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Circulating TNF Receptors 1 and 2 Predict Stage 3 CKD in Type 1 Diabetes

医学 肾功能 内科学 四分位数 蛋白尿 危险系数 2型糖尿病 内分泌学 糖尿病 比例危险模型 置信区间 泌尿科
作者
Tomohito Gohda,Monika A. Niewczas,Linda Ficociello,William H. Walker,Jan Skupień,Florencia Rosetti,Xavier Culleré,Amanda C. Johnson,Gordon S. Crabtree,Adam M. Smiles,Tanya N. Mayadas,James H. Warram,Andrzej S. Królewski
出处
期刊:Journal of The American Society of Nephrology [American Society of Nephrology]
卷期号:23 (3): 516-524 被引量:349
标识
DOI:10.1681/asn.2011060628
摘要

Elevated plasma concentrations of TNF receptors 1 and 2 (TNFR1 and TNFR2) predict development of ESRD in patients with type 2 diabetes without proteinuria, suggesting these markers may contribute to the pathogenesis of renal decline. We investigated whether circulating markers of the TNF pathway determine GFR loss among patients with type 1 diabetes. We followed two cohorts comprising 628 patients with type 1 diabetes, normal renal function, and no proteinuria. Over 12 years, 69 patients developed estimated GFR less than 60 mL/min per 1.73 m(2) (16 per 1000 person-years). Concentrations of TNFR1 and TNFR2 were strongly associated with risk for early renal decline. Renal decline was associated only modestly with total TNFα concentration and appeared unrelated to free TNFα. The cumulative incidence of estimated GFR less than 60 mL/min per 1.73 m(2) for patients in the highest TNFR2 quartile was 60% after 12 years compared with 5%-19% in the remaining quartiles. In Cox proportional hazards analysis, patients with TNFR2 values in the highest quartile were threefold more likely to experience renal decline than patients in the other quartiles (hazard ratio, 3.0; 95% confidence interval, 1.7-5.5). The risk associated with high TNFR1 values was slightly less than that associated with high TNFR2 values. TNFR levels were unrelated to baseline free TNFα level and remained stable over long periods within an individual. In conclusion, early GFR loss in patients with type 1 diabetes without proteinuria is strongly associated with circulating TNF receptor levels but not TNFα levels (free or total).
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