Time-resolved Mendelian randomization detects substantial variation in the detrimental effect of obesity throughout life

The global burden of disease attributable to obesity continues to rise. The disease incidence is substantially higher in elderly populations, but how obesity affects disease risk across a lifetime is largely unknown. To quantify the long-term temporal impact of obesity, access to large-scale longitudinal cohorts spanning many decades would typically be required. However, these longitudinal studies are rare and may be heavily biased by the presence of unaccountable confounding. Here, we develop a method-time-resolved Mendelian randomization-to estimate the cumulative effect of body mass index on disease risk at different ages. Using the UK Biobank, we find strong age-varying patterns for type 2 diabetes mellitus, coronary artery disease, and atrial fibrillation, as well as for osteoarthritis. We demonstrate that some of the most notable temporal characteristics are sex specific, while other features are shared between sexes. Analyses suggest that these features can be manifestations of primary prevention strategies.

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Journal
Science Advances
Published
2025-10-24
DOI
https://doi.org/10.1126/sciadv.adv0926
Primary Topic
Genetic Associations and Epidemiology
Type
article
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article

Time-resolved Mendelian randomization detects substantial variation in the detrimental effect of obesity throughout life

Daniel Schmitz, Torgny Karlsson, Åsa Johansson, Fatemeh Hadizadeh et al.
Science Advances
Genetic Associations and Epidemiology
article

Time-resolved Mendelian randomization detects substantial variation in the detrimental effect of obesity throughout life

Daniel Schmitz, Torgny Karlsson, Åsa Johansson, Fatemeh Hadizadeh, Mathias Rask‐Andersen
article en

Abstract

The global burden of disease attributable to obesity continues to rise. The disease incidence is substantially higher in elderly populations, but how obesity affects disease risk across a lifetime is largely unknown. To quantify the long-term temporal impact of obesity, access to large-scale longitudinal cohorts spanning many decades would typically be required. However, these longitudinal studies are rare and may be heavily biased by the presence of unaccountable confounding. Here, we develop a method-time-resolved Mendelian randomization-to estimate the cumulative effect of body mass index on disease risk at different ages. Using the UK Biobank, we find strong age-varying patterns for type 2 diabetes mellitus, coronary artery disease, and atrial fibrillation, as well as for osteoarthritis. We demonstrate that some of the most notable temporal characteristics are sex specific, while other features are shared between sexes. Analyses suggest that these features can be manifestations of primary prevention strategies.

Science AdvancesVol. 11(43)
Uppsala University (SE), Science for Life Laboratory (SE)
Openalex Percentile: Top 67%
Genetic Associations and Epidemiology
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