- 1Department of Pharmacy, Health, and Nutritional Sciences, University of Calabria, Arcavacata di Rende, Italy
- 2Centro Sanitario, University of Calabria, Arcavacata di Rende, Italy
- 3Health Center SRL, Cosenza, Italy
- 4School of Specialization in Food Sciences, University of Rome Tor Vergata, Rome, Italy
- 5Department of Clinical and Experimental Medicine, University Magna Graecia, Catanzaro, Italy
- 6Department of Mathematics, University of Calabria, Arcavacata di Rende, Italy
Adherence to Mediterranean diet (MD) and physical activity (PA) in adolescence represent powerful indicators of healthy lifestyles in adulthood. The aim of this longitudinal study was to investigate the impact of nutrition education program (NEP) on the adherence to the MD and on the inflammatory status in healthy adolescents, categorized into three groups according to their level of PA (inactivity, moderate intensity, and vigorous intensity). As a part of the DIMENU (Dieta Mediterranea & Nuoto) study, 85 adolescents (aged 14–17 years) participated in the nutrition education sessions provided by a team of nutritionists and endocrinologists at T0. All participants underwent anthropometric measurements, bio-impedentiometric analysis (BIA), and measurements of inflammatory biomarkers such as ferritin, erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP) levels. Data were collected at baseline (T0) and 6 months after NEP (T1). To assess the adherence to the MD, we used KIDMED score. In our adolescents, we found an average MD adherence, which was increased at T1 compared with T0 (T0: 6.03 ± 2.33 vs. T1: 6.96 ± 2.03, p = 0.002), with an enhanced percentage of adolescents with optimal (≥8 score) MD adherence over the study period (T0: 24.71% vs. T1: 43.52%, p = 0.001). Interestingly, in linear mixed-effects models, we found that NEP and vigorous-intensity PA levels independently influenced KIDMED score (β = 0.868, p < 0.0001 and β = 1.567, p = 0.009, respectively). Using ANOVA, NEP had significant effects on serum ferritin levels (p < 0.001), while either NEP or PA influenced ESR (p = 0.035 and 0.002, respectively). We also observed in linear mixed-effects models that NEP had a negative effect on ferritin and CRP (β = −14.763, p < 0.001 and β = −0.714, p = 0.02, respectively). Our results suggest the usefulness to promote healthy lifestyle, including either nutrition education interventions, or PA to improve MD adherence and to impact the inflammatory status in adolescence as a strategy for the prevention of chronic non-communicable diseases over the entire lifespan.
Introduction
Adherence to the Mediterranean diet (MD) and physical activity (PA) in adolescence represent powerful indicators of healthy lifestyles in adulthood (1–3).
The MD, characterized by a high intake of vegetables, fruits, legumes, dairy products, and nuts, a moderate intake of fish and poultry, along with a low intake of red meat, processed foods, and saturated lipids (4), has been accepted as one of the healthiest dietary patterns in the world (5). The inverse association between the MD adherence and a wide range of chronic and metabolic diseases is well-known (6), and it may be, at least in part, attributed to the anti-inflammatory properties of MD components (7). For instance, it has been reported that low adherence to the MD is directly associated with a worse profile of circulating inflammation-related biomarkers (8). Although, the relationship between MD and inflammatory markers within a population of European adolescents has been recently investigated (9), the impact of MD and PA on inflammatory status in healthy adolescents remains to be clarified.
The spectrum of PA is broad, ranging from physical inactivity/sedentary behavior to different levels of PA intensities. Particularly, the sedentary behavior has been reported to be implicated in unhealthy conditions (10), while moderate- to vigorous-intensity PA during adolescence leads to chronic disease benefits that can be attributed to the anti-inflammatory effects of exercise (11–14).
Over the last years, the impact of PA on inflammation has received great attention for the identification of biologically active substances, secreted by myocytes (myokines) after skeletal muscle contraction, which can exert beneficial influence on systemic inflammatory responses, and to have positive health effects (15, 16). It has been widely recognized that among myokines interleukin (IL)-6 is locally produced in working skeletal muscle in larger amounts than any other cytokines, and it can account for the increase in plasma IL-6 during exercise (17). Muscle-derived IL-6, along with other classical pro-inflammatory cytokines, such as tumor necrosis factor (TNF)-α and IL-1β, is accompanied by the secretion of other cytokines, such as IL-10, which can create an anti-inflammatory environment (18–20).
Convincing evidence indicates the need to promote healthy nutrition and PA to achieve benefits in terms of the prevention of risk factors for metabolic and chronic diseases. In this context, a carefully designed nutrition education program (NEP) aiming to enhance the knowledge of the MD principles for empowering adolescents toward healthy dietary habits may represent a useful tool to ensure a better quality of life in adulthood.
Thus, the aim of this longitudinal study was to assess over a 6-month period the impact of NEP and PA on MD adherence and on inflammatory status in a cohort of healthy adolescents of a Mediterranean area.
Materials and Methods
Study Population
The DIMENU (Dieta Mediterranea & Nuoto) project was funded by the EU Regional Operational Programme Calabria, Italy (prot. #52243/2017), for investigating the impact of the adherence of MD and PA on health status in a sample of adolescents from Southern Italy. Based on an in-depth collaboration with the public high school “Istituto Istruzione Superiore”—Castrolibero, and three swim and sport centers (sports club in Cosenza, Paola, and Crotone of Calabria Region, Italy), we were able to recruit and to select sedentary adolescents and subjects performing recreational sport activities or competitive sports, between December 2018 and January 2019 (21). The exclusion criteria were cognitive or physical/motor limitation, health-related problems, use of medications, restrictive diet (i.e., hypocaloric, low carbohydrate, and low fat). All participants and their parents received a detailed explanation of study purposes. Prior to the enrolment of adolescents in the DIMENU trial, their parents provided written informed consent. All adolescents were subjected to study visits and data collection at baseline (T0) in which the NEP on MD-related issues and sports nutrition was also included. This study was conducted according to the guidelines laid down in the Declaration of Helsinki and approved by the Ethic Committee of the University of Calabria, Italy (#5727/2018).
Nutritional History Assessment and Nutrition Education Sessions
To collect the nutritional and medical history, participants were orally interviewed at baseline and after 6 months by a team of nutritionists through a nutritional history record, as previously reported (21). Using the KIDMED test (4, 22), we assessed the adherence to the MD in the study population. The score of MD adherence, ranging from 0 to 12, was based on a 16-point paper questionnaire in which a value of +1 was assigned for the consumption of fruits, vegetables, fish, legumes, whole cereals or grain, nuts, oil, dairy products, and yogurt and a negative value −1 for skipping breakfast, consumption of baked goods, sweets, and going to fast food. At baseline, two 30/40-min education sessions, consisting of seminars and interactive lectures structured to cover knowledge of food sources of macro- and micronutrients included in the healthy eating pattern and benefits of MD (basic nutrition concepts, eat at regular intervals, maintain adequate hydration, healthy food choices), were provided for all participants by study nutritionists (EA, AG, GC, EM, and SF) and by three endocrinologists (DB, SA, and SC). In addition, we have created an official website of DIMENU project (https://www.dimenu.it/) (23) and a Facebook page (https://www.facebook.com/dimenu2019) (24) as innovative ways for assuring additional support and information on MD-related issues to all participants.
Physical Activity Intensity Levels
The intensity of PA levels was estimated following WHO recommendations (25) as physical inactivity [<3 metabolic equivalents (METs)], moderate-intensity (3–6 METs), and vigorous-intensity PA (>6 METs). Specifically, using a questionnaire to assess PA habits that we have described elsewhere (21), the enrolled adolescents were classified into three groups: physical inactivity (PAi = 23), moderate-intensity PA (Pam = 34) [subjects performing at least 60min daily of bicycling (n = 2), dancing (n = 2), brisk walking (n = 2), gymnastics (n = 4), aquatic aerobics (n = 3), recreational swimming (n = 21)] and vigorousintensity PA (PAv = 28) [subjects engaged in at least 60 min daily of jogging or running (n = 2), boxing (n = 1), tennis (n = 1), soccer (n = 2), basketball (n = 2), squash (n = 1), swimming (n = 16), aerobic dancing (n = 2), and volleyball (n = 1)]. The same PA intensity levels of adolescents were confirmed through the interview at T1.
Anthropometric Parameters and Bioelectrical Impedance Analysis
A detailed description of the anthropometric measurements and bio-impedentiometric analysis (BIA) performed has been reported elsewhere (21). BIA estimated phase angle (PhA), total body water (TBW), body cell mass (BCM), fat-free mass (FFM), and fat mass (FM). Data obtained by BIA test were analyzed using version 1.2.2.8. of the software Bodygram Plus (Akern Srl; Florence, Italy).
Biochemical Measurements, Erythrocyte Sedimentation Rate, and Interleukin Assays
In the detailed explanation of study purposes, participants were informed to have not eaten at least for 8 h before blood collection. Additionally, participants were reminded 1 week before the study visit. Venous blood samples were collected at T0 and T1, and in order to obtain serum, samples were centrifuged as previously reported (21). ESR was measured by Wintrobe method. Serum C-reactive protein (CRP) levels were detected by immunonephelometry (GOLDSITE Diagnostics, Inc., Shenzhen, China). Serum ferritin levels were measured by enzyme-linked immunosorbent assay (ELISA) (Monobind Inc., Lake Forest, CA, United States), with a detection sensitivity limit of 0.17 ng/ml. Serum iron was determined on a Konelab 20i Chemistry Analyzer (Thermo Electron Corporation, Vantaa, Finland) according to the standardized procedures (Method Iron “Ferene S,” Sclavo Diagnostics, Siena, Italy). Quantification of interleukins was performed using ELISA kits for human IL-6, human TNF-α, human IL-1β, and human IL-10 (Merck Life Sciences, Darmstadt, Germany). The respective sensitivities of these assays were 1.6 pg/ml for IL-6, 0.2 pg/ml for TNF-α, 0.2 pg/ml for IL-1β, and 2 pg/ml for IL-10.
Mediterranean Diet Meal Plan
All participants received a personalized MD meal plan according to their different PA intensity levels. During the entire period of the NEP, the nutritionists gave verbal and written dietary instructions on the choice of typical Mediterranean foods. The dietary approach was based on the MD pattern according to the last guidelines (26, 27). Each diet plan provides 15–20% of calories through protein, 45–60% of calories through carbohydrates, and 25–30% of calories through fat, with the respective distribution of macro- and micronutrients according to the different energy expenditure of each subject. We calculated the total daily energy expenditure (TDEE) using the formula: TDEE = Basal Metabolic Rate × Physical Activity Level, as recommended by the Italian Society of Human Nutrition (https://sinu.it/2019/07/09/fabbisogno-energetico-medio-ar-nellintervallo-deta-1-17-anni/) (28). Meals included an abundance of plant food (fruits, vegetables, whole grains, nuts, and legumes); fish, poultry, and eggs in moderate amounts; olive oil as the primary source of fat; low consumption of red meats, saturated fats, and sweets. Meals and food plans were designed using MetaDieta software version 4.2.1. (Meteda S.r.l, Roma, Italy).
Statistical Analysis
Sample size was calculated by considering the whole adolescent population (aged 14–17 years) living in the Mediterranean area of Calabria region (76,000 adolescents) by fixing the confidence level to 95% and the confidence interval to 10% (https://www.surveysystem.com/sscalc.htm). Post-hoc power analysis was performed, by G*Power software version 3.1.9.4 (University of Heinrich-Heine, Germany), to evaluate the adequacy of the analyzed sample; the effect size was calculated on a website (https://campbellcollaboration.org/escalc/html/EffectSizeCalculator-SMD1.php) on the mean values and standard deviation obtained at baseline (T0) and after 6-month follow-up (T1) for KIDMED score (d = 0.4210), ESR (d = 0.3621), and ferritin levels (d = 0.6584) using Cohen's d formula. Data were analyzed by SigmaPlot for Windows version 12.0 (Systat, San Jose, CA, United States) and reported as the mean and SD. Data normality was verified by Kolmogorov–Smirnov test (with Lilliefors' correction). The statistical differences between variables T0 and T1 were evaluated by using paired t-test. Frequencies (%) were used to describe qualitative variables that were graphically represented in radar plots. McNemar's chi-squared test was applied to evaluate the statistical differences. Two-way repeated-measures ANOVA was used to test for significant differences between KIDMED score with respect to NEP and PA and for their interaction. Spearman's correlation test was used to assess the association between variables. Linear mixed-effects models were used to test the association between dependent variables (KIDMED, ferritin, ESR, CRP, and cytokines) and independent variables such as NEP and PA along with a set of anthropometric parameters to improve the robustness of our analyses. In the modeling analysis, the p-value was adjusted with the Holm–Šidák method (extension of Holm–Bonferroni method). The latter analyses were carried out in a Python 3 environment taking advantage of the statsmodels module. Results are considered statistically significant when p < 0.05.
Results
Characteristics of Participants
The longitudinal DIMENU project was conducted in 85 adolescents (44 girls and 41 boys) who completed the scheduled monitoring visit at T0 and T1. The enrolment at T0 included 92 adolescents, but seven participants dropped out over the course of the study. Table 1 summarizes the anthropometric characteristics and body composition parameters of 85 subjects categorized according to the intensity level of PA into the following three groups: inactivity (PAi), moderate-intensity (PAm), and vigorous-intensity (PAv) PA at T0 and T1. We observed that either NEP or PA had statistically significant effects on the majority of anthropometric measurements and body composition parameters, while no combined effects were found (Table 1).
Table 1. Anthropometric characteristics and body composition parameters of participants according to the three physical activity (PA) groups at baseline (T0) and after 6 months (T1).
Impact of NEP and PA on the Adherence to the Mediterranean Diet
Over the study period, we found that adherence to the MD evaluated by KIDMED score increased at T1 compared with T0 (T0: 6.03 ± 2.33 vs. T1: 6.96 ± 2.03, p = 0.002) in all adolescents. Based on the KIDMED values, we divided the population into optimal (score ≥8), medium (score 4–7), and poor (score ≤ 3) adherence to the MD (22), and we observed that the proportion of adolescents having optimal adherence to the MD was significantly higher after nutritional intervention with respect to baseline (T0: 24.71% vs. T1: 43.52%, p = 0.001).
In Figure 1, we reported the compliance with items from KIDMED test in the three separate PA groups. No significant changes were observed in the comparison between T0 and T1 for most of items with the exception of an increase in the consumption of “a fruit/day” in PAi group and “second fruit/day” in PAv group (65 vs. 91%, p = 0.03 and 32 vs. 60%, p = 0.03, respectively). Statistical analyses evidenced that KIDMED score is influenced by NEP (p < 0.001) and not by either PA or by NEP+PA (Figure 1).
Figure 1. Compliance with items from KIDMED test according to the three physical activity (PA) groups (PAi: inactive; PAm: moderate; PAv: vigorous) at baseline (T0) and after 6 months (T1). The radar chart plots the values of each item of Mediterranean diet score along a separate axis that starts in the center of the chart (0% compliance) and ends at the outer ring (100% compliance). KIDMED score is presented as Mean ± SD; statistical differences were evaluated by two-way repeated-measures ANOVA. NEP, Nutrition Education Program.
To evaluate the impact of NEP and PA on the adherence to the MD, we performed linear mixed-effects models including a set of anthropometric parameters (age, gender, weight, height, BMI, and PhA) as independent variables. Results show that NEP had a significant positive effect on the KIDMED score (p < 0.001), considering constant all the other variables. Furthermore, PAv had a greater impact on the MD adherence with respect to PAi (p = 0.009), while there were no significant differences in KIDMED scores between PAm and PAi (Table 2). To further study these associations, we investigated the interaction between NEP and PA on the KIDMED score, concluding that there were no significant effects between the two variables (Table 2).
Table 2. Mixed-effect linear regression model for the association between KIDMED score and NEP, PA, and a set of anthropometric parameters, considering T0 and T1 as a unique longitudinal dataset.
Correlations Between Inflammatory Biomarkers and Body Composition Parameters
Evaluating the inflammatory status by measuring ferritin, ESR, and CRP along with a panel of serum cytokines in our population longitudinally, we observed that ferritin and CRP levels were significantly reduced in all adolescents (50.66 ± 33.90 vs. 17.79 ± 16.75, p < 0.001 and 1.94 ± 3.07 vs. 1.53 ± 2.76, p = 0.028, respectively). Using ANOVA, we found that NEP significantly influenced ferritin, ESR, and serum IL-6 as well as TNF-α levels, and PA had effects on ESR, while NEP in combination with PA exerted the effects on serum TNF-α (Table 3). Using the correlation analysis, we found that the pro-inflammatory IL-1β, IL-6, and TNF-α cytokines were significantly associated with the anti-inflammatory IL-10 levels at both times of observation (Figure 2). As expected, serum IL-6, IL-1β, and TNF-α levels were also directly correlated (Supplementary Figure 1).
Table 3. Serum inflammatory markers in adolescents according to the three physical activity (PA) groups at baseline (T0) and after 6 months (T1).
Figure 2. Correlations between interleukin-10 and interleukin-1β, interleukin-6, or tumor necrosis factor (TNF)-α in all sample at baseline (T0) and after 6 months (T1). Association of interleukin (IL)-10 with IL-1β (A,D), IL-6 (B,E), and TNF-α (C,F) in all samples at baseline (T0) and after 6 months (T1) were analyzed by Spearman's correlation test. For each linear regression graph, the linear equation (Y), the correlation coefficient (r), and the statistical significance (p) are reported.
As shown in Table 4, ferritin was positively associated with BCM and FFM (both expressed in kg) at baseline and after 6 months of follow-up. Serum ESR and CRP values were positively correlated with FM (expressed in kg or percentage) and negatively correlated with FFM (expressed in kg or percentage) and TBW at baseline, while serum CRP levels also directly correlated with BMI and inversely with PhA and BCM (expressed in percentage) (Table 4). After 6 months, ESR values showed a positive correlation with FM (expressed in kg or percentage) and an inverse correlation with PhA, TBW, BCM, and FFM (both these latter parameters expressed in kg or percentage), whereas, serum CRP levels were directly correlated with BMI. There were no statistically significant correlations between other inflammatory markers and body composition measurements (data not shown).
Table 4. Correlations between serum ferritin, ESR, and CRP levels with body composition parameters in all the sample at baseline (T0) and after 6 months (T1).
Impact of NEP and PA on Inflammatory Biomarker Levels
Finally, we investigated the influence of NEP and PA on the levels of inflammatory markers ferritin, ESR, and CRP using linear mixed-effects models with a set of anthropometric parameters (age, gender, weight, height, BMI, and PhA). Table 5 shows that NEP had a negative effect on ferritin (p < 0.0001) and CRP (p = 0.02) levels. There were no significant effects of PA on the ferritin, ESR, and CRP levels over the study period. NEP and PA interaction had no effects on ferritin, ESR, and CRP (Supplementary Table 1) as well as on cytokine levels (Supplementary Table 2).
Table 5. Mixed-effect linear regression model for the association between ferritin, ESR, CRP, and NEP, PA, and a set of anthropometric parameters, considering T0 and T1 as a unique longitudinal dataset.
Discussion
In the present study, we highlighted the impact of nutrition education intervention and PA on the adherence to the MD and on inflammatory status in healthy adolescents living in a Mediterranean area of Southern Italy.
In adolescents, Sahingoz and Sanlier (29) have reported that poor nutrition knowledge related to food sources of macro- and micronutrients was associated with low adherence to the MD. Conflicting data are reported in previous observations on the adherence to the MD in adolescent athletes following nutrition education since only in few studies the intervention resulted in improvements in food choices, and it was correlated with most successful sports performance (30–32). Recently, a systematical review of the scientific literature available on MD adherence in adolescents showed the direct association between adherence to the MD and PA (and possibly with diet adequacy) and the inverse correlation with sedentary behavior, while the results for other variables such as gender, age, weight, and socioeconomic status were not consistent (33).
In our population sample, the KIDMED score showed a medium adherence to the MD with the proportion of subjects having an optimal score, which was significantly improved over the study period (T0: 24.7% vs. T1: 43.5%), underlining that they have translated nutrition knowledge into healthier eating habits. This finding is supported by the evidence that using ANOVA NEP had a positive effect on the MD adherence, while PA alone or in combination with NEP did not exert any influence. Using linear mixed-effects models, we confirmed that nutrition education intervention had a positive effect on the adherence of the MD, and interestingly, we were also able to evidence that vigorous PA intensity positively influenced healthy dietary pattern. Surprisingly, the main effects of NEP and PA lose their statistical significance when the model includes the interaction term. We hypothesize that the introduction of the interaction effect increases the model complexity, which would require a larger population sample to potentially obtain significant results. Data on the MD adherence are in agreement with those reported among adolescents and adults living within the Mediterranean area (34–37) as well as in children and adolescents outside of the Mediterranean region (38, 39). Importantly, the positive implications of nutrition education sessions by a team of nutritionists and endocrinologists were observed on increased KIDMED score and a better compliance to the recommendation of the Mediterranean food choices. This seems to be very important at this age range, representing the most appropriate regime for disease prevention (40). Evidence suggests that adhering to the MD and performing regular PA, as an integral part of the traditional Mediterranean lifestyle, have been linked to health benefits (25, 41). For instance, their combined promotion may be a useful means to reduce metabolic risk and obesity in adult populations (42). Specifically, systematic reviews and meta-analyses have reported that high adherence to the MD and PA decreased the risk factors related to several metabolic and chronic diseases, such as type 2 diabetes, metabolic syndrome, neurodegenerative diseases, and cancers, and was associated with a reduced mortality (38, 39). Low-grade inflammation has emerged as critical in the pathogenesis of these chronic diseases being characterized by abnormal cytokine production and the activations of inflammatory signaling pathways (43). The protection provided by the MD pattern against the diseases associated with chronic low-grade inflammation can probably be due to its antioxidant and anti-inflammatory properties (7, 44). Inflammatory process is associated with changes in the production of serum cytokine levels that may either increase (pro-inflammatory) or decrease (anti-inflammatory) in response to inflammation. In our study, serum levels of both pro-inflammatory and anti-inflammatory cytokines were higher in adolescents at T1 compared with T0 irrespective of different levels of PA. Moreover, we found a direct correlation between the assayed pro-inflammatory IL-6, IL-1β, and TNF-α with the anti-inflammatory cytokine IL-10, which may be responsible to control the balance of inflammation in healthy population at both times of observation. Thus, we speculate that these findings are not related to the impact of NEP or PA but are probably due to other factors contributing to maintain inflammatory balance in adolescents.
In clinical practice, ESR and CRP biomarkers are widely used for identifying and monitoring individuals with inflammatory systemic activity (45–49). Evidence from previous studies suggests that ESR, when elevated in adolescence, is positively associated with premature mortality, making it a suitable marker of inflammation when collecting large amounts of data (50, 51). In adolescents, CRP is inversely related to vigorous-intensity levels of PA, showing that exercise may protect against low-grade systemic inflammation in youth (48). In a recent cross-sectional design, Cayres et al. (52) demonstrated that in adolescents both previous sports participation and regular engagement in PA are inversely related to CRP levels, indicating that frequency and intensity of sports are important factors associated with CRP levels. In line with these observations, we also found that CRP and ESR levels were correlated with several body composition parameters indicative of healthier status, CRP levels were significantly reduced over the study period, while ESR was influenced by either PA or NEP in our adolescents. In the past couple of decades, also ferritin, first discovered as an iron storage protein, has been considered a marker of inflammation, used for predicting and even diagnosing many chronic diseases, including cardiovascular disease, diabetes, and various forms of cancer (49, 53–55). Particularly, elevated serum ferritin levels have been demonstrated to be associated with worse metabolic profile and with an increased cardiometabolic risk in adolescence (49), indicating ferritin as a marker of inflammatory-related diseases. Our results showed that ferritin levels were significantly decreased in all adolescents longitudinally. This latter finding is in agreement with a recent investigation in which ferritin was positively and longitudinally associated with worse health conditions at the adolescent stage (55). Finally, NEP was inversely correlated with both CRP and ferritin levels, suggesting the usefulness to measure these inflammatory biomarkers in the young population from a clinical health perspective.
The limitations of the study include the lack of a control group, the relatively small population studied, and the evaluation of the adherence of MD using only KIDMED test. On the other hand, our longitudinal study strengthens the importance to improve healthy dietary habits in adolescents generating useful data for further investigations in a large number of individuals.
Conclusions
In summary, this longitudinal study demonstrates the effectiveness to improve nutrition education and to foster an adequate PA intensity levels in adolescents in order to enhance MD adherence and to impact inflammatory marker levels as a strategy for assuring the prevention and control of chronic non-communicable diseases over the entire lifespan.
Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics Statement
The study involving human participants was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Ethic Committee of the University of Calabria, Italy 384 (#5727/2018). Written informed consent was provided by the participants' legal guardian/next of kin.
Author Contributions
CM and EA involved in data collection, study design, analysis and interpretation of data, and writing the manuscript. AG, GC, EM, and SF performed nutritional analyses. AC and DD performed blood analyses. IB, SC, and SA performed analyses and involved in the interpretation of data. CA and GG performed statistical analyses. DS, CG, and DB involved in conception of idea, study design, and reviewing manuscript. All authors have read and agreed to the published version of the manuscript.
Funding
The authors declare that this study received funding from EU Regional Operational Programme Calabria, Italy (POR Calabria FESR-FSE 2014-2020), DIMENU (prot. #52243/2017), and from Department of Excellence (Italian Law no. 232/2016), Department of Pharmacy, Health, and Nutritional Sciences, University of Calabria, Italy. The funder was not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.
Conflict of Interest
EA, AG, GC, EM, and SF were employed by the company Health Center srl.
The remaining 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.
Acknowledgments
We sincerely thank all our participants enrolled from High School Istituto Istruzione Superiore—Castrolibero and from sports teams of Cosenza, Paola, and Crotone, located in Calabria Region, Italy. We are thankful to all partners of DIMENU project (Amphiios S.C.R. L., Istituto Istruzione Superiore—Castrolibero, ELLE 17 S.R.L.). We also thank Dr. Francesco Grandinetti for helpful administrative support.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnut.2021.685247/full#supplementary-material
References
1. Lake AA, Mathers JC, Rugg-Gunn AJ, Adamson AJ. Longitudinal change in food habits between adolescence (11-12 years) and adulthood (32-33 years): the ASH30 study. J Public Health. (2006) 28:10–6. doi: 10.1093/pubmed/fdi082
2. Sawyer SM, Afifi RA, Bearinger LH, Blakemore SJ, Dick B, Ezeh AC, et al. Adolescence: a foundation for future health. Lancet. (2012) 379:1630–40. doi: 10.1016/S0140-6736(12)60072-5
3. Twig G, Yaniv G, Levine H, Leiba A, Goldberger N, Derazne E, et al. Body-mass index in 2.3 million adolescents and cardiovascular death in adulthood. N Engl J Med. (2016) 374:2430–40. doi: 10.1056/NEJMoa1503840
4. Mediterranean Diet. Proceeding of the 1st World Conference on the Mediterranean Diet, Milan, Italy, 6-8 July 2016. Milan (2016). Available online at: http://www.ifmed.org/1st-world-conference-on-the-mediterranean-diet (accessed March 16, 2021).
5. Serra-Majem L, Roman B, Estruch R. Scientific evidence of interventions using the Mediterranean diet: a systematic review. Nutr Rev. (2006) 64(2 Pt. 2):S27–47. doi: 10.1301/nr.2006.feb.S27-S47
6. Schwingshackl L, Schwedhelm C, Galbete C, Hoffmann G. Adherence to mediterranean diet and risk of cancer: an updated systematic review and meta-analysis. Nutrients. (2017) 9:1063. doi: 10.3390/nu9101063
7. Estruch R. Anti-inflammatory effects of the Mediterranean diet: the experience of the PREDIMED study. Proc Nutr Soc. (2010) 69:333–40. doi: 10.1017/S0029665110001539
8. Sureda A, Bibiloni MDM, Julibert A, Bouzas C, Argelich E, Llompart I, et al. Adherence to the Mediterranean diet and inflammatory markers. Nutrients. (2018) 10:62. doi: 10.3390/nu10010062
9. Arouca A, Michels N, Moreno LA, Gonzalez-Gil EM, Marcos A, Gomez S, et al. Associations between a Mediterranean diet pattern and inflammatory biomarkers in European adolescents. Eur J Nutr. (2018) 57:1747–60. doi: 10.1007/s00394-017-1457-4
10. Yates T, Wilmot EG, Khunti K, Biddle S, Gorely T, Davies MJ. Stand up for your health: is it time to rethink the physical activity paradigm? Diabetes Res Clin Pract. (2011) 93:292–4. doi: 10.1016/j.diabres.2011.03.023
11. Nimmo MA, Leggate M, Viana JL, King JA. The effect of physical activity on mediators of inflammation. Diabetes Obes Metab. (2013) 15(Suppl. 3):51–60. doi: 10.1111/dom.12156
12. Cayres SU, de Lira FS, Machado-Rodrigues AM, Freitas Junior IF, Barbosa MF, Fernandes RA. The mediating role of physical inactivity on the relationship between inflammation and artery thickness in prepubertal adolescents. J Pediatr. (2015) 166:924–9. doi: 10.1016/j.jpeds.2014.12.057
13. Garcia-Hermoso A, Sanchez-Lopez M, Escalante Y, Saavedra JM, Martinez-Vizcaino V. Exercise-based interventions and C-reactive protein in overweight and obese youths: a meta-analysis of randomized controlled trials. Pediatr Res. (2016) 79:522–7. doi: 10.1038/pr.2015.274
14. Cayres SU, de Lira FS, Kemper HCG, Codogno JS, Barbosa MF, Fernandes RA. Sport-based physical activity recommendations and modifications in C-reactive protein and arterial thickness. Eur J Pediatr. (2018) 177:551–8. doi: 10.1007/s00431-018-3101-6
15. Pedersen BK, Febbraio MA. Muscles, exercise and obesity: skeletal muscle as a secretory organ. Nat Rev Endocrinol. (2012) 8:457–65. doi: 10.1038/nrendo.2012.49
16. Pedersen BK. Muscle as a secretory organ. Compr Physiol. (2013) 3:1337–62. doi: 10.1002/cphy.c120033
17. Pedersen BK, Febbraio MA. Muscle as an endocrine organ: focus on muscle-derived interleukin-6. Physiol Rev. (2008) 88:1379–406. doi: 10.1152/physrev.90100.2007
18. Ostrowski K, Schjerling P, Pedersen BK. Physical activity and plasma interleukin-6 in humans–effect of intensity of exercise. Eur J Appl Physiol. (2000) 83:512–5. doi: 10.1007/s004210000312
19. Petersen AM, Pedersen BK. The anti-inflammatory effect of exercise. J Appl Physiol. (2005) 98:1154–62. doi: 10.1152/japplphysiol.00164.2004
20. Rubin DA, Hackney AC. Inflammatory cytokines and metabolic risk factors during growth and maturation: influence of physical activity. Med Sport Sci. (2010) 55:43–55. doi: 10.1159/000321971
21. Morelli C, Avolio E, Galluccio A, Caparello G, Manes E, Ferraro S, et al. Impact of vigorous-intensity physical activity on body composition parameters, lipid profile markers, and irisin levels in adolescents: a cross-sectional study. Nutrients. (2020) 12:742. doi: 10.3390/nu12030742
22. Garcia Cabrera S, Herrera Fernandez N, Rodriguez Hernandez C, Nissensohn M, Roman-Vinas B, Serra-Majem L. Kidmed test prevalence of low adherence to the mediterranean diet in children and young a systematic review. Nutr Hosp. (2015) 32:2390–9. doi: 10.3305/nh.2015.32.6.9828
23. Dieta Mediterranea e Nuoto,. (2019). Available online at: https://www.dimenu.it/ (accessed March 16, 2021).
24. Dieta Mediterranea e Nuoto Facebook Page,. (2019). Available online at: https://www.facebook.com/dimenu2019 (accessed March 16, 2021).
25. World Health Organization. Global Recommendations on Physical Activity for Health. WHO Geneva, Switzerland (2010). Available online at: https://www.who.int/dietphysicalactivity/factsheet_recommendations/en/ (accessed March 16, 2021).
26. Dernini S, Berry EM, Serra-Majem L, La Vecchia C, Capone R, Medina FX, et al. Med Diet 4.0: the Mediterranean diet with four sustainable benefits. Public Health Nutr. (2017) 20:1322–30. doi: 10.1017/S1368980016003177
27. Revitalizing the Mediterranean Diet from a Healthy Dietary Pattern to a Healthy Mediterranean Sustainable Lifestyle. Milan. (2016). Available online at: https://www.ifmed.org/1st-world-conference-on-the-mediterranean-diet/ (accessed March 16, 2021).
28. Società Italiana di Nutrizione Umana. (2014). Available online at: https://sinu.it/2019/07/09/fabbisogno-energetico-medio-ar-nellintervallo-deta-1-17-anni/ (accessed March 16, 2021).
29. Sahingoz SA, Sanlier N. Compliance with Mediterranean Diet Quality Index (KIDMED) and nutrition knowledge levels in adolescents. A case study from Turkey. Appetite. (2011) 57:272–7. doi: 10.1016/j.appet.2011.05.307
30. Reading KJ, McCargar LJ, Marriage BJ. Adolescent and young adult male hockey players: nutrition knowledge and education. Can J Diet Pract Res. (1999) 60:166–9.
31. Doyle-Lucas AF, Davy BM. Development and evaluation of an educational intervention program for pre-professional adolescent ballet dancers: nutrition for optimal performance. J Dance Med Sci. (2011) 15:65–75.
32. Philippou E, Middleton N, Pistos C, Andreou E, Petrou M. The impact of nutrition education on nutrition knowledge and adherence to the Mediterranean Diet in adolescent competitive swimmers. J Sci Med Sport. (2017) 20:328–32. doi: 10.1016/j.jsams.2016.08.023
33. Iaccarino Idelson P, Scalfi L, Valerio G. Adherence to the Mediterranean diet in children and adolescents: a systematic review. Nutr Metab Cardiovasc Dis. (2017) 27:283–99. doi: 10.1016/j.numecd.2017.01.002
34. Grosso G, Marventano S, Buscemi S, Scuderi A, Matalone M, Platania A, et al. Factors associated with adherence to the Mediterranean diet among adolescents living in Sicily, Southern Italy. Nutrients. (2013) 5:4908–23. doi: 10.3390/nu5124908
35. Santomauro F, Lorini C, Tanini T, Indiani L, Lastrucci V, Comodo N, et al. Adherence to Mediterranean diet in a sample of Tuscan adolescents. Nutrition. (2014) 30:1379–83. doi: 10.1016/j.nut.2014.04.008
36. Grosso GGF. Mediterranean diet adherence in children and adolescents in southern European countries. NFS Journal. (2016) 3:13–9. doi: 10.1016/j.nfs.2016.02.004
37. Caparello G, Galluccio A, Giordano C, Lofaro D, Barone I, Morelli C, et al. Adherence to the Mediterranean diet pattern among University staff: a cross-sectional web-based epidemiological study in Southern Italy. Int J Food Sci Nutr. (2020) 71:581–92. doi: 10.1080/09637486.2019.1686753
38. Muros JJ, Cofre-Bolados C, Arriscado D, Zurita F, Knox E. Mediterranean diet adherence is associated with lifestyle, physical fitness, and mental wellness among 10-y-olds in Chile. Nutrition. (2017) 35:87–92. doi: 10.1016/j.nut.2016.11.002
39. Galan-Lopez P, Ries F, Gisladottir T, Dominguez R, Sanchez-Oliver AJ. Healthy lifestyle: relationship between Mediterranean diet, body composition and physical fitness in 13 to 16-years old icelandic students. Int J Environ Res Public Health. (2018) 15:2632. doi: 10.3390/ijerph15122632
40. D'Innocenzo S, Biagi C, Lanari M. Obesity and the Mediterranean diet: a review of evidence of the role and sustainability of the mediterranean diet. Nutrients. (2019) 11:1306. doi: 10.3390/nu11061306
41. Dinu M, Pagliai G, Casini A, Sofi F. Mediterranean diet and multiple health outcomes: an umbrella review of meta-analyses of observational studies and randomised trials. Eur J Clin Nutr. (2018) 72:30–43. doi: 10.1038/ejcn.2017.58
42. Malakou E, Linardakis M, Armstrong MEG, Zannidi D, Foster C, Johnson L, et al. The combined effect of promoting the mediterranean diet and physical activity on metabolic risk factors in adults: a systematic review and meta-analysis of randomised controlled trials. Nutrients. (2018) 10:1577. doi: 10.3390/nu10111577
43. Hotamisligil GS. Inflammation and metabolic disorders. Nature. (2006) 444:860–7. doi: 10.1038/nature05485
44. Casas R, Sacanella E, Estruch R. The immune protective effect of the Mediterranean diet against chronic low-grade inflammatory diseases. Endocr Metab Immune Disord Drug Targets. (2014) 14:245–54. doi: 10.2174/1871530314666140922153350
45. Warnoff C, Lekander M, Hemmingsson T, Sorjonen K, Melin B, Andreasson A. Is poor self-rated health associated with low-grade inflammation in 43,110 late adolescent men of the general population? A cross-sectional study. BMJ Open. (2016) 6:e009440. doi: 10.1136/bmjopen-2015-009440
46. Imhof A, Frohlich M, Loewel H, Helbecque N, Woodward M, Amouyel P, et al. Distributions of C-reactive protein measured by high-sensitivity assays in apparently healthy men and women from different populations in Europe. Clin Chem. (2003) 49:669–72. doi: 10.1373/49.4.669
47. Rifai N, Ridker PM. Population distributions of C-reactive protein in apparently healthy men and women in the United States: implication for clinical interpretation. Clin Chem. (2003) 49:666–9. doi: 10.1373/49.4.666
48. Sabiston CM, Castonguay A, Low NC, Barnett T, Mathieu ME, O'Loughlin J, et al. Vigorous physical activity and low-grade systemic inflammation in adolescent boys and girls. Int J Pediatr Obes. (2010) 5:509–15. doi: 10.3109/17477160903572019
49. Khan A, Khan WM, Ayub M, Humayun M, Haroon M. ferritin is a marker of inflammation rather than iron deficiency in overweight and obese people. J Obes. (2016) 2016:1937320. doi: 10.1155/2016/1937320
50. Toss F, Nordstrom A, Nordstrom P. Inflammation in young adulthood is associated with myocardial infarction later in life. Am Heart J. (2013) 165:164–9. doi: 10.1016/j.ahj.2012.10.030
51. Kantor ED, Udumyan R, Giovannucci EL, Valdimarsdottir UA, Signorello LB, Montgomery S, et al. Association of blood marker of inflammation in late adolescence with premature mortality. JAMA Pediatr. (2019) 173:1095–7. doi: 10.1001/jamapediatrics.2019.2835
52. Cayres SU, Werneck AO, Urban JB, Turi-Lynch BC, Barbosa MF, Fernandes RA. Sports participation is inversely associated with C-reactive protein levels in adolescents: ABCD growth study. Scand J Med Sci Sports. (2019) 29:1000–5. doi: 10.1111/sms.13418
53. Fang X, Min J, Wang F. A dose-response association between serum ferritin and metabolic syndrome? Atherosclerosis. (2018) 279:130–1. doi: 10.1016/j.atherosclerosis.2018.10.016
54. Balla J, Balla G, Zarjou A. Ferritin in kidney and vascular related diseases: novel roles for an old player. Pharmaceuticals. (2019) 12:96. doi: 10.3390/ph12020096
Keywords: Mediterranean diet, physical activity, ferritin, C-reactive protein, body composition parameters, healthy lifestyle
Citation: Morelli C, Avolio E, Galluccio A, Caparello G, Manes E, Ferraro S, Caruso A, De Rose D, Barone I, Adornetto C, Greco G, Catalano S, Andò S, Sisci D, Giordano C and Bonofiglio D (2021) Nutrition Education Program and Physical Activity Improve the Adherence to the Mediterranean Diet: Impact on Inflammatory Biomarker Levels in Healthy Adolescents From the DIMENU Longitudinal Study. Front. Nutr. 8:685247. doi: 10.3389/fnut.2021.685247
Received: 24 March 2021; Accepted: 18 June 2021;
Published: 19 July 2021.
Edited by:
Nora L. Nock, Case Western Reserve University, United StatesReviewed by:
Emily Ricker, Henry M. Jackson Foundation for the Advancement of Military Medicine (HJF), United StatesErsilia Nigro, University of Naples Federico II, Italy
Anil K. Verma, Marche Polytechnic University, Italy
Copyright © 2021 Morelli, Avolio, Galluccio, Caparello, Manes, Ferraro, Caruso, De Rose, Barone, Adornetto, Greco, Catalano, Andò, Sisci, Giordano and Bonofiglio. 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: Daniela Bonofiglio, ZGFuaWVsYS5ib25vZmlnbGlvJiN4MDAwNDA7dW5pY2FsLml0
†These authors have contributed equally to this work
‡These authors share senior authorship