Key result
Increases in BMI (Beta -0.216) and IL-6 (Beta -0.130) were independently associated with declining beta-cell function over time, whereas higher baseline adiponectin (Beta 0.150) was protective.
Cohort (n=361)
Yes
In Mexican Americans at risk for type 2 diabetes, weight gain and increasing IL-6 are associated with declining beta-cell function, while higher baseline adiponectin is protective independent of insulin resistance.
Obesity and adipokines are associated with development of type 2 diabetes. However, limited longitudinal studies have examined their roles on declining β-cell function over time. This report assessed three adiposity measures (BMI, percent body fat, trunk fat), insulin resistance, and fifteen adipokines in relationship to longitudinal change in β-cell function measured by disposition index (DI) from frequently-sampled-intravenous-glucose-tolerance testing. The results showed that three factors were significantly and independently associated with rate of change in DI over time: rate of change in BMI (negative), rate of change in IL-6 (negative), and baseline adiponectin (positive). The association was the strongest for changing BMI and was largely explained by changing insulin resistance; the association with changing IL-6 was also largely explained by changing insulin resistance. Baseline adiponectin remained positively associated after adjustment for changing insulin resistance, suggesting an independent effect of adiponectin to preserve or improve β-cell function. These findings provide evidence and potential mechanisms for the role of obesity in promoting β-cell dysfunction, highlighting the potential importance of mitigating obesity and its metabolic effects in preventing and treating type 2 diabetes.
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Xiang et al. (2018) conducted a cohort in At risk for type 2 diabetes (n=361). Weight gain and adipokines was evaluated on Rate of change in disposition index (DI) (Beta -0.216, p=<0.001). Increases in BMI (Beta -0.216) and IL-6 (Beta -0.130) were independently associated with declining beta-cell function over time, whereas higher baseline adiponectin (Beta 0.150) was protective.
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