- Research article
- Open Access
Low prevalence of lipodystrophy in HIV-infected Senegalese children on long-term antiretroviral treatment: the ANRS 12279 MAGGSEN Pediatric Cohort Study
BMC Infectious Diseases volume 18, Article number: 374 (2018)
The long-term benefits of antiretroviral treatment (ART) are associated with metabolic complications, especially lipodystrophy, which has been well described among HIV-infected adults and children on ART in developed settings. Specifically, stavudine, and to a lesser extent zidovudine and protease inhibitors (PI), have been consistently implicated in the development of lipodystrophy. In 2006, following advice from the WHO, Senegal began phasing out stavudine from first-line ART. The objectives of this cross-sectional analysis are to assess and identify risk factors affecting the prevalence of lipodystrophy in Senegalese children and adolescents on long-term ART participating in a cohort study.
Lipodystrophy was clinically assessed in two- to 18-year-old children on ART for at least six months and with no concurrent severe acute malnutrition. Risk factors for lipodystrophy were identified using stepwise multivariable logistic regression. Explanatory variables included clinical and personal data, immunovirologic status, and therapeutic history.
Overall, 254 children were assessed for lipodystrophy. The median age was 10.9 years (IQR: 8.1–14.2) and the median duration on ART was 54 months (32–84). Only 18% had been previously treated with stavudine, with a median treatment duration of 8 months (5–25). Ongoing treatment included 76% of children receiving zidovudine (median duration of 48 months (26–74)) and 27% receiving PI (lopinavir/ritonavir; median duration of 49 months (23–59)). Mild signs of lipodystrophy were observed in 33 children (13%): 28 with lipoatrophy, 4 with lipohypertrophy and one with combined type. Boys were more likely to present with lipoatrophy than girls (aOR: 4.3, 95% CI: 1.6–11.7). Children previously treated with stavudine for ≥1 year had a greater risk for lipoatrophy than those never exposed (3.8, 1.0–14.0), although the association was weak. There was no association between lipodystrophy and age or current or cumulative treatment with lopinavir/ritonavir or zidovudine.
We report low prevalence of mild lipodystrophy in children and adolescents on long-term ART receiving a stavudine-sparing regimen. These findings are reassuring for clinicians in low-income settings where zidovudine is massively prescribed and lopinavir/ritonavir is the only widely available PI.
The long-term benefits of antiretroviral treatment (ART) are associated with metabolic complications, especially lipodystrophy, which has been well described among HIV-infected adults and children on ART. Lipodystrophy diagnosis involves changes in regional fat distribution, including peripheral fat loss (lipoatrophy), central fat accumulation (lipohypertrophy), or a combination of both. Because lipodystrophy, and in particular the potentially disfiguring effects of lipoatrophy, may negatively affect treatment adherence and effectiveness , such effects are of major concern in children and adolescents who may require life-long ART.
In studies published over the past decade, the prevalence of lipodystrophy in children receiving ART has ranged widely, from 10 to 84% [2,3,4,5,6,7,8,9], depending on the detection method. Stavudine, and to a lesser extent zidovudine, both of which are thymidine-analogue nucleoside reverse transcriptase inhibitors (NRTI), have consistently been associated with lipoatrophy, affecting between 8 to 28% of children, after 2–5 years of treatment [2, 3, 7, 10]. Protease inhibitors (PI) have been previously implicated in the development of both fat loss and accumulation [11, 12], thus complicating the study of risk factors, as these drugs may be administered together. Lastly, lipodystrophy development is likely multifactorial, including other risk factors, such as puberty [5, 6, 13], ethnicity [2, 3], HIV disease progression [3, 8] and host factors .
Compared to high to middle-income settings, much less is known about lipodystrophy in African children and especially adolescents. Two recent cross-sectional studies in Uganda and Tanzania reported mild lipoatrophy in 27%  and 30%  of children aged one to 18 years, after substantial stavudine exposure. Conversely, moderate to severe lipoatrophy was reported in 36% of prepubescent South African children following a median treatment duration of 41 months with stavudine . Data on fat distribution abnormalities among HIV-infected children and adolescents in other regions of Africa are unavailable.
A 2006 World Health Organization (WHO) report highlighted stavudine-associated toxicities and advised that stavudine be substituted with abacavir in patients with lipoatrophy . In response, from 2007 to 2008 the Senegalese National Program phased out stavudine from first-line pediatric treatment. Due to the prohibitive cost of abacavir, most children were switched to zidovudine. Thereafter, stavudine was used sparingly until 2012, due to lack of alternative options in some patients or as a substitution drug for six months in children with severe anemia. In 2015, it was estimated that 4800 (4000–5600) children aged 0 to 14 years were living with HIV in Senegal, of whom 26% (19–31%) were receiving ART .
The ANRS 12279 Maggsen Pediatric Cohort Study aims to investigate growth and metabolic disorders among HIV-infected Senegalese children and adolescents on long-term ART and under active follow-up at the country’s two earliest and most important pediatric HIV clinics, Albert Royer and Roi Baudouin Hospitals, which account for 30% of all children on ART at the country level. Our present objectives are to characterize and assess the prevalence of lipodystrophy and to identify risk factors in cross-sectional analyses conducted at mid-term of the cohort study.
Full details of the rationale for the Maggsen Pediatric Cohort Study and methods are provided elsewhere . Briefly, the study includes HIV-1-infected children aged two to < 16 years under active follow-up in two Senegalese HIV clinics from April 2013. Children were seen every three months for a complete clinical assessment, and every six months for laboratory monitoring/fasting blood analyses. The present cross-sectional analysis includes study patients under active follow-up from May to December 2015, who had at least six months on ART. As it might be difficult to distinguish between lipoatrophy and wasting syndrome, children experiencing severe acute malnutrition were excluded from the analysis. Severe acute malnutrition is defined for both weight-for-height z scores (WHZ) in children < 5 years or body mass index-for-age z score (BMIZ) in children ≥5 years as being <− 3 [20, 21].
In May 2015, four pediatricians at the clinics (three from Albert Royer Hospital and one from Roi Baudouin Hospital) received practical and collective training for lipodystrophy diagnosis followed by clinical assessment of 102 children in the cohort. These sessions were conducted and supervised by a senior researcher and pediatrician (SB) experienced in pediatric lipodystrophy, who was both blind to children’s ART regimen and independent from the cohort study. Diagnosis of the remaining children was then assigned to the permanent pediatrician at each site and performed when the children came to their scheduled visit. Lipoatrophy was defined as fat loss in one or more of the following sites: face, arm, leg, or buttocks. Lipohypertrophy was defined as fat gain in one or more of the following sites: abdomen, neck, or breast. Children with at least one sign of lipoatrophy and one sign of lipohypertrophy were defined as combined type . Body fat redistribution was rated as none – no fat changes; mild – possible minor changes, noticeable only on close inspection; moderate – moderate changes, readily noticeable to an experienced clinician or a close relative who knows the child well; severe – major changes, readily noticeable to a casual observer . Clinical assessment used a scoring sheet included in the child’s medical file. At Albert Royer Hospital, in case of doubt between a grade mild and a grade moderate, or a grade moderate and grade severe, the procedure was to require an additional diagnosis from another trained pediatrician and if discordant, to grade at the lower score. At Roi Baudouin Hospital, however, there was only one pediatrician in charge of HIV care and grades were assigned at their discretion.
Variables and definitions
Data recorded from medical files included WHZ or BMIZ scores, puberty onset (defined as a child reaching stage 2 of the Tanner classification ), WHO stage at ART initiation and therapeutic history, CD4 cell counts and viral load (undetectable defined as HIV RNA < 40 copies per milliliter), total cholesterol, LDL cholesterol and triglycerides. Dyslipidemia was defined as total cholesterol and/or isolated HDL and/or triglycerides abnormalities. Clinical and laboratory variables were those collected just prior to the lipodystrophy assessment visit (< 3 and < 6 months, respectively).
The primary outcomes investigated were fat redistribution (any form) and lipoatrophy. Children characteristics including, age, sex, puberty onset, nutritional status, WHO stage at ART initiation, stavudine, zidovudine and PI treatments and durations, CD4 count, virologic suppression and lipid profiles were compared with the primary outcomes. For each ART drug, recent drug treatment (defined as current treatment or treatment ending within the previous six months), any treatment (defined as drug ever used) and exposure duration were included as separate variables. Associations from univariable analyses were assessed using the Kruskal-Wallis and Wilcoxon rank-sum tests, Chi-square and Fisher’s exact, and univariable logistic regression, as appropriate. Risk factors for the primary outcomes were identified using a stepwise multivariable logistic regression. Explanatory variables with P < 0.25 in univariable analysis were included in the multivariable models and exited by the stepwise procedure at P ≥ 0.20. Continuous explanatory variables were categorized before entering the models.
Continuous variables are expressed as median with interquartile range (IQR). Odds ratios (OR) and adjusted OR (aOR) are given with their 95% confidence interval (CI) in univariable and multivariable analyses, respectively. Differences were considered statistically significant at P < 0.05. All statistical analyses were performed in SAS version 9.3 (SAS Institute, Cary, North Carolina, USA).
Ethics clearance for the cohort study was given by the Ethics and Regulatory Committees in Senegal and the Ethics Committee of the Institute of Research for Development in France. All parents or legal guardians provided written informed consent on behalf of their children. The cohort was registered with ClinicalTrials.gov: NCT01771562 on 01/18/2013.
Size and characteristics of the study population
Between May and December 2015, among 335 children included in the cohort, 323 were still in care in the study facilities. Of these, 42 children were on ART for less than six months and 27 presented with severe acute malnutrition. Therefore, the study population for this analysis comprised 254 patients (Table 1). The median age was 10.9 years (8.1–14.2). Overall, 74% of children were on first-line ART, 26% on second-line ART and one child was on third-line ART. There were no differences between boys and girls with regard to therapeutic and immunovirologic data, however, boys were more likely than girls to present moderate wasting (33% vs 14%, P = 0.0007) and prepubescent status (72% vs 50%, P = 0.0004).
Prevalence and characterization of fat redistribution
Overall, 33 cases (13%) of lipodystrophy were clinically reported, all in children older than five years of age. Signs of fat loss were observed in 28 children (11%), signs of fat accumulation in four children (2%), and only one child presented with combined type (Table 2). All signs of fat redistribution were graded “mild” (grade 1). While there is often inherent uncertainty in grading mild lipodystrophy, there were no examples of doubt in a clinical diagnosis between mild versus moderate (grade 2) or severe (grade 3) signs of lipodystrophy reported in the study.
In 28 children with signs of lipoatrophy, 22 presented with only prominent veins in the arms while the remaining six presented with additional signs of fat loss (six with sunken cheeks, two with prominent veins in the legs and two with sunken buttocks). Abdominal fat accumulation was present in the four children with lipohypertrophy. Fat redistribution was not associated with age categories (< 10 and ≥ 10 years) or any lipid abnormality.
Fat redistribution by treatment with ART drugs
Signs of lipodystrophy were weakly associated with prior treatment with stavudine and longer PI treatment duration (Table 3). Few children (18%) had been previously treated with stavudine and for a limited median treatment duration of 8 months (5–25). Stavudine treatment in these children could only have occurred at any time between September 2003 and November 2012, so that at enrollment in the cohort study, no child was still receiving stavudine. Almost all children had been treated with zidovudine, and 76% were currently receiving this ART drug in their backbone regimen, for a median treatment duration of 48 months (26–74). The median duration of current treatment with PI, essentially lopinavir/ritonavir (lopinavir/r), was 49 months (23–59). Treatment with other PI was marginal: six children had previously received a nelfinavir-based ART for a median duration of 61 months (53–87) and eight were currently treated with an atazanavir/ritonavir-based regimen.
Factors associated with lipoatrophy
To identify risk factors for lipoatrophy, we ran a stepwise logistic regression model with ‘lipoatrophy + combined type’ as the dependent variable. Univariable analyses identified sex, moderate wasting, exposure to stavudine (no vs. < 1 year vs. ≥ 1 year), and recent exposure to lopinavir/r (no vs. < 3 years vs. ≥ 3 years) for inclusion in the model (Table 4). Forcing age (< 10 years and ≥ 10 years) and moderate wasting (yes/no) to remain in the model did not change the results. Boys were more likely to present with lipoatrophy (aOR: 4.3, 95% CI: 1.6–11.7) than girls. Children exposed to stavudine for ≥1 year had a greater risk for lipoatrophy than those never exposed (aOR: 3.8, 95% CI: 1.0–14.0), although the association was weak. Results were similar from a model including all cases of lipodystrophy (n = 33).
The prevalence of clinical lipodystrophy was very low, 13%, in a cohort of HIV-infected Senegalese children and adolescents on ART for a median duration of 54 months. First, we observed only mild signs of lipodystrophy, by definition corresponding strictly to possible minor changes. Second, prior treatment with stavudine was limited in this Senegalese cohort, regarding both the proportion of children concerned, 18%, and the duration on treatment, eight months on average. However, children previously treated with stavudine for more than one year were at greater risk to present with possible sign(s) of lipoatrophy than those never exposed. Most studies are based on clinical examination for fat redistribution, which might be subjective. Some have coupled clinical assessment with various objective techniques including skin-fold thickness, dual energy X-ray absorptiometry (DEXA) and magnetic resonance imaging. These methods are prohibitively expensive and/or complex, if not unavailable, for routine use in low-income settings. Clinical assessment of fat redistribution in HIV-infected children is further complicated by the normal, dynamic alterations in body shape and composition occurring during childhood and adolescence. Hence some studies have considered only grades moderate to severe, because of uncertainty in providing a definitive diagnosis of mild grade lipodystrophy. Acknowledging the inherent uncertainty in the diagnosis of the mild grade, we found no instance of doubt in clinical diagnosis between mild versus moderate or severe signs of lipodystrophy.
There is overwhelming evidence that lipoatrophy is an adverse drug reaction to stavudine, with potential mechanisms including mitochondrial damage in adipocytes and inhibition of adipogenesis [24, 25]. Recent southern African studies reporting on the association between lipodystrophy and stavudine treatment in children are conflicting. Innes et al. found an alarmingly high prevalence, 36%, of moderate to severe lipoatrophy in prepubescent South African children after a median treatment duration of 41 months on stavudine . They also reported that current treatment with stavudine was the predominant risk factor for lipoatrophy, as well as finding a cumulative effect, by year of exposure, on arm fat loss. Studies in Uganda and Tanzania reported lipodystrophy in 27% (mostly lipoatrophy, of all grades) and 30% (mostly mild lipoatrophy) of children aged two to 18 years [13, 15]. In the Ugandan study, involving children with a median of 3.8 years on ART of whom 20% had an ongoing exposition to stavudine, risk factors identified were older age, puberty onset and any exposure to stavudine . Similarly, the Tanzanian study reported older age and longer exposure to stavudine as predictors of lipodystrophies in children under current exposure to stavudine for approximatively 3 years . In 2012, most African children were still receiving stavudine-based ART. Thus a distinguishing feature between these studies and ours is the context of long-term and ongoing exposure to stavudine.
The effect of stavudine in causing lipoatrophy appears to be strongly dose-related . The CHAPAS-3 trial, where stavudine was notably prescribed at lower doses  than in the previously cited studies, reported only 1% of lipodystrophy (lipoatrophies grade 2 and 3) in children previously treated with stavudine for a median of 3 years and randomized to continue with a stavudine-based regimen over 96 weeks .
In recent years, WHO reiterated recommendations for countries to phase out stavudine and today it is no longer considered in first-line options. Nonetheless, estimates suggest stavudine still contributed to between 7 to 9% of the NRTI procurement forecasted for pediatric use in low and middle-income countries in 2016 . The early promotion of stavudine-sparing first-line regimen in Senegal since 2007 certainly contributed to limiting the occurrence of lipoatrophy in this cohort.
It had been suggested that zidovudine, which like stavudine, is a thimidine-analogue NRTI, could also lead to lipodystrophy, although to a lesser extent [13, 15, 30]. Zidovudine treatment was predominant in these Senegalese children’s ART regimen, and our results are consistent with those of the ARROW trial which reported, three years after randomization to lamivudine+abacavir+zidovudine, an extremely low rate of mainly mild lipoatrophy in children aged three to 19 years of less than 2% . In that study, the use of stavudine (as a first-line substitution) and protease inhibitor (as second line) was minimal. In addition, substitution of stavudine with zidovudine significantly decreased severity or promoted resolution of mild to moderate lipoatrophy in HIV-infected Thaï children after 96 weeks  or more . In the present study, thirty months had passed since the date of last individual exposure to stavudine and inclusion in the assessment. We suspect that a process of reversal of lipodystrophy figures occurred in this cohort. Together, these results provide reassurance on the substantially lower potential of zidovudine for lipoatrophy, in settings where stavudine has been massively replaced by zidovudine in first-line treatment.
The first generation of PI has also been associated with fat redistribution, both loss [12, 34, 35] and accumulation [11, 36, 37] in adults, and with similarly conflicting results in children [5, 7, 9, 38,39,40]. However, the role played by ART, and especially by the PI, in the pathogenesis of lipohypertrophy is less clear. The most accepted hypothesis is that PI impair adipocyte differentiation resulting in hypertrophy of adipose tissue, particularly in visceral tissue [2, 9, 12]. Although past and current exposure to lopinavir/r was substantial in this cohort, we did not find an association with lipodystrophy in multivariable analysis.
Ultimately, male sex was the main risk factor for lipoatrophy in the cohort. Boys were more likely to present with moderate wasting and a prepubescent status than girls at the time of the evaluation. Having excluded children with severe wasting from our study population, moderate wasting remained at rather high level, particularly among adolescents, and is consistent with figures reported from a recent study conducted in similar context in Mali . Explanations for persistent wasting in the Senegalese adolescents on ART may lie in a therapeutic history of drug resistance development and late switch to second-line ART , a potentially high level of household food insecurity  and a substantial level of undernutrition in the general school population of the Dakar suburbs . However, wasting was not associated with lipoatrophy in either univariable or multivariable analyses.
Some studies in high to middle-income countries reported that females were more likely to develop lipodystrophy than males [3, 7, 44]. In those settings, lipohypertrophy and combined type were more common than lipoatrophy. In recent studies reporting a high prevalence of lipoatrophy, sex was not identified as an independent risk factor [3, 15, 16]. Boys accumulate less subcutaneous fat mass than girls during childhood  and adolescence . In addition, boys might have looked generally thinner than girls in this cohort. Combined, such considerations could have influenced the clinical assessment towards an overestimation of lipoatrophy in boys and/or under diagnosis in girls.
Lipodystrophies are frequently associated with metabolic disturbances, presented as a lipodystrophic syndrome . It is recognized that PI may induce dyslipidemia, which may increase the risk of cardiovascular disease in adulthood [7, 38]. The rate of hypercholesterolemia was high, mainly led by elevated LDL-cholesterol, while hypertriglyceridemia was marginal in the cohort. As have others [13, 48], we found no association between lipodystrophy and dyslipidemia. Longitudinal analyses of blood lipid profile evolution are currently ongoing in the cohort (data not shown).
This study has several limitations. First, our cross-sectional study design does not allow for controlling the trend in evolution of reported lipodystrophy cases. However, the temporality of data, as well as the children’s profiles, suggest that the risk for an increase in prevalence or a development towards more severe forms of lipoatrophy are unlikely. Second, due to the small number of fat redistribution cases, a limited number of explanatory variables could be included in the multivariable model and statistical power might be limited. Third, the number of patients not included in this ANRS study cohort due to death or being lost to follow-up before enrollment is unknown, and the results might primarily apply to patients who remained in care.
We report low prevalence of mild lipodystrophy in children and adolescents on long-term ART with limited exposure to stavudine. The responsiveness of the national Senegalese HIV programme to the 2007 WHO recommendations to phase out stavudine due to concerns over treatment toxicity, presumably helped to prevent the occurrence and/or the progression of lipodystrophy in these HIV-infected children and adolescents. Moreover, we found that consistent exposure to lopinavir/r and zidovudine did not lead to such adverse drug reaction in our cohort. These findings bring a reassuring message to clinicians in low-income settings where zidovudine is still massively prescribed in the NRTI backbone combination of pediatric ART and lopinavir/r is the most widely available PI.
adjusted odds ratio
Body mass index for age z-score
Non nucleoside reverse transcriptase inhibitor
Nucleoside/nucleotide reverse transcriptase inhibitor
World health organization
Weight for height z-score
Duran S, et al. Failure to maintain long-term adherence to highly active antiretroviral therapy: the role of lipodystrophy. AIDS. 2001;15(18):2441–4.
Beregszaszi M, et al. Longitudinal evaluation and risk factors of lipodystrophy and associated metabolic changes in HIV-infected children. J Acquir Immune Defic Syndr. 2005;40(2):161–8.
Alam N, et al. Body fat abnormality in HIV-infected children and adolescents living in Europe: prevalence and risk factors. J Acquir Immune Defic Syndr. 2012;59(3):314–24.
Vigano A, et al. Increased lipodystrophy is associated with increased exposure to highly active antiretroviral therapy in HIV-infected children. J Acquir Immune Defic Syndr. 2003;32(5):482–9.
Taylor P, et al. Natural history of lipid abnormalities and fat redistribution among human immunodeficiency virus-infected children receiving long-term, protease inhibitor-containing, highly active antiretroviral therapy regimens. Pediatrics. 2004;114(2):e235–42.
Jaquet D, et al. Clinical and metabolic presentation of the lipodystrophic syndrome in HIV-infected children. AIDS. 2000;14(14):2123–8.
European Paediatric Lipodystrophy Group. Antiretroviral therapy, fat redistribution and hyperlipidaemia in HIV-infected children in Europe. AIDS. 2004;18(10):1443–51.
Arpadi SM, et al. Lipodystrophy in HIV-infected children is associated with high viral load and low CD4+ -lymphocyte count and CD4+ -lymphocyte percentage at baseline and use of protease inhibitors and stavudine. J Acquir Immune Defic Syndr. 2001;27(1):30–4.
Ene L, et al. Prevalence of lipodystrophy in HIV-infected children: a cross-sectional study. Eur J Pediatr. 2007;166(1):13–21.
Hartman K, et al. Detection of lipoatrophy in human immunodeficiency virus-1-infected children treated with highly active antiretroviral therapy. Pediatr Infect Dis J. 2006;25(5):427–31.
Kotler DP. HIV lipodystrophy etiology and pathogenesis. Body composition and metabolic alterations: etiology and pathogenesis. AIDS Read. 2003;13(4 Suppl):S5–9.
Martinez E, Gatell J. Metabolic abnormalities and use of HIV-1 protease inhibitors. Lancet. 1998;352(9130):821–2.
Piloya T, et al. Lipodystrophy among HIV-infected children and adolescents on highly active antiretroviral therapy in Uganda: a cross sectional study. J Int AIDS Soc. 2012;15(2):17427.
Zanone Poma B, et al. Genetic polymorphisms differently influencing the emergence of atrophy and fat accumulation in HIV-related lipodystrophy. AIDS. 2008;22(14):1769–78.
Kinabo GD, et al. Prevalence of lipodystrophy in HIV-infected children in Tanzania on highly active antiretroviral therapy. Pediatr Infect Dis J. 2013;32(1):39–44.
Innes S, et al. High prevalence of lipoatrophy in pre-pubertal South African children on antiretroviral therapy: a cross-sectional study. BMC Pediatr. 2012;12:183.
WHO, Antiretroviral therapy for HIV infection in adults and adolescents. Recommendations for a public health approach. Geneva: World Health Organization; 2006.
UNAIDS. Country factsheets Senegal. 2016 [cited 2018 05/05/2018]; Available from: http://www.unaids.org/fr/regionscountries/countries/senegal.
Cames C, et al. Risk Factors for Growth Retardation in HIV-Infected Senegalese Children on Antiretroviral Treatment: The ANRS 12279 MAGGSEN Pediatric Cohort Study. Pediatr Infect Dis J. 2017;36(4):e87–e92.
WHO. Child growth standards: WHO Anthro (version 3.2.2, January 2011) and macros. 2006 [cited 2012 07/30/2012]; Available from: http://www.who.int/childgrowth/software/en/.
WHO. Growth reference 5–19 years: WHO Anthro Plus software and macros. 2007 [cited 2012 07/30/2012]; Available from: http://www.who.int/growthref/tools/en/.
Carr A, et al. An objective case definition of lipodystrophy in HIV-infected adults: a case-control study. Lancet. 2003;361(9359):726–35.
Tanner JM. Growth at adolescence. Oxford: Blackwell Scientific; 1962. 325 p.
Hammond E, McKinnon E, Nolan D. Human immunodeficiency virus treatment-induced adipose tissue pathology and lipoatrophy: prevalence and metabolic consequences. Clin Infect Dis. 2010;51(5):591–9.
Mallal SA, et al. Contribution of nucleoside analogue reverse transcriptase inhibitors to subcutaneous fat wasting in patients with HIV infection. AIDS. 2000;14(10):1309–16.
Hill A, et al. Systematic review of clinical trials evaluating low doses of stavudine as part of antiretroviral treatment. Expert Opin Pharmacother. 2007;8(5):679–88.
WHO, Consolidated guidelines on the use of antiretroviral drugs for treating and preventing HIV infection. Recommendations for a public health approach. 2013: Geneva.
Mulenga V, et al. Abacavir, zidovudine, or stavudine as paediatric tablets for African HIV-infected children (CHAPAS-3): an open-label, parallel-group, randomised controlled trial. Lancet Infect Dis. 2015;
WHO. Antiretroviral medicines in low- and middle-income countries: forecasts of global and regional demand for 2013–2016. Geneva: World Health Organization; 2014.
de Waal R, Cohen K, Maartens G. Systematic review of antiretroviral-associated lipodystrophy: lipoatrophy, but not central fat gain, is an antiretroviral adverse drug reaction. PLoS One. 2013;8(5):e63623.
Bwakura-Dangarembizi M, et al. Prevalence of lipodystrophy and metabolic abnormalities in HIV-infected African children after 3 years on first-line antiretroviral therapy. Pediatr Infect Dis J. 2015;34(2):e23–31.
Aurpibul L, et al. Recovery from lipodystrophy in HIV-infected children after substitution of stavudine with zidovudine in a non-nucleoside reverse transcriptase inhibitor-based antiretroviral therapy. Pediatr Infect Dis J. 2012;31(4):384–8.
Sawawiboon N, et al. Lipodystrophy and reversal of facial lipoatrophy in perinatally HIV-infected children and adolescents after discontinuation of stavudine. Int J STD AIDS. 2012;23(7):497–501.
Carr A, et al. Pathogenesis of HIV-1-protease inhibitor-associated peripheral lipodystrophy, hyperlipidaemia, and insulin resistance. Lancet. 1998;351(9119):1881–3.
Domingo P, et al. Subcutaneous adipocyte apoptosis in HIV-1 protease inhibitor-associated lipodystrophy. AIDS. 1999;13(16):2261–7.
Brown TT, et al. Longitudinal increases in waist circumference are associated with HIV-serostatus, independent of antiretroviral therapy. AIDS. 2007;21(13):1731–8.
Sax PE, Kumar P. Tolerability and safety of HIV protease inhibitors in adults. J Acquir Immune Defic Syndr. 2004;37(1):1111–24.
Arpadi S, et al. Metabolic abnormalities and body composition of HIV-infected children on Lopinavir or Nevirapine-based antiretroviral therapy. Arch Dis Child. 2013;98(4):258–64.
Dos Reis LC, et al. Anthropometry and body composition of vertically HIV-infected children and adolescents under therapy with and without protease inhibitors. Public Health Nutr. 2014;18(7):1255–61.
Ramalho LC, et al. Abnormalities in body composition and nutritional status in HIV-infected children and adolescents on antiretroviral therapy. Int J STD AIDS. 2011;22(8):453–6.
Jesson J, et al. Evaluation of a Nutritional Support Intervention in Malnourished HIV-Infected Children in Bamako, Mali. J Acquir Immune Defic Syndr. 2017;76(2):149–57.
Cames C, et al. Acceptability of Outpatient Ready-To-Use Food-Based Protocols in HIV-Infected Senegalese Children and Adolescents Within the MAGGSEN Cohort Study. Food Nutr Bull. 2017;38(1):27–36.
Fiorentino M, et al. Anthropometric and micronutrient status of school-children in an urban West Africa setting: a cross-sectional study in Dakar (Senegal). PLoS One. 2013;8(12):e84328.
Aurpibul L, et al. Lipodystrophy and metabolic changes in HIV-infected children on non-nucleoside reverse transcriptase inhibitor-based antiretroviral therapy. Antivir Ther. 2007;12(8):1247–54.
Fomon SJ, et al. Body composition of reference children from birth to age 10 years. Am J Clin Nutr. 1982;35(5 Suppl):1169–75.
Haschke F. In: Klish WJ, Kretchmer N, editors. Body composition during adolescence, in Body composition measurements in infants and children - Report of the 98th Ross Conference on Pediatric Research. Colombus Ohio: Ross Laboratories; 1989. p. 76–82.
McComsey GA, Leonard E. Metabolic complications of HIV therapy in children. AIDS. 2004;18(13):1753–68.
Innes S, et al. High Prevalence of Dyslipidemia and Insulin Resistance in HIV-infected Prepubertal African Children on Antiretroviral Therapy. Pediatr Infect Dis J. 2016;35(1):e1–7.
We would like to thank all the participating children and their caregivers.
The ANRS 12279 MAGGSEN Cohort Study Group.
Centre Hospitalier National d’Enfants Albert Royer, Dakar, Senegal:
Haby, Sy Signate; Aminata, Diack; Helene, Mbodj; Ndeye Fatou, Diallo; Aissata, Ba; Aicha, Dia; Ndeye Ngone, Have; Astou, Dieye; Oumy, Fall; Rosine, Sonko.
Synergie pour l’Enfance/Centre Hospitalier Roi Baudouin, Guediawaye, Senegal:
Ngagne, Mbaye; Baly, Ouattara; Abdou, K, Niang; Alhadji, B, Diom; Adama, Ndour; Bigue, Badiane.
Institut de Recherche pour le Développement, Montpellier, France: Cecile, Cames; Lea, Pascal; Philippe, Msellati; Caroline, Desclaux Sall; Suzanne, Izard.
Centre de Recherche et de Formation à la Prise en Charge Clinique, Dakar, Senegal: Amady, Ndiaye; Ousseynou, Ndiaye; Binta, Seck.
Financial support was provided by the Agence Nationale de Recherche sur le SIDA et les hépatites virales (ANRS). The ANRS had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Availability of data and materials
The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.
Ethics approval and consent to participate
Ethics clearance for the cohort study was given by the Ethics and Regulatory Committees in Senegal (Ministry of Health) and the Ethics Committee of the Institute of Research for Development in France. All parents or legal guardians provided written informed consent on behalf of their children.
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The authors declare that they have no competing interests.
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Cames, C., Pascal, L., Ba, A. et al. Low prevalence of lipodystrophy in HIV-infected Senegalese children on long-term antiretroviral treatment: the ANRS 12279 MAGGSEN Pediatric Cohort Study. BMC Infect Dis 18, 374 (2018). https://doi.org/10.1186/s12879-018-3282-7
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