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饮酒与骨折风险:前瞻性队列研究的系统评价和剂量反应荟萃分析。

Alcohol Consumption and Risk of Fractures: A Systematic Review and Dose-Response Meta-Analysis of Prospective Cohort Studies.

机构信息

Department of General Practice, The Affiliated Luohu Hospital of Shenzhen University Medical School, Shenzhen, Guangdong, China, 47 Youyi Road, Luohu District, Shenzhen, Guangdong, 518001, People's Republic of China.

Department of Epidemiology and Biostatistics, College of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China.

出版信息

Adv Nutr. 2023 Jul;14(4):599-611. doi: 10.1016/j.advnut.2023.03.008. Epub 2023 Mar 24.

Abstract

Alcohol consumption remains inconsistently correlated with fracture risk, and a dose-response meta-analysis for specific outcomes is lacking. The objective of this study was to quantitatively integrate the data on the relationship between alcohol consumption and fracture risk. Pertinent articles were identified in PubMed, Web of Science, and Embase databases up to 20 February 2022. Combined RRs and 95% CIs were estimated by random- or fixed-effects models. Restricted cubic splines were used to model linear or nonlinear relationships. Forty-four articles covering 6,069,770 participants and 205,284 cases of fracture were included. The combined RRs and 95% CIs for highest compared with lowest alcohol consumption were 1.26 (1.17-1.37), 1.24 (1.13-1.35), and 1.20 (1.03-1.40) for total, osteoporotic, and hip fractures, respectively. A linear positive relationship between alcohol consumption and total fracture risk was detected (P = 0.057); the risk was correlated with a 6% increase (RR, 1.06; 95% CI: 1.02, 1.10) per 14 g/d increment of alcohol consumption. J-shaped relationships of alcohol consumption with risk of osteoporotic fractures (P < 0.001) and hip fractures (P < 0.001) were found. Alcohol consumption of 0 to 22 g/d was linked to a reduced risk of osteoporotic fractures and hip fractures. Our findings show that any level of alcohol consumption is a risk factor for total fractures. Moreover, this dose-response meta-analysis shows that an alcohol consumption level of 0 to 22 g/d is related to a reduction in the risk of osteoporotic and hip fractures. The protocol was registered in the International Prospective Register of Systematic Reviews (CRD42022320623).

摘要

饮酒与骨折风险的相关性不一致,且缺乏针对特定结局的剂量-反应荟萃分析。本研究旨在定量整合关于饮酒与骨折风险之间关系的数据。截至 2022 年 2 月 20 日,在 PubMed、Web of Science 和 Embase 数据库中检索相关文献。采用随机或固定效应模型估计合并 RR 和 95%CI。采用限制性立方样条模型来拟合线性或非线性关系。纳入 44 篇文献,涵盖 6069770 名参与者和 205284 例骨折。最高与最低饮酒量相比的合并 RR 和 95%CI 分别为 1.26(1.17-1.37)、1.24(1.13-1.35)和 1.20(1.03-1.40),用于总骨折、骨质疏松性骨折和髋部骨折。饮酒与总骨折风险之间呈线性正相关(P = 0.057);风险与每增加 14 g/d 饮酒量导致风险增加 6%(RR,1.06;95%CI:1.02,1.10)相关。饮酒与骨质疏松性骨折(P < 0.001)和髋部骨折(P < 0.001)风险的关系呈 J 形。饮酒量为 0 至 22 g/d 与骨质疏松性骨折和髋部骨折风险降低相关。我们的研究结果表明,任何水平的饮酒均是总骨折的危险因素。此外,这种剂量-反应荟萃分析表明,饮酒量为 0 至 22 g/d 与降低骨质疏松性和髋部骨折风险相关。该方案已在国际前瞻性系统评价注册库(CRD42022320623)中注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/620e/10334160/c76491949fac/gr1.jpg

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