Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Madrid, Spain.
Plataforma de Laboratorio, Hospital General Universitario "Gregorio Marañón", Madrid, Spain.
J Acquir Immune Defic Syndr. 2020 Dec 15;85(5):659-664. doi: 10.1097/QAI.0000000000002485.
HIV/AIDS progression is linked to vitamin D, which is regulated by several key cytochromes P450 (CYP). Single nucleotide polymorphisms (SNPs) in CYP genes influence vitamin D metabolism and serum levels. The objective of this study was to evaluate the association between CYP SNPs and the clinical AIDS progression in antiretroviral treatment (ART)-naïve HIV-infected patients.
We performed a retrospective study in 661 ART-naïve HIV-infected patients who were stratified by their AIDS progression pattern [181 long-term nonprogressors (LTNPs), 332 moderate progressors, and 148 rapid progressors (RPs)]. Four CYP SNPs (CYP2R1 rs10500804, CYP2R1 rs1993116, CYP27B1 rs10877012, and CYP24A1 rs6013897) were genotyped using Agena Bioscience's MassARRAY platform. Correction for multiple testing was performed using the false discovery rate (Benjamini-Hochberg procedure).
The adjusted regression showed a significant association only for CYP27B1 rs10877012 SNP. When analyzing all HIV patients, the rs10877012 T allele was protective against AIDS progression (ordinal outcome) under the dominant [adjusted odds ratio (aOR) = 0.69; P = 0.021) and additive (aOR) = 0.75; P = 0.025] inheritance models. When analyzing LTNPs versus RPs, the rs10877012 T allele also showed a significant protective association under the dominant (aOR = 0.45; P = 0.004) and additive (aOR = 0.54; P = 0.008) inheritance models. P values remained significant after correcting by multiple comparisons only for the comparison of LTNPs versus RPs (extreme phenotypes).
The CYP27B1 rs10877012 T allele was linked to non-AIDS progression in ART-naïve HIV-infected patients. The rs10877012 SNP seems to have an impact on the clinical AIDS progression, possibly modifying vitamin D levels, which could be relevant for the pathogenesis of HIV infection.
HIV/AIDS 的进展与维生素 D 有关,而维生素 D 又受到几种关键细胞色素 P450(CYP)的调节。CYP 基因中的单核苷酸多态性(SNP)会影响维生素 D 的代谢和血清水平。本研究旨在评估 CYP SNP 与未经抗逆转录病毒治疗(ART)的 HIV 感染者的临床 AIDS 进展之间的关系。
我们对 661 名未经 ART 治疗的 HIV 感染者进行了回顾性研究,这些患者根据 AIDS 进展模式进行分层[181 名长期非进展者(LTNPs)、332 名中度进展者和 148 名快速进展者(RPs)]。使用 Agena Bioscience 的 MassARRAY 平台对四个 CYP SNP(CYP2R1 rs10500804、CYP2R1 rs1993116、CYP27B1 rs10877012 和 CYP24A1 rs6013897)进行了基因分型。使用错误发现率(Benjamini-Hochberg 程序)对多重检测进行了校正。
调整后的回归分析仅显示 CYP27B1 rs10877012 SNP 存在显著相关性。在分析所有 HIV 患者时,rs10877012 T 等位基因在显性[调整优势比(aOR)=0.69;P=0.021]和加性(aOR)=0.75;P=0.025]遗传模型下对 AIDS 进展(有序结局)具有保护作用。在分析 LTNPs 与 RPs 时,rs10877012 T 等位基因在显性(aOR=0.45;P=0.004)和加性(aOR=0.54;P=0.008)遗传模型下也显示出显著的保护相关性。只有在 LTNPs 与 RPs 之间的比较中,经过多重比较校正后,P 值仍然具有统计学意义(极端表型)。
未经 ART 治疗的 HIV 感染者的 CYP27B1 rs10877012 T 等位基因与非 AIDS 进展相关。rs10877012 SNP 似乎对临床 AIDS 进展有影响,可能通过改变维生素 D 水平来影响 HIV 感染的发病机制。