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ORIGINAL RESEARCH article

Front. Reprod. Health, 20 July 2023
Sec. HIV and STIs

Correlates of physical activity among people living with and without HIV in rural Uganda

\r\nSmart Z. Mabweazara
Smart Z. Mabweazara1*Jennifer Manne-Goehler,Jennifer Manne-Goehler2,3Prossy BibangambahProssy Bibangambah4June-Ho Kim,June-Ho Kim2,5Sentongo RuthSentongo Ruth4Linda C. HemphillLinda C. Hemphill2Samson Okello,Samson Okello4,7Mark HamerMark Hamer8Mark J. Siedner,,,,\r\nMark J. Siedner1,2,4,6,9
  • 1Clinical Research Department, Africa Health Research Institute, KwaZulu-Natal, South Africa
  • 2Department of Medicine, Harvard Medical School, Boston MA, United States
  • 3Department of Medicine Brigham and Women's Hospital Boston, MA, United States
  • 4Faculties of Medicine and Radiology, Mbarara University of Science and Technology, Mbarara, Uganda
  • 5Ariadne Labs, Brigham and Women's Hospital, Boston, MA, United States
  • 6Department of Medicine, Massachusetts General Hospital, Boston, MA, United States
  • 7Department of Epidemiology, University of North Carolina, Chapel Hill, NC, United States
  • 8Division of Surgery & Interventional Science, University College London, London, United Kingdom
  • 9Faculty of Medical Sciences, University of KwaZulu-Natal, Durban, South Africa

Background: Antiretroviral therapy (ART) has led to diminishing AIDS-related mortality but a concomitant increase in non-communicable diseases (NCDs) for people with HIV (PWH). Whereas physical activity (PA) has been shown to help prevent NCDs and NCD outcomes in other settings, there are few data on PA and its correlates among PWH in high-endemic settings. We aimed to compare PA by HIV serostatus in rural Uganda.

Methods: We analysed data from the UGANDAC study, an observational cohort including PWH in ambulatory HIV care in Mbarara, Uganda, and age- and gender-matched people without HIV (PWOH). Our primary outcome of interest was PA, which we assessed using the International Physical Activity Questionnaire and considered as a continuous measure of metabolic equivalents in minutes/week (MET-min/week). Our primary exposure of interest was HIV serostatus. We fit univariable and multivariable linear regression models to estimate the relationship between HIV and PA levels, with and without addition of sociodemographic and clinical correlates of PA (MET-min/week). In secondary analyses, we explored relationships restricted to rural residents, and interactions between gender and serostatus.

Results: We enrolled 309 participants, evenly divided by serostatus and gender. The mean age of PWH was 52 [standard deviation (SD) 7.2] and 52.6 (SD 7.3) for PWOH. In general, participants engaged in high levels of PA regardless of serostatus, with 81.2% (251/309) meeting criteria for high PA. However, PWOH reported higher mean levels of PA met-minutes/week than PWH (9,128 vs 7,152, p ≤ 0.001), and a greater proportion of PWOH (88.3%; 136/154) met the criteria for high PA compared to PWH (74.2%; 115/155). In adjusted models, lower levels of PA persisted among PWH (β = −1,734, 95% CI: −2,645, −824, p ≤ 0.001). Results were similar in a sensitivity analysis limited to people living in rural areas.

Conclusion: In a rural Ugandan cohort, PWOH had higher levels of PA than PWH. Interventions that encourage PA among PWH may have a role in improving NCD risk profiles among PWH in the region.

Introduction

Antiretroviral therapy (ART) has led to a narrowing gap in life expectancy between people with HIV and people without HIV (1, 2). As AIDS-related mortality has decreased, people with HIV are at increasing risk of non-communicable diseases (NCDs), including cardiovascular disease (CVD) (35). In the global north, people with HIV have been observed to have a 1.5- to 2-fold greater risk of CVD than people without HIV (5). A combination of determinants is thought to cause this increased risk, including traditional CVD risk factors (6), HIV-specific factors such as chronic immune activation and inflammation (7, 8), ART-related dyslipidemia and other metabolic comorbidities (9, 10), behavioural factors such as smoking and physical inactivity (1113) and inequalities in access to health care (1416). A particular concern is the effect of modern ART regimens, such as dolutegravir- to cause significant increases in weight, especially when in combination with tenofovir alafenamide fumarate (17).

The rising tide of CVD morbidity among people with HIV necessitates exploration of scalable interventions that can help improve health, particularly in high-burden HIV endemic settings. There is an abundance of evidence showing the health-related benefits of physical activity (PA) in the general population, including decreasing the risk of CVD among people with HIV (18). Physical activity has multiple benefits, including reducing many modifiable CVD risk factors that are increased because of HIV infection and/or treatment (19, 20). For example, benefits of PA in CVD risk reduction include elevated serum HDL-C, decreased triglycerides and total cholesterol (21, 22), and a reduction in BMI, waist-to-hip ratio, and total body fat (23). People with HIV who regularly engage in PA also have significantly lower advanced glycation end products, lower waist circumference (WC) (24), and less lipodystrophy than non-active people with HIV (25). In people with HIV, PA has been beneficial for maintaining good health (26), improving metabolic profiles and cardiorespiratory fitness (27), maintaining lean muscle tissue, improving cardiopulmonary function and immune status, enhancing quality of life (28), controlling inflammation, and improving cardio-metabolic health (27, 29).

However, despite the numerous known benefits of PA for people with HIV and for CVD risk reduction, and its potential as a focus of health interventions, there is little data on PA levels among people in HIV endemic settings, particularly in sub-Saharan Africa. There is substantial inter- and intra-regional variation in PA, and PA also differs significantly by social determinants (3033). Furthermore, since HIV serostatus presents unique barriers to PA among rural or underserved people with HIV (34), comparing PA levels and determinants to people without HIV will also be a crucial step towards designing PA interventions for this population.

Thus, our overarching aim was to describe the distribution and determinants of PA in a cohort of adult people with HIV on ART and age-matched people without HIV in Uganda. We additionally aimed to explore how PA differs by demographic and cardiometabolic factors, and whether these factors confound relationships with HIV serostatus. We hypothesize that people with HIV engage in lower levels of PA and lower intensity PA than people without HIV and that, women, individuals who are older, those with higher blood pressure and HbA1c ≥ 7 and of low educational attainment, wealth quartile and living in an urban location will also engage in less PA.

Materials and methods

Population and study design

The UGANDAC study was a longitudinal observational cohort study of people with HIV in ambulatory HIV care in Mbarara, Uganda, and a group of age- and gender-matched people without HIV comparators (NCT 02445079) (35). The objective of the study was to test hypotheses related to associations between HIV and NCD risk, including cardiovascular and pulmonary disease, in an HIV-endemic setting in sub-Saharan Africa in an aging population. Thus, our study uses a population of people aged 40 years of age and older. To be included in the study, people with HIV had to meet the following criteria: (1) in ambulatory care at the Immune Suppression Syndrome Clinic at Mbarara Regional Referral Hospital, (2) age ≥40 years and (3) duration of ART use ≥3 years (36, 37). After enrolment of people with HIV, age and gender-matched people without HIV comparators living in the clinic catchment area were recruited from their homes using a population census. Since this was a longitudinal study, for this study we use data from visit one (i.e., first year of the study). The only data which we carried forward were for wealth quartile since this data only started to be collected in visit two (i.e., in the second year of the study). Since this was a secondary data analysis from a parent cohort study. The parent study was initially powered to test for a difference in the progression of carotid intima media thickness by HIV serostatus in Uganda (35). In keeping with best practices, a post-hoc power calculation was not conducted for this analysis, given their known pitfalls and strong recommendations from experts in the field not to be undertaken in this scenario (38).

Data collection

Trained study nurses conducted interviews between December 2013 and May 2018 to capture sociodemographic data, history of CVD diagnosis and its management, CVD risk factors (including, hypertension, diabetes mellitus, atherosclerosis and dyslipidemia) (39). Study nurses also measured weight using standardized scales (seca 762, Hanover, USA) and height using roll-up measuring stadiometers (seca 206, Hanover, USA) (39). Height was measured to the nearest 0.1 cm and weight was measured to the nearest kilogram (39). Height and weight were then used to calculate body mass (BMI) as weight (in kilograms) divided by the square of height (in meters), and categorized BMI as underweight (30 kg/m2), normal weight (18.5–24.9 kg/m2), overweight (25–29.9 kg/m2), or obese (>30 kg/m2) (39). Bilateral, resting blood pressure was collected using automated digital upper arm sphygmomanometers (Omron Healthcare Inc., Bannockburn, USA) with small (<21 cm), normal (22 cm–32 cm), and large cuffs (35 cm–44 cm). This was done with participants seated in a chair and allowed to rest for 5 min. The average of the measurements from both arms was used to determine the blood pressure of each participant (39). Blood for HBA1c testing was collected using Siemens Vantage A1c testing kits (Siemens Medical Solutions USA, Malvern, PA) (40). To measure relative wealth in our study population, we collected data on ownership of assets as described previously and used in Demographic Health Surveys across the region (41). In summary, we used principal component methods and selected the first principal component applied to multiple binary indicators for household-owned assets (e.g., bicycle, radio) and housing characteristics (e.g., type of toilet facilities, water source). We then constructed four quartiles from this variable to enable relative and interpretable comparisons in wealth (lowest, low, high, highest) within the cohort.

Physical activity, the primary outcome of this study was assessed using an adapted version of the International Physical Activity Questionnaire (IPAQ) short form, which was developed to assess PA across all domains of leisure-time, work, transportation, and household tasks (42). It has been previously validated compared to PA (43). Specifically, a study that collected reliability and validity data on the IPAQ short form showed that its reliability is within acceptable levels with 75% of correlation coefficients observed above 0.65 (44). Similarly, using a total of 781 adults, fair to moderate agreement between the IPAQ short form data against accelerometers was shown in the same study (pooled correlation coefficient 0.3 (95% CI: 0.23–0.36) (44). Respondents report frequency and duration of walking, moderate-intensity and vigorous-intensity activity performed for at least 10 min duration per session. Our adapted questionnaire captured PA relating to activities of daily living such as work and travel-related PA which were specific to the Ugandan rural population context. As such, activities which were captured were a combination of aerobic and anaerobic activity of low and moderate-to-vigorous intensity.

Statistical analysis

We analysed the first visit for each participant with available data on PA. Descriptive statistics were used to summarize sociodemographic (age, sex, educational attainment, wealth quartile, and residential location) and clinical factors (blood pressure, HbA1c, and BMI) by HIV serostatus. These were reported as mean [standard deviation (SD)] or median and interquartile range (IQR) for continuous variables and as frequencies (n and percent) for categorical variables. Measures of association by HIV serostatus were computed using non-parametric log-rank testing for continuous variables and Pearson chi squared testing for categorical variables.

Our outcome of interest was PA. To estimate PA levels, we first calculated the weekly minutes of walking, moderate-intensity and vigorous-intensity activity by multiplying the number of days/weeks by the duration on an average day. Reported minutes per week in each category were weighted by a metabolic equivalent (MET; multiples of resting energy expenditure) resulting in a PA estimate independent of body weight, expressed in MET-minutes/week and calculated by multiplying METs by minutes/week (44). Physical activity was defined in two ways: (1) for our primary analysis we considered PA as a continuous variable (MET-minutes/week) and (2) for a pre-specified secondary analysis, we dichotomized PA into high PA versus low or moderate PA. To do so, we used standardized criteria (42), in which we considered walking to be 3.3 METS, moderate PA to be 4 METS and vigorous PA to be 8 METS and 2) categorized as “low” (physically inactive), “moderate” and “high” physical activity, based on the following definitions: Low: Meets neither ‘moderate’ nor ‘high’ criteria; Moderate: Meets any of the following three criteria: (a) 3 days of vigorous activity of at least 20 min/day; (b) 5 days of moderate-intensity activity or walking of >30 min/day for >10 min at a time; or (c) 5 days of any combination of walking, moderate-intensity or vigorous-intensity activities achieving at least 600 MET-minutes/week; High: Meets either of two criteria: (a) vigorous-intensity activity on >3 days/week and accumulating at least 1,500 MET-minutes/week; or (b) >5 days of any combination of walking, moderate-intensity, or vigorous-intensity activities achieving at least 3,000 MET-minutes/week. We adapted the questionnaire to reflect the rural Ugandan context. In the adapted PA questionnaire, vigorous activities included cutting or carrying wood, cutting crops, shovelling, grinding or pounding millet, or digging. Moderate physical activities included carrying water or a load on your head while walking, scrubbing, washing clothes, or tending animals. These activities were categorised according to the compendium of physical activities.

For our primary analysis we considered PA as a continuous measure of MET-minutes/week. We fitted univariable and multivariable linear regression models, with HIV as the primary exposure of interest, with and without additional confounding variables, including sociodemographic (age, gender, educational attainment, residential location, and wealth quartile) and clinical factors (HbA1c, blood pressure, and BMI). We used purposeful selection (45) in the regression model and included all items in the univariable model with a p-value of <0.25 in the multivariable model and included HIV in both models a priori because it was our primary explanatory variable of interest. In pre-specified secondary analyses, we then repeated these steps, but with analysis restricted to individuals living in rural areas because most people without HIV participants in the cohort were recruited from a rural location. We also repeated these steps to identify those with the highest level of PA, by dichotomizing PA as either high or low as the outcome of interest and fitting logistic regression models to assess associations with HIV and the same confounding variables as above. Further, analysis was also done to identify correlates of PA with interaction terms on gender and serostatus. All analyses were conducted using Stata version 16 (College Station, TX).

Ethical considerations

Study procedures were reviewed and approved by the Institutional Review Board of Mass General Brigham (2014P001928) and the Research Ethics Committee of the Mbarara University of Science and Technology (06/04–14). All participants gave written informed consent. Permission to conduct this secondary data analysis was also granted by the University of KwaZulu Natal Biomedical Research Ethics Committee (BREC/00003396/2021).

Results

Study population

Sociodemographic, PA and clinical factors of participants are summarized in Table 1. Of the 309 participants in our study, approximately half (155/309, 50%) of the participants were people with HIV and the cohort was nearly evenly divided by sex [158/309 (51%) male]. Most participants had primary or less education (255/309, 83%) and most lived in a rural residential location (263/309; 85%). People with HIV tended to have higher asset ownership, with a greater proportion of people in the highest quartile (34% vs 13%) and lower proportion of people in the lowest quartile (20% vs 32%) of asset ownership (p < 0.001). Most participants had a HbA1c < 7, which was similar for people with HIV and people without HIV. The mean systolic and diastolic blood pressures for people with HIV were 114 [standard deviation (SD) 20] and 71.6 (SD 12) respectively whilst that for people without HIV was 120 (SD 18) and 76 (SD 12), respectively. In terms of BMI, a greater proportion (43/155, 28%) of people with HIV were in the overweight/obese BMI category, compared to 37/154, 24% in people without HIV, even though the proportions were statistically similar. In terms of PA, both people with HIV (115/155, 74%) and people without HIV (136/154, 88%), had a greater proportion of people reporting high PA than low or moderate PA and this proportion was higher in people without HIV. For people with HIV, the median CD4 was 458 cell/ml (IQR: 336–559), whilst 86% had a suppressed viral load.

TABLE 1
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Table 1. Cohort sociodemographic and clinical characteristics.

Distributions of physical activity by serostatus

In general, the study cohort engaged in high levels of PA, with 81.2% (251/309) meeting criteria for high PA (Figure 1). When we compared PA by HIV serostatus, we found that the mean number of metabolic equivalents/weeks was higher in people without HIV than people with HIV (9,128 vs 7,152, p ≤ 0.001), and that a greater proportion of people without HIV (88.3%; 136/154) met the criteria for high PA category compared to people with HIV (74.2%; 115/155, Figure 2A and Table 1). The higher level of PA seen in people without HIV was present in both males and females, across strata of age, and across strata of BMI (Figures 2B–D).

FIGURE 1
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Figure 1. Categorical physical activity level stratified by serostatus, gender, age, and BMI.

FIGURE 2
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Figure 2. Distribution of physical activity level, stratified by (A) serostatus (B) gender (C) age (D) BMI.

In unadjusted models, having secondary and greater education (β = −1,967, 95% CI: −3,340, −595, p = 0.005), living in an urban location (β = −2,223, 95% CI: −3,632, −814, p = 0.002), being in the middle (β = −1,531, 95% CI: −2,748, −313, p = 0.014) or highest quartile of asset ownership (β = −3,934, 95% CI: −5,179, −2,690, p < 0.001), having a higher mean diastolic blood pressure (β = −450, 95% CI: −841, −68, p = 0.021), and being HIV positive (β = −19,76, 95% CI: −2,876, −1,076, p < 0.001) were significantly associated with lower PA levels (Table 2). In multivariable models, female sex remained significantly associated with higher PA levels (β = 931, 95% CI: 49, 1,813, p = 0.039), as did being in the highest quartile of asset ownership (β = −3,054, 95% CI: −44,348, −1,760, p < 0.001), having a higher mean diastolic blood pressure (β = −416, 95% CI: −790, −42, p = 0.030) and being HIV-positive (β = −1,734, 95% CI: −2,645, −824, p ≤ 0.001) (Table 2). These results were similar in a sensitivity analysis limited to people living in rural areas (Supplementary Table S1).

TABLE 2
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Table 2. Univariable and multivariable linear regression models to identify sociodemographic and clinical correlates of physical activity in people with and without HIV.

When we considered PA as a categorical variable, with high PA as the outcome, we found that having secondary or greater education (OR = 0.40, 95% CI: 0.19, 0.84, p = 0.015), living in an urban location (OR = 0.42, 95% CI: 0.19, 0.92, p = 0.030), having the highest quartile of asset ownership (OR = 0.11, 95% CI: 0.04, 0.29, p < 0.001), and being HIV-positive (OR = 0.38, 95% CI: 0.21, 0.70, p = 0.002) were each 50–90 percent lower odds of high physical activity (Table 3). In adjusted models, being in the highest quartile of asset ownership (OR = 0.12, 95% CI: 0.04, 0.34, p < 0.001) remained associated with an approximately 90% lower odds of having high physical activity (Table 3). We did not find evidence of interaction by gender, age, or BMI in models that included interaction terms for each of these (Supplementary Table S2).

TABLE 3
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Table 3. Univariable and multivariable logistic regression models to identify correlates of high physical activity in rural Uganda.

Discussion

In an observational cohort study from Uganda, including people with HIV on ART and age and gender-matched people without HIV from the same community, we found that people without HIV reported higher mean levels of PA energy expenditure compared to people with HIV and that a greater proportion of people without HIV met criteria for high levels of PA than people with HIV. These results remained consistent after adjusting for gender, age, BMI, and cardiovascular disease risk factors, as well as in a sub-sample limited to residents of rural areas. This finding holds relevance in the context of growing reports of CVD as a primary cause of morbidity and mortality among people with HIV globally (46). Although our data were collected prior to the integrase-inhibitor era, they remain relevant in light of an increasing obesity epidemic among people with HIV taking dolutegravir (47). If confirmed in other settings, these findings signal a need for consideration of PA counselling and behaviour change interventions for people with HIV in the region to help realize the multifaceted beneficial impacts of PA on health for this population (27).

Despite the reported benefits of PA for people with HIV in terms of improving metabolic profile, quality of life (27), and functional status (48), studies of people with HIV in sub-Saharan Africa (SSA) have generally demonstrated poor engagement in PA to improve health (49). Indeed, our finding that most people with HIV engage in less PA compared to people without HIV is consistent with the findings of most other studies conducted in SSA (5054). Although our study did not explore perceptions or behaviours related to PA, we hypothesize that the observed lower levels of PA among people with HIV may be attributed to context-specific barriers to PA among people with HIV. Other studies in the region have suggested that HIV-related symptoms and medications, community safety, depression, cultural beliefs, lack of knowledge about PA and motivation to engage in PA, and fear of negative physical effects of exercise (34, 55) all may be contributors. With sizeable increases in obesity reported among people with HIV taking integrase-inhibitors based therapies (56), future studies should better elucidate the barriers and facilitators of PA among people with HIV in Uganda to assist in design of interventions to promote PA among people with HIV.

There were a number of secondary findings of interest in our study. For example, we found that the study cohort engaged in comparatively high levels of PA regardless of serostatus. This finding is consistent with a national survey of PA data collected as part of a Ugandan national NCD risk factor analysis, which found that 73% of rural participants had high levels of PA, largely achieved through travel and work-related activities (57). Residing in a rural location has also been found to be associated with higher odds of active transportation (58) and intense agricultural activities and manual work as part of employment (59). We similarly found lower levels of PA among urban-dwelling residents compared to rural-dwelling residents in unadjusted models, although the effect was dampened after adjustment for confounders. A number of studies conducted elsewhere in sub-Saharan Africa have also reported increased PA among rural populations (6063). However, notably, this pattern is not consistent throughout the continent. For example, in South Africa, individuals in urban settings were more likely to engage in moderate PA than rural participants (64), whilst (65) reported that being from a rural formal location reduced the prospect of engaging in vigorous PA. Similar relationships have also been reported outside the African continent (66), and may support the presence of distinct relationships in urbanicity and PA, by broader socioeconomic status.

We also found that female gender was associated with higher PA levels. We hypothesize that the relationship between female gender and PA is due to our study setting in a largely rural area, and high dependence on the agricultural sector for food (67), in a setting where women contribute the highest share of labour (67). Additionally, in many African countries, rural women often are charged with domestic chores, such as collecting water and firewood, processing and preparing food, travelling, and transporting, and caregiving (68). Notably, our results contrast with numerous studies conducted elsewhere in SSA who report that women engage in less PA compared to men (50, 51, 6265, 6972). This may be in part, due to some studies only reporting specific domains of PA such as frequency, intensity, and duration (Craft et al., 2014), and not reporting PA as a whole. For example (64), investigated the prevalence and socio-demographic correlates of PA among adults in urban and rural communities in South Africa, specifically reports that women were less likely to engage in vigorous PA and does not report the low and moderate PA.

Similarly, we observed that people with greater wealth had lower levels of PA. This is in contrast with studies who typically report that individuals of higher socioeconomic status (SES) engage in more PA than those of low SES (e.g.,) (65, 7376). In general, evidence suggests a positive relationship between an individual's economic resources and PA. However, it has recently been suggested that the observed positive relationship between higher SES and PA is mainly a relationship between leisure-time PA and SES, and may be unique of high-income settings (77). By contrast, in our low-income setting, we suspect the opposite relationship may be driven by inherent PA requirements to participation in an agrarian economy (57).

Finally, we found an association between higher diastolic blood pressure and lower levels of PA. Physical inactivity is a risk factor for development of hypertension (78). Moreover, the beneficial effects of PA on hypertension and reduction in both systolic and diastolic blood pressure are well documented (7983). Thus, the relationship here is not unexpected, and highlights the need for context-specific PA interventions to help improve CVD risk prevention in this region.

Our study should be interpreted in the context of its limitations. We conducted a cross-sectional analysis, as such causal inference cannot be made. We also used a self-reported measure of PA, which may be prone to social desirability bias and less accurate than some objective measures, such as motion sensors. The IPAQ scale is also meant to be a quantitative measure to estimate the magnitude of PA undertaken, but does not provide contextual information about the types of activities being taken (e.g., aerobic versus anaerobic or PA for pleasure versus occupation). Future work should better describe types of and preferences for PA undertaken by PWH to promote intervention development. Comparisons with other studies are limited due to a paucity of research comparing PA and its correlates between people with HIV and people without HIV in sub-Saharan Africa. Finally, given that about half of our study sample were females of menopausal age, adverse health effects that frequently accompany the menopausal transition, such as increases in body weight and mood changes must be considered when interpreting their PA levels.

In summary, this study highlights differences in PA levels between people with HIV and people without HIV. In particular, the development of effective PA interventions, may entail first understanding the factors that facilitate and hinder PA participation, including those that may be unique to people with HIV in rural locations such as HIV-infection related barriers, those that are a consequence of ART, and socioeconomic factors. Most importantly, the emergence of NCDs among people with HIV also calls for an understanding of NCD risk factors among this population and the use of PA as an adjunct therapeutic measure to minimise these risk factors and prevent NCDs. Future studies are recommended to focus on both PA intensity and PA domain so that researchers are able to develop domain-specific interventions.

Data availability statement

The datasets presented in this article are not readily available because this study was a secondary analysis of data. Requests to access the datasets should be directed to mark.siedner@ahri.org.

Ethics statement

The studies involving human participants were reviewed and approved by Institutional Review Board of Mass General Brigham (2014P001928) and the Research Ethics Committee of the Mbarara University of Science and Technology (06/04–14). Permission to conduct this secondary data analysis was also granted by the University of KwaZulu Natal Biomedical Research Ethics Committee (BREC/00003396/2021). The patients/participants provided their written informed consent to participate in this study.

Author contributions

SM and MS: contributed to the conception, design, and statistical analysis of the first draft of the manuscript. SM wrote the first draft of the manuscript. JM-G and MH contributed to the conception and design of the study. BP, JK, RS, LH, and SO contributed to the manuscript revision. All authors contributed to the article and approved the submitted version.

Funding

This study was funded by the US National Institutes of Health (P30AI060354; R21HL124712; R01HL141053; R24AG044325; P30AG024409). MJS reports additional support from K24 HL166024. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Acknowledgment

The authors would like to thank Alexander Tsai, for his contribution in the parent study and the staff at the Immune Suppression Syndrome (ISS) clinic and the Uganda Non-Communicable Diseases and Aging Cohort study staff, including: Alan Babweteera, Zulaika Namboga, Sheila Abaasabyoona, and Doreen Kyomuhendo.

Conflict of interest

The reviewer [CS] declared a shared affiliation with the authors [MH, MJS] to the handling Editor at the time of review.

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.

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.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/frph.2023.1093298/full#supplementary-material

Supplemental Table 1
Multivariable linear regression models to identify sociodemographic and clinical correlates of physical activity in people with and without HIV restricted to individuals living in rural areas

Supplemental Table 2
Multivariable linear regression models to identify sociodemographic and clinical correlates of physical activity in people with and without HIV living with interaction terms on sex, BMI, age, mean diastolic blood pressure and serostatus

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Keywords: physical activity, HIV, correlates, cardiovascular disease, socioeconomic status

Citation: Mabweazara SZ, Manne-Goehler J, Bibangambah P, Kim J-H, Ruth S, Hemphill LC, Okello S, Hamer M and Siedner MJ (2023) Correlates of physical activity among people living with and without HIV in rural Uganda. Front. Reprod. Health 5:1093298. doi: 10.3389/frph.2023.1093298

Received: 8 November 2022; Accepted: 7 June 2023;
Published: 20 July 2023.

Edited by:

Stephen Ojiambo Wandera, Makerere University, Uganda

Reviewed by:

Caroline Sabin, Institute for Global Health, University College London, United Kingdom
Leah Helane Rubin, Johns Hopkins University, United States
Hellen Myezwa, University of the Witwatersrand, South Africa

© 2023 Mabweazara, Manne-Goehler, Bibangambah, Kim, Ruth, Tsai, Hemphill, Okello, Hamer and Siedner. 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: Smart Z. Mabweazara smart.mabweazara@ahri.org

Disclaimer: 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.