Key result
Age, sex, and alcohol modify genetic effects on cardiometabolic traits with up to ~47% heritability.
Why the study?
Little is known about the heritable basis of gene-environment interactions in humans for cardiometabolic traits.
Cohort (n=16,430)
Effect estimate: h2 24% to 47%
p-value: p=<0.001
Age, sex, and alcohol intake are major modifiers of genetic effects for cardiometabolic traits, which may help identify specific loci modifying lifestyle effects in cardiometabolic disease.
May inform personalized cardiometabolic risk models; leaves open validation in prospective cohorts before clinical adoption.
AIMS/HYPOTHESIS: Little is known about the heritable basis of gene-environment interactions in humans. We therefore screened multiple cardiometabolic traits to assess the probability that they are influenced by genotype-environment interactions. METHODS: Fourteen established environmental risk exposures and 11 cardiometabolic traits were analysed in the VIKING study, a cohort of 16,430 Swedish adults from 1682 extended pedigrees with available detailed genealogical, phenotypic and demographic information, using a maximum likelihood variance decomposition method in Sequential Oligogenic Linkage Analysis Routines software. RESULTS: ) ranging from 24% to 47%. Genotype-environment interactions were detected for age and sex (for the majority of traits), physical activity (for triacylglycerols, 2 h glucose and diastolic BP), smoking (for weight), alcohol intake (for weight, BMI and 2 h glucose) and diet pattern (for weight, BMI, glycaemic traits and systolic BP). Genotype-age interactions for weight and systolic BP, genotype-sex interactions for BMI and triacylglycerols and genotype-alcohol intake interactions for weight remained significant after multiple test correction. CONCLUSIONS/INTERPRETATION: Age, sex and alcohol intake are likely to be major modifiers of genetic effects for a range of cardiometabolic traits. This information may prove valuable for studies that seek to identify specific loci that modify the effects of lifestyle in cardiometabolic disease.
No takes yet. Share an insight, caveat, or question.
Poveda et al. (2016) conducted a cohort in Cardiometabolic traits (n=16,430). Environmental exposures (age, sex, physical activity, smoking, alcohol intake, diet pattern) vs. Different levels of exposure was evaluated on Narrow-sense heritability (h2) of cardiometabolic traits and genotype-environment interactions (h2 24% to 47%, p=<0.001). Age, sex, and alcohol intake significantly modify the genetic effects on a range of cardiometabolic traits, which demonstrated narrow-sense heritabilities ranging from 24% to 47%.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: