Key result
Genetically predicted type-2 diabetes is linked to ~11% higher CHD risk per unit increase.
Observational
Mendelian randomization
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In observational studies, type-2 diabetes (T2D) is associated with an increased risk of coronary heart disease (CHD), yet interventional trials have shown no clear effect of glucose-lowering on CHD. Confounding may have therefore influenced these observational estimates. Here we use Mendelian randomization to obtain unconfounded estimates of the influence of T2D and fasting glucose (FG) on CHD risk. Using multiple genetic variants associated with T2D and FG, we find that risk of T2D increases CHD risk (odds ratio (OR)=1.11 (1.05-1.17), per unit increase in odds of T2D, P=8.8 × 10(-5); using data from 34,840/114,981 T2D cases/controls and 63,746/130,681 CHD cases/controls). FG in non-diabetic individuals tends to increase CHD risk (OR=1.15 (1.00-1.32), per mmol·per l, P=0.05; 133,010 non-diabetic individuals and 63,746/130,681 CHD cases/controls). These findings provide evidence supporting a causal relationship between T2D and CHD and suggest that long-term trials may be required to discern the effects of T2D therapies on CHD risk.
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Ahmad et al. (2015) conducted an observational in Type-2 diabetes and coronary heart disease. Genetic predisposition to type-2 diabetes and fasting glucose vs. Lower genetic risk of type-2 diabetes / lower fasting glucose was evaluated on Coronary heart disease (CHD) risk (OR 1.11, 95% CI 1.05-1.17, p=8.8 × 10(-5)). Genetically predicted type-2 diabetes increased coronary heart disease risk.
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