group, School of Life Sciences, University of Westminster, London, United Kingdom
  • 3Active Ageing Research Group, Institute of Health, University of Cumbria, Lancaster, United Kingdom
  • 4Lancaster Medical School, Lancaster University, Lancaster, United Kingdom
  • 5The Centre for Ageing Research, Lancaster University, Lancaster, United Kingdom
  • 6Department of Psychology, Lancaster University, Lancaster, United Kingdom
  • 7AGE Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom
  • 8National Institute for Health Research Newcastle Biomedical Research Centre, Newcastle upon Tyne Hospitals National Health Service Foundation Trust and Newcastle University, Newcastle upon Tyne, United Kingdom

Background: Sarcopenia is defined as a progressive and generalized loss of skeletal muscle quantity and function associated predominantly with aging. Physical activity appears the most promising intervention to attenuate sarcopenia, yet physical activity guidelines are rarely met. In recent years high intensity interval training (HIIT) has garnered interested in athletic populations, clinical populations, and general population alike. There is emerging evidence of the efficacy of HIIT in the young old (i.e. seventh decade of life), yet data concerning the oldest old (i.e., ninth decade of life onwards), and those diagnosed with sarcopenic are sparse.

Objectives: In this scoping review of the literature, we aggregated information regarding HIIT as a potential intervention to attenuate phenotypic characteristics of sarcopenia.

Eligibility Criteria: Original investigations concerning the impact of HIIT on muscle function, muscle quantity or quality, and physical performance in older individuals (mean age ≥60 years of age) were considered.

Sources of Evidence: Five electronic databases (Medline, EMBASE, Web of Science, Scopus, and the Cochrane Central Register of Controlled Trials [CENTRAL]) were searched.

Methods: A scoping review was conducted using the Arksey and O'Malley methodological framework (2005). Review selection and characterization were performed by two independent reviewers using pretested forms.

Results: Authors reviewed 1,063 titles and abstracts for inclusion with 74 selected for full text review. Thirty-two studies were analyzed. Twenty-seven studies had a mean participant age in the 60s, two in the 70s, and three in the 80s. There were 20 studies which examined the effect of HIIT on muscle function, 22 which examined muscle quantity, and 12 which examined physical performance. HIIT was generally effective in Improving muscle function and physical performance compared to non-exercised controls, moderate intensity continuous training, or pre-HIIT (study design-dependent), with more ambiguity concerning muscle quantity.

Conclusions: Most studies presented herein utilized outcome measures defined by the European Working Group on Sarcopenia in Older People (EWGSOP). However, there are too few studies investigating any form of HIIT in the oldest old (i.e., ≥80 years of age), or those already sarcopenic. Therefore, more intervention studies are needed in this population.

Key Points

• A variety of intensity prescriptions were utilized in previous experiments, which included “all-out” effort, percentage of maximal heart rate, perceived a percentage of peak oxygen uptake, percentage of intensity at termination of a ramped exercise test, percentage of peak instantaneous power, rating of perceived exertion, and percentage of maximum gait speed.

• Twenty-seven studies had a mean participant age in the 60s, two in the 70s, and three in the 80s. There were 20 studies which examined the effect of HIIT on muscle function, 22 studies which examined the effect of HIIT on muscle quantity, and 12 studies which examined the effect of HIIT on physical function (which are the outcomes used to diagnose sarcopenia).

• No previous investigation had considered HIIT in a sarcopenic or pre-sarcopenic population, and only three studies were in the oldest old humans.

Introduction

Rationale

Sarcopenia is a progressive skeletal muscle disorder, characterized by reduced skeletal muscle quantity and function which is associated with a range of negative health outcomes including frailty, falls, reduced quality of life, and mortality (Cruz-Jentoft and Sayer, 2019; Cruz-Jentoft et al., 2019). In addition to these individual health impacts, sarcopenia places a considerable economic burden on healthcare systems with the associated costs in the UK estimated at £2.5 billion per year (Pinedo-Villanueva et al., 2019). Taken together, these effects highlight the need to develop treatment strategies to counteract the deleterious consequences of sarcopenia.

Factors including chronic inflammation, mitochondrial dysfunction, and reduced satellite cell function contribute to the onset and progression of sarcopenia (Ziaaldini et al., 2017). Exercise training has the potential to counteract these cellular, molecular, and neural alterations (Marzetti et al., 2017; Seo and Hwang, 2020) with aerobic and resistance exercise capable of inducing differential adaptations (Hawley et al., 2014). Previous work has demonstrated that resistance exercise has multisystem effects, acting at both the physiological [e.g., improvements in mitochondrial function (Melov et al., 2007) and reduced inflammation (Beyer et al., 2012)] and the functional level [e.g., improvements in muscle strength and physical performance (Peterson et al., 2010; Steib et al., 2010)]. To date there remains no pharmacological treatment approved for the treatment of sarcopenia and resistance exercise training is recommended as its primary treatment (Dent et al., 2018). Given the multi-factorial nature of sarcopenia, exercise programmes for older adults living with sarcopenia often involve a combination of exercise modes (Witham et al., 2020) with the aim of simultaneously improving muscular and cardiorespiratory function (Hurst et al., 2019a). Offering a range of alternative exercise training approaches which can simultaneously improve multiple outcomes (e.g., muscle strength, physical performance, and cardiorespiratory fitness) could help to maximize the potential of exercise as a therapeutic strategy for older people living with sarcopenia.

High intensity interval training (HIIT) has previously been shown to exert substantial cardio-protective effects, across a range of population groups (Knowles et al., 2015; Hwang et al., 2016; Batacan et al., 2017; Füzéki and Banzer, 2018; Hannan et al., 2018; Hayes et al., 2020; Herbert et al., 2021). In the clinical context, HIIT has been shown to be a safe, feasible and effective therapeutic strategy in patients living with diabetes (Little et al., 2011), heart failure (Angadi et al., 2015) and coronary artery disease (Warburton et al., 2005). From a pragmatic perspective, HIIT can be embedded within the clinical pathway (Way et al., 2020) and can be delivered using a range of exercise modes (e.g., stair climbing, stepping, cycling, walking).

Despite this, much less is known about how HIIT could improve elements of muscular structure and function. A recent narrative review (Callahan et al., 2021) outlined several mechanistic explanations as to why HIIT might be anabolic in nature. These authors called for further investigation of HIIT in populations of different age groups and training status to explore this phenomenon further. Moreover, they proposed HIIT may be beneficial in middle and older age where physical conditioning (i.e., aerobic fitness) and increased muscle quantity were simultaneously desired. Whether HIIT could provide the necessary improvements in muscle quantity, quality, and strength, in addition to cardioprotective effects however, remain unclear (Hurst et al., 2019b). The potential for HIIT to simultaneously induce improvements in cardiometabolic health and muscular health is an appealing strategy. However, until now there has not been a comprehensive review of HIIT within older adults pertaining to phenotypic characteristics of sarcopenia using a systematic search strategy.

Given that exercise programmes delivered to older people with sarcopenia in clinical practice are varied and often poorly prescribed (Witham et al., 2020), delivering effective and engaging exercise programmes to older people is of prime concern (Dismore et al., 2020; Collado-Mateo et al., 2021). HIIT is reportedly enjoyable (Thum et al., 2017), can be completed without gym equipment (Blackwell et al., 2017; Dunford et al., 2021; Yasar et al., 2021), and deliver self-perceived health and fitness improvements (Knowles et al., 2015). However, before HIIT can be proposed as a viable countermeasure to phenotypic characteristics of sarcopenia, it is important to consider the existing literature in terms of methodologies, quality of research and heterogeneity, to determine whether a systematic review and meta-analysis is possible, and if not to identify the areas in which the current literature is deficient. A comprehensive review of HIIT and its effect on phenotypic characteristics of sarcopenia is important for clinicians and exercise practitioners to ensure they are equipped to support community-dwelling older adults and their families/caregivers. Therefore, it seemed prudent to conduct a scoping review in this area to map the existing literature in terms of the volume, nature, and characteristics of the primary research (Arksey and O'Malley, 2005). We used a scoping review rather than systematic review and meta-analysis because our aim was not to ask a precise question and were more interested in the characteristics of investigations conducted (Munn et al., 2018). Moreover, the topic has not yet been extensively reviewed and may have been complex or heterogeneous in nature. If existing research was heterogeneous, a systematic review and meta-analysis would not have been possible, and therefore we opted to scope the area in this manuscript (Mays et al., 2001).

Objectives

We aimed to provide an overview of existing literature relating to phenotypic characteristics of sarcopenia pre- and post-HIIT in older adults. The four specific objectives of this scoping review were to (1) conduct a systematic search of the published literature for the effect of HIIT on muscle strength, muscle quantity or quality, and physical performance [aligned to the 2018 operational definition of sarcopenia (Cruz-Jentoft et al., 2019)] in older adults, (2) map characteristics and methodologies used and classified as “HIIT” within the interventions, (3) outline the range and characteristics of outcome variables used, and (4) provide recommendations for the advancement of the investigative area.

Methods

Protocol and Registration

The review was conducted and reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for scoping reviews (PRISMA-ScR) guidelines (Tricco et al., 2018) and the five-stage framework outlined in Arksey and O'Malley (Arksey and O'Malley, 2005). A review protocol was not published.

Eligibility Criteria

Studies that met the following criteria were included: (1) involvement of human participants with a mean age of ≥ 60 years [considered the start of old age (United Nations, 2020)]; (2) not a review; (3) an intervention which included bouts of high intensity exercise interspersed with periods of recovery, including exercise defined as HIIT or sprint interval training (SIT). We defined high intensity as exercise >85% peak oxygen uptake (VO2peak) or 85% maximal heart rate (HRmax) or equivalent perception-based approaches (e.g., Borg 6–20 scale or similar); (4) employing an intervention design and include an exercise training period of >2 weeks; (5) including HIIT in isolation or performed in combination with another form of exercise; (6) including outcome measures related to either (i) muscle function (either strength or power), (ii) muscle quantity, or (iii) physical performance.

Search Strategy

The search strategy consisted of a combination of free-text and MeSH terms relating to “high-intensity interval training,” “sarcopenia,” and “older adults” which were developed through examination of previously published original and review articles (e.g., screening of titles, abstracts, keywords). Filters were applied to ensure that only records published in English language involving human participants were included in the search results. Full search terms and the complete search strategy can be found in the online Supplementary Material associated with this article (Supplementary Material 1).

Information Sources

Five electronic databases (Medline, EMBASE, Web of Science, Scopus, and the Cochrane Central Register of Controlled Trials [CENTRAL]) were searched to identify original research articles published from the earliest available up until 12th March 2020. Reference lists from included studies and previously published review articles were examined for potentially eligible papers.

Study Selection

Data were extracted by two reviewers (LH & CH) independently and compared in an unblinded and standardized manner. Once each database search was completed and manuscripts were sourced, all studies were downloaded into a single reference list with duplicates removed. Titles and abstracts were then screened for eligibility and full texts were only retrieved for studies with HIIT incorporated. Two reviewers then read and coded all the included articles using the PEDro scale (de Morton, 2009). Full texts were then thoroughly assessed using the complete eligibility criteria with first (LH) and last (CH) authors confirming inclusion and exclusion. Following this quality assessment, the same reviewers read and coded each of the studies and assessed the following moderators: design method (randomized control trial; RCT, controlled trial; CT or uncontrolled trial; UCT), combined or HIIT in isolation, and outcome variable. Furthermore, participant descriptions and training programme variables were extracted with as much detail provided by the authors. Any disagreement between reviewers was discussed in a consensus meeting, and unresolved items were addressed by a third reviewer.

Data Items

Data extracted from each study included sample size, group descriptions, study design, analysis method, and outcome data. Methodological quality was assessed using the modified 0–10 PEDro scale (de Morton, 2009). The primary outcome variables were defined as muscle strength or power, muscle quantity or quality, and physical performance, pre- and post-intervention. There was heterogeneity in study inclusion criteria, interventions, assessment tools, and outcomes, thus a pooled analysis was not appropriate.

Results

Study Selection

Following the initial database search, 1,267 records were identified (Figure 1). Once duplicates were removed, 1,063 titles and abstracts remained, and were screened for inclusion, resulting in 74 full-text articles being screened. Of these, 42 were excluded and 32 remained.

FIGURE 1
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Figure 1. Schematic flow diagram describing exclusions of potential studies and final number of studies.

Study Characteristics

Of the 32 studies included, 14 were RCTs (Adamson et al., 2014, 2020; Hwang et al., 2016; Coetsee and Terblanche, 2017; Sculthorpe et al., 2017; Aboarrage Junior et al., 2018; Malin et al., 2018; Martins et al., 2018; Ballesta-García et al., 2019; Hurst et al., 2019c; Jiménez-García et al., 2019; Nunes et al., 2019; Taylor et al., 2019; Coswig et al., 2020), one was a quasi-experimental, non-randomized, single-blinded controlled study (Losa-Reyna et al., 2019), 16 were observational cohort studies (Bruseghini et al., 2015, 2019; Boereboom et al., 2016; Guadalupe-Grau et al., 2017; Hayes et al., 2017; Herbert et al., 2017a,b; Robinson et al., 2017; Wyckelsma et al., 2017; Andonian et al., 2018; Bartlett et al., 2018; Buckinx et al., 2018, 2019; Søgaard et al., 2018, 2019; Snijders et al., 2019), and one was a pilot study (although randomized; (Beetham et al., 2019) (Table 1). Where a study had multiple outcome measures, they were examined separately. Three out of 32 (9%) included HIIT in a multicomponent intervention (Guadalupe-Grau et al., 2017; Losa-Reyna et al., 2019; Snijders et al., 2019). Sixteen studies included HIIT on a cycle ergometer, six included HIIT on a treadmill, seven included resistance exercise HIIT (including bodyweight exercises), two included HIIT on an elliptical trainer, and one study did not detail the intervention. Three studies used an “all-out” intensity, 15 used a percentage of HRmax or heart rate reserve (HRR) to prescribe intensity, four used a percentage of VO2peak to prescribe intensity, three used a percentage of intensity at termination of a ramped incremental exercise protocol to prescribe intensity, four used percentage of peak power output to prescribe intensity, one used the Borg scale to prescribe intensity, one study used a percentage of maximum gait speed to prescribe intensity, and one study did not detail the intervention. Twenty-seven studies had a mean age in the 60s, two in the 70s, and three in the 80s. One study considered frail participants. There were 20 studies which examined the effect of HIIT on muscle function, 22 studies which examined the effect of HIIT on muscle quantity, and 12 studies which examined the effect of HIIT on physical function (Figure 2). Several studies investigated more than one parameter, thus why the sum of the studies above is greater than the number of included studies.

TABLE 1
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Table 1. General study information of investigations concerning HIIT and phenotypic characteristics of sarcopenia.

FIGURE 2
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Figure 2. Schematic representation of frequency of outcome examined (n = 54) within the 32 included studies concerning HIIT and phenotypic characteristics of sarcopenia.

HIIT and Muscle Function

There were 20 studies which examined the effect of HIIT on muscle function using one or more of the criteria outline by EWGSOP (Cruz-Jentoft et al., 2019) (Table 2). Of these, 18 measured muscle strength, and five measured muscle power (some studies measured both, thus why this total is not 20). Of those reporting strength, six used the handgrip test, one used a 30 s arm curl test, five used a 30 s chair stand test, four used the 5 repetitions chair stand test, one used a 10 repetition chair stand test, two used knee extensor isokinetic dynamometry, one used a strain gauge for the knee extensors, four used a leg press, two used a chest press, three used a knee extension machine (which was not a dynamometer), and one used latissimus dorsi pull-down, horizontal row, and shoulder press. Of the 20 studies examining strength outcomes, 15 reported ≥1 strength parameter having been improved by HIIT compared to pre-training or compared to a moderate intensity continuous training (MICT) or non-exercise control. Of the remaining three (Robinson et al., 2017; Martins et al., 2018; Nunes et al., 2019), they all reported strength had improved more in a combined aerobic and resistance training group than a HIIT group.

TABLE 2
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Table 2. Summary of study details concerning HIIT and muscle function.

There were five studies which examined the effect of HIIT on muscle power, with two studies examining peak power output during cycle ergometry, and the remaining three determined power during a resistance training exercise (leg extension or leg-press). One investigation examined power during a 5 repetition chair stand test (Losa-Reyna et al., 2019). Of these studies, all reported improved power output post-HIIT. There was no evident association between change in muscle function (either 5 rep chair stand, 30 s chair stand, or grip strength) and number of bouts completed (Supplementary Figures 1a–c).

HIIT and Muscle Quantity or Quality

There were 22 studies which examined the effect of HIIT on muscle quantity or a surrogate (fat free mass, lean mass, thigh volume; Table 3). Of these, 13 measured whole body lean mass by dual-energy X-ray absorptiometry (DEXA), nine measured leg lean mass by DEXA (of these, all nine also reported whole body lean mass), one measured whole body lean mass by air plethysmography, one measured M. vastus lateralis muscle thickness by ultrasonography, two measured quadriceps muscle volume by magnetic resonance imaging (MRI), two measured quadriceps cross-sectional area (CSA) or anatomical CSA (ACSA) by MRI, one measured whole body lean mass by MRI, one measured thigh muscle area by peripheral quantitative computed tomography (pQCT), and six measured whole body lean mass by bioelectrical impedance analysis (BIA). Of the 22 studies examining muscle quantity or quality outcomes, 11 reported ≥1 muscle quantity parameter was improved by HIIT, 14 reported no difference in ≥1 measure from pre-intervention or vs. a no exercise control, two reported inferior adaptation following HIIT compared to a group undertaking resistance training in ≥1 measure, one study reported lean mass was lost post-HIIT to a similar extent as a non-exercise control, and one did not report post-intervention lean mass (some studies measured several outcomes, thus why this total is not 22). There was no evident relationship between change in muscle quantity (as measured by lean mass) and number of bouts completed (Supplementary Figure 1d).

TABLE 3
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Table 3. Summary of study details concerning HIIT and muscle quantity or quality.

HIIT and Physical Performance

There were 12 studies which examined the effect of HIIT on physical function (Table 4). One used the short physical performance battery (SPPB), eight used gait speed or the 6 min walk test (6MWT), nine used the timed up and go (TUG) test, and one used the 400 m walk test (some studies utilized more than one outcome). Of the 12 studies examining physical performance, all reported ≥1 parameter was improved by HIIT. The only study examining SPPB reported HIIT improved SPPB performance.

TABLE 4
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Table 4. Summary of study details concerning HIIT and physical performance.

There was no evident relationship between change in muscle performance (as measured by TUG and 6MWT) and number of bouts completed (Supplementary Figures 1e,f).

Discussion

This scoping review provided an overview of existing literature pertaining to HIIT and phenotypic characteristics of sarcopenia. We examined outcomes according to the revised EWGSOP definition (Cruz-Jentoft et al., 2019) to facilitate translation of research findings into clinical practice. Firstly, the earliest article cited was Adamson et al. (2014) published in 2014, which speaks to this rapidly emerging area of research. This review catalogs existing literature, with a view to facilitating discussion of research opportunities and issues that need to be addressed in future studies.

In relation to our first objective, which was to search the literature for the effect of HIIT on phenotypic characteristics of sarcopenia in older adults, we observed most studies reported at least one positive change in characteristics when compared to vs. pre-HIIT, vs. non-exercise control, or vs. MICT. In this context, 19 of 20 studies reported an improvement to ≥1 muscle function outcome for ≥1 comparisons examined (vs. pre-HIIT, vs. non-exercise control, or vs. MICT) (Bruseghini et al., 2019). Similarly, twelve of 22 reported an improvement to ≥1 muscle quantity outcome for ≥1 comparison examined, and 11 of 12 reported an improvement to for ≥1 physical performance outcome for ≥1 comparison examined.

In relation to our second objective, training programmes ranged in duration from 2 to 24 weeks (median = 9.5 weeks), incorporated resistance training based HIIT, running/walking HIIT, cycling HIIT, and HIIT combined with other exercise modes (i.e., resistance training). Populations studied were commonly in the 7th decade of life, and mostly living independently. In relation to our third objective, muscle quantity, or quality was most frequently studied in the included literature. DEXA was the most utilized measurement method, which is in line with the EWGSOP algorithm for sarcopenia case findings in clinical practice (Cruz-Jentoft et al., 2019). However, these are only routinely found in research facilities and hospitals and would likely require a referral from primary care before an individual received a DEXA scan. Importantly, none of the included studies involved participants who had been diagnosed with sarcopenia using a formalized definition. This limits the clinical significance of the included literature and clearly highlights a need for further work in this population.

HIIT and Muscle Function

According to the revised EWGSOP definition of sarcopenia (Cruz-Jentoft et al., 2019), muscle function is primarily considered as muscle strength. Yet, the chair stand test (or its variations) is named as a parameter that measures muscle strength. However, as the chair stand test relies on the ability to generate force over a short period of time, this could be considered a test of muscle power, rather than a measure of maximal force. The term dynapenia [i.e., the age-associated reduction in muscle strength and power (Clark and Manini, 2012; Manini and Clark, 2012)] was originally used to differentiate itself from sarcopenia (Clark and Manini, 2008), which has its roots in age-related reduced muscle mass [Greek translation = “poverty of flesh” (Kim and Choi, 2013)]. However, more recent definitions and diagnoses of sarcopenia have broadened to include muscle function. In this context, when one measures muscle strength using non-isometric movements (i.e., when work occurs), force, distance, and time can be extracted, which is quantification of power. Thus, we believed it pertinent to include studies which concerned muscle power within this review. In fact, muscle power associates more strongly with physical performance and independence than muscle quantity (Clark and Manini, 2010; Trombetti et al., 2016), which may explain why the chair stand test is at the forefront of the revised EWGSOP algorithm for diagnosing and quantifying sarcopenia (Cruz-Jentoft et al., 2019). Moreover, as this is a scoping review, our a priori aim was to outline the range and characteristics of outcome variables examined.

In this review, only six studies used grip strength as an outcome measure (Guadalupe-Grau et al., 2017; Buckinx et al., 2019; Hurst et al., 2019c; Jiménez-García et al., 2019). This is interesting to note as EWGSOP propose grip strength as the primary measurement of muscle strength in clinical practice and research studies (Cruz-Jentoft et al., 2019). However, of these six investigations, two were published before the revised EWGSOP guidelines, and four were published the same year, so data collection may have been pre-update. Wiśniowska-Szurlej et al. (2019) examined handgrip strength and other mobility parameters including gait speed, balance, and chair stand and observed weak correlations between handgrip strength and mobility in older adults under long-term care facilities. Yee et al. (2021) corroborated this finding reporting weak correlations between chair stand test and handgrip strength in community-dwelling older adults. Similarly, changes in handgrip strength do correlate with changes in leg muscle strength of physical performance during an exercise intervention program in frail older people (Tieland et al., 2015), suggesting it is not a good surrogate of mobility, muscle function, or change in muscle function of muscle other than those involved in gripping. If the two proposed measures of muscle strength to diagnose sarcopenia are not in agreement, then an alternative method for measuring muscle strength is necessary in this population. This may explain why most studies in this review have not measured handgrip and instead opted for isokinetic dynamometry, considered the gold standard for assessing muscle strength but not commonly used in a clinical setting. When considering the body of studies examining muscle function, the majority report increased strength (70% of studies) or power (100% of studies) following HIIT.

Considering reduced muscle function is at the forefront of the recent update on the definition and treatment of sarcopenia (Cruz-Jentoft et al., 2019), any intervention targeting the prevention or reversal of phenotypic characteristics of sarcopenia must be capable of enhancing muscle strength. To our knowledge, Losa-Reyna et al. (2019) is the only investigation to examine an exercise intervention containing HIIT in frail older adults. These authors examined the influence of a 6-week multicomponent exercise intervention (including walking-based HIIT) focused on enhancing muscle power in ~84-year olds (range 77–96 years; 75% females; 35% pre-frail and 65% frail). Post-intervention, leg press strength had improved by 34%, and muscle power improved by 47%. Moreover, load at peak power on the force-velocity curve increased by 23%, which suggests this type of intervention may improve muscle strength and power in frail and pre-frail elderly.

HIIT and Muscle Quantity or Quality

In this review, 20/21 (95%) of studies report appendicular skeletal muscle mass measured by DEXA, BIA, or MRI, or cross-sectional area of the thigh by MRI or pQCT scan, which are the primary measurement of muscle quantity proposed by EWGSOP in clinical practice and research (Cruz-Jentoft et al., 2019). The remaining investigation used air plethysmography to determine whole body lean mass (Andonian et al., 2018). When considering the body of studies examining total body lean mass, several reported no increase from pre-HIIT (Bruseghini et al., 2015; Boereboom et al., 2016; Hwang et al., 2016; Andonian et al., 2018; Malin et al., 2018; Søgaard et al., 2018; Beetham et al., 2019; Buckinx et al., 2019; Jiménez-García et al., 2019; Nunes et al., 2019; Snijders et al., 2019; Coswig et al., 2020), whereas some reported an increase post-HIIT compared to pre-HIIT (Hayes et al., 2017; Herbert et al., 2017a; Sculthorpe et al., 2017). To add further uncertainty, two studies which observed no increase in whole body lean quantity observed increased thigh lean mass (Boereboom et al., 2016; Bruseghini et al., 2019). Taken together, it is unclear whether HIIT can significantly increase muscle quantity or quality, and the result may be determined by measurement technique of muscle quantity.

There are no data concerning the effect of HIIT on skeletal muscle quantity or its surrogates (e.g., fat free mass [FFM], lean body mass) in adults diagnosed with sarcopenia, or oldest old humans, despite emerging evidence in the rodent model (Seldeen et al., 2018). Thus, data from the middle old and young old must be extrapolated until these studies exist. In this context, and despite no changes in muscle strength, Robinson et al. (Robinson et al., 2017) observed a ~1 kg increase in FFM in sedentary ~71 year olds following 3 days/week cycling HIIT and 2 days/week of treadmill walking. This increase was greater in a resistance training only group, however. Interestingly, FFM was also increased to the same extend in a young (~25 years old) sedentary cohort, suggesting HIIT can increase FFM in the young and old to equal magnitude. This can be interpreted in two ways: 1) sedentary older adults maintain muscle plasticity and sensitivity to HIIT into older age, and 2) HIIT can increase FFM quantity in young sedentary adults who have not experienced muscle wastage. However, as all participants were untrained, increased FFM could be attributed to both young and old participants being HIIT-naïve.

It would have been a reasonable a priori hypothesis to predict HIIT performed at the greatest relative intensity (i.e., all-out or SIT) would result in the greatest increases in muscle quantity, as intensities closer to maximal voluntary contraction are known to induce muscle hypertrophy (Schoenfeld, 2010; Krzysztofik et al., 2019). However, this was not observed as Aboarrage Junior et al. (2018) utilized an all-out protocol, with no reported increases in lean mass. Likewise, it may have been expected untrained participants would exhibit the greatest increase in muscle quantity. However, Herbert et al. (2017a) examined the body composition changes in a group of previously sedentary older males and masters athletes, and reported FFM increased ~3% (from ~67 to ~69 kg) and ~4% (from ~65 to ~68 kg), respectively. This suggests HIIT may be efficacious at increasing FFM in highly active older males and previously sedentary older male, if they are HIIT-naïve. Yet, these data are not ubiquitous through the included literature of this review. Adequate intake of dietary protein is also an important consideration for older adults and any potential exercise induced increases in muscle mass are likely to be influenced by this (Beaudart et al., 2019).

HIIT and Physical Performance

In this review, all of the studies assessing physical performance reported gait speed (part of the SPPB), the SPPB, or the TUG test as an outcome, which are the primary measurements of physical performance proposed by EWGSOP in clinical practice and research (Cruz-Jentoft et al., 2019). Four investigations also reported the 5 repetitions chair stand test separately (Adamson et al., 2014, 2020; Losa-Reyna et al., 2019; Nunes et al., 2019). However, this is one element of the SPPB, so those reporting SPPB values will have conducted this test. When considering the body of literature examining physical performance, all studies reported improvements post-HIIT. When considering studies examining physical performance, all studies report increased physical performance of ≥1 parameter following HIIT. In some instances HIIT did not improve performance more than another training method, where investigations had a parallel arm (Martins et al., 2018; Ballesta-García et al., 2019; Nunes et al., 2019). Physical performance represents a multidimensional construct involving a range of physiological systems across the whole-body (Beaudart et al., 2019) and is a key component in the definition of severe sarcopenia (Cruz-Jentoft et al., 2019).

Losa-Reyna et al. (2019) observed that a 6-week multicomponent exercise intervention (including walking-based HIIT) focused on enhancing muscle power improved the frailty phenotype by 1.6 points, muscle strength by 34%, and muscle power by 47%, suggesting this type of intervention is feasible in frail and pre-frail elderly. As this intervention was multicomponent, it is not possible to quantify the contribution of HIIT to the overall improvement, and therefore it is difficult to ascertain whether adaptations would have occurred were HIIT examined in isolation, rather than simultaneously with a resistance training programme.

Strengths and Limitations

In cataloging the research concerning HIIT and phenotypic characteristics of sarcopenia, several issues and considerations came to light, all of which have important implications for the interpretation of this body of literature, and improvement of future investigations. Firstly, the use of exercise terminology requires clarity. In this context, we mean the definition of “HIIT.” HIIT has previously been described as periods of work >85% VO2peak or 85% HRmax or equivalent perception-based approaches, interspersed by recovery periods (Gibala et al., 2012). Only articles matching this description were included in this article. Several articles were returned from our database searching which termed the exercise intervention HIIT, but often these did not reach this threshold of intensity. Similarly, when exercise is described as “all-out,” this should be termed SIT, which although a subcategory of HIIT, is unique in its prescription (Weston et al., 2014). It is imperative to classify protocols based on the nature of exercise prescription as different interval exercise classifications will alter experience and potentially subsequent adaptation to the exercise (Biddle and Batterham, 2015). Penultimately, the majority of studies considered small samples sized, which limits interpretation. Finally, the major limitation of the present scoping review is the lack of studies in older adults diagnosed with sarcopenia. Whilst the literature assessment was comprehensive, it is possible that studies may have been missed from the analysis, but as three databases were searched, it is unlikely enough were missed to create a large void in the included literature.

One questions that cannot be answered in the current scoping review is the effect of age on adaptations in physical performance, muscle function, or muscle quantity with HIIT. Whilst we attempted to examine results by decade (60–69, 70–79, and ≥80 years of age), it was noted that most published results were performed in “younger old” participants between 60 and 70 years of age. Further meta-analytical subgroup analysis or meta-regression may thus be required to examine differing responses by age group. In a similar manner, another limitation noted is the inability to examine potential sex differences in responses to HIIT for any outcome. Whilst most studies utilized both male and female participants, groups were typically mixed and thus no insight into sex difference of HIIT responses is attempted here. With a need to better describe and report female physiology in exercise physiology literature (Elliott-Sale et al., 2021), more work in this area may this be called for.

It is also important to acknowledge that the studies included in this review were delivered across a range of settings and involved a diverse range of older adults of varying health and fitness status. While this makes generalizing findings difficult, it does suggest that HIIT may be feasible across a broad range of settings with a wide range of older people. However, it is important to make clear that HIIT may not be suitable for all older people and all exercise programmes should be individually prescribed based on the characteristics of the individual.

Recommendations for Advancement of the Investigative Area

In relation to our fourth objective (provide recommendations for the advancement of the investigative area), this review revealed a dearth of studies considering participants diagnosed with sarcopenia. Therefore, our primary recommendation for advancement of the research area is to increase studies that recruit participants or patients with sarcopenia, or those who are at risk from sarcopenia (i.e., the oldest old). These studies could be feasibility trials, as there is little information as to whether HIIT is a feasible exercise approach in older people. Secondly, given the issue regarding terminology and exercise intensity discussed above, authors are encouraged to be consistent in the use of exercise terminology by adhering to the consensus on exercise reporting template [CERT; (Slade et al., 2016)] in future investigations, which would permit assessment of intervention heterogeneity. Thirdly, studies included within this review had a sample size ranging from 8 to 82 participants, possibly due to resource commitments associated with having large sample sizes and/or rigorous research design. We suggest multicentre RCTs to improve (a) statistical power, and (b) the quality of available evidence, as only 17/32 studies achieved ≥5 on the PEDro scale. Finally, although this review focused directly on phenotypic characteristics of sarcopenia (i.e., quantitative assessment), qualitative investigations on the perceptions of adults with phenotypic characteristics of sarcopenia on this type of exercise and how it could be delivered to this population with minimizing any barriers will be beneficial for the field of gerontology.

Conclusions and Practical Recommendations

In conclusion, most studies presented herein utilized outcome measures defined by the revised EWGSOP guidelines. There was divergence observed in exercise interventions, with HIIT interventions involving a range of exercise modes delivered in a range of settings. Currently, there is some evidence suggesting HIIT may improve phenotypic characteristics of sarcopenia. However, there are few studies investigating any form of HIIT in the very old, or those diagnosed with sarcopenia. Therefore, more intervention studies are needed in this population to confirm this phenomenon and confidently quantify the effectiveness of HIIT. In addition, we need to understand if this is a safe and feasible training approach in this population. In a practical context, combined interventions involving HIIT and resistance training are a worthy avenue for investigation as resistance training is the most potent stimulus to increase muscle quantity and studies herein showed divergent results concerning HIIT and muscle quantity. Finally, HIIT or SIT that is easy to apply (i.e., without equipment needs, travel, specialist training, and intensity monitoring such as heart rate or power output) or can be supported virtually is likely needed to promote the transition of HIIT from the laboratory to the real world.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.

Author Contributions

LH and CH: conceptualization, methodology, investigation, and project administration. LH and NS-H: formal analysis and investigation. LH, BE, ZY, TB, NS, NS-H, and CH: writing—original draft preparation. LH, BE, TB, NS, NS-H, and CH: writing—review and editing. LH and BE: visualization. LH and CH: funding acquisition. All authors contributed to the article and approved the submitted version.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Acknowledgments

The authors wish to acknowledge the support of respective employers in preparation of this review.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphys.2021.715044/full#supplementary-material

Supplementary Figure 1. Percent change (Δ%) in outcome measures for muscle function (a) 5 s chair stand, (b) 30 s chair stand, (c) grip strength, muss quality (d) lean mass, or muscle performance (e) timed up and go (TUG), and (f) 6 min walk test (6MWT), all as a function of the number of bouts completed. Dashed lines indicate 95% confidence intervals.

References

Aboarrage Junior, A. M., Teixeira, C. V. L. S., Dos Santos, R. N., Machado, A. F., Evangelista, A. L., Rica, R. L., et al. (2018). A high-intensity jump-based aquatic exercise program improves bone mineral density and functional fitness in postmenopausal women. Rejuvenation Res. 21, 535–540. doi: 10.1089/rej.2018.2069

PubMed Abstract | CrossRef Full Text | Google Scholar

Adamson, S., Kavaliauskas, M., Lorimer, R., and Babraj, J. (2020). The impact of sprint interval training frequency on blood glucose control and physical function of older adults. IJERPH. 17:454. doi: 10.3390/ijerph17020454

PubMed Abstract | CrossRef Full Text | Google Scholar

Adamson, S. B., Lorimer, R., Cobley, J. N., and Babraj, J. A. (2014). Extremely short-duration high-intensity training substantially improves the physical function and self-reported health status of elderly adults. J. Am. Geriatr. Soc. 62, 1380–1381. doi: 10.1111/jgs.12916

PubMed Abstract | CrossRef Full Text | Google Scholar

Andonian, B. J., Bartlett, D. B., Huebner, J. L., Willis, L., Hoselton, A., Kraus, V. B., et al. (2018). Effect of high-intensity interval training on muscle remodeling in rheumatoid arthritis compared to prediabetes. Arthritis Res Ther. 20:283. doi: 10.1186/s13075-018-1786-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Angadi, S. S., Mookadam, F., Lee, C. D., Tucker, W. J., Haykowsky, M. J., and Gaesser, G. A. (2015). High-intensity interval training vs. moderate-intensity continuous exercise training in heart failure with preserved ejection fraction: a pilot study. J. Appl. Physiol. 119, 753–758. doi: 10.1152/japplphysiol.00518.2014

PubMed Abstract | CrossRef Full Text | Google Scholar

Arksey, H., and O'Malley, L. (2005). Scoping studies: towards a methodological framework. Int J Soc Res Methodol.8:19–32. doi: 10.1080/1364557032000119616

CrossRef Full Text | Google Scholar

Ballesta-García, I., Martínez-González-Moro, I., Rubio-Arias, J. Á., and Carrasco-Poyatos, M. (2019). High-intensity interval circuit training versus moderate-intensity continuous training on functional ability and body mass index in middle-aged and older women: a randomized controlled trial. IJERPH 16:4205. doi: 10.3390/ijerph16214205

PubMed Abstract | CrossRef Full Text | Google Scholar

Bartlett, D. B., Willis, L. H., Slentz, C. A., Hoselton, A., Kelly, L., Huebner, J. L., et al. (2018). Ten weeks of high-intensity interval walk training is associated with reduced disease activity and improved innate immune function in older adults with rheumatoid arthritis: a pilot study. Arthritis Res. Ther. 20:127. doi: 10.1186/s13075-018-1624-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Batacan, R. B., Duncan, M. J., Dalbo, V. J., Tucker, P. S., and Fenning, A. S. (2017). Effects of high-intensity interval training on cardiometabolic health: a systematic review and meta-analysis of intervention studies. Br. J. Sports Med. 51, 494–503. doi: 10.1136/bjsports-2015-095841

PubMed Abstract | CrossRef Full Text | Google Scholar

Beaudart, C., Rolland, Y., Cruz-Jentoft, A. J., Bauer, J. M., Sieber, C., Cooper, C., et al. (2019). Assessment of muscle function and physical performance in daily clinical practice: a position paper endorsed by the european society for clinical and economic aspects of osteoporosis, osteoarthritis and Musculoskeletal Diseases (ESCEO). Calcif Tissue Int. 105, 1–14. doi: 10.1007/s00223-019-00545-w

PubMed Abstract | CrossRef Full Text | Google Scholar

Beetham, K. S., Howden, E. J., Fassett, R. G., Petersen, A., Trewin, A. J., Isbel, N. M., et al. (2019). High-intensity interval training in chronic kidney disease: a randomized pilot study. Scand. J. Med. Sci. Sports. 26, 1197–1204. doi: 10.1111/sms.13436

PubMed Abstract | CrossRef Full Text | Google Scholar

Beyer, I., Mets, T., and Bautmans, I. (2012). Chronic low-grade inflammation and age-related sarcopenia. Curr Opin Clin Nutrition Metabolic Care 15, 12–22. doi: 10.1097/MCO.0b013e32834dd297

PubMed Abstract | CrossRef Full Text | Google Scholar

Biddle, S. J. H., and Batterham, A. M. (2015). High-intensity interval exercise training for public health: a big HIT or shall we HIT it on the head? Int. J. Behav. Nutr. Phys. Act. 12:95. doi: 10.1186/s12966-015-0254-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Blackwell, J., Atherton, P. J., Smith, K., Doleman, B., Williams, J. P., Lund, J. N., et al. (2017). The efficacy of unsupervised home-based exercise regimens in comparison to supervised laboratory-based exercise training upon cardio-respiratory health facets. Physiol. Rep. 5:e13390. doi: 10.14814/phy2.13390

PubMed Abstract | CrossRef Full Text | Google Scholar

Boereboom, C. L., Phillips, B. E., Williams, J. P., and Lund, J. N. (2016). A 31-day time to surgery compliant exercise training programme improves aerobic health in the elderly. Tech. Coloproctol. 20, 375–382. doi: 10.1007/s10151-016-1455-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Bruseghini, P., Calabria, E., Tam, E., Milanese, C., Oliboni, E., Pezzato, A., et al. (2015). Effects of eight weeks of aerobic interval training and of isoinertial resistance training on risk factors of cardiometabolic diseases and exercise capacity in healthy elderly subjects. Oncotarget. 6, 16998–17015. doi: 10.18632/oncotarget.4031

PubMed Abstract | CrossRef Full Text | Google Scholar

Bruseghini, P., Capelli, C., Calabria, E., Rossi, A. P., and Tam, E. (2019). Effects of high-intensity interval training and isoinertial training on leg extensors muscle function, structure, and intermuscular adipose tissue in older adults. Front Physiol. 10:1260. doi: 10.3389/fphys.2019.01260

PubMed Abstract | CrossRef Full Text | Google Scholar

Buckinx, F., Gouspillou, G., Carvalho, L., Marcangeli, V., El Hajj Boutros, G., Dulac, M., et al. (2018). Effect of high-intensity interval training combined with L-citrulline supplementation on functional capacities and muscle function in dynapenic-obese older adults. JCM. 7:561. doi: 10.3390/jcm7120561

PubMed Abstract | CrossRef Full Text | Google Scholar

Buckinx, F., Marcangeli, V., Pinheiro Carvalho, L., Dulac, M., Hajj Boutros, G., Gouspillou, G., et al. (2019). Initial dietary protein intake influence muscle function adaptations in older men and women following high-intensity interval training combined with citrulline. Nutrients 11:1685. doi: 10.3390/nu11071685

PubMed Abstract | CrossRef Full Text | Google Scholar

Callahan, M. J., Parr, E. B., Hawley, J. A., and Camera, D. M. (2021). Can high-intensity interval training promote skeletal muscle anabolism? Sports Med. 51, 405–421. doi: 10.1007/s40279-020-01397-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Clark, B. C., and Manini, T. M. (2008). Sarcopenia =/= dynapenia. J. Gerontol Biol. Sci. Med. Sci. 63, 829–834. doi: 10.1093/gerona/63.8.829

PubMed Abstract | CrossRef Full Text | Google Scholar

Clark, B. C., and Manini, T. M. (2010). Functional consequences of sarcopenia and dynapenia in the elderly. Curr. Opin. Clin. Nutr. Metab. Care 13, 271–276. doi: 10.1097/MCO.0b013e328337819e

PubMed Abstract | CrossRef Full Text | Google Scholar

Clark, B. C., and Manini, T. M. (2012). What is dynapenia? Nutrition 28, 495–503. doi: 10.1016/j.nut.2011.12.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Coetsee, C., and Terblanche, E. (2017). The effect of three different exercise training modalities on cognitive and physical function in a healthy older population. Eur. Rev. Aging Phys. Act. 14:13. doi: 10.1186/s11556-017-0183-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Collado-Mateo, D., Lavín-Pérez, A. M., Peñacoba, C., Del Coso, J., Leyton-Román, M., Luque-Casado, A., et al. (2021). Key factors associated with adherence to physical exercise in patients with chronic diseases and older adults: an umbrella review. Int. J. Environ. Res. Public Health 18:2023. doi: 10.3390/ijerph18042023

PubMed Abstract | CrossRef Full Text | Google Scholar

Coswig, V. S., Barbalho, M., Raiol, R., Del Vecchio, F. B., Ramirez-Campillo, R., and Gentil, P. (2020). Effects of high vs moderate-intensity intermittent training on functionality, resting heart rate and blood pressure of elderly women. J. Transl. Med. 18:88. doi: 10.1186/s12967-020-02261-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Cruz-Jentoft, A. J., Bahat, G., Bauer, J., Boirie, Y., Bruyère, O., Cederholm, T., et al. (2019). Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing 48, 16–31. doi: 10.1093/ageing/afy169

PubMed Abstract | CrossRef Full Text | Google Scholar

Cruz-Jentoft, A. J., and Sayer, A. A. (2019). Sarcopenia. Lancet 393, 2636–2646. doi: 10.1016/S0140-6736(19)31138-9

PubMed Abstract | CrossRef Full Text | Google Scholar

de Morton, N. A. (2009). The PEDro scale is a valid measure of the methodological quality of clinical trials: a demographic study. Aust. J. Physiother. 55, 129–133. doi: 10.1016/S0004-9514(09)70043-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Dent, E., Morley, J. E., Cruz-Jentoft, A. J., Arai, H., Kritchevsky, S. B., Guralnik, J., et al. (2018). International clinical practice guidelines for Sarcopenia (ICFSR): screening, diagnosis and management. J. Nutr. Health Aging. 22, 1148–1161. doi: 10.1007/s12603-018-1139-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Dismore, L., Hurst, C., Sayer, A. A., Stevenson, E., Aspray, T., and Granic, A. (2020). Study of the older adults' motivators and barriers engaging in a nutrition and resistance exercise intervention for sarcopenia: an embedded qualitative project in the MIlkMAN Pilot study. Gerontol. Geriatr. Med. 6:2333721420920398. doi: 10.1177/2333721420920398

PubMed Abstract | CrossRef Full Text | Google Scholar

Dunford, E. C., Valentino, S. E., Dubberley, J., Oikawa, S. Y., McGlory, C., Lonn, E., et al. (2021). Brief vigorous stair climbing effectively improves cardiorespiratory fitness in patients with coronary artery disease: a randomized trial. Front Sports Act Living. 3:630912. doi: 10.3389/fspor.2021.630912

PubMed Abstract | CrossRef Full Text | Google Scholar

Elliott-Sale, K. J., Minahan, C. L., de Jonge, X. A. K. J., Ackerman, K. E., Sipil,ä, S, Constantini, N. W., et al. (2021). Methodological considerations for studies in sport and exercise science with women as participants: a working guide for standards of practice for research on women. Sports Med. 51, 843–861. doi: 10.1007/s40279-021-01435-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Füzéki, E., and Banzer, W. (2018). Physical activity recommendations for health and beyond in currently inactive populations. Int J Environ Res Public Health. 15:1042. doi: 10.3390/ijerph15051042

PubMed Abstract | CrossRef Full Text | Google Scholar

Gibala, M. J., Little, J. P., MacDonald, M. J., and Hawley, J. A. (2012). Physiological adaptations to low-volume, high-intensity interval training in health and disease. J. Physiol. 590, 1077–1084. doi: 10.1113/jphysiol.2011.224725

PubMed Abstract | CrossRef Full Text | Google Scholar

Guadalupe-Grau, A., Aznar-Laín, S., Mañas, A., Castellanos, J., Alcázar, J., Ara, I., et al. (2017). Short- and long-term effects of concurrent strength and HIIT training in octogenarians with COPD. J. Aging Phys. Activity. 25, 105–115. doi: 10.1123/japa.2015-0307

PubMed Abstract | CrossRef Full Text | Google Scholar

Hannan, A. L., Hing, W., Simas, V., Climstein, M., Coombes, J. S., Jayasinghe, R., et al. (2018). High-intensity interval training versus moderate-intensity continuous training within cardiac rehabilitation: a systematic review and meta-analysis. Open Access J. Sports Med. 9, 1–17. doi: 10.2147/OAJSM.S150596

PubMed Abstract | CrossRef Full Text | Google Scholar

Hawley, J. A., Hargreaves, M., Joyner, M. J., and Zierath, J. R. (2014). Integrative biology of exercise. Cell 159, 738–749. doi: 10.1016/j.cell.2014.10.029

PubMed Abstract | CrossRef Full Text | Google Scholar

Hayes, L. D., Herbert, P., Sculthorpe, N., and Grace, F. (2020). High intensity interval training (HIIT) produces small improvements in fasting glucose, insulin, and insulin resistance in sedentary older men but not masters athletes. Exp. Gerontol. 140:111074. doi: 10.1016/j.exger.2020.111074

PubMed Abstract | CrossRef Full Text | Google Scholar

Hayes, L. D., Herbert, P., Sculthorpe, N. F., and Grace, F. M. (2017). Exercise training improves free testosterone in lifelong sedentary aging men. Endocr Connect. 6, 306–310. doi: 10.1530/EC-17-0082

PubMed Abstract | CrossRef Full Text | Google Scholar

Herbert, P., Hayes, L., Sculthorpe, N., and Grace, F. (2017b). HIIT produces increases in muscle power and free testosterone in male masters athletes. Endocrine Connect. 6, 430–436. doi: 10.1530/EC-17-0159

PubMed Abstract | CrossRef Full Text | Google Scholar

Herbert, P., Hayes, L. D., Beaumont, A. J., Grace, F. M., and Sculthorpe, N. F. (2021). Six weeks of high intensity interval training (HIIT) preserves aerobic capacity in sedentary older males and male masters athletes for four years: a reunion study. Exp. Gerontol. 150:111373. doi: 10.1016/j.exger.2021.111373

PubMed Abstract | CrossRef Full Text | Google Scholar

Herbert, P., Hayes, L. D., Sculthorpe, N., and Grace, F. M. (2017a). High-intensity interval training (HIIT) increases insulin-like growth factor-I (IGF-I) in sedentary aging men but not masters' athletes: an observational study. Aging Male. 20, 54–59. doi: 10.1080/13685538.2016.1260108

PubMed Abstract | CrossRef Full Text | Google Scholar

Hurst, C., Scott, J. P. R., Weston, K. L., and Weston, M. (2019b). High-intensity interval training: a potential exercise countermeasure during human spaceflight. Front Physiol. 10:581. doi: 10.3389/fphys.2019.00581

PubMed Abstract | CrossRef Full Text | Google Scholar

Hurst, C., Weston, K. L., McLaren, S. J., and Weston, M. (2019a). The effects of same-session combined exercise training on cardiorespiratory and functional fitness in older adults: a systematic review and meta-analysis. Aging Clin. Exp. Res. 31, 1701–1717. doi: 10.1007/s40520-019-01124-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Hurst, C., Weston, K. L., and Weston, M. (2019c). The effect of 12 weeks of combined upper- and lower-body high-intensity interval training on muscular and cardiorespiratory fitness in older adults. Aging Clin. Exp. Res. 31, 661–671. doi: 10.1007/s40520-018-1015-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Hwang, C.-L., Yoo, J.-K., Kim, H.-K., Hwang, M.-H., Handberg, E. M., Petersen, J. W., et al. (2016). Novel all-extremity high-intensity interval training improves aerobic fitness, cardiac function and insulin resistance in healthy older adults. Exp. Gerontol. 82, 112–119. doi: 10.1016/j.exger.2016.06.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiménez-García, J., Martínez-Amat, A., De la Torre-Cruz, M., Fábrega-Cuadros, R., Cruz-Díaz, D., Aibar-Almazán, A., et al. (2019). Suspension training HIIT improves gait speed, strength and quality of life in older adults. Int. J. Sports Med. 40, 116–124. doi: 10.1055/a-0787-1548

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, T. N., and Choi, K. M. (2013). Sarcopenia: definition, epidemiology, and pathophysiology. J. Bone Metab. 20, 1–10. doi: 10.11005/jbm.2013.20.1.1

PubMed Abstract | CrossRef Full Text | Google Scholar

Knowles, A.-M., Herbert, P., Easton, C., Sculthorpe, N., and Grace, F. M. (2015). Impact of low-volume, high-intensity interval training on maximal aerobic capacity, health-related quality of life and motivation to exercise in ageing men. Age 37:25. doi: 10.1007/s11357-015-9763-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Krzysztofik, M., Wilk, M., Wojdała, G., and Gołaś, A. (2019). Maximizing muscle hypertrophy: a systematic review of advanced resistance training techniques and methods. Int J Environ Res Public Health. 34, 364–380. doi: 10.3390/ijerph16244897

PubMed Abstract | CrossRef Full Text | Google Scholar

Little, J. P., Gillen, J. B., Percival, M. E., Safdar, A., Tarnopolsky, M. A., Punthakee, Z., et al. (2011). Low-volume high-intensity interval training reduces hyperglycemia and increases muscle mitochondrial capacity in patients with type 2 diabetes. J. Appl. Physiol. 111, 1554–1560. doi: 10.1152/japplphysiol.00921.2011

PubMed Abstract | CrossRef Full Text | Google Scholar

Losa-Reyna, J., Baltasar-Fernandez, I., Alcazar, J., Navarro-Cruz, R., Garcia-Garcia, F. J., Alegre, L. M., et al. (2019). Effect of a short multicomponent exercise intervention focused on muscle power in frail and pre frail elderly: a pilot trial. Exp Gerontol. 115, 114–121. doi: 10.1016/j.exger.2018.11.022

PubMed Abstract | CrossRef Full Text | Google Scholar

Malin, S. K., Francois, M. E., Eichner, N. Z. M., Gilbertson, N. M., Heiston, E. M., Fabris, C., et al. (2018). Impact of short-term exercise training intensity on β-cell function in older obese adults with prediabetes. J. Appl. Physiol. 125, 1979–1986. doi: 10.1152/japplphysiol.00680.2018

PubMed Abstract | CrossRef Full Text | Google Scholar

Manini, T. M., and Clark, B. C. (2012). Dynapenia and aging: an update. J. Gerontol. A Biol. Sci. Med. Sci. 67A, 28–40. doi: 10.1093/gerona/glr010

PubMed Abstract | CrossRef Full Text | Google Scholar

Martins, F. M., de Paula Souza, A., Nunes, P. R. P., Michelin, M. A., Murta, E. F. C., Resende, E. A. M. R., et al. (2018). High-intensity body weight training is comparable to combined training in changes in muscle mass, physical performance, inflammatory markers and metabolic health in postmenopausal women at high risk for type 2 diabetes mellitus: a randomized controlled clinical trial. Exp. Gerontol. 107, 108–115. doi: 10.1016/j.exger.2018.02.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Marzetti, E., Calvani, R., Tosato, M., Cesari, M., Di Bari, M., Cherubini, A., et al. (2017). Physical activity and exercise as countermeasures to physical frailty and sarcopenia. Aging Clin. Exp. Res. 29, 35–42. doi: 10.1007/s40520-016-0705-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Mays, N., Roberts, E., and Popay, J. (2001). “Synthesising research evidence,” in Studying the Organisation and Delivery of Health Services: Research Methods, eds N. Fulop, P. Allen, A. Clarke, N. Black (City of London: Routledge), 188–220.

Melov, S., Tarnopolsky, M. A., Beckman, K., Felkey, K., and Hubbard, A. (2007). Resistance exercise reverses aging in human skeletal muscle. PLoS ONE. 2:e465. doi: 10.1371/journal.pone.0000465

PubMed Abstract | CrossRef Full Text | Google Scholar

Munn, Z., Peters, M. D. J., Stern, C., Tufanaru, C., McArthur, A., and Aromataris, E. (2018). Systematic review or scoping review? Guidance for authors when choosing between a systematic or scoping review approach. BMC Med Res Methodol. 18:143. doi: 10.1186/s12874-018-0611-x

PubMed Abstract | CrossRef Full Text

Nunes, P. R. P., Martins, F. M., Souza, A. P., Carneiro, M. A. S., Nomelini, R. S., Michelin, M. A., et al. (2019). Comparative effects of high-intensity interval training with combined training on physical function markers in obese postmenopausal women: a randomized controlled trial. Menopause 26, 1242–1249. doi: 10.1097/GME.0000000000001399

PubMed Abstract | CrossRef Full Text | Google Scholar

Peterson, M. D., Rhea, M. R., Sen, A., and Gordon, P. M. (2010). Resistance exercise for muscular strength in older adults: a meta-analysis. Ageing Res Rev. 9, 226–237. doi: 10.1016/j.arr.2010.03.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Pinedo-Villanueva, R., Westbury, L. D., Syddall, H. E., Sanchez-Santos, M. T., Dennison, E. M., Robinson, S. M., et al. (2019). Health care costs associated with muscle weakness: a UK population-based estimate. Calcified Tissue Int. 104, 137–144. doi: 10.1007/s00223-018-0478-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Robinson, M. M., Dasari, S., Konopka, A. R., Johnson, M. L., Manjunatha, S., Esponda, R. R., et al. (2017). Enhanced protein translation underlies improved metabolic and physical adaptations to different exercise training modes in young and old humans. Cell Metab. 25, 581–592. doi: 10.1016/j.cmet.2017.02.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Schoenfeld, B. J. (2010). The mechanisms of muscle hypertrophy and their application to resistance training. J. Strength Cond Res. 24, 2857–2872. doi: 10.1519/JSC.0b013e3181e840f3

PubMed Abstract | CrossRef Full Text | Google Scholar

Sculthorpe, N. F., Herbert, P., and Grace, F. (2017). One session of high-intensity interval training (HIIT) every 5 days, improves muscle power but not static balance in lifelong sedentary ageing men: a randomized controlled trial. Medicine 96:e6040. doi: 10.1097/MD.0000000000006040

PubMed Abstract | CrossRef Full Text | Google Scholar

Seldeen, K. L., Lasky, G., Leiker, M. M., Pang, M., Personius, K. E., and Troen, B. R. (2018). High intensity interval training improves physical performance and frailty in aged mice. J. Gerontol. A Biol. Sci. Med. Sci. 73, 429–437. doi: 10.1093/gerona/glx120

PubMed Abstract | CrossRef Full Text | Google Scholar

Seo, D. Y., and Hwang, B. G. (2020). Effects of exercise training on the biochemical pathways associated with sarcopenia. Phys. Act. Nutr. 24, 32–38. doi: 10.20463/pan.2020.0019

PubMed Abstract | CrossRef Full Text | Google Scholar

Slade, S. C., Dionne, C. E., Underwood, M., Buchbinder, R., Beck, B., Bennell, K., et al. (2016). Consensus on exercise reporting template (CERT): modified delphi study. Phys. Ther. 96, 1514–1524. doi: 10.2522/ptj.20150668

PubMed Abstract | CrossRef Full Text | Google Scholar

Snijders, T., Nederveen, J. P., Bell, K. E., Lau, S. W., Mazara, N., Kumbhare, D. A., et al. (2019). Prolonged exercise training improves the acute type II muscle fibre satellite cell response in healthy older men. J. Physiol. 597, 105–119. doi: 10.1113/JP276260

PubMed Abstract | CrossRef Full Text | Google Scholar

Søgaard, D., Baranowski, M., Larsen, S., Taulo Lund, M., Munk Scheuer, C., Vestergaard Abildskov, C., et al. (2019). Muscle-saturated bioactive lipids are increased with aging and influenced by high-intensity interval training. IJMS 20:1240. doi: 10.3390/ijms20051240

PubMed Abstract | CrossRef Full Text | Google Scholar

Søgaard, D., Lund, M. T., Scheuer, C. M., Dehlbaek, M. S., Dideriksen, S. G., Abildskov, C. V., et al. (2018). High-intensity interval training improves insulin sensitivity in older individuals. Acta Physiol. 222:e13009. doi: 10.1111/apha.13009

PubMed Abstract | CrossRef Full Text | Google Scholar

Steib, S., Schoene, D., and Pfeifer, K. (2010). Dose–response relationship of resistance training in older adults: a meta-analysis. Br. J. Sports Med. 42, 902–914. doi: 10.1249/MSS.0b013e3181c34465

PubMed Abstract | CrossRef Full Text | Google Scholar

Taylor, J., Coombes, J. S., Leveritt, M. D., Holland, D. J., and Keating, S. E. (2019). Effect of high intensity interval training on visceral adiposity and body composition in patients with coronary artery disease. Obesity Res. Clinical Pract. 13:265. doi: 10.1016/j.orcp.2018.11.086

CrossRef Full Text

Thum, J. S., Parsons, G., Whittle, T., and Astorino, T. A. (2017). High-intensity interval training elicits higher enjoyment than moderate intensity continuous exercise. PLoS ONE 12:e0166299. doi: 10.1371/journal.pone.0166299

PubMed Abstract | CrossRef Full Text | Google Scholar

Tieland, M., Verdijk, L. B., de Groot, L. C., and van Loon, L. J. C. (2015). Handgrip strength does not represent an appropriate measure to evaluate changes in muscle strength during an exercise intervention program in frail older people. Int. J. Sport. Nutr. Exerc. Metab. 25, 27–36. doi: 10.1123/ijsnem.2013-0123

PubMed Abstract | CrossRef Full Text | Google Scholar

Tricco, A. C., Lillie, E., Zarin, W., O'Brien, K. K., Colquhoun, H., Levac, D., et al. (2018). PRISMA extension for scoping reviews (PRISMA-ScR): checklist and explanation. Ann Intern. Med. Am. College Physic. 169, 467–473. doi: 10.7326/M18-0850

PubMed Abstract | CrossRef Full Text | Google Scholar

Trombetti, A., Reid, K. F., Hars, M., Herrmann, F. R., Pasha, E., Phillips, E. M., et al. (2016). Age-associated declines in muscle mass, strength, power, and physical performance: impact on fear of falling and quality of life. Osteoporos Int. 27, 463–471. doi: 10.1007/s00198-015-3236-5

PubMed Abstract | CrossRef Full Text | Google Scholar

United Nations (2020). Department of Economic and Social Affairs, Population Division. World population ageing.

Google Scholar

Warburton, D. E. R., McKenzie, D. C., Haykowsky, M. J., Taylor, A., Shoemaker, P., Ignaszewski, A. P., et al. (2005). Effectiveness of high-intensity interval training for the rehabilitation of patients with coronary artery disease. Am. J. Cardiol. 95, 1080–1084. doi: 10.1016/j.amjcard.2004.12.063

PubMed Abstract | CrossRef Full Text | Google Scholar

Way, K. L., Vidal-Almela, S., Keast, M.-L., Hans, H., Pipe, A. L., and Reed, J. L. (2020). The feasibility of implementing high-intensity interval training in cardiac rehabilitation settings: a retrospective analysis. BMC Sports Sci. Med. Rehabil. 12:38. doi: 10.1186/s13102-020-00186-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Weston, K. S., Wisløff, U., and Coombes, J. S. (2014). High-intensity interval training in patients with lifestyle-induced cardiometabolic disease: a systematic review and meta-analysis. Br. J. Sports Med. 48, 1227–1234. doi: 10.1136/bjsports-2013-092576

PubMed Abstract | CrossRef Full Text | Google Scholar

Wiśniowska-Szurlej, A., Cwirlej-Sozańska, A., Wołoszyn, N., Sozański, B., and Wilmowska-Pietruszyńska, A. (2019). Association between handgrip strength, mobility, leg strength, flexibility, and postural balance in older adults under long-term care facilities. BioMed Res. Int. 2019:e1042834. doi: 10.1155/2019/1042834

PubMed Abstract | CrossRef Full Text | Google Scholar

Witham, M. D., Chawner, M., De Biase, S., Offord, N., Todd, O., Clegg, A., et al. (2020). Content of exercise programmes targeting older people with sarcopenia or frailty – findings from a UK survey. JFSF 5, 17–23. doi: 10.22540/JFSF-05-017

PubMed Abstract | CrossRef Full Text | Google Scholar

Wyckelsma, V. L., Levinger, I., Murphy, R. M., Petersen, A. C., Perry, B. D., Hedges, C. P., et al. (2017). Intense interval training in healthy older adults increases skeletal muscle [3 H]ouabain-binding site content and elevates Na +,K + -ATPase α 2 isoform abundance in Type II fibers. Physiol. Rep. 5:e13219. doi: 10.14814/phy2.13219

PubMed Abstract | CrossRef Full Text | Google Scholar

Yasar, Z., Elliott, B. T., Kyriakidou, Y., Nwokoma, C. T., Postlethwaite, R. D., Gaffney, C. J., et al. (2021). Sprint interval training (SIT) reduces serum epidermal growth factor (EGF), but not other inflammatory cytokines in trained older men. Eur. J. Appl. Physiol. 121:1909–19. doi: 10.1007/s00421-021-04635-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Yee, X. S., Ng, Y. S., Allen, J. C., Latib, A., Tay, E. L., Abu Bakar, H. M., et al. (2021). Performance on sit-to-stand tests in relation to measures of functional fitness and sarcopenia diagnosis in community-dwelling older adults. Eur Rev Aging Phys Activity 18:1. doi: 10.1186/s11556-020-00255-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Ziaaldini, M. M., Marzetti, E., Picca, A., and Murlasits, Z. (2017). Biochemical pathways of sarcopenia and their modulation by physical exercise: a narrative review. Front Med. 4:167. doi: 10.3389/fmed.2017.00167

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: aging, exercise, HIIT, high intensity, power, sarcopenia, sprint, strength

Citation: Hayes LD, Elliott BT, Yasar Z, Bampouras TM, Sculthorpe NF, Sanal-Hayes NEM and Hurst C (2021) High Intensity Interval Training (HIIT) as a Potential Countermeasure for Phenotypic Characteristics of Sarcopenia: A Scoping Review. Front. Physiol. 12:715044. doi: 10.3389/fphys.2021.715044

Received: 26 May 2021; Accepted: 20 July 2021;
Published: 24 August 2021.

Edited by:

Hamdi Chtourou, University of Sfax, Tunisia

Reviewed by:

Ellen Freiberger, University of Erlangen Nuremberg, Germany
J. Matthew Hinkley, AdventHealth, United States

Copyright © 2021 Hayes, Elliott, Yasar, Bampouras, Sculthorpe, Sanal-Hayes and Hurst. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Lawrence D. Hayes, TGF3cmVuY2UuSGF5ZXMmI3gwMDA0MDtVV1MuYWMudWs=

ORCID: Lawrence D. Hayes orcid.org/0000-0002-6654-0072
Bradley T. Elliott orcid.org/0000-0003-4295-3785
Zerbu Yasar orcid.org/0000-0001-8838-7286
Theodoros M. Bampouras orcid.org/0000-0002-8991-4655
Nicholas F. Sculthorpe orcid.org/0000-0001-8235-8580
Nilihan E. M. Sanal-Hayes orcid.org/0000-0003-4979-9653
Christopher Hurst orcid.org/0000-0002-7239-6599

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