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本文引用的文献

1
Circulating Selenium and Prostate Cancer Risk: A Mendelian Randomization Analysis.循环硒与前列腺癌风险:一项孟德尔随机化分析。
J Natl Cancer Inst. 2018 Sep 1;110(9):1035-1038. doi: 10.1093/jnci/djy081.
2
Childhood BMI and Adult Type 2 Diabetes, Coronary Artery Diseases, Chronic Kidney Disease, and Cardiometabolic Traits: A Mendelian Randomization Analysis.儿童 BMI 与成人 2 型糖尿病、冠状动脉疾病、慢性肾脏病和心脏代谢特征:孟德尔随机分析。
Diabetes Care. 2018 May;41(5):1089-1096. doi: 10.2337/dc17-2141. Epub 2018 Feb 26.
3
Diet/lifestyle and risk of diabetes and glycemic traits: a Mendelian randomization study.饮食/生活方式与糖尿病和血糖特征风险:一项孟德尔随机化研究。
Lipids Health Dis. 2018 Jan 29;17(1):18. doi: 10.1186/s12944-018-0666-z.
4
Vitamin supplements in type 2 diabetes mellitus management: A review.2型糖尿病管理中的维生素补充剂:一项综述。
Diabetes Metab Syndr. 2017 Dec;11 Suppl 2:S589-S595. doi: 10.1016/j.dsx.2017.04.009. Epub 2017 Apr 12.
5
Dairy consumption, systolic blood pressure, and risk of hypertension: Mendelian randomization study.乳制品消费、收缩压与高血压风险:孟德尔随机化研究
BMJ. 2017 Mar 16;356:j1000. doi: 10.1136/bmj.j1000.
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Genetic variation at 16q24.2 is associated with small vessel stroke.16号染色体长臂24.2区域的基因变异与小血管性卒中有关。
Ann Neurol. 2017 Mar;81(3):383-394. doi: 10.1002/ana.24840.
7
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.53个基因座的遗传关联揭示了与肾功能相关的细胞类型和生物学途径。
Nat Commun. 2016 Jan 21;7:10023. doi: 10.1038/ncomms10023.
8
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.一项基于千人基因组计划的冠心病全基因组关联荟萃分析。
Nat Genet. 2015 Oct;47(10):1121-1130. doi: 10.1038/ng.3396. Epub 2015 Sep 7.
9
Circulating tocopherols and risk of coronary artery disease: A systematic review and meta-analysis.循环生育酚与冠状动脉疾病风险:一项系统评价与荟萃分析。
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10
Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression.使用无效工具变量的孟德尔随机化:通过Egger回归进行效应估计和偏差检测
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循环维生素E与心脏代谢指标:孟德尔随机化分析

Circulating vitamin E and cardiometabolic measures: a Mendelian randomization analysis.

作者信息

Fan Chuanlong, Huang Tao, Kong Xuejun, Zhang Xiaohong, Zou Zuquan, Xiao Jing

机构信息

Medical School, Ningbo University, 818 Fenghua Road, Ningbo, Zhejiang 315211, China.

Department of Epidemiology & Biostatistics, School of Public Health, Peking University, 5 Summer Palace Road, Haidian District, Beijing 100000, China.

出版信息

J Clin Biochem Nutr. 2019 Sep;65(2):160-169. doi: 10.3164/jcbn.19-12. Epub 2019 Aug 9.

DOI:10.3164/jcbn.19-12
PMID:31592210
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6769411/
Abstract

Although a large body of literature reported that high intake of vitamin E played a possible role in reducing risk of cardiometabolic diseases, conflicting results were also found in some observational studies due to confounding factors. Hence, we used a Mendelian randomization study as an alternative way to examine the causality between circulating vitamin E and cardiometabolic diseases. Summary-level data were extracted from consortia and three single nucleotide polymorphisms were used as instrumental variables. Our study showed that a one-SD increase in circulating vitamin E levels was causally associated with an increased risk of coronary artery disease [odds ratio (OR) 3.16 (95%CI 1.74, 5.73);  = 1.91 × 10] at the Bonferroni-adjusted level of significance (<0.005). Moreover, a one-SD increase in circulating vitamin E levels was associated with a 0.572-SD increase in low density lipoprotein cholesterol (mg/dl), a 0.693-SD increase in total cholesterol (mg/dl), and a 1.45-SD increase in triglyceride (mg/dl), but a 0.502-SD decrease in high density lipoprotein cholesterol (mg/dl) at the Bonferroni-adjusted level of significance (<0.0028). Our findings indicated that genetically elevated vitamin E was associated with increased risk of coronary artery disease, suggesting an adverse causality between circulating vitamin E and coronary artery disease.

摘要

尽管大量文献报道,高摄入维生素E在降低心血管代谢疾病风险方面可能发挥作用,但由于混杂因素,一些观察性研究也发现了相互矛盾的结果。因此,我们采用孟德尔随机化研究作为另一种方法来检验循环维生素E与心血管代谢疾病之间的因果关系。从联盟中提取汇总水平的数据,并使用三个单核苷酸多态性作为工具变量。我们的研究表明,在Bonferroni校正的显著性水平(<0.005)下,循环维生素E水平每增加一个标准差,与冠状动脉疾病风险增加相关[比值比(OR)3.16(95%CI 1.74,5.73); = 1.91×10]。此外,在Bonferroni校正的显著性水平(<0.0028)下,循环维生素E水平每增加一个标准差,与低密度脂蛋白胆固醇(mg/dl)增加0.572个标准差、总胆固醇(mg/dl)增加0.693个标准差和甘油三酯(mg/dl)增加1.45个标准差相关,但与高密度脂蛋白胆固醇(mg/dl)降低0.502个标准差相关。我们的研究结果表明,基因水平升高的维生素E与冠状动脉疾病风险增加相关,提示循环维生素E与冠状动脉疾病之间存在不良因果关系。