학술논문

Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose
Document Type
article
Source
PLOS ONE. 15(5)
Subject
Biological Sciences
Biomedical and Clinical Sciences
Genetics
Epidemiology
Health Sciences
Pharmacology and Pharmaceutical Sciences
Tobacco
Aging
Tobacco Smoke and Health
Human Genome
Nutrition
Diabetes
Clinical Research
Prevention
Aetiology
2.1 Biological and endogenous factors
Good Health and Well Being
Adult
Aged
Black People
Blood Glucose
Cigarette Smoking
Cohort Studies
Diabetes Mellitus
Type 2
Fasting
Feasibility Studies
Female
Genetic Loci
Genome-Wide Association Study
Genotype
Humans
Incidence
Male
Middle Aged
Polymorphism
Single Nucleotide
Risk
White People
General Science & Technology
Language
Abstract
Smoking is a potentially causal behavioral risk factor for type 2 diabetes (T2D), but not all smokers develop T2D. It is unknown whether genetic factors partially explain this variation. We performed genome-environment-wide interaction studies to identify loci exhibiting potential interaction with baseline smoking status (ever vs. never) on incident T2D and fasting glucose (FG). Analyses were performed in participants of European (EA) and African ancestry (AA) separately. Discovery analyses were conducted using genotype data from the 50,000-single-nucleotide polymorphism (SNP) ITMAT-Broad-CARe (IBC) array in 5 cohorts from from the Candidate Gene Association Resource Consortium (n = 23,189). Replication was performed in up to 16 studies from the Cohorts for Heart Aging Research in Genomic Epidemiology Consortium (n = 74,584). In meta-analysis of discovery and replication estimates, 5 SNPs met at least one criterion for potential interaction with smoking on incident T2D at p