| Literature DB >> 28159780 |
Viji Nair1, Cassianne Robinson-Cohen2, Michelle R Smith1, Keith A Bellovich3, Zeenat Yousuf Bhat4, Maria Bobadilla5, Frank Brosius1, Ian H de Boer2, Laurent Essioux6, Ivan Formentini6, Crystal A Gadegbeku7, Debbie Gipson8, Jennifer Hawkins1, Jonathan Himmelfarb2, Bryan Kestenbaum2, Matthias Kretzler1,9, Maria Chiara Magnone6, Kalyani Perumal10, Susan Steigerwalt8, Wenjun Ju11,9, Nisha Bansal12.
Abstract
Growth differentiation factor-15 (GDF-15) is a member of the TGF-β 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 GDF15 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 GDF15 transcript levels (r=0.54, P=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; P=0.003) and 65% higher (95% confidence interval, 1.08 to 2.50; P=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 GDF15 and significantly associated with increased risk of CKD progression in two independent cohorts. Circulating GDF-15 may be a marker for intrarenal GDF15-related signaling pathways associated with CKD and CKD progression.Entities:
Keywords: chronic kidney disease; end-stage renal disease; gene expression; glomerular filtration rate; kidney biopsy
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Year: 2017 PMID: 28159780 PMCID: PMC5491285 DOI: 10.1681/ASN.2016080919
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121