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Obesity, Type 2 Diabetes, Lifestyle Factors, and Risk of Gallstone Disease: A Mendelian Randomization Investigation.肥胖、2型糖尿病、生活方式因素与胆结石疾病风险:一项孟德尔随机化研究
Clin Gastroenterol Hepatol. 2022 Mar;20(3):e529-e537. doi: 10.1016/j.cgh.2020.12.034. Epub 2021 Jan 6.
2
A comprehensive survey of genetic variation in 20,691 subjects from four large cohorts.对来自四个大型队列的20691名受试者的基因变异进行全面调查。
PLoS One. 2017 Mar 16;12(3):e0173997. doi: 10.1371/journal.pone.0173997. eCollection 2017.
3
Origin, Methods, and Evolution of the Three Nurses' Health Studies.三项护士健康研究的起源、方法与演变
Am J Public Health. 2016 Sep;106(9):1573-81. doi: 10.2105/AJPH.2016.303338. Epub 2016 Jul 26.
4
Determinants for gallstone formation - a new data cohort study and a systematic review with meta-analysis.胆结石形成的决定因素——一项新的数据队列研究及一项荟萃分析的系统评价
Scand J Gastroenterol. 2016 Oct;51(10):1239-48. doi: 10.1080/00365521.2016.1182583. Epub 2016 May 27.
5
Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies.在一项全基因组关联研究的荟萃分析中确定的胆结石疾病的四个易感基因座。
Gastroenterology. 2016 Aug;151(2):351-363.e28. doi: 10.1053/j.gastro.2016.04.007. Epub 2016 Apr 16.
6
Tobacco smoking and the risk of gallbladder disease.吸烟与胆囊疾病风险
Eur J Epidemiol. 2016 Jul;31(7):643-53. doi: 10.1007/s10654-016-0124-z. Epub 2016 Feb 22.
7
Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.在乳腺癌和前列腺癌队列联盟中,全基因组关联研究确定的易感性单核苷酸多态性与乳腺癌风险因素之间的加性相互作用。
Am J Epidemiol. 2014 Nov 15;180(10):1018-27. doi: 10.1093/aje/kwu214. Epub 2014 Sep 25.
8
The ABCG5/8 cholesterol transporter and myocardial infarction versus gallstone disease.ABCG5/8 胆固醇转运蛋白与心肌梗死和胆石病。
J Am Coll Cardiol. 2014 May 27;63(20):2121-2128. doi: 10.1016/j.jacc.2013.12.055. Epub 2014 Mar 19.
9
Elevated body mass index as a causal risk factor for symptomatic gallstone disease: a Mendelian randomization study.体重指数升高是症状性胆石病的一个因果风险因素:一项孟德尔随机化研究。
Hepatology. 2013 Dec;58(6):2133-41. doi: 10.1002/hep.26563. Epub 2013 Oct 11.
10
Likelihood ratio test for detecting gene (G)-environment (E) interactions under an additive risk model exploiting G-E independence for case-control data.基于病例对照数据中基因(G)-环境(E)独立性,利用加性风险模型检测基因(G)-环境(E)相互作用的似然比检验。
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根据遗传易感性探讨肥胖、脂肪过多与有症状胆结石疾病风险的关系。

Obesity, Adiposity, and Risk of Symptomatic Gallstone Disease According to Genetic Susceptibility.

作者信息

Lim Junghyun, Wirth Janine, Wu Kana, Giovannucci Edward, Kraft Peter, Turman Constance, Song Mingyang, Jovani Manol, Chan Andrew T, Joshi Amit D

机构信息

Clinical and Translational Epidemiology Unit, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts; Department of Medicine, University of Miami Leonard M. Miller School of Medicine, Miami, Florida.

Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts; UCD Institute of Food and Health, School of Agriculture and Food Science, University College Dublin, Dublin, Ireland.

出版信息

Clin Gastroenterol Hepatol. 2022 May;20(5):e1083-e1120. doi: 10.1016/j.cgh.2021.06.044. Epub 2021 Jul 2.

DOI:
10.1016/j.cgh.2021.06.044
PMID:34217876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8720320/
Abstract

BACKGROUND & AIMS: Adiposity has been consistently associated with gallstone disease risk. We aimed to characterize associations of anthropometric measures (body mass index [BMI], recent weight change, long-term weight change, waist circumference, and waist-to-hip ratio) with symptomatic gallstone disease according to strata of gallstone disease polygenic risk score (PRS).

METHODS

We conducted analysis among 34,626 participants with available genome-wide genetic data within 3 large, prospective, U.S. cohorts-the Nurses' Health Study (NHS), Health Professionals Follow-Up Study, and NHS II. We characterized joint associations of PRS and anthropometric measures and tested for interactions on the relative and absolute risk scales.

RESULTS

Women in the highest BMI and PRS categories (BMI ≥30 kg/m and PRS ≥1 SD above mean) had odds ratio for gallstone disease of 5.55 (95% confidence interval, 5.29 to 5.81) compared with those in the lowest BMI and PRS categories (BMI <25 kg/m and PRS <1 SD below the mean). The corresponding odds ratio among men was 1.65 (95% confidence interval, 1.02 to 2.29). Associations for BMI did not vary within strata of PRS on the relative risk scale. On the absolute risk scale, the incidence rate difference between obese and normal-weight individuals was 1086 per 100,000 person-years within the highest PRS category, compared with 666 per 100,000 person-years in the lowest PRS category, with strong evidence for interaction with the ABCG8 locus.

CONCLUSIONS

While maintenance of a healthy body weight reduces gallstone disease risk among all individuals, risk reduction is higher among the subset with greater genetic susceptibility to gallstone disease.

摘要

背景与目的

肥胖一直与胆结石疾病风险相关。我们旨在根据胆结石疾病多基因风险评分(PRS)分层,描述人体测量指标(体重指数[BMI]、近期体重变化、长期体重变化、腰围和腰臀比)与症状性胆结石疾病之间的关联。

方法

我们对美国3个大型前瞻性队列(护士健康研究[NHS]、卫生专业人员随访研究和NHS II)中34626名有全基因组遗传数据的参与者进行了分析。我们描述了PRS和人体测量指标的联合关联,并在相对和绝对风险量表上测试了相互作用。

结果

BMI和PRS最高类别(BMI≥30 kg/m²且PRS高于平均值1个标准差)的女性患胆结石疾病的比值比为5.55(95%置信区间,5.29至5.81),而BMI和PRS最低类别(BMI<25 kg/m²且PRS低于平均值1个标准差)的女性为1。男性相应的比值比为1.65(95%置信区间,1.02至2.29)。在相对风险量表上,BMI的关联在PRS各层内没有变化。在绝对风险量表上,最高PRS类别中肥胖与正常体重个体之间的发病率差异为每10万人年1086例,而最低PRS类别中为每10万人年666例,有强有力的证据表明与ABCG8基因座存在相互作用。

结论

虽然保持健康体重可降低所有人患胆结石疾病的风险,但在对胆结石疾病遗传易感性较高的亚组中,风险降低幅度更大。