Homogeneity in the association of body mass index with type 2 diabetes across the UK Biobank: A Mendelian randomization study

被引:0
|
作者
Wainberg, Michael [1 ]
Mahajan, Anubha [2 ,3 ]
Kundaje, Anshul [1 ]
McCarthy, Mark I. [2 ,3 ,5 ,11 ]
Ingelsson, Erik [6 ,7 ,8 ,9 ]
Sinnott-Armstrong, Nasa [4 ]
Rivas, Manuel A. [10 ]
机构
[1] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
[2] Univ Oxford, Wellcome Ctr Human Genet, Oxford, England
[3] Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Churchill Hosp, Oxford, England
[4] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[5] Churchill Hosp, NIHR Oxford Biomed Res Ctr, Oxford, England
[6] Uppsala Univ, Dept Med Sci, Mol Epidemiol, Uppsala, Sweden
[7] Uppsala Univ, Sci Life Lab, Uppsala, Sweden
[8] Stanford Univ, Sch Med, Dept Med, Div Cardiovasc Med, Stanford, CA 94305 USA
[9] Stanford Univ, Stanford Cardiovasc Inst, Stanford, CA 94305 USA
[10] Stanford Univ, Dept Biomed Data Sci, Stanford, CA 94305 USA
[11] Genentech Inc, OMNI Human Genet, San Francisco, CA 94080 USA
基金
加拿大自然科学与工程研究理事会;
关键词
LIFE-STYLE; WEIGHT-LOSS; RISK; OBESITY; BIAS; INTERVENTION; OVERWEIGHT; RATIO;
D O I
10.1371/journal.pmed.1002982; 10.1371/journal.pmed.1002982.r001; 10.1371/journal.pmed.1002982.r002; 10.1371/journal.pmed.1002982.r003; 10.1371/journal.pmed.1002982.r004; 10.1371/journal.pmed.1002982.r005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Lifestyle interventions to reduce body mass index (BMI) are critical public health strategies for type 2 diabetes prevention. While weight loss interventions have shown demonstrable benefit for high-risk and prediabetic individuals, we aimed to determine whether the same benefits apply to those at lower risk. Methods and findings We performed a multi-stratum Mendelian randomization study of the effect size of BMI on diabetes odds in 287,394 unrelated individuals of self-reported white British ancestry in the UK Biobank, who were recruited from across the United Kingdom from 2006 to 2010 when they were between the ages of 40 and 69 years. Individuals were stratified on the following diabetes risk factors: BMI, diabetes family history, and genome-wide diabetes polygenic risk score. The main outcome measure was the odds ratio of diabetes per 1-kg/m(2) BMI reduction, in the full cohort and in each stratum. Diabetes prevalence increased sharply with BMI, family history of diabetes, and genetic risk. Conversely, predicted risk reduction from weight loss was strikingly similar across BMI and genetic risk categories. Weight loss was predicted to substantially reduce diabetes odds even among lower-risk individuals: for instance, a 1-kg/m(2) BMI reduction was associated with a 1.37-fold reduction (95% CI 1.12-1.68) in diabetes odds among non-overweight individuals (BMI < 25 kg/m(2)) without a family history of diabetes, similar to that in obese individuals (BMI >= 30 kg/m(2)) with a family history (1.21-fold reduction, 95% CI 1.13-1.29). A key limitation of this analysis is that the BMI-altering DNA sequence polymorphisms it studies represent cumulative predisposition over an individual's entire lifetime, and may consequently incorrectly estimate the risk modification potential of weight loss interventions later in life. Conclusions In a population-scale cohort, lower BMI was consistently associated with reduced diabetes risk across BMI, family history, and genetic risk categories, suggesting all individuals can substantially reduce their diabetes risk through weight loss. Our results support the broad deployment of weight loss interventions to individuals at all levels of diabetes risk. Author summaryWhy was this study done? Excessive body weight is a key risk factor for type 2 diabetes, and weight loss is known to dramatically reduce risk, at least among people who were at high risk to begin with. However, even people without obvious risk factors like excessive weight or a family history of the disease still have a relatively large chance (about 1 percent) of developing type 2 diabetes: Could these individuals also reduce their risk of type 2 diabetes through weight loss? What did the researchers do and find? We looked at inherited genetic mutations that predispose people to lower body weight, and asked how much these mutations tend to protect people from type 2 diabetes, across 287,394 self-reported white British individuals from the UK Biobank cohort. We found that these mutations seem to offer about the same degree of protection against type 2 diabetes regardless of a person's body weight, family history of type 2 diabetes, or genetic risk for type 2 diabetes, suggesting that weight loss would have a similarly uniform protective effect for all individuals. What do these findings mean? These findings suggest that all individuals can substantially reduce their type 2 diabetes risk through weight loss, and support the broad deployment of weight loss interventions to individuals at all levels of diabetes risk as a public health measure. However, a key limitation to keep in mind is that genetic mutations, because they act across an individual's entire lifespan, are not a perfect proxy for weight loss interventions that happen only later in life.
引用
收藏
页数:15
相关论文
共 50 条
  • [31] Body mass index and the risk of abdominal hernia: a Mendelian randomization study
    Z. Li
    L. Xia
    X. Li
    Y. Guan
    H. He
    L. Jin
    Hernia, 2023, 27 : 423 - 429
  • [32] Age at menarche and adult body mass index: a Mendelian randomization study
    Dipender Gill
    Christopher F. Brewer
    Fabiola Del Greco M
    Prasanthi Sivakumaran
    Jack Bowden
    Nuala A. Sheehan
    Cosetta Minelli
    International Journal of Obesity, 2018, 42 : 1574 - 1581
  • [33] Body Mass Index and Risk of Diabetic Nephropathy: A Mendelian Randomization Study
    Lu, Jingru
    Liu, Xiaoshuang
    Jiang, Song
    Kan, Shuyan
    An, Yu
    Zheng, Chunxia
    Li, Xiang
    Liu, Zhihong
    Xie, Guotong
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2022, 107 (06): : 1599 - 1608
  • [34] The Association of Hyperuricemia and Gout With the Risk of Cardiovascular Diseases: A Cohort and Mendelian Randomization Study in UK Biobank
    Zhu, Jianwei
    Zeng, Yu
    Zhang, Hanyue
    Qu, Yuanyuan
    Ying, Zhiye
    Sun, Yajing
    Hu, Yao
    Chen, Wenwen
    Yang, Huazhen
    Yang, Jing
    Song, Huan
    FRONTIERS IN MEDICINE, 2022, 8
  • [35] Investigating the association of testosterone with survival in men and women using a Mendelian randomization study in the UK Biobank
    C. M. Schooling
    J. V. Zhao
    Scientific Reports, 11
  • [36] Investigating the association of testosterone with survival in men and women using a Mendelian randomization study in the UK Biobank
    Schooling, C. M.
    Zhao, J., V
    SCIENTIFIC REPORTS, 2021, 11 (01)
  • [37] Effects of body mass index on relationship status, social contact and socio-economic position: Mendelian randomization and within-sibling study in UK Biobank
    Howe, Laura D.
    Kanayalal, Roshni
    Harrison, Sean
    Beaumont, Robin N.
    Davies, Alisha R.
    Frayling, Timothy M.
    Davies, Neil M.
    Hughes, Amanda
    Jones, Samuel E.
    Sassi, Franco
    Wood, Andrew R.
    Tyrrell, Jessica
    INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2020, 49 (04) : 1173 - 1184
  • [38] Body mass index may not have causal association with thyroid cancer risk: A Mendelian randomization study
    Kim, Jeongseon
    Lee, Soo Ji
    Nguyen, Quy N.
    Lee, Jeonghee
    Lee, Eun Kyung
    Hwangbo, Yul
    Sung, Joohon
    CANCER RESEARCH, 2018, 78 (13)
  • [39] Association between temperatures and type 2 diabetes: A prospective study in UK Biobank
    Wang, ShengYuan
    Lei, YaTing
    Wang, XiaoLi
    Ma, Kun
    Wang, Cheng
    Sun, ChangHao
    Han, TianShu
    DIABETES RESEARCH AND CLINICAL PRACTICE, 2024, 215
  • [40] Educational attainment and drinking behaviors: Mendelian randomization study in UK Biobank
    Tao Zhou
    Dianjianyi Sun
    Xiang Li
    Hao Ma
    Yoriko Heianza
    Lu Qi
    Molecular Psychiatry, 2021, 26 : 4355 - 4366