Association of urinary EGF, FABP3, and VCAM1 levels with the progression of early diabetic kidney disease.

IF 2.3 4区 医学 Q2 PERIPHERAL VASCULAR DISEASE Kidney & blood pressure research Pub Date : 2024-11-07 DOI:10.1159/000542267
Felix Keller, Sara Denicolò, Johannes Leierer, Maren Kruus, Andreas Heinzel, Michael Kammer, Wenjun Ju, Viji Nair, Frederic Burdet, Mark Ibberson, Rajasree Menon, Edgar Otto, Ye Ji Choi, Laura Pyle, Patricia Ladd, Petter M Bjornstad, Susanne Eder, Laszlo Rosivall, Patrick Barry Mark, Andrzej Wiecek, Hiddo J Lamber Heerspink, Matthias Kretzler, Rainer Oberbauer, Gert Mayer, Paul Perco
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Abstract

Introduction Diabetic kidney disease (DKD) is a common cause of chronic kidney disease with around 25-40% of patients with diabetes being affected. The course of DKD is variable and estimated glomerular filtration rate (eGFR) and albuminuria, the currently used clinical markers, are not able to accurately predict the individual disease trajectory, in particular in early stages of the disease. The aim of this study was to assess the association of urine levels of selected protein biomarkers with the progression of DKD at an early stage of disease. Methods We measured 22 protein biomarkers using the Mesoscale Discovery platform in 461 urine samples of the PROVALID cohort, an observational study of patients with type 2 diabetes mellitus followed at the primary health care level for a minimum of four years. Odds ratios (OR) were estimated for the effect of marker values above median on fast progression using unadjusted and adjusted logistic regression models. RNA expression at the single cell level in kidney biopsy samples obtained from a cohort of young persons with type 2 diabetes mellitus was in addition determined for markers showing significant associations with disease progression. Results Increased urinary levels of epidermal growth factor (EGF) were linked to lower odds of fast progression (defined as annual eGFR decline greater than 2.58 ml/min per 1.73 m2) with an odds ratio (OR) of 0.60 (95% CI 0.46, 0.78). The association with outcome was even stronger when adjusting for a set of 14 baseline clinical parameters including age, biological sex, eGFR, body mass index, albuminuria, and HbA1c. Elevated urinary levels of fatty acid binding protein 3 (FABP3) and vascular cell adhesion molecule 1 (VCAM1) were each significantly associated with fast progression with an OR of 1.44 (95% CI 1.11, 1.87) and an OR of 1.41 (95% CI 1.08, 1.83), respectively. Enriched expression of EGF and FABP3 was observed in distal convoluted tubular cells and VCAM1 in parietal epithelial cells at single cell level from biopsies of patients with early DKD. Conclusion In summary we show that lower urinary levels of EGF and higher urinary levels of FABP3 and VCAM1 are significantly associated with DKD progression in early-stage disease.

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尿液中 EGF、FABP3 和 VCAM1 水平与早期糖尿病肾病进展的关系。
导言 糖尿病肾病(DKD)是慢性肾病的常见病因,约有 25%-40% 的糖尿病患者受到影响。糖尿病肾病的病程多变,目前使用的临床标记物--估计肾小球滤过率(eGFR)和白蛋白尿并不能准确预测个体疾病的发展轨迹,尤其是在疾病的早期阶段。本研究旨在评估尿液中特定蛋白质生物标志物的水平与疾病早期阶段 DKD 进展的关系。方法 我们使用 Mesoscale Discovery 平台测量了 PROVALID 队列 461 份尿液样本中的 22 种蛋白质生物标志物。使用未调整和调整后的逻辑回归模型估算了标记物值高于中位数对快速进展的影响的比值比(OR)。此外,还测定了从 2 型糖尿病患者队列中获取的肾活检样本中单细胞水平的 RNA 表达,以确定与疾病进展有显著关联的标记物。结果 尿液中表皮生长因子(EGF)水平的升高与疾病快速进展(定义为 eGFR 年下降率大于 2.58 毫升/分钟/1.73 平方米)的几率降低有关,其几率比 (OR) 为 0.60(95% CI 0.46,0.78)。如果对包括年龄、生理性别、eGFR、体重指数、白蛋白尿和 HbA1c 在内的 14 项基线临床参数进行调整,则与结果的关联性更强。尿液中脂肪酸结合蛋白 3 (FABP3) 和血管细胞粘附分子 1 (VCAM1) 水平的升高与快速进展显著相关,OR 值分别为 1.44(95% CI 1.11,1.87)和 1.41(95% CI 1.08,1.83)。从早期 DKD 患者的活检组织中观察到 EGF 和 FABP3 在远端曲细管细胞中大量表达,VCAM1 在顶叶上皮细胞中单细胞水平上大量表达。结论 总之,我们的研究表明,尿液中 EGF 水平较低、FABP3 和 VCAM1 水平较高与早期 DKD 病程进展密切相关。
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来源期刊
Kidney & blood pressure research
Kidney & blood pressure research 医学-泌尿学与肾脏学
CiteScore
4.80
自引率
3.60%
发文量
61
审稿时长
6-12 weeks
期刊介绍: This journal comprises both clinical and basic studies at the interface of nephrology, hypertension and cardiovascular research. The topics to be covered include the structural organization and biochemistry of the normal and diseased kidney, the molecular biology of transporters, the physiology and pathophysiology of glomerular filtration and tubular transport, endothelial and vascular smooth muscle cell function and blood pressure control, as well as water, electrolyte and mineral metabolism. Also discussed are the (patho)physiology and (patho) biochemistry of renal hormones, the molecular biology, genetics and clinical course of renal disease and hypertension, the renal elimination, action and clinical use of drugs, as well as dialysis and transplantation. Featuring peer-reviewed original papers, editorials translating basic science into patient-oriented research and disease, in depth reviews, and regular special topic sections, ''Kidney & Blood Pressure Research'' is an important source of information for researchers in nephrology and cardiovascular medicine.
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