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  4. Circulating Wnt/β-catenin signalling inhibitors and uraemic vascular calcifications
 
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Circulating Wnt/β-catenin signalling inhibitors and uraemic vascular calcifications

Journal
Nephrology Dialysis Transplantation
Journal Volume
30
Journal Issue
8
Pages
1356-1363
Date Issued
2015
Author(s)
Yang C.-Y.
ZEE-FEN CHANG  
Chau Y.-P.
Chen A.
Yang W.-C.
Yang A.-H.
Lee O.K.-S.
DOI
10.1093/ndt/gfv043
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84939602614&doi=10.1093%2fndt%2fgfv043&partnerID=40&md5=f6463753baca16de619a8de3cb7e5f67
https://scholars.lib.ntu.edu.tw/handle/123456789/564347
Abstract
The process of vascular calcification has been associated with the canonical Wnt/β-catenin signalling pathway in cell cultures and animal studies. The relationship between circulating Wnt/β-catenin inhibitors and vascular calcification in dialysis patients is unknown. The aim of this study was to investigate the associations between serum dickkopf-1 (Dkk-1) and sclerostin, two circulating inhibitors of the Wnt/β-catenin signalling pathway, and the severity of aortic calcification (AoC) and cardiovascular outcomes in dialysis patients. This was a prospective observational cohort study. One hundred and twenty-five patients on maintenance haemodialysis participated in the study. Serum levels of Dkk-1 and sclerostin were measured. AoC scores were calculated from plain films of both posterior-anterior and lateral views. The patients were followed up for 2 years or until death or withdrawal. The circulating sclerostin level was inversely associated with the severity of AoC (P = 0.035) and indicators of the bone turnover rate including serum alkaline phosphatase (ALP) (r = -0.235, P = 0.008) and intact parathyroid hormone (r = -0.523, P < 0.001). Furthermore, Cox regression analysis indicated that the patients with high circulating sclerostin levels were less likely to experience future cardiovascular events [1 pmol/L sclerostin increase, hazard ratio 0.982 (95% CI, 0.967-0.996), P = 0.015] after adjusting for a propensity score. In contrast, serum Dkk-1 was not associated with AoC and clinical outcomes. In long-term haemodialysis patients, circulating sclerostin but not Dkk-1 is inversely associated with AoCs and future cardiovascular events. Our findings suggest that sclerostin, as a bone-related protein, might act as a communicator between uraemic bone and vasculature.
SDGs

[SDGs]SDG3

Publisher
Oxford University Press
Type
journal article

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