Kelso Natalie E, Sheps David S, Cook Robert L
a Department of Epidemiology , College of Public Health and Health Professions and College of Medicine, University of Florida , Gainesville , FL , USA.
Am J Drug Alcohol Abuse. 2015;41(6):479-88. doi: 10.3109/00952990.2015.1058812. Epub 2015 Jul 30.
People living with HIV-infection (PLWH) have higher prevalence and earlier onset of cardiovascular disease (CVD), compared to uninfected populations. It is unclear how alcohol consumption is related to CVD among PLWH.
To summarize the current literature and strength of evidence regarding alcohol consumption as a risk factor for CVD among PLWH, to generate summary estimates for the effect of alcohol consumption on CVD outcomes, and to make recommendations for clinical practice and future research based on the findings and limitations of existing studies.
A systematic review was conducted using Pubmed/Medline to identify relevant peer-reviewed articles published between 1 January 1999 and 1 January 2014. After critical review of the literature, 13 studies were identified. Risk ratios were extracted or calculated and sample size weighted summary estimates were calculated.
The prevalence of a CVD diagnosis or event ranged from 5.7-24.0%. The weighted pooled crude effect sizes were 1.75 (95% CI 1.06, 3.17) for general and 1.78 (95% CI 1.09, 2.93) for heavy alcohol use on CVD. The pooled adjusted effect size was 1.37 (95% CI 1.02, 1.84) for heavy alcohol use on CVD. Pooled estimates differed by CVD outcome and alcohol measure; alcohol consumption was most significant for cerebral/ischemic events.
HIV clinicians should consider risk factors that are not included in the traditional risk factor framework, particularly heavy alcohol consumption. Neglect of this risk factor may lead to underestimation of risk, and thus under-treatment among PLWH.
与未感染人群相比,感染人类免疫缺陷病毒(HIV)的人(PLWH)心血管疾病(CVD)的患病率更高且发病更早。目前尚不清楚饮酒与PLWH中的CVD之间的关系。
总结当前关于饮酒作为PLWH中CVD危险因素的文献和证据强度,对饮酒对CVD结局的影响进行汇总估计,并根据现有研究的结果和局限性为临床实践和未来研究提出建议。
使用PubMed/Medline进行系统综述,以识别1999年1月1日至2014年1月1日期间发表的相关同行评审文章。在对文献进行严格审查后,确定了13项研究。提取或计算风险比,并计算样本量加权汇总估计值。
CVD诊断或事件的患病率在5.7%-24.0%之间。一般饮酒和大量饮酒对CVD的加权合并粗效应大小分别为1.75(95%CI 1.06,3.17)和1.78(95%CI 1.09,2.93)。大量饮酒对CVD的合并调整效应大小为1.37(95%CI 1.02,1.84)。汇总估计因CVD结局和饮酒量测量方法而异;饮酒对脑/缺血性事件影响最为显著。
HIV临床医生应考虑传统危险因素框架中未包括的危险因素,特别是大量饮酒。忽视这一危险因素可能导致对风险的低估,从而导致PLWH治疗不足。