Department of Occupational and Environmental Health, Key Laboratory of Environment and Health, Ministry of Education and State Key Laboratory of Environmental Health (Incubating), School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
School of Public Health, Guangzhou Medical University, Guangzhou 511436, China.
J Clin Endocrinol Metab. 2023 Feb 15;108(3):736-744. doi: 10.1210/clinem/dgac586.
Impairment of immune and inflammatory homeostasis is reported to be one of the causal factors of diabetes. However, the association of complement C3 levels with incident diabetes in humans remains unclear.
This study aimed to examine the association between C3 levels and incident type 2 diabetes mellitus (T2DM), and further explore the potential mediating role of body mass index (BMI) in C3-T2DM associations.
We determined serum C3 levels of 2662 nondiabetic middle-aged and elderly (64.62 ± 7.25 years) individuals from the Dongfeng-Tongji cohort at baseline. Cox regression was employed to examine the incidence of T2DM in relationship to C3 levels during 10 years of follow-up. Mediation analysis was further applied to assess potential effect of BMI on the C3-T2DM associations.
Overall, 711 (26.7%) participants developed T2DM during 23 067 person-years of follow-up. Higher serum C3 was significantly associated with higher risk of incident T2DM after full adjustment (HR [95% CI] = 1.16 [1.05, 1.27]; per SD higher). Compared with the first quartile of C3 levels, the HR in the fourth quartile was 1.52 (95% CI = [1.14, 2.02]; Ptrend = 0.029). Robust significant linear dose-response relationship was observed between C3 levels and BMI (Poverall < 0.001, Pnonlinear = 0.96). Mediation analyses indicated that BMI might mediate 41.0% of the associations between C3 and T2DM.
The present prospective study revealed that C3 could be an early biomarker for incident T2DM, and that BMI might play a potential mediating role in the C3-T2DM associations, which provided clues for the pathogenesis of diabetes.
据报道,免疫和炎症稳态的损害是糖尿病的一个病因因素。然而,补体 C3 水平与人类 2 型糖尿病(T2DM)的发病之间的关联尚不清楚。
本研究旨在研究 C3 水平与 2 型糖尿病发病的关系,并进一步探讨 BMI 在 C3-T2DM 关联中的潜在中介作用。
我们在基线时测定了 2662 名无糖尿病的中老年(64.62±7.25 岁)个体的血清 C3 水平。Cox 回归分析用于检查 10 年随访期间 C3 水平与 T2DM 发病的关系。进一步应用中介分析评估 BMI 对 C3-T2DM 关联的潜在影响。
在 23067 人年的随访中,共有 711 名(26.7%)参与者发生了 T2DM。在充分调整后,较高的血清 C3 与更高的 T2DM 发病风险显著相关(HR [95%CI] = 1.16 [1.05, 1.27];每 SD 更高)。与 C3 水平的第一四分位数相比,第四四分位数的 HR 为 1.52(95%CI=[1.14, 2.02];Ptrend=0.029)。在 C3 水平和 BMI 之间观察到稳健的显著线性剂量反应关系(Poverall<0.001,Pnonlinear=0.96)。中介分析表明,BMI 可能介导了 C3 与 T2DM 之间 41.0%的关联。
本前瞻性研究表明,C3 可能是 T2DM 发病的早期生物标志物,BMI 可能在 C3-T2DM 关联中发挥潜在的中介作用,为糖尿病的发病机制提供了线索。