Joseph Banks Laboratories, College of Health and Science, University of Lincoln, Lincoln, U.K.
Calico Life Sciences LLC, South San Francisco, CA.
Diabetes. 2024 Jun 1;73(6):1012-1025. doi: 10.2337/db23-1005.
We aimed to unravel the mechanisms connecting adiposity to type 2 diabetes. We used MR-Clust to cluster independent genetic variants associated with body fat percentage (388 variants) and BMI (540 variants) based on their impact on type 2 diabetes. We identified five clusters of adiposity-increasing alleles associated with higher type 2 diabetes risk (unfavorable adiposity) and three clusters associated with lower risk (favorable adiposity). We then characterized each cluster based on various biomarkers, metabolites, and MRI-based measures of fat distribution and muscle quality. Analyzing the metabolic signatures of these clusters revealed two primary mechanisms connecting higher adiposity to reduced type 2 diabetes risk. The first involves higher adiposity in subcutaneous tissues (abdomen and thigh), lower liver fat, improved insulin sensitivity, and decreased risk of cardiometabolic diseases and diabetes complications. The second mechanism is characterized by increased body size and enhanced muscle quality, with no impact on cardiometabolic outcomes. Furthermore, our findings unveil diverse mechanisms linking higher adiposity to higher disease risk, such as cholesterol pathways or inflammation. These results reinforce the existence of adiposity-related mechanisms that may act as protective factors against type 2 diabetes and its complications, especially when accompanied by reduced ectopic liver fat.
我们旨在揭示肥胖与 2 型糖尿病之间的关联机制。我们使用 MR-Clust 根据与 2 型糖尿病相关的独立遗传变异对体脂肪百分比(388 个变异)和 BMI(540 个变异)的影响进行聚类。我们确定了与更高的 2 型糖尿病风险相关的五个肥胖增加等位基因簇(不利肥胖)和三个与更低的风险相关的簇(有利肥胖)。然后,我们根据各种生物标志物、代谢物以及基于 MRI 的脂肪分布和肌肉质量测量值来描述每个簇的特征。分析这些簇的代谢特征揭示了两种将更高的肥胖与降低的 2 型糖尿病风险联系起来的主要机制。第一个机制涉及腹部和大腿等皮下组织的更高肥胖,更低的肝脂肪,改善的胰岛素敏感性,以及减少心血管代谢疾病和糖尿病并发症的风险。第二个机制的特点是身体尺寸增加和肌肉质量增强,对心血管代谢结果没有影响。此外,我们的研究结果揭示了将更高的肥胖与更高的疾病风险联系起来的不同机制,例如胆固醇途径或炎症。这些结果强化了存在与肥胖相关的机制,这些机制可能作为 2 型糖尿病及其并发症的保护因素,尤其是在伴有异位肝脂肪减少的情况下。