Levesque Christine, Sanger Nitika, Edalati Hanie, Sohi Ivneet, Shield Kevin D, Sherk Adam, Stockwell Tim, Butt Peter R, Paradis Catherine
Canadian Centre on Substance Use and Addiction, Ottawa, Ontario, Canada.
Institute for Mental Health Policy Research, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Alcohol Clin Exp Res (Hoboken). 2023 Jul;47(7):1238-1255. doi: 10.1111/acer.15121. Epub 2023 Jul 9.
Alcohol use is causally linked to the development of and mortality from numerous diseases. The aim of this study is to provide an update to a previous systematic review of meta-analyses that quantify the sex-specific dose-response risk relationships between chronic alcohol use and disease occurrence and/or mortality. An updated systematic search of multiple databases was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses criteria to identify meta-analyses published from January 1, 2017, to March 8, 2021, which quantified the risk relationships between chronic alcohol use and the risk of disease occurrence and/or mortality. This systematic review was not preregistered. The comparator was people who have never consumed at least one standard drink of alcohol. Measurements included relative risks, odds ratios, and hazard ratios of disease occurrence and/or mortality based on long-term alcohol intake measured in grams per day. The systematic search yielded 5953 articles, of which 14 were included in the narrative review. All diseases showed an increased risk of occurrence as alcohol use increased. At all doses examined, alcohol had a significant detrimental effect on tuberculosis, lower respiratory infections, oral cavity and pharyngeal cancers, esophageal cancer, colorectal cancer, liver cancer, laryngeal cancer, epilepsy, hypertension, liver cirrhosis, and pancreatitis (among men). For ischemic heart disease, ischemic stroke, and intracerebral hemorrhage, protective effects from low-dose chronic alcohol use among both men and women were observed. Low-dose alcohol consumption also had a protective effect for diabetes mellitus and pancreatitis among women (approximately to 50 g/day and 30 g/day, respectively). Alcohol use increases the risk of numerous infectious and noncommunicable diseases in a dose-response manner. Higher levels of alcohol use have a clear detrimental impact on health; however, at lower levels of use, alcohol can have both disease-specific protective and detrimental effects.
饮酒与多种疾病的发生及死亡率存在因果关联。本研究旨在更新之前一项系统综述中的荟萃分析,该综述量化了慢性饮酒与疾病发生和/或死亡率之间的性别特异性剂量反应风险关系。按照系统评价与荟萃分析的首选报告项目标准,对多个数据库进行了更新的系统检索,以识别2017年1月1日至2021年3月8日期间发表的、量化慢性饮酒与疾病发生风险和/或死亡率之间风险关系的荟萃分析。本系统综述未进行预注册。对照对象为从未饮用过至少一杯标准酒精饮料的人群。测量指标包括基于每日酒精摄入量(以克为单位)测量的疾病发生和/或死亡率的相对风险、比值比和风险比。系统检索共获得5953篇文章,其中14篇纳入叙述性综述。所有疾病均显示随着饮酒量增加,发病风险升高。在所有检测剂量下,酒精对结核病、下呼吸道感染、口腔和咽喉癌、食管癌、结直肠癌、肝癌、喉癌、癫痫、高血压、肝硬化和胰腺炎(男性)均有显著有害影响。对于缺血性心脏病、缺血性中风和脑出血,观察到男性和女性低剂量慢性饮酒均有保护作用。低剂量饮酒对女性糖尿病和胰腺炎也有保护作用(分别约为每日50克和30克)。饮酒以剂量反应方式增加多种传染病和非传染病的风险。较高水平的饮酒对健康有明显有害影响;然而,在较低饮酒水平时,酒精对特定疾病既有保护作用,也有有害作用。