Institute of Genetic Epidemiology, Faculty of Medicine and Medical Center-University of Freiburg, Freiburg, Germany.
Department of Medicine IV-Nephrology and Primary Care, Faculty of Medicine and Medical Center-University of Freiburg, Freiburg, Germany.
Nephrol Dial Transplant. 2023 Jan 23;38(1):70-79. doi: 10.1093/ndt/gfac187.
The progression of chronic kidney disease (CKD), a global public health burden, is accompanied by a declining number of functional nephrons. Estimation of remaining nephron mass may improve assessment of CKD progression. Uromodulin has been suggested as a marker of tubular mass. We aimed to identify metabolites associated with uromodulin concentrations in urine and serum to characterize pathophysiologic alterations of metabolic pathways to generate new hypotheses regarding CKD pathophysiology.
We measured urinary and serum uromodulin levels (uUMOD, sUMOD) and 607 urinary metabolites and performed cross-sectional analyses within the German Chronic Kidney Disease study (N = 4628), a prospective observational study. Urinary metabolites significantly associated with uUMOD and sUMOD were used to build weighted metabolite scores for urine (uMS) and serum uromodulin (sMS) and evaluated for time to adverse kidney events over 6.5 years.
Metabolites cross-sectionally associated with uromodulin included amino acids of the tryptophan metabolism, lipids and nucleotides. Higher levels of the sMS [hazard ratio (HR) = 0.73 (95% confidence interval 0.64; 0.82), P = 7.45e-07] and sUMOD [HR = 0.74 (95% confidence interval 0.63; 0.87), P = 2.32e-04] were associated with a lower risk of adverse kidney events over time, whereas uUMOD and uMS showed the same direction of association but were not significant.
We identified urinary metabolites associated with urinary and serum uromodulin. The sUMOD and the sMS were associated with lower risk of adverse kidney events among CKD patients. Higher levels of sUMOD and sMS may reflect a higher number of functional nephrons and therefore a reduced risk of adverse kidney outcomes.
慢性肾脏病(CKD)是一种全球公共卫生负担,其进展伴随着功能性肾单位数量的减少。估计剩余肾单位质量可能会改善对 CKD 进展的评估。尿调蛋白已被认为是肾小管质量的标志物。我们旨在确定与尿和血清中尿调蛋白浓度相关的代谢物,以描述代谢途径的病理生理改变,从而产生关于 CKD 病理生理学的新假设。
我们测量了尿和血清中尿调蛋白水平(uUMOD、sUMOD)和 607 种尿代谢物,并在德国慢性肾脏病研究(N=4628)中进行了横断面分析,这是一项前瞻性观察性研究。与 uUMOD 和 sUMOD 显著相关的尿代谢物被用于构建尿液的加权代谢物评分(uMS)和血清尿调蛋白评分(sMS),并在 6.5 年内评估其对不良肾脏事件的时间。
与尿调蛋白相关的代谢物包括色氨酸代谢、脂质和核苷酸的氨基酸。较高的 sMS [风险比(HR)=0.73(95%置信区间 0.64;0.82),P=7.45e-07] 和 sUMOD [HR=0.74(95%置信区间 0.63;0.87),P=2.32e-04] 与不良肾脏事件的风险随着时间的推移而降低相关,而 uUMOD 和 uMS 则显示出相同的关联方向,但没有统计学意义。
我们鉴定出与尿和血清尿调蛋白相关的尿代谢物。sUMOD 和 sMS 与 CKD 患者不良肾脏事件的风险降低相关。较高的 sUMOD 和 sMS 水平可能反映了更多的功能性肾单位,因此降低了不良肾脏结局的风险。