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单核细胞趋化蛋白-1可预测糖尿病肾病的发生。

Monocyte chemoattractant protein-1 predicts the development of diabetic nephropathy.

作者信息

Scurt Florian G, Menne Jan, Brandt Sabine, Bernhardt Anja, Mertens Peter R, Haller Hermann, Chatzikyrkou Christos

机构信息

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.

出版信息

Diabetes Metab Res Rev. 2022 Feb;38(2):e3497. doi: 10.1002/dmrr.3497. Epub 2021 Oct 12.

Abstract

AIM

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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