Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York.
Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
JAMA Cardiol. 2019 Dec 1;4(12):1239-1249. doi: 10.1001/jamacardio.2019.4025.
Lipid metabolism disruption and excess risk of cardiovascular disease (CVD) have been observed in HIV-infected individuals, but the associations among HIV infection, plasma lipidome, and CVD risk have not been well understood.
To evaluate plasma lipidomic profiles and their associations with carotid artery atherosclerosis in individuals with HIV and individuals without HIV.
DESIGN, SETTING, AND PARTICIPANTS: Prospective analysis in the Women's Interagency HIV Study and Multicenter AIDS Cohort Study during a 7-year follow-up (from 2004-2006 to 2011-2013) at multicenter HIV cohorts in the United States. The study included 737 participants aged 35 to 55 years (520 with HIV and 217 without HIV) without CVD or carotid artery plaque at baseline. Data were analyzed between April 2017 and July 2019.
Two hundred eleven plasma lipid species.
Poisson regression was used to examine the associations of baseline lipid species with risk of plaque measured by repeated B-mode carotid artery ultrasonography imaging.
Of the 737 included participants, 398 (54%) were women, 351 (48%) were African American (non-Hispanic), 156 of 737 (21%) were nonwhite Hispanic, and the mean (SD) age was 45 (6) years. After adjusting for demographic and behavioral factors, we identified 12 lipid species, representing independent signals for 10 lipid classes, associated with risk of plaque. Nine lipid species remained significant after further adjusting for conventional CVD risk factors, although many of them showed moderate to high association with conventional blood lipids (eg, total and low-density lipoprotein cholesterols and triglycerides). Cholesteryl ester (16:1) (risk ratio [RR] per standard deviation, 1.28; 95% CI, 1.08-1.52), ceramide (16:0) (RR, 1.29; 95% CI, 1.02-1.63), lysophosphatidylcholine (20:4) (RR, 1.28; 95% CI, 1.05-1.58), lysophosphatidylethanolamine (16:0) (RR, 1.28; 95% CI, 1.05-1.57), phosphatidylethanolamine (38:6) (RR, 1.33; 95% CI, 1.08-1.64), phosphatidylethanolamine-plasmalogen (36:2) (RR, 1.25; 95% CI, 1.04-1.52), phosphatidylserine-plasmalogen (36:3) (RR, 1.19; 95% CI, 1.00-1.43), and triacylglycerol (54:6) (RR, 1.26; 95% CI, 1.04-1.54) were associated with increased risk of plaque, while phosphatidylcholine (36:4) (RR, 0.65; 95% CI, 0.54-0.77) was associated with decreased risk of plaque. Most of these plaque-increased lipid species showed higher levels in individuals with HIV, particularly among individuals with HIV using antiretroviral therapy compared with individuals without HIV. Network analysis identified 9 lipid modules, and 2 modules composed of triacylglycerols and phosphatidylcholines with long and unsaturated acyl chains, respectively, showed the strongest associations with increased risk of plaque.
This study identified multiple plasma lipid species associated with carotid artery atherosclerosis, and alterations in these lipid species might be associated with HIV infection and antiretroviral therapy. Our data suggest unfavorable associations of long-chain and unsaturated triacylglycerols and phosphatidylcholines with carotid artery plaque formation.
在感染 HIV 的个体中观察到脂质代谢紊乱和心血管疾病(CVD)风险增加,但 HIV 感染、血浆脂质组学和 CVD 风险之间的关联尚未得到很好的理解。
评估 HIV 感染者和未感染者的血浆脂质组谱及其与颈动脉粥样硬化的关系。
设计、地点和参与者:在美国多个 HIV 队列的多中心 AIDS 队列研究和妇女机构 HIV 研究中的前瞻性分析,在 7 年的随访期间(2004-2006 年至 2011-2013 年)进行。研究包括 737 名年龄在 35 至 55 岁之间的参与者(520 名 HIV 感染者和 217 名未感染者),基线时无 CVD 或颈动脉斑块。数据分析于 2017 年 4 月至 2019 年 7 月进行。
211 种血浆脂质种类。
泊松回归用于检查基线脂质种类与通过重复 B 型颈动脉超声成像测量的斑块风险之间的关联。
在纳入的 737 名参与者中,398 名(54%)为女性,351 名(48%)为非裔美国人(非西班牙裔),156 名(21%)为非白西班牙裔,平均(SD)年龄为 45(6)岁。在调整了人口统计学和行为因素后,我们确定了 12 种脂质种类,代表 10 种脂质类别的独立信号,与斑块风险相关。在进一步调整了传统 CVD 危险因素后,仍有 9 种脂质种类具有统计学意义,尽管其中许多与传统血脂(如总胆固醇和低密度脂蛋白胆固醇以及甘油三酯)具有中度至高度关联。胆固醇酯(16:1)(每标准差风险比[RR],1.28;95%CI,1.08-1.52)、神经酰胺(16:0)(RR,1.29;95%CI,1.02-1.63)、溶血磷脂酰胆碱(20:4)(RR,1.28;95%CI,1.05-1.58)、溶血磷脂酰乙醇胺(16:0)(RR,1.28;95%CI,1.05-1.57)、磷脂酰乙醇胺(38:6)(RR,1.33;95%CI,1.08-1.64)、磷脂酰乙醇胺-血小板(36:2)(RR,1.25;95%CI,1.04-1.52)、磷脂酰丝氨酸-血小板(36:3)(RR,1.19;95%CI,1.00-1.43)和三酰甘油(54:6)(RR,1.26;95%CI,1.04-1.54)与斑块风险增加相关,而磷脂酰胆碱(36:4)(RR,0.65;95%CI,0.54-0.77)与斑块风险降低相关。这些与斑块增加相关的脂质种类中,大多数在 HIV 感染者中水平较高,特别是在接受抗逆转录病毒治疗的 HIV 感染者中,与未感染 HIV 的个体相比。网络分析确定了 9 个脂质模块,分别由具有长链和不饱和酰基的三酰甘油和磷脂酰胆碱组成的 2 个模块与斑块风险增加呈最强关联。
本研究确定了与颈动脉粥样硬化相关的多种血浆脂质种类,这些脂质种类的改变可能与 HIV 感染和抗逆转录病毒治疗有关。我们的数据表明,长链和不饱和三酰甘油和磷脂酰胆碱与颈动脉斑块形成呈不利关联。