科研之友
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摘要
Objective: Macrophage inhibitory cytokine-1 (MIC-1) belongs to the transforming growth factor (TGF)-beta superfamily, and has been reported to be involved in energy homoeostasis and weight loss and to have anti-inflammatory properties. We hypothesized that decreased concentrations of MIC-1 would be associated with higher risk of developing type 2 diabetes.
Design and methods: We designed a nested case-control study within the Whitehall II cohort and measured serum concentrations of MIC-1 by ELISA in 180 individuals without type 2 diabetes at baseline who developed type 2 diabetes during the follow-up period of 11.5 +/- 3.0 years and in 372 controls frequency-matched for age, sex, and body mass index with normal glucose tolerance throughout the study.
Results: MIC-1 concentrations at baseline were higher in cases (median (25/75th percentiles) 537.1 (452.7-677.4) pg/ml) than in controls (499.7 (413.8-615.4) pg/ml; P=0.0044). In the age- and sex-adjusted model, a 1-S.D. increase in MIC-1 (206.0 pg/ml) was associated with an odds ratio (95% confidence interval) of 1.21 (0.997; 1.46; P=0.054) for type 2 diabetes. Adjustment for waist circumference, cardiovascular risk factors, socioeconomic status, proinflammatory mediators, and glycemia abolished the association.
Conclusions: Baseline MIC-1 concentrations were increased, not decreased, in individuals before type 2 diabetes manifestation, but not independently associated with incident type 2 diabetes in multivariable analyses. This upregulation of MIC-1 could be part of an anti-inflammatory response preceding the onset of type 2 diabetes, which has been described before for interleukin-1 receptor antagonist and TGF-beta 1.
- 出版日期2010-5
