Fasting lipid profile of HIV-infected children on antiretroviral therapy living in an area of prolonged armed conflict
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Abstract
Background. Armed conflict of over a decade in north-eastern Nigeria has led to interrupted access to antiretroviral therapy (ART) among HIV-positive children in this region.
Objective. To determine the prevalence of lipid abnormalities among HIV-positive children on ART in an area experiencing prolonged armed conflict.
Methods. This descriptive cross-sectional study involved 249 children aged 2 - 15 years on ART presenting at the University of Maiduguri Teaching Hospital between April 2021 and March 2022. Sociodemographic and clinical characteristics were obtained through a questionnaire, while serum lipid levels were determined from blood samples.
Results. Dyslipidaemia was found in 63.1% of the study sample. Hypertriglyceridaemia was the most prevalent abnormality (38.6%), followed by hypercholesterolaemia (32.3%), high levels of low-density lipoprotein cholesterol (24.9%) and low levels of high-density lipoprotein cholesterol (21.3%). Significant associations were found between dyslipidaemia and prolonged ART (>5 years) (p<0.001), increasing clinical disease stage (p=0.031) and use of protease inhibitors (p=0.016). All patients whose treatment had been interrupted (n=55) owing to the conflict experienced treatment failure and were switched to protease inhibitor-based regimens, although treatment interruption was not significantly associated with dyslipidaemia.
Conclusion. Almost two-thirds of the study sample (63.1%) presented with dyslipidaemia. We recommend a pragmatic strategy to ensure continuation of treatment in a conflict zone and routine determination of fasting serum lipid profiles in HIV-positive children, especially those who have been on ART for 5 years or more, patients receiving protease inhibitors, and children whose disease has progressed to stage II or beyond.
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References
1. Veenstra N, Whiteside A, Lalloo D, Gibbs A. Unplanned antiretroviral treatment interruptions in southern Africa: How should we be managing these? Global Health 2010;6:4.
2. Vreeman R, Nyandiko W, Sang E, Musick B, Braitstein P, Wiehe S. Impact of the Kenya postelection crisis on clinic attendance and medication adherence for HIV-infected children in western Kenya. Confl Health 2009;3:5.
3. Loewenberg S. Famine fears in northeast Nigeria as Boko Haram fight rages. Lancet 2017;389:352.
4. WHO. HIV/AIDS -Disease Burden. WHO 2021. https://www.afro.who.int/ health-topics/hivaids (accessed 5 August 2025).
5. Joint United Nations Programme of HIV/AIDS. Global HIV Statistics – Fact Sheet 2021. https://embargo.unaids.org/static/files/uploaded_files/UNAIDS_2021_ factsheet_en_em.pdf (accessed 5 August 2025).
6. Statista. People living with HIV in Nigeria in 2021. Statista, 2021. https://www. statista.com/statisticss/1128675/people-living-with-hiv-receiving-treatment- in-nigeria/
7. Irira EM, Rune NP, Joshua YM, et al. Dyslipidaemia in HIV-infected children and adolescents on antiretroviral therapy receiving care at Kilimanjaro Christian Medical Centre in Tanzania: A cross-sectional study. Infect Dis (Auckl) 2020;13:1178633720948860.
8. Mandal A, Mukherjee A, Lakshmy R, Kabra SK, Lodha R. Dyslipidaemia in HIV infected children receiving highly active antiretroviral therapy. Indian J Pediatr 2016;83:226-231.
9. Kanjanavanit S, Puthanakit T, Vibol U, et al. High prevalence of lipid abnormalities among antiretroviral-naive HIV-infected Asian children with mild-to moderate immunosuppression. Antivir Ther 2011;16(8):1351-1355.
10. Viljoen E, MacDougall C, Mathibe M, Veldman F, Mda S. Dyslipidaemia among HIV-infected children on antiretroviral therapy in Garankuwa, Pretoria. S Afr J Clin Nutr 2019;33(3):1-8.
11. Aliu-Isah O, Hassan-Hanga F, Yahaya I, Oyelami O, Aikhionbare H. The prevalence and risk factors for dyslipidaemia in human immunodeficiency virus-infected children on highly active antiretroviral therapy in Kano, Nigeria. Ann Afri Med Res 2020;3. https://doi.org/10.4081/aamr.2020.103
12. Blazquez D, Ramos-Amador JT, Sainz T, et al. Lipid and glucose alterations in perinatally-acquired HIV-infected adolescents and young adults. BMC Infect Dis 2015;15:119.
13. Santiprabhob J, Tanchaweng S, Maleesatharn S, et al. Metabolic disorders in HIV-infected adolescents receiving protease inhibitors. Biomed Res Inter 2017:7481597.
14. Innes S, Abdullah KL, Haubrich R, Cotton MF, Browse SH. High prevalence of dyslipidaemia and insulin resistance in HIV-infected prepubertal African children on antiretroviral therapy. Pediatr Infect Dis J 2016;35(1)::e1-7.
15. Tadesse BT, Foster BA, Chala A, et al. HIV and cART-associated dyslipidaemia among HIV-infected children. J Clin Med 2019;(8):430.
16. Nampijja D, Kumbakumba E, Bajunirwe F, Kiwanuka J. Dyslipidaemia and its correlates among HIV infected children on HAART attending Mbarara Regional Referral Hospital. Int Clin Pathol J 2017;4(3):00098.
17. Dejkhamron P, Unachak K, Aurpibul L, Sirisanthana V. Insulin resistance and lipid profiles in HIV-infected Thai children receiving lopinavir/ritonavir- based highly active antiretroviral therapy. J Pediatr Endocrinol Metab 2014;27(5-6):403-412.
18. Padmapriyadarsini C, Shet A, Srinivasan R, et al. High prevalence of lipid abnormalities and insulin resistance among antiretroviral naive HIV-infected children in India. Pediatr Infect Dis J 2018;37(3):253-257.
19. Jao J, Yu W, Patel K, et al. Improvement in lipids after switch to boosted atazanavir or darunavir in children/adolescents with perinatally acquired HIV on older protease inhibitors: Results from the Pediatric HIV/AIDS Cohort Study. HIV Med 2018;19(3):175-183.
20. Hammond CK, Eley B, Wieselthaler N, Ndondo A, Wilmshurst JM. Cerebrovascular disease in children with HIV-1 infection. Dev Med Child Neurol 2016;58:452-460.
21. Dapena M, Jiménez B, Noguera-Julian A, Soler-Palacín P, Fortuny C, Lahoz R, et al. Metabolic disorders in vertically HIV-infected children: Future adults at risk for cardiovascular disease. J Pediatr Endocrinol Metab 2012;25:529-535.
22. Babayemi OO, Daniel AA, Sabastine SW, Tolulope TO, Chamberlin E. Quantification of the effect of terrorism on the HIV response in Nigeria. Lancet 2018;391(10127):1257-1258.
23. Mann M, Lurie MN, Kimaiyo S, Kantor R. Effects of political conflict induced treatment interruption on HIV drug resistance. AIDS Rev 2013;15(1):15-24.
24. Gardner EM, Burman WJ, Steiner JF, Anderson PL, Bangsberg DR. Antiretroviral medication adherence and the development of class-specific antiretroviral resistance. AIDS 2009;23:1035-1046.
25. Federal Ministry of Health. National guidelines for HIV prevention, treatment and care – National AIDS and STIs control programme. Abuja: Federal Ministry of Health, 2016.
26. Federal Ministry of Health. National guidelines for HIV prevention, treatment and care – National AIDS and STIs control programme. Abuja: Federal Ministry of Health, 2020.
27. Cochrane WG. Sampling Technique. 2nd edition, New York: John Wiley and Sons; 1963.
28. Ige OO, Yilgwan CS, Ebonyi OA, et al. Serum lipid and glucose profiles in HIV- positive Nigerian children. J Virus Erad 2017;3:157-162.
29. Oyedeji GA. Socio-economic and cultural background of hospitalised children in Ilesha. Nig J Paediatr 1995;1:111-117.
30. Kranzer K, Lewis JJ, Ford N, et al. Treatment interruption in a primary care antiretroviral therapy programme in South Africa: Cohort analysis of trends and risk factor. J Acquir Immune Defic Syndr 2010;55(3):e17-23. https://doi. org/10.1097/OAI.0b013e3181f275fd
31. World Health Organization. Guide to physical measurement. The WHO STEPS Surveillance Manual. Geneva: WHO, 2014. https://cdn.who.int/ media/docs/default-source/ncds/ncd-surveillance/steps/part3-section5. pdf ?sfvrsn=a46653c7_2
32. World Health Organization. WHO AnthroPlus Software. Geneva: WHO, 2007.
https://www.who.int/tools/growth-reference-data-for-5to19-years/application-
tools
33. Croft TN, Aileen MJM, Courtney KA, et al. 2018.Nutritional status in: Guide to DHS Statistics, DHS-7(version 2). Rockville, Maryland, USA: ICF, 2018:11.50-11.58. https://www.dhsprogram.com/pubs/pdf/DHSG1/Guide_to_DHS_statistics_ DHS7_V2.pdf
34. Fossati P, Prencipe L. Serum triglycerides determined colorimetrically with an enzyme that produces hydrogen peroxide. Clin Chem 1982;28(10):2077-2080. 35. Friedwald WT, Levy RI, Fredrickson DS. Estimation of the concentration
of low-density lipoprotein cholesterol in plasma, without the use of the
preparative ultracentrifuge. Clin Chem 1972;18(6):499-502.
36. Expert Panel on Integrated Guidelines for Cardiovascular Health and Risk Reduction in Children and Adolescents, National Heart, Lung, and Blood Institute. Expert panel on integrated guidelines for cardiovascular health and risk reduction in children and adolescents: Summary report. Pediatrics
2011;128 Suppl 5: S213-S256.
37. Okechukwu AA, Lawson J, Dalilo M. Dyslipidemia in HIV infected children
and adolescents on highly active antiretroviral therapy in Abuja, Nigeria. J Adv
Med Med Res 2017;24(3):1-11.
38. Dressman J, Kincer J, Matveev SV, et al. HIV protease inhibitors promote
atherosclerotic lesion formation independent of dyslipidaemia by increasing CD36-dependent cholesteryl ester accumulation in macrophages. J Clin Invest 2003;111(3):389-397.
39. Paganella MP, Cohen RA, Harris DR, et al. Association of dyslipidemia and glucose abnormalities with antiretroviral treatment in a cohort of HIV-infected Latin American children. J Acquir Immune Defic Syndr 2017;74(1):e1-8.
40. Calza L, Manfredi R, Chiodo F. Hyperlipidaemia in patients with HIV-1 infection receiving highly active antiretroviral therapy: Epidemiology, pathogenesis, clinical course and management. Int J Antimicrob Agents 2003;22(2):89-99.
41. Rhoads MP, Lanigan J, Smith CJ, Hermione EG. Effect of specific ART drugs on lipid changes and the need for lipid management in children with HIV. J Acquir Immune Defic Syndr 2011;57:404-412.