Genetic markers associated to dyslipidemia in HIV-infected individuals on HAART
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Updated: May 6, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Rosmeri K Lazzaretti1, Aline S Gasparotto, Marina G de M Sassi
1Serviço de Cardiologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, 90035-903 Porto Alegre, RS, Brazil.
Insights
Genetic factors significantly influence lipid levels in HIV patients on antiretroviral therapy (ART). Specific gene polymorphisms, including APOE and APOA5, are linked to dyslipidemia, suggesting genotyping may guide ART selection.
Area of Science:
- Genetics
- Cardiovascular Health
- Infectious Diseases
Background:
- Dyslipidemia is a common complication in HIV-infected patients undergoing antiretroviral therapy (ART).
- Genetic predisposition may play a role in lipid level variations among these patients.
Purpose of the Study:
- To investigate the association between single nucleotide polymorphisms (SNPs) in candidate genes and dyslipidemia in HIV-infected patients on stable ART.
- To identify specific genetic variants that impact lipid profiles (triglycerides, LDL-C, HDL-C) in this population.
Main Methods:
- Genotyping of 9 SNPs across 6 genes (APOB, APOA5, APOE, APOC3, SCAP, LDLR) in 614 HIV-infected patients.
- Analysis of associations between genotypes and lipid parameters (total cholesterol, LDL-C, HDL-C, triglycerides).
- Utilized conventional and real-time polymerase chain reaction (PCR) for SNP genotyping.
Main Results:
- High prevalence of dyslipidemia (79%) observed in patients treated with protease inhibitors.
- APOE genotypes (rs429358, rs7412) and APOA5 -1131T>C (rs662799) associated with triglyceride and LDL-C levels.
- APOA5 -1131T>C (rs662799) and SCAP 2386A>G (rs12487736) linked to HDL-C levels.
- APOB polymorphisms (rs17240441, rs693) associated with total cholesterol and LDL-C.
Conclusions:
- Genetic factors are crucial in determining lipid levels in HIV-infected individuals.
- The findings support the potential benefit of pre-treatment genotyping to guide the selection of personalized antiretroviral therapy (ART) regimens.
- Further studies are warranted to explore the clinical implications of these genetic associations for ART management.
Abstract:
This study evaluated the impact of 9 single nucleotide polymorphisms (SNPs) in 6 candidate genes (APOB, APOA5, APOE, APOC3, SCAP, and LDLR) over dyslipidemia in HIV-infected patients on stable antiretroviral therapy (ART) with undetectable viral loads. Blood samples were collected from 614 patients at reference services in the cities of Porto Alegre, Pelotas, and Rio Grande in Brazil. The SNPs were genotyped by conventional polymerase chain reaction (PCR) and real-time PCR. The prevalence of dyslipidemia was particularly high among the protease inhibitors-treated patients (79%). APOE (rs429358 and rs7412) genotypes and APOA5 -1131T>C (rs662799) were associated with plasma triglycerides (TG) and low-density-lipoprotein cholesterol levels (LDL-C). The APOA5 -1131T>C (rs662799) and SCAP 2386A>G (rs12487736) polymorphisms were significantly associated with high-density-lipoprotein cholesterol levels. The mean values of the total cholesterol and LDL-C levels were associated with both the APOB SP Ins/Del (rs17240441) and APOB XbaI (rs693) polymorphisms. In conclusion, our data support the importance of genetic factors in the determination of lipid levels in HIV-infected individuals. Due to the relatively high number of carriers of these risk variants, studies to verify treatment implications of genotyping before HAART initiation may be advisable to guide the selection of an appropriate antiretroviral therapy regimen.
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