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Serum fetuin-A is associated with the components of MIAC (malnutrition, inflammation, atherosclerosis, calcification) syndrome in different stages of chronic kidney disease.

Authors :
MUTLUAY, Rüya
KONCA DEĞERTEKİN, Ceyla
IŞIKTAŞ SAYILAR, Emel
DERİCİ, Ülver
GÜLTEKİN, Serap
GÖNEN, Sevim
ARINSOY, Selim Turgay
SİNDEL, Mahmut Şükrü
Source :
Turkish Journal of Medical Sciences; 2019, Vol. 49 Issue 1, p327-335, 9p
Publication Year :
2019

Abstract

Background/aim: Fetuin-A, a circulating inhibitor of calcification, is a marker of inflammatory-nutritional state. We evaluated the association between serum fetuin-A levels and vascular calcification, intima-media thickness, and nutritional and inflammatory markers in different stages of chronic kidney disease (CKD). Materials and methods: CKD patients were sampled for calcium-phosphate parameters and nutritional and inflammatory markers [highly sensitive C-reactive protein (hs-CRP)], and serum fetuin-A levels. Intima-media thicknesses of the common carotid arteries (CIMT) were measured. Peripheral artery calcification scores were obtained. Results: A total of 238 patients were included in the study. Fetuin-A levels in patients with end-stage renal disease were significantly lower than those in patients with stage-3 and stage-4 CKD (stage-5 vs. stage-4, P < 0.001; stage-5 vs. stage-3, P < 0.001). Fetuin-A was negatively correlated with creatinine (P < 0.001), Ca × P product (P < 0.001), hs-CRP (P = 0.01), vascular calcification score (P < 0.001), and CIMT (P < 0.001), and positively correlated with BMI (P < 0.001, r = 0.30) and serum albumin (P < 0.001). Conclusion: Lower levels of fetuin-A were associated with higher vascular calcification scores, CIMT, hs-CRP levels, and lower BMI and albumin. Fetuin-A deficiency may be a key element for MIAC syndrome. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13000144
Volume :
49
Issue :
1
Database :
Complementary Index
Journal :
Turkish Journal of Medical Sciences
Publication Type :
Academic Journal
Accession number :
134815720
Full Text :
https://doi.org/10.3906/sag-1809-43