Recent abacavir use and incident cardiovascular disease in contemporary-treated people with HIV

医学 阿巴卡韦 优势比 四分位间距 内科学 比率 肾脏疾病 置信区间 队列 危险系数 入射(几何) 队列研究 心肌梗塞 人类免疫缺陷病毒(HIV) 免疫学 病毒载量 抗逆转录病毒疗法 物理 光学
作者
Nadine Jaschinski,Lauren Greenberg,Bastian Neesgaard,José M. Miró,Katharina Grabmeier‐Pfistershammer,Gilles Wandeler,Colette Smith,Stéphane De Wit,Ferdinand Wit,Annegret Pelchen‐Matthews,Cristina Mussini,Antonella Castagna,Christian Pradier,Antonella d’Arminio Monforte,Jörg Janne Vehreschild,Anders Sönnerborg,Alain Volny Anne,Andrew Carr,Loveleen Bansi‐Matharu,Jens Lundgren
出处
期刊:AIDS [Lippincott Williams & Wilkins]
卷期号:37 (3): 467-475 被引量:18
标识
DOI:10.1097/qad.0000000000003373
摘要

Assessing whether the previously reported association between abacavir (ABC) and cardiovascular disease (CVD) remained amongst contemporarily treated people with HIV.Multinational cohort collaboration.RESPOND participants were followed from the latest of 1 January 2012 or cohort enrolment until the first of a CVD event (myocardial infarction, stroke, invasive cardiovascular procedure), last follow-up or 31 December 2019. Logistic regression examined the odds of starting ABC by 5-year CVD or chronic kidney disease (CKD) D:A:D risk score. We assessed associations between recent ABC use (use within the past 6 months) and risk of CVD with negative binomial regression models, adjusted for potential confounders.Of 29 340 individuals, 34% recently used ABC. Compared with those at low estimated CVD and CKD risks, the odds of starting ABC were significantly higher among individuals at high CKD risk [odds ratio 1.12 (95% confidence interval = 1.04-1.21)] and significantly lower for individuals at moderate, high or very high CVD risk [0.80 (0.72-0.88), 0.75 (0.64-0.87), 0.71 (0.56-0.90), respectively]. During 6.2 years of median follow-up (interquartile range; 3.87-7.52), there were 748 CVD events (incidence rate 4.7 of 1000 persons-years of follow up (4.3-5.0)]. The adjusted CVD incidence rate ratio was higher for individuals with recent ABC use [1.40 (1.20-1.64)] compared with individuals without, consistent across sensitivity analyses. The association did not differ according to estimated CVD (interaction P = 0.56) or CKD ( P = 0.98) risk strata.Within RESPOND's contemporarily treated population, a significant association between CVD incidence and recent ABC use was confirmed and not explained by preferential ABC use in individuals at increased CVD or CKD risk.

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