Coffee and tea consumption and the risk for subarachnoid hemorrhage: A meta-analysis

被引:5
|
作者
Rui, Qin [1 ]
Ni, Haibo [2 ]
Liu, Huixiang [2 ]
Zhu, Xiaojue [1 ]
Gao, Rong [2 ]
机构
[1] First Peoples Hosp Zhangjiagang City, Dept Lab, Suzhou, Jiangsu, Peoples R China
[2] First Peoples Hosp Zhangjiagang City, Dept Neurosurg, Suzhou, Jiangsu, Peoples R China
关键词
Coffee; Tea; Subarachnoid hemorrhage; Meta-analysis; Epidemiology; CARDIOVASCULAR-DISEASE; GREEN TEA; CASE-FATALITY; STROKE; CAFFEINE; RUPTURE; HEALTH; REGION;
D O I
10.1016/j.nut.2018.06.026
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Objectives: Reports on the association between coffee or tea consumption and subarachnoid hemorrhage (SAH) risk are inconsistent. The aim of this study was to determine if an association exists between consumption of coffee or tea and the risk for SAH. Methods: A random-effects model was used to estimate the summary relative risks (RRs) and 95% confidence intervals (CIs). Heterogeneity among studies was assessed using the statistics Cochran's Q and I-2. Seven studies on coffee consumption and five on tea consumption were included in the meta-analysis. Results: The pooled RRs of SAH for the highest versus the lowest categories of coffee and tea consumption were 1.31 (95% CI, 0.84-2.05) and 0.83 (95% CI, 0.65-1.08), respectively. There was evidence of heterogeneity among studies of coffee consumption (P-heterogeneity = 0.002, I-2 = 71.7%) but not among studies of tea consumption (P-heterogeneity = 0.34, I-2 = 11.3%). Omitting one study that substantially contributed to the heterogeneity among studies of coffee consumption yielded a pooled RR of 1.51 (95% Cl, 1.10-2.06). Dose-response analysis showed that the summary RRs of SAH for an increase of one cup of coffee and tea consumption per day were 1.00 (95% CI, 0.96-1.04) and 0.97 (95% CI, 0.85-1.11), respectively. There was no evidence of publication bias. Conclusion: Our meta-analysis of current evidence does not support an association between the consumption of coffee or tea and SAH risk. Further studies with prospective designs that control for important confounders and provide sufficient data for dose-response analysis are warranted. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:21 / 28
页数:8
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