Scurt Florian G, Menne Jan, Brandt Sabine, Bernhardt Anja, Mertens Peter R, Haller Hermann, Chatzikyrkou Christos
Clinic of Nephrology, Hypertension, Diabetes and Endocrinology, Otto-von-Guericke University Magdeburg, Magdeburg, Germany.
Department of Nephrology, KRH Hospital Siloah, Klinikum Region Hannover GmbH, Hanover, Germany.
Diabetes Metab Res Rev. 2022 Feb;38(2):e3497. doi: 10.1002/dmrr.3497. Epub 2021 Oct 12.
Diabetic nephropathy (DN) is a devastating complication of diabetes mellitus (DM). Therefore, screening strategies in order to prevent its development and/or retard its progression are of paramount importance. We investigated if monocyte chemoattractant protein-1 (MCP-1) was associated with new onset microalbuminuria-the earliest sign of the albuminuric phenotype of DN- in patients with type 2 DM and normoalbuminuria.
We measured MCP-1 in serum and urine samples from patients of the Randomized Olmesartan And Diabetes Microalbuminuria Prevention (ROADMAP) study and its Observational Follow-up (OFU) cohort. A case control design was used with inclusion of 172 patients who developed microalbuminuria (MA) and of 188 well matched controls who remained normoalbuminuric.
The median duration of follow-up for the ROADMAP cohorts was 6.5 years, whereas the mean time until occurrence of MA was 53.2 months. In the multivariate analysis, serum and urine MCP-1 remained significant predictors of new onset MA. The risk for MA increased continuously with increasing serum and urine MCP-1 levels but reached statistical significance only in the highest quartiles. The risk associations were stronger with serum MCP-1.
MCP-1 is a marker and possibly a mediator of early diabetic nephropathy. Further prospective studies are necessary to test whether diabetic patients with elevated MCP-1 levels would benefit from specific therapeutic interventions.
糖尿病肾病(DN)是糖尿病(DM)的一种严重并发症。因此,为预防其发生和/或延缓其进展而采取的筛查策略至关重要。我们研究了单核细胞趋化蛋白-1(MCP-1)是否与2型糖尿病和正常白蛋白尿患者新发微量白蛋白尿(DN白蛋白尿表型的最早迹象)相关。
我们在随机奥美沙坦与糖尿病微量白蛋白尿预防(ROADMAP)研究及其观察性随访(OFU)队列的患者血清和尿液样本中测量了MCP-1。采用病例对照设计,纳入172例发生微量白蛋白尿(MA)的患者和188例匹配良好的仍为正常白蛋白尿的对照。
ROADMAP队列的中位随访时间为6.5年,而发生MA的平均时间为53.2个月。在多变量分析中,血清和尿液MCP-1仍然是新发MA的显著预测因子。MA的风险随着血清和尿液MCP-1水平的升高而持续增加,但仅在最高四分位数时达到统计学显著性。与血清MCP-1的风险关联更强。
MCP-1是早期糖尿病肾病的一个标志物,可能也是其介导因子。有必要进行进一步的前瞻性研究,以测试MCP-1水平升高的糖尿病患者是否能从特定治疗干预中获益。