Research Division, Joslin Diabetes Center, Boston, MA 02215, USA.
Department of Medicine, Harvard Medical School, Boston, MA 02215, USA.
Sci Transl Med. 2021 Jun 30;13(600). doi: 10.1126/scitranslmed.abd2699.
Diabetic kidney disease (DKD) and its major clinical manifestation, progressive renal decline that leads to end-stage renal disease (ESRD), are a major health burden for individuals with diabetes. The disease process that underlies progressive renal decline comprises factors that increase risk as well as factors that protect against this outcome. Using untargeted proteomic profiling of circulating proteins from individuals in two independent cohorts with type 1 and type 2 diabetes and varying stages of DKD followed for 7 to 15 years, we identified three elevated plasma proteins-fibroblast growth factor 20 (OR, 0.69; 95% CI, 0.54 to 0.88), angiopoietin-1 (OR, 0.72; 95% CI, 0.57 to 0.91), and tumor necrosis factor ligand superfamily member 12 (OR, 0.75; 95% CI, 0.59 to 0.95)-that were associated with protection against progressive renal decline and progression to ESRD. The combined effect of these three protective proteins was demonstrated by very low cumulative risk of ESRD in those who had baseline concentrations above median for all three proteins, whereas the cumulative risk of ESRD was high in those with concentrations below median for these proteins at the beginning of follow-up. This protective effect was shown to be independent from circulating inflammatory proteins and clinical covariates and was confirmed in a third cohort of diabetic individuals with normal renal function. These three protective proteins may serve as biomarkers to stratify diabetic individuals according to risk of progression to ESRD and might also be investigated as potential therapeutics to delay or prevent the onset of ESRD.
糖尿病肾病(DKD)及其主要临床表现,即导致终末期肾病(ESRD)的进行性肾脏衰退,是糖尿病患者的主要健康负担。导致进行性肾脏衰退的疾病过程包括增加风险的因素和保护免受这种结果的因素。我们使用来自两个独立队列的个体的循环蛋白的非靶向蛋白质组学分析,这些个体患有 1 型和 2 型糖尿病以及不同阶段的 DKD,并进行了 7 至 15 年的随访,我们确定了三种升高的血浆蛋白 - 成纤维细胞生长因子 20(OR,0.69;95%CI,0.54 至 0.88),血管生成素-1(OR,0.72;95%CI,0.57 至 0.91)和肿瘤坏死因子配体超家族成员 12(OR,0.75;95%CI,0.59 至 0.95) - 与防止进行性肾脏衰退和进展到 ESRD 相关。这三种保护性蛋白的联合作用通过在基线时三种蛋白的浓度均高于中位数的患者中,ESRD 的累积风险非常低来证明,而在随访开始时这些蛋白的浓度低于中位数的患者中,ESRD 的累积风险很高。这种保护作用被证明与循环炎症蛋白和临床协变量无关,并在肾功能正常的糖尿病患者的第三个队列中得到证实。这三种保护性蛋白可以作为根据进展到 ESRD 的风险对糖尿病患者进行分层的生物标志物,也可以作为潜在的治疗方法来延迟或预防 ESRD 的发生。