BMI and Mortality in UK Biobank: Revised Estimates Using Mendelian Randomization

Obesity (Silver Spring). 2018 Nov;26(11):1796-1806. doi: 10.1002/oby.22313.

Abstract

Objective: The aim of this study was to obtain estimates of the causal relationship between BMI and mortality.

Methods: Mendelian randomization (MR) with BMI-associated genotypic variation was used to test the causal effect of BMI on all-cause and cause-specific mortality in UK Biobank participants of White British ancestry.

Results: MR analyses supported a causal association between higher BMI and greater risk of all-cause mortality (hazard ratio [HR] per 1 kg/m2 : 1.03; 95% CI: 0.99-1.07) and mortality from cardiovascular diseases (HR: 1.10; 95% CI: 1.01-1.19), specifically coronary heart disease (HR: 1.12; 95% CI: 1.00-1.25) and those excluding coronary heart disease/stroke/aortic aneurysm (HR: 1.24; 95% CI: 1.03-1.48), stomach cancer (HR: 1.18; 95% CI: 0.87-1.62), and esophageal cancer (HR: 1.22; 95% CI: 0.98-1.53), and a decreased risk of lung cancer mortality (HR: 0.96; 95% CI: 0.85-1.08). Sex stratification supported the causal role of higher BMI increasing bladder cancer mortality risk (males) but decreasing respiratory disease mortality risk (males). The J-shaped observational association between BMI and mortality was visible with MR analyses, but the BMI at which mortality was minimized was lower and the association was flatter over a larger BMI range.

Conclusions: Results support a causal role of higher BMI in increasing the risk of all-cause mortality and mortality from several specific causes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Specimen Banks / standards*
  • Body Mass Index*
  • Female
  • Humans
  • Male
  • Mendelian Randomization Analysis / methods*
  • Middle Aged
  • Mortality
  • United Kingdom