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Serum myeloid-related protein 8/14 complex is associated with microalbuminuria in patients with type 2 diabetes

机译:血清髓样相关蛋白8/14复合物与2型糖尿病患者的微量白蛋白尿有关

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Microalbuminuria (MA) is associated independently with cardiovascular risk and progression of renal disease in patients with diabetes and the normal population. MA is an accepted factor for microvascular defects, in particular in patients with diabetes, and is associated with inflammation. Activated transmigrating macrophages are key cells in these inflammatory processes. Based on the theory that myeloid-related protein 8/14 complex (MRP8/14) is secreted by transmigrating macrophages, we hypothesized that MA was accompanied by elevated MRP8/14 and investigated whether MA predicts MRP8/14 in patients with type 2 diabetes. A total of 86 men with type 2 diabetes were grouped according to urinary albumin excretion in normoalbuminuria and MA. Serum MRP8/14 levels were measured by enzyme-linked immunosorbent assay. Established cardiovascular risk factors were quantified in both groups and compared with urinary albumin excretion. Albuminuria (mg/day) was positively associated with MRP8/14 (r = 0.34) and systemic blood pressure (r = 0.33). Patients with type 2 diabetes and MA demonstrated significantly higher MRP8/14 levels than patients with normoalbuminuria [median (interquartile range), 1.24 (0.97–2.28) μg/ml versus 0.97 (0.67–1.35) μg/ml, p β = 0.454) as well as SBP (β = 0.625) and haemoglobin A1c (β = 0.322). Our data demonstrate that albumin excretion is associated with the process of macrophage activation determined by MRP8/14 levels. These data not only suggest tissue inflammation as a factor for elevated cardiovascular risk in patients with type 2 diabetes, they further point to a role of macrophage activation in this process.
机译:在糖尿病患者和正常人群中,微量白蛋白尿(MA)与心血管风险和肾脏疾病的进展独立相关。 MA是导致微血管缺损(尤其是在糖尿病患者中)的公认因素,并且与炎症相关。活化的迁移巨噬细胞是这些炎症过程中的关键细胞。基于迁移的巨噬细胞分泌髓样相关蛋白8/14复合物(MRP8 / 14)的理论,我们假设MA伴随MRP8 / 14升高,并调查了MA是否可预测2型糖尿病患者的MRP8 / 14。根据正常白蛋白尿和MA中尿白蛋白排泄,对86名2型糖尿病男性进行了分组。通过酶联免疫吸附测定法测定血清MRP8 / 14水平。在两组中确定已建立的心血管危险因素,并与尿白蛋白排泄进行比较。蛋白尿(mg /天)与MRP8 / 14(r = 0.34)和全身性血压(r = 0.33)呈正相关。 2型糖尿病和MA患者的MRP8 / 14水平明显高于正常白蛋白尿患者[中位(四分位间距),1.24(0.97–2.28)μg/ ml,而0.97(0.67–1.35)μg/ ml,pβ= 0.454)以及SBP(β= 0.625)和血红蛋白A1c(β= 0.322)。我们的数据表明白蛋白排泄与由MRP8 / 14水平决定的巨噬细胞活化过程有关。这些数据不仅表明组织炎症是导致2型糖尿病患者心血管风险升高的因素,而且进一步指出了巨噬细胞激活在此过程中的作用。

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