Prospective Study of the Association Between the Proline to Alanine Codon 12 Polymorphism in the PPARγ Gene and Type 2 Diabetes

Author:

Memisoglu Asli1,Hu Frank B.2,Hankinson Susan E.13,Liu Simin4,Meigs James B.5,Altshuler David M.6,Hunter David J.137,Manson JoAnn E.134

Affiliation:

1. Department of Epidemiology, Harvard School of Public Health, Boston, Massachusetts

2. Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts

3. Channing Laboratory, Department of Medicine, Harvard Medical School and Brigham and Women’s Hospital, Boston, Massachusetts

4. Division of Preventive Medicine, Department of Medicine, Harvard Medical School and Brigham and Women’s Hospital, Boston, Massachusetts

5. General Medicine Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts

6. Department of Genetics, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts

7. Harvard School of Public Health, Center for Cancer Prevention, Boston, Massachusetts

Abstract

OBJECTIVE—To determine whether the Pro12Ala polymorphism in the PPARγ gene was associated with risk of type 2 diabetes in the Nurses’ Health Study. RESEARCH DESIGN AND METHODS—The study was a nested case-control study of 387 incident cases of type 2 diabetes and 771 matching control subjects nested within the Nurses’ Health Study, a prospective cohort study. Association between PPARγ genotype and incident type 2 diabetes was estimated using logistic regression. RESULTS—Carriers of the PPARγ variant 12Ala allele had reduced risk of type 2 diabetes compared with noncarriers. Unadjusted and adjusted odds ratios of type 2 diabetes were 0.74 (95% CI 0.55–1.00) and 0.72 (0.52–0.99), respectively. CONCLUSIONS—The results of this study provide further support for an inverse association between the PPARγ variant 12Ala allele and risk of type 2 diabetes.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

Cited by 52 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. PPARG (Pro12Ala) genetic variant and risk of T2DM: a systematic review and meta-analysis;Scientific Reports;2020-07-29

2. Adventures in the environment and genes;European Journal of Epidemiology;2019-12

3. FADS and PPARG2 Single Nucleotide Polymorphisms are Associated with Plasma Lipids in 9-Mo-Old Infants;The Journal of Nutrition;2019-05-01

4. Genetic Basis for Increased Risk for Vascular Diseases in Diabetes;Mechanisms of Vascular Defects in Diabetes Mellitus;2017

5. Role of PPARG (Pro12Ala) in Malaysian type 2 diabetes mellitus patients;International Journal of Diabetes in Developing Countries;2016-01-15

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3