饮酒及其与癌症、心血管疾病、肝病和脑病的关系:孟德尔随机研究的系统回顾。

Frontiers in epidemiology Pub Date : 2024-11-07 eCollection Date: 2024-01-01 DOI:10.3389/fepid.2024.1385064
Naouras Bouajila, Cloé Domenighetti, Henri-Jean Aubin, Mickael Naassila
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引用次数: 0

摘要

背景:关于饮酒对健康的影响,尤其是与戒酒相比,轻度至中度饮酒可能具有的保护作用,仍是一个争论不休的话题。然而,流行病学研究由于暴露测量不精确以及残余混杂和反向因果关系可能造成的偏差而面临局限性。为了解决这些局限性,我们对孟德尔随机化(MR)研究进行了系统性回顾,考察了饮酒与癌症、心血管疾病、肝脏疾病和神经系统疾病之间的因果关系:我们检索了 PubMed、ScienceDirect 和 Embase 以及欧洲 PMC(截至 2024 年 5 月)上有关调查基因预测饮酒量与癌症、心血管疾病、肝脏疾病和神经系统疾病之间关系的 MR 研究。我们根据遗传关联研究工具 MR 设计的关键要素对方法学质量进行了评估:我们纳入了 70 项符合纳入标准的 MR 研究。我们的综述显示,饮酒与多种癌症(如口腔癌、口咽癌、食管癌、结直肠癌、肝细胞癌和皮肤黑色素瘤)有明显关联。虽然现有研究并未一致证实酒精对其他癌症(如肺癌)的不利或保护作用,但观察性研究表明了这一点。此外,磁共振研究证实,酒精对高血压、心房颤动、心肌梗塞和血管疾病的风险可能有因果影响。然而,没有证据支持观察性研究报告的轻度至中度饮酒对认知功能、老年痴呆症和肌萎缩性脊髓侧索硬化症的保护作用,而我们的综述显示癫痫和多发性硬化症的风险增加。关于饮酒与肝病之间的联系,现有研究提供的结果有限:尽管 MR 研究对饮酒与各种健康结果之间的因果关系提供了有价值的见解,但值得注意的是,由于遗传工具变量区分戒酒者、轻度饮酒者和中度饮酒者的能力不一致,因此很难区分暴露与结果之间的 U 型或 J 型关系与线性关系。有必要开展更多研究,为MR研究建立正式的质量评估工具,并在包括非欧洲血统在内的不同人群中开展更多研究。系统综述注册:www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42021246154,识别码:prospero (crd42021):prospero(CRD42021246154)。
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Alcohol consumption and its association with cancer, cardiovascular, liver and brain diseases: a systematic review of Mendelian randomization studies.

Background: The health effects of alcohol consumption, particularly regarding potential protective benefits of light to moderate intake compared to abstinence, remain a subject of ongoing debate. However, epidemiological studies face limitations due to imprecise exposure measurements and the potential for bias through residual confounding and reverse causation. To address these limitations, we conducted a systematic review of Mendelian Randomization (MR) studies examining the causal relationship between alcohol consumption and cancers, cardiovascular, liver, and neurological diseases.

Methodology: We searched PubMed, ScienceDirect and Embase and Europe PMC up to 05/2024 for MR studies investigating the association of genetically predicted alcohol consumption with cancers, cardiovascular, liver and neurological diseases. We assessed methodological quality based on key elements of the MR design a genetic association studies tool.

Results: We included 70 MR studies that matched our inclusion criteria. Our review showed a significant association of alcohol consumption with multiple cancers such as oral and oropharyngeal, esophageal, colorectal cancers, hepatocellular carcinoma and cutaneous melanoma. While the available studies did not consistently confirm the adverse or protective effects of alcohol on other cancers, such as lung cancer, as suggested by observational studies. Additionally, MR studies confirmed a likely causal effect of alcohol on the risk of hypertension, atrial fibrillation, myocardial infraction and vessels disease. However, there was no evidence to support the protective effects of light to moderate alcohol consumption on cognitive function, Alzheimer's disease, and amyotrophic lateral sclerosis, as reported in observational studies while our review revealed an increased risk of epilepsy and multiple sclerosis. The available studies provided limited results on the link between alcohol consumption and liver disease.

Conclusions: Despite the valuable insights into the causal relationship between alcohol consumption and various health outcomes that MR studies provided, it is worth noting that the inconsistent ability of genetic instrumental variables to distinguish between abstainers, light and moderate drinkers makes it difficult to differentiate between U or J-shaped vs. linear relationships between exposure and outcome. Additional research is necessary to establish formal quality assessment tools for MR studies and to conduct more studies in diverse populations, including non-European ancestries.

Systematic review registration: www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42021246154, Identifier: PROSPERO (CRD42021246154).

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