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. 2022 Jun 17;21:109. doi: 10.1186/s12933-022-01540-6

Table 1.

Characteristics of the GWASs used in present study

Phenotype PMID Consortium Sample
size
Ancestry Exclusion criteria Adjusted covariates
Exposure
 IR 27841877 MAGIC for fasting insulin adjusting BMI 108,557 European Individuals had a physician diagnosis of diabetes, were on diabetes treatment (oral or insulin), or had a fasting plasma glucose equal to or greater than 7 mmol/l Age, sex, BMI
29046328 GLGC for TGs and HDL-C 188,577 European Individuals known to be on lipid-lowering medications Age, sex
 HbA1c 28898252 MAGIC 123,665 European Individuals had a physician diagnosis of diabetes, were on diabetes treatment (oral or insulin), or had a fasting plasma glucose equal to or greater than 7 mmol/l Study-specific covariates, age, sex, and genomic control
 Fasting insulin 22885924 MAGIC 108,557 European Individuals had a physician diagnosis of diabetes, were on diabetes treatment (oral or insulin), or had a fasting plasma glucose equal to or greater than 7 mmol/l Age, sex, BMI
 Fasting glucose 133,010
Outcomes
 LV end-diastolic volume 31554410 UK Biobank 16,920 European Individuals with prevalent myocardial infarction, heart failure, or LV ejection fraction < 50% to minimize the confounding influence of these preexisting conditions were excluded Age, sex, height, weight, systolic blood pressure, phenotype-derivation method, array type, and imaging center
 LV end-systolic volume 16,920
 LV ejection fraction 16,923
 LV mass 16,920
 LV mass to end-diastolic volume ratio 16,884
 Heart failure 31919418 HERMES 47,309 cases and 930,014 controls European Non-European ancestry individuals were excluded Age, sex, genotyping array and the first 10 principal components

GWAS genome-wide association studies, IR insulin resistance, HDL-C high-density lipoprotein cholesterol, TGs triglycerides, HbA1c hemoglobin A1c, LV left ventricular, BMI body mass index, MAGIC the Meta-Analyses of Glucose and Insulin-related traits Consortium, GLGC Global Lipids Genetics Consortium, HERMES the Heart Failure Molecular Epidemiology for Therapeutic Targets