Relationship of high circulating cystatin c to biochemical markers of bone turnover and bone mineral density in elderly males with a chronic heart failure
Autor: | Božić-Nedeljković Biljana, Lončar Goran, Vizin Tjaša, Radojičić Zoran, Popović-Brkić Vera, Kos Janko |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: | |
Zdroj: | Journal of Medical Biochemistry, Vol 38, Iss 1, Pp 53-62 (2019) |
Druh dokumentu: | article |
ISSN: | 1452-8258 1452-8266 |
Popis: | Background: The aim of the study was to investigate the association of Cystatin C (CysC) to biochemical markers of bone turnover and bone mass, and to evaluate its prognostic significance in elderly males with chronic heart failure (CHF). Methods: A prospective cohort study was executed on sixtyeight males (mean age 68±7 years) with mild to moderate CHF, together with 19 of corresponding ageand body mass index-matched healthy individuals who underwent cardiovascular, bone mineral density (BMD), and body composition assessment. Biochemical assessment of all subjects included NT-pro-BNP, parathyroid hormone (PTH), 25-hydroxy vitamin D (25(O h )D), CysC, and biochemical markers of bone turnover including osteocalcin (OC), alkaline phosphatase (ALP), b-CrossLaps (b-CTx), osteoprotegerin (OPG), and receptor activator of nuclear factor k B ligand (RANKL). Results: Serum CysC was significantly increased in males with CHF in comparison to healthy control ones. A significant positive association was found between CysC levels and OC in males with CHF, while OC and b-CTx increased in increasing CysC tertiles. In multivariate regression analysis, OC and smoking were a significant determinant of CysC in males with CHF Level of CysC was found to be positively associated with an increased fatal risk in males with CHF. Conclusions: Serum osteocalcin is an independent predictor of CysC level in elderly males with CHF. Higher CysC level showed a negative relation to survival and bone loss in males with CHF. Further research is needed to confirm the potential role of CysC in the crosstalk between heart, kidney, bone, and energy metabolism in CHF. |
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