Laura Llamosas-Falcón, Charlotte Probst, Charlotte Buckley, Huan Jiang, Aurélie M Lasserre, Klajdi Puka, Alexander Tran, Jürgen Rehm
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A total of 24 studies were included in the analysis. There were collectively 2,112,476 females and 924,853 males, and a total of 4,301 and 4,231 cases of LC for females and males, respectively. We identified a non-linear dose-response relationship. Females showed a higher risk for LC compared to males with the same amount of alcohol consumed daily. For instance, drinking 40 g/day showed RRs of 9.35 (95% CI 7.64-11.45) in females and 2.82 (95% CI 2.53-3.14) in males, while drinking 80 g/day presented RRs of 23.32 (95% CI 18.24-29.82) in females and 7.93 (95% CI 7.12-8.83) in males. Additional analyses showed that a higher risk for females was found for morbidity and for mortality. 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引用次数: 0
摘要
不同的研究表明,与男性相比,女性在较低的酒精摄入量下就会罹患肝病。我们的目的是按性别量化酒精消耗量与肝硬化风险之间的剂量-反应关系,并确定女性与男性之间的差异。我们使用PubMed/Medline和Embase进行了系统性回顾,以确定分析饮酒水平与肝硬化(LC)发病率和死亡率(ICD-8和ICD-9代码571和ICD-10代码K70、K73、K74)之间关系的纵向和病例对照研究。采用随机效应模型计算汇总相对风险(RR)。剂量-反应关系采用限制性三次样条模型。共有 24 项研究被纳入分析。共有 2,112,476 名女性和 924,853 名男性,女性和男性的 LC 病例数分别为 4,301 和 4,231 例。我们发现了一种非线性的剂量-反应关系。在每日饮酒量相同的情况下,女性患低血糖症的风险高于男性。例如,每天饮酒 40 克,女性的 RR 值为 9.35(95% CI 7.64-11.45),男性为 2.82(95% CI 2.53-3.14),而每天饮酒 80 克,女性的 RR 值为 23.32(95% CI 18.24-29.82),男性为 7.93(95% CI 7.12-8.83)。其他分析表明,女性发病和死亡的风险较高。需要了解性别对饮酒与 LC 风险关系的影响,以制定预防和治疗建议及临床指南。系统综述注册:https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022299680,标识符为 CRD42022299680。
Sex-specific association between alcohol consumption and liver cirrhosis: An updated systematic review and meta-analysis.
Different studies have shown that females develop liver diseases at lower levels of alcohol consumption than males. Our aim was to quantify the dose-response relationship between alcohol consumption and the risk of liver cirrhosis by sex and identify the differences between females and males. A systematic review was conducted using PubMed/Medline and Embase to identify longitudinal and case-control studies that analyzed the relationship between the level of alcohol use and liver cirrhosis (LC) incidence, and mortality (ICD-8 and ICD-9 codes 571 and ICD-10 codes K70, K73, K74). Pooled relative risks (RR) were calculated by random effects models. Restricted cubic splines were used to model the dose-response relationship. A total of 24 studies were included in the analysis. There were collectively 2,112,476 females and 924,853 males, and a total of 4,301 and 4,231 cases of LC for females and males, respectively. We identified a non-linear dose-response relationship. Females showed a higher risk for LC compared to males with the same amount of alcohol consumed daily. For instance, drinking 40 g/day showed RRs of 9.35 (95% CI 7.64-11.45) in females and 2.82 (95% CI 2.53-3.14) in males, while drinking 80 g/day presented RRs of 23.32 (95% CI 18.24-29.82) in females and 7.93 (95% CI 7.12-8.83) in males. Additional analyses showed that a higher risk for females was found for morbidity and for mortality. Understanding the influence of sex on the association of alcohol consumption and the risk of LC is needed to develop recommendations and clinical guidelines for prevention and treatment.