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Elevated Urinary Connective Tissue Growth Factor in Diabetic Nephropathy Is Caused by Local Production and Tubular Dysfunction

机译:糖尿病肾病中尿路结缔组织生长因子升高是由局部生产和肾小管功能障碍引起的

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摘要

Connective tissue growth factor (CTGF; CCN2) plays a role in the development of diabetic nephropathy (DN). Urinary CTGF (uCTGF) is elevated in DN patients and has been proposed as a biomarker for disease progression, but it is unknown which pathophysiological factors contribute to elevated uCTGF. We studied renal handling of CTGF by infusion of recombinant CTGF in diabetic mice. In addition, uCTGF was measured in type 1 DN patients and compared with glomerular and tubular dysfunction and damage markers. In diabetic mice, uCTGF was increased and fractional excretion (FE) of recombinant CTGF was substantially elevated indicating reduced tubular reabsorption. FE of recombinant CTGF correlated with excretion of endogenous CTGF. CTGF mRNA was mainly localized in glomeruli and medullary tubules. Comparison of FE of endogenous and recombinant CTGF indicated that 60% of uCTGF had a direct renal source, while 40% originated from plasma CTGF. In DN patients, uCTGF was independently associated with markers of proximal and distal tubular dysfunction and damage. In conclusion, uCTGF in DN is elevated as a result of both increased local production and reduced reabsorption due to tubular dysfunction. We submit that uCTGF is a biomarker reflecting both glomerular and tubulointerstitial hallmarks of diabetic kidney disease.
机译:结缔组织生长因子(CTGF; CCN2)在糖尿病性肾病(DN)的发展中发挥作用。 DN患者尿CTGF(uCTGF)升高,并被提议作为疾病进展的生物标志物,但尚不清楚哪些病理生理因素促成uCTGF升高。我们研究了通过在糖尿病小鼠中输注重组CTGF对肾脏处理CTGF的方法。此外,在1型DN患者中测量uCTGF,并将其与肾小球和肾小管功能障碍和损伤标志物进行比较。在糖尿病小鼠中,uCTGF增加,重组CTGF的分数排泄(FE)显着升高,表明肾小管重吸收减少。重组CTGF的FE与内源性CTGF的排泄相关。 CTGF mRNA主要位于肾小球和髓小管。内源性和重组CTGF的FE值比较表明,uCTGF的60%具有直接的肾脏来源,而40%来源于血浆CTGF。在DN患者中,uCTGF与近端和远端肾小管功能障碍和损伤的标志物独立相关。总之,由于肾小管功能障碍,由于局部产量增加和重吸收减少,DN中的uCTGF升高。我们认为,uCTGF是一种反映糖尿病肾病肾小球和肾小管间质标志的生物标志物。

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