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Genetic and baseline metabolic factors for incident diabetes and HbA(1c) at follow-up: The healthy twin study

Cited 3 time in Web of Science Cited 8 time in Scopus
Authors

Sung, Joohon; Lee, Kayoung; Song, Yun-Mi; Lee, Mikyeong; Kim, Jina

Issue Date
2015-05
Publisher
John Wiley & Sons Inc.
Citation
Diabetes/Metabolism Research and Reviews, Vol.31 No.4, pp.376-384
Abstract
BackgroundWe investigated baseline anthropometric/metabolic traits predicting incident diabetes, genetic/environmental relationships between these traits and HbA(1c) at follow-up and the contribution of genetics, covariates and environments to variance in HbA(1c) at follow-up and incident diabetes. MethodsNondiabetic twins (n=869) and their family members (n=949) were followed over 3.71.4years (44.312.8years of age); baseline anthropometric/metabolic traits were measured. Fasting plasma glucose and HbA(1c) were measured at follow-up. Incident diabetes was defined as HbA(1c) 6.5% or fasting plasma glucose 7mmol/L. ResultsAge-adjusted incident diabetes was 4.9% in men and 4.1% in women. Odd ratio for incident diabetes was 2.34-2.40, 1.25-1.28, 1.22-1.27 and 1.89 per standard deviation of baseline fasting plasma glucose, white blood cell (WBC), triglycerides and waist circumference, respectively, in multivariate generalized estimating equation models (p<0.05). Age-adjusted and sex-adjusted heritability was 0.85 for diabetes and 0.72 for HbA(1c). In bivariate analyses adjusted for age, sex and body mass index at baseline, HbA(1c) at follow-up showed significant genetic and environmental correlations with baseline glucose (0.44, 0.17), significant genetic correlation with baseline waist circumference (0.16) and triglycerides (0.30) and significant environmental correlation with baseline WBC (0.09). Variance in HbA(1c) at follow-up and incident diabetes was explained by genetics (33% and 28%, respectively), covariates (36% and 48%, respectively), shared environments (7% and 0%, respectively) and errors (24% and 24%, respectively). ConclusionsHigh values for baseline fasting plasma glucose, WBC, triglycerides and waist circumference are independent risk factors for incident diabetes. While genetic influences strongly contribute to variance in HbA(1c) at follow-up and incident diabetes, these risk factors significantly contribute to the remaining variance. Copyright (c) 2014 John Wiley & Sons, Ltd.
ISSN
1520-7552
Language
English
URI
https://hdl.handle.net/10371/94766
DOI
https://doi.org/10.1002/dmrr.2619
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