Current Smoking Dose-Dependently Associated with Decreased β-Cell Function in Chinese Men without Diabetes

The aim of this study was to evaluate the associations between chronic smoking and insulin resistance and β-cell function in Chinese men without diabetes. A total of 1,568 participants were recruited by multistage sampling. Using homeostatic model assessment (HOMA), geometric means of insulin resist...

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Veröffentlicht in:Journal of Diabetes Research 2015-01, Vol.2015 (2015), p.1-9
Hauptverfasser: Yu, Shali, Chen, Gang, Xiang, Quanyong, Wang, Xiaoke, Lin, Ping, Lv, Shurong, Zhu, Ying, Liu, Suyi, Wu, Junxia, Wang, Yijun, Wang, Chun, Xu, Yan
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Sprache:eng
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Zusammenfassung:The aim of this study was to evaluate the associations between chronic smoking and insulin resistance and β-cell function in Chinese men without diabetes. A total of 1,568 participants were recruited by multistage sampling. Using homeostatic model assessment (HOMA), geometric means of insulin resistance (HOMA-IR) and β-cell function (HOMA-β) with 95% confidence interval (CI) were calculated by general linear model. Odds ratios (ORs) with 95% CI were estimated to evaluate the associations between smoking status and insulin resistance and β-cell deficiency under a logistic regression model. Current smokers had higher levels of 2 h glucose (6.66 versus 6.48 mmol/L) for oral glucose tolerance test and lower levels of fasting insulin (5.68 versus 6.03 mU/L) than never smokers. The adjusted means for HOMA-β (%) were 54.86 in current smokers and 58.81 in never smokers (P=0.0257). Current smoking was associated with β-cell deficiency (OR 1.29, 95% CI 1.01–1.64) compared to never smoking. The β-cell function gradually decreased with increasing smoking intensity (Ptrend=0.0026), and the differences were statistically significant when the pack-year of smoking was 20 or above. No association was observed between smoking status and HOMA-IR. Our study suggested that chronic smoking may dose-dependently suppress insulin secretion in Chinese men.
ISSN:2314-6745
2314-6753
DOI:10.1155/2015/841768