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Type 2 diabetes and cause-specific mortality in Mexico City: a Mendelian randomisation analysis

Abstract:
Background
Observational epidemiological studies in Mexico have shown high mortality risks associated with type 2 diabetes (T2D). However, it is unclear whether these relationships are wholly causal. We aimed to assess the association of genetically-predicted T2D liability with risk of death in Mexico.

Methods
Between 1998 and 2004, 150,000 men and women were recruited from Mexico City and followed-up until September 2022 for cause-specific mortality. Mendelian randomisation analyses, using a genetic risk score (GRS) comprising 1055 established T2D-associated risk variants, estimated associations with risk of all-cause and cause-specific mortality at ages 35–74.

Findings
Among 121,433 included participants with a mean (standard deviation) age of 51 (11), 68% (n = 82,249) were women and 18% (n = 21,371) had T2D. The GRS explained 6.3% of T2D liability and was not associated with major potential confounders of the T2D-mortality relationship. During a median (interquartile range) of 20.2 (19.4–21.4) years’ follow-up, 12,293 participants died. Genetically-predicted T2D liability was associated with a death rate ratio (RR) of 1.29 (95% confidence interval [CI] 1.23–1.36) per trebling in genetically-predicted odds of T2D. There were particularly strong associations with death from renal disease (n = 1696; RR 2.29 [95% CI 1.99–2.64]) and acute diabetic crises (n = 509; RR 2.27 [1.75–2.93]) and weaker, but still strong, associations with death from vascular disease (n = 3226; RR 1.31 [1.19–1.46]) and infection (n = 2437; RR 1.21 [1.07–1.36]). Genetically-predicted T2D liability was not clearly associated with death from cancer (n = 2016; RR 1.00 [95% CI 0.88–1.14]) or cirrhosis (n = 895; RR 0.90 [0.74–1.10]).

Interpretation
T2D is causally associated with death from vascular, renal and infectious diseases. Its prevention and effective management could substantially reduce premature deaths in Mexico, where T2D is common.

Funding
Wellcome Trust, the Mexican Health Ministry, the National Council for Science and Technology (CONACyT) for Mexico, Cancer Research UK, British Heart Foundation, Kidney Research UK, UK Medical Research Council, AstraZeneca, Regeneron.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.lana.2025.101082

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Clinical Trial Service Unit
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Clinical Trial Service Unit
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Clinical Trial Service Unit
Role:
Author


More from this funder
Funder identifier:
https://ror.org/029chgv08
Grant:
058299/Z/99
More from this funder
Funder identifier:
https://ror.org/02kx7se86
Grant:
MR/R007764/1
More from this funder
Funder identifier:
https://ror.org/02wdwnk04
Grant:
RE/13/1/30181
More from this funder
Funder identifier:
https://ror.org/03x94j517
Grant:
MC_UU_00017/2
MR/Z504543/1
More from this funder
Funder identifier:
https://ror.org/02f51rf24


Publisher:
Elsevier
Journal:
Lancet Regional Health Americas More from this journal
Volume:
45
Article number:
101082
Publication date:
2025-04-06
Acceptance date:
2025-03-18
DOI:
EISSN:
2667-193X
ISSN:
2667-193X


Language:
English
Keywords:
Pubs id:
2095268
Local pid:
pubs:2095268
Deposit date:
2025-03-19
ARK identifier:

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