Nair Viji, Robinson-Cohen Cassianne, Smith Michelle R, Bellovich Keith A, Bhat Zeenat Yousuf, Bobadilla Maria, Brosius Frank, de Boer Ian H, Essioux Laurent, Formentini Ivan, Gadegbeku Crystal A, Gipson Debbie, Hawkins Jennifer, Himmelfarb Jonathan, Kestenbaum Bryan, Kretzler Matthias, Magnone Maria Chiara, Perumal Kalyani, Steigerwalt Susan, Ju Wenjun, Bansal Nisha
Department of Internal Medicine, Division of Nephrology.
Kidney Research Institute, Division of Nephrology, University of Washington, Seattle, Washington.
J Am Soc Nephrol. 2017 Jul;28(7):2233-2240. doi: 10.1681/ASN.2016080919. Epub 2017 Feb 3.
Growth differentiation factor-15 (GDF-15) is a member of the TGF- cytokine superfamily that is widely expressed and may be induced in response to tissue injury. Elevations in GDF-15 may identify a novel pathway involved in loss of kidney function among patients with CKD. Among participants in the Clinical Phenotyping and Resource Biobank (C-PROBE) study and the Seattle Kidney Study (SKS), we tested whether kidney tissue expression of mRNA correlates with circulating levels of GDF-15 and whether elevations in circulating GDF-15 are associated with decline in kidney function. In matching samples of 24 patients with CKD from the C-PROBE study, circulating GDF-15 levels significantly correlated with intrarenal transcript levels (=0.54, =0.01). Among the 224 C-PROBE and 297 SKS participants, 72 (32.1%) and 94 (32.0%) patients, respectively, reached a composite end point of 30% decline in eGFR or progression to ESRD over a median of 1.8 and 2.0 years of follow up, respectively. In multivariable models, after adjusting for potential confounders, every doubling of GDF-15 level associated with a 72% higher (95% confidence interval, 1.21 to 4.45; =0.003) and 65% higher (95% confidence interval, 1.08 to 2.50; =0.02) risk of progression of kidney disease in C-PROBE and SKS participants, respectively. These results show that circulating GDF-15 levels strongly correlated with intrarenal expression of and significantly associated with increased risk of CKD progression in two independent cohorts. Circulating GDF-15 may be a marker for intrarenal -related signaling pathways associated with CKD and CKD progression.
生长分化因子-15(GDF-15)是转化生长因子-β细胞因子超家族的成员,广泛表达,可能在组织损伤时被诱导产生。GDF-15水平升高可能揭示了慢性肾脏病(CKD)患者肾功能丧失的一条新途径。在临床表型与资源生物样本库(C-PROBE)研究和西雅图肾脏研究(SKS)的参与者中,我们测试了肾脏组织中mRNA的表达是否与循环中GDF-15水平相关,以及循环中GDF-15水平升高是否与肾功能下降有关。在C-PROBE研究中选取的24例匹配的CKD患者样本中,循环GDF-15水平与肾内转录水平显著相关(r = 0.54,P = 0.01)。在224例C-PROBE研究参与者和297例SKS研究参与者中,分别有72例(32.1%)和94例(32.0%)患者在中位随访时间1.8年和2.0年后达到了估计肾小球滤过率(eGFR)下降30%或进展为终末期肾病(ESRD)的复合终点。在多变量模型中,在调整潜在混杂因素后,GDF-15水平每升高一倍,C-PROBE研究和SKS研究参与者发生肾病进展的风险分别升高72%(95%置信区间为1.21至4.45;P = 0.003)和65%(95%置信区间为1.08至2.50;P = 0.02)。这些结果表明,循环GDF-15水平与肾内表达密切相关,并且在两个独立队列中与CKD进展风险增加显著相关。循环GDF-15可能是与CKD及其进展相关的肾内相关信号通路的标志物。