Factors Affecting High-density Lipoprotein Cholesterol in HIV-infected Patients on Nevirapine-based Antiretroviral Therapy
Overview
Authors
Affiliations
Background & Objectives: Cardiovascular disease (CVD) risk with low high-density lipoprotein cholesterol (HDL-C) and high triglycerides is common in the general population in India. As nevirapine (NVP)-based antiretroviral therapy (ART) tends to increase HDL-C, gene polymorphisms associated with HDL-C metabolism in HIV-infected adults on stable NVP-based ART were studied.
Methods: A cross-sectional study was conducted between January 2013 and July 2014 among adults receiving NVP-based ART for 12-15 months. Blood lipids were estimated and gene polymorphisms in apolipoprotein C3 (APOC3), cholesteryl ester transfer protein (CETP) and lipoprotein lipase (LPL) genes were analyzed by real-time polymerase chain reaction. Framingham's 10-yr CVD risk score was estimated. Logistic regression was done to show factors related to low HDL-C levels.
Results: Of the 300 patients included (mean age: 38.6±8.7 yr; mean CD4 count 449±210 cell/μl), total cholesterol (TC) >200 mg/dl was observed in 116 (39%) patients. Thirty nine per cent males and 47 per cent females had HDL-C levels below normal while 32 per cent males and 37 per cent females had TC/HDL ratio of 4.5 and 4.0, respectively. Body mass index [adjusted odds ratio (aOR)=1.70, 95% confidence interval (CI) 1.01-2.84, P=0.04] and viral load (aOR=3.39, 95% CI: 1.52-7.52, P=0.003) were negatively associated with serum HDL-C levels. The 10-yr risk score of developing CVD was 11-20 per cent in 3 per cent patients. Allelic variants of APOC3 showed a trend towards low HDL-C.
Interpretation & Conclusions: High-risk lipid profiles for atherosclerosis and cardiovascular disease were common among HIV-infected individuals, even after 12 months of NVP-based ART. Targeted interventions to address these factors should be recommended in the national ART programmes.
Inflammatory and Immune Mechanisms for Atherosclerotic Cardiovascular Disease in HIV.
Hmiel L, Zhang S, Obare L, Santana M, Wanjalla C, Titanji B Int J Mol Sci. 2024; 25(13).
PMID: 39000373 PMC: 11242562. DOI: 10.3390/ijms25137266.
Human Immunodeficiency Virus as a Risk Factor for Cardiovascular Disease.
Lembas A, Zaleski A, Peller M, Mikula T, Wiercinska-Drapalo A Cardiovasc Toxicol. 2023; 24(1):1-14.
PMID: 37982976 PMC: 10838226. DOI: 10.1007/s12012-023-09815-4.
Jumare J, Dakum P, Sam-Agudu N, Memiah P, Nowak R, Bada F BMC Endocr Disord. 2023; 23(1):160.
PMID: 37507703 PMC: 10375691. DOI: 10.1186/s12902-023-01419-x.
Hamooya B, Musonda P, Mutale W, Masenga S, Halwiindi H, Mutengo K PLoS One. 2021; 16(2):e0247004.
PMID: 33592027 PMC: 7886128. DOI: 10.1371/journal.pone.0247004.
Chen Z, Liu Y, Wang H, Chen Z, Liu J, Liu H Food Sci Biotechnol. 2019; 28(2):519-528.
PMID: 30956864 PMC: 6431327. DOI: 10.1007/s10068-018-0466-2.