MacCann Rachel, Li Junhui, Leon Alejandro Abner Garcia, Negi Riya, Alalwan Dana, Tinago Willard, McGettrick Padraig, Cotter Aoife G, Landay Alan, Sabin Caroline, O'Toole Paul W, Mallon Patrick W G
School of Medicine, University College Dublin.
Department of Infectious Diseases, St Vincent's University Hospital.
J Infect Dis. 2025 Apr 15;231(4):e781-e791. doi: 10.1093/infdis/jiaf043.
Inflammation and innate immune activation are associated with chronic human immunodeficiency virus (HIV) infection, despite effective treatment. Although gut microbiota alterations are linked to systemic inflammation, their relationship with HIV infection the relationships between the gut microbiome, inflammation, and HIV remains unclear.
The HIV UPBEAT Coronary Artery Disease sub-study evaluated cardiovascular disease (CVD) in people with and without HIV. Subclinical CVD was assessed using coronary computed tomography angiography (CCTA). Thirty-four biomarkers were measured using quantitative immunoassays. Stool samples underwent 16S rRNA sequencing. Differentially abundant species were identified by analysis of compositions of microbiomes with bias correction (ANCOM-BC) and correlated to biomarkers, diet, and CCTA outcomes using Spearman correlation.
Among 81 participants (median age, 51 years; 73% male), people with HIV (n = 44) had higher rates of hypercholesterolemia (P < .025). Gut microbiome β-diversity differed significantly by HIV status. Enriched Bifidobacterium pseudocatenulatum, Megamonas hypermegale, and Selenomonas ruminantium correlated with lower plaque burden, while depleted Ruminococcus bromii correlated with higher plaque burden and fat intake. Depleted Bacteroides spp and Alistepes spp correlated with elevated biomarkers (D-dimer, CD40 ligand, C-reactive protein, and interferon-γ).
Gut microbiota differences in people with HIV were linked to subclinical CVD, diet, and inflammation, highlighting the microbiome's role in cardiovascular risk in HIV infection.
尽管有有效的治疗方法,但炎症和先天免疫激活与慢性人类免疫缺陷病毒(HIV)感染相关。虽然肠道微生物群的改变与全身炎症有关,但其与HIV感染之间的关系,以及肠道微生物组、炎症和HIV之间的关系仍不清楚。
HIV乐观冠状动脉疾病子研究评估了有无HIV感染者的心血管疾病(CVD)。使用冠状动脉计算机断层扫描血管造影(CCTA)评估亚临床CVD。使用定量免疫测定法测量34种生物标志物。粪便样本进行16S rRNA测序。通过偏差校正微生物组组成分析(ANCOM-BC)确定差异丰富的物种,并使用Spearman相关性将其与生物标志物、饮食和CCTA结果相关联。
在81名参与者(中位年龄51岁;73%为男性)中,HIV感染者(n = 44)的高胆固醇血症发生率更高(P <.025)。肠道微生物组的β多样性因HIV状态而异。丰富的假链双歧杆菌、巨大巨单胞菌和反刍月形单胞菌与较低的斑块负荷相关,而减少的布鲁氏瘤胃球菌与较高的斑块负荷和脂肪摄入相关。减少的拟杆菌属和阿里斯特佩斯属与生物标志物(D-二聚体、CD40配体、C反应蛋白和干扰素-γ)升高相关。
HIV感染者的肠道微生物群差异与亚临床CVD、饮食和炎症有关,突出了微生物组在HIV感染心血管风险中的作用。