Chen Yanyan, Wang Shanshan, Guo Hang, Han Fei, Sun Bei, Li Nan, Yang Hongxi, Chen Liming
NHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin, China.
Research Center of Clinical Epidemiology, Peking University Third Hospital, Peking, China.
J Diabetes. 2025 May;17(5):e70097. doi: 10.1111/1753-0407.70097.
To explore the influence of the serum total bilirubin to total cholesterol (TBIL/TC) ratio on the progression of chronic kidney disease (CKD) in people with type 2 diabetes.
The present retrospective discovery cohort investigated 4282 patients. The exposure was baseline TBIL/TC ratio. The outcome was the first time to progressing CKD, defined by a drop in the estimated glomerular filtration rate (eGFR) category, along with a reduction in eGFR of at least 25% compared to the baseline value. Hazard ratios (HRs) for CKD progression were evaluated based on the Cox proportional hazards approach. Dose-response relationships were conducted using Restricted Cubic Splines (RCS). Additionally, 758 patients were enrolled as an independent validation cohort.
During a median observation period of 2.4 years (interquartile range 1.3-3.8 years) within the discovery cohort, 522 individuals showed progression in CKD. The analysis revealed a negative association between the TBIL/TC ratio and the risk of CKD progression, with an adjusted HR of 0.17 and a 95% CI ranging from 0.07 to 0.41. After adjusting for confounding variables, the HRs for the second, third, and fourth quartiles of the TBIL/TC ratio were recorded at 0.61 (95% CI 0.48, 0.78), 0.55 (95% CI 0.42, 0.72), and 0.55 (95% CI 0.41, 0.74), respectively. Analysis with RCS indicated an optimal TBIL/TC ratio threshold of 0.25%. Similar results were also observed in the validation cohort.
A higher TBIL/TC ratio was significantly associated with a reduced risk of CKD progression in patients with type 2 diabetes.
探讨血清总胆红素与总胆固醇比值(TBIL/TC)对2型糖尿病患者慢性肾脏病(CKD)进展的影响。
本回顾性发现队列研究纳入了4282例患者。暴露因素为基线TBIL/TC比值。观察终点为首次进展为CKD,定义为估计肾小球滤过率(eGFR)分级下降,且与基线值相比eGFR降低至少25%。基于Cox比例风险模型评估CKD进展的风险比(HR)。采用限制性立方样条(RCS)分析剂量反应关系。此外,纳入758例患者作为独立验证队列。
在发现队列中位2.4年(四分位间距1.3 - 3.8年)的观察期内,522例个体出现CKD进展。分析显示TBIL/TC比值与CKD进展风险呈负相关,校正后HR为0.17,95%置信区间为0.07至0.41。调整混杂变量后,TBIL/TC比值第二、第三和第四四分位数的HR分别为0.61(95%CI 0.48, 0.78)、0.55(95%CI 0.42, 0.72)和0.55(95%CI 0.41, 0.74)。RCS分析表明最佳TBIL/TC比值阈值为0.25%。在验证队列中也观察到了类似结果。
较高的TBIL/TC比值与2型糖尿病患者CKD进展风险降低显著相关。