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Cystatin C as a potential predictor of osteoprotegerin levels in healthy men, a cross-sectional, observational study

BACKGROUND: The aim of the present study is to evaluate serum osteoprotegerin (OPG) and soluble receptor activator of nuclear factor κB ligand (sRANKL) levels in a randomly selected male cohort over 50 years of age and its association with cystatin C, a cysteine proteinase inhibitor that decreases f...

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Autores principales: Kulcsar-Jakab, Eva, Petho, Zsofia, Pap, Zoltan, Kalina, Edit, Foldesi, Roza, Balogh, Adam, Antal-Szalmas, Peter, Bhattoa, Harjit Pal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551745/
https://www.ncbi.nlm.nih.gov/pubmed/26311162
http://dx.doi.org/10.1186/s12891-015-0684-1
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author Kulcsar-Jakab, Eva
Petho, Zsofia
Pap, Zoltan
Kalina, Edit
Foldesi, Roza
Balogh, Adam
Antal-Szalmas, Peter
Bhattoa, Harjit Pal
author_facet Kulcsar-Jakab, Eva
Petho, Zsofia
Pap, Zoltan
Kalina, Edit
Foldesi, Roza
Balogh, Adam
Antal-Szalmas, Peter
Bhattoa, Harjit Pal
author_sort Kulcsar-Jakab, Eva
collection PubMed
description BACKGROUND: The aim of the present study is to evaluate serum osteoprotegerin (OPG) and soluble receptor activator of nuclear factor κB ligand (sRANKL) levels in a randomly selected male cohort over 50 years of age and its association with cystatin C, a cysteine proteinase inhibitor that decreases formation of osteoclasts by interfering at a late stage of pre-osteoclast differentiation, apart from being a marker of renal function independent of gender, muscle mass and age; in addition to known predictors such as age, sex hormones, vitamin D, bone mineral density (BMD) and biochemical markers of bone turnover. METHODS: We determined serum OPG and sRANKL levels and examined its relationship with cystatin C, age, osteocalcin, C-terminal telopeptides of type-I collagen, procollagen type 1 amino-terminal propeptide, 25-hydroxyvitamin D, parathyroid hormone, total 17β-estradiol (E2), total testosterone and L1–L4 (LS) and femur neck (FN) BMD data available from 194 (age, range: 51–81 years) randomly selected ambulatory men belonging to the HunMen cohort. RESULTS: OPG correlated significantly with age (Spearman’s rho (r) = 0.359, p < 0.001), cystatin C (r = 0.298, p < 0.001), E2 (r = 0.160, p = 0.028) and free testosterone index (FTI) (r = −0.230, p = 0.001). Compared to the middle-aged (age: ≤ 59 years, n = 98), older men (age > 59 years, n = 96) had significantly higher serum OPG (4.6 pmol/L vs. 5.4 pmol/L; p < 0.001), and lower sRANKL (0.226 pmol/L vs. 0.167 pmol/L; p = 0.048) levels. The older men showed a significant correlation between serum OPG levels and cystatin C (Spearman’s rho = 0.322, p = 0.002), and E2 (Spearman’s rho = 0.211, p = 0.043). Including cystatin C and E2 in a regression model showed that cystatin C (standard regression coefficient (β) = 0.345; p = 0.002) was the only significant predictor of serum OPG levels in the older men. CONCLUSIONS: The results of this study demonstrated that in addition to age (which was the stronger predictor), other modifiable factors such as cystatin C, FTI and E2 were also significant predictors of OPG, and that the association between cystatin C and OPG was more evident with increased age (older age group). As such, cystatin C is a significant predictor of OPG independently of age, FTI and E2. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12891-015-0684-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-45517452015-08-29 Cystatin C as a potential predictor of osteoprotegerin levels in healthy men, a cross-sectional, observational study Kulcsar-Jakab, Eva Petho, Zsofia Pap, Zoltan Kalina, Edit Foldesi, Roza Balogh, Adam Antal-Szalmas, Peter Bhattoa, Harjit Pal BMC Musculoskelet Disord Research Article BACKGROUND: The aim of the present study is to evaluate serum osteoprotegerin (OPG) and soluble receptor activator of nuclear factor κB ligand (sRANKL) levels in a randomly selected male cohort over 50 years of age and its association with cystatin C, a cysteine proteinase inhibitor that decreases formation of osteoclasts by interfering at a late stage of pre-osteoclast differentiation, apart from being a marker of renal function independent of gender, muscle mass and age; in addition to known predictors such as age, sex hormones, vitamin D, bone mineral density (BMD) and biochemical markers of bone turnover. METHODS: We determined serum OPG and sRANKL levels and examined its relationship with cystatin C, age, osteocalcin, C-terminal telopeptides of type-I collagen, procollagen type 1 amino-terminal propeptide, 25-hydroxyvitamin D, parathyroid hormone, total 17β-estradiol (E2), total testosterone and L1–L4 (LS) and femur neck (FN) BMD data available from 194 (age, range: 51–81 years) randomly selected ambulatory men belonging to the HunMen cohort. RESULTS: OPG correlated significantly with age (Spearman’s rho (r) = 0.359, p < 0.001), cystatin C (r = 0.298, p < 0.001), E2 (r = 0.160, p = 0.028) and free testosterone index (FTI) (r = −0.230, p = 0.001). Compared to the middle-aged (age: ≤ 59 years, n = 98), older men (age > 59 years, n = 96) had significantly higher serum OPG (4.6 pmol/L vs. 5.4 pmol/L; p < 0.001), and lower sRANKL (0.226 pmol/L vs. 0.167 pmol/L; p = 0.048) levels. The older men showed a significant correlation between serum OPG levels and cystatin C (Spearman’s rho = 0.322, p = 0.002), and E2 (Spearman’s rho = 0.211, p = 0.043). Including cystatin C and E2 in a regression model showed that cystatin C (standard regression coefficient (β) = 0.345; p = 0.002) was the only significant predictor of serum OPG levels in the older men. CONCLUSIONS: The results of this study demonstrated that in addition to age (which was the stronger predictor), other modifiable factors such as cystatin C, FTI and E2 were also significant predictors of OPG, and that the association between cystatin C and OPG was more evident with increased age (older age group). As such, cystatin C is a significant predictor of OPG independently of age, FTI and E2. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12891-015-0684-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-28 /pmc/articles/PMC4551745/ /pubmed/26311162 http://dx.doi.org/10.1186/s12891-015-0684-1 Text en © Kulcsar-Jakab et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kulcsar-Jakab, Eva
Petho, Zsofia
Pap, Zoltan
Kalina, Edit
Foldesi, Roza
Balogh, Adam
Antal-Szalmas, Peter
Bhattoa, Harjit Pal
Cystatin C as a potential predictor of osteoprotegerin levels in healthy men, a cross-sectional, observational study
title Cystatin C as a potential predictor of osteoprotegerin levels in healthy men, a cross-sectional, observational study
title_full Cystatin C as a potential predictor of osteoprotegerin levels in healthy men, a cross-sectional, observational study
title_fullStr Cystatin C as a potential predictor of osteoprotegerin levels in healthy men, a cross-sectional, observational study
title_full_unstemmed Cystatin C as a potential predictor of osteoprotegerin levels in healthy men, a cross-sectional, observational study
title_short Cystatin C as a potential predictor of osteoprotegerin levels in healthy men, a cross-sectional, observational study
title_sort cystatin c as a potential predictor of osteoprotegerin levels in healthy men, a cross-sectional, observational study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551745/
https://www.ncbi.nlm.nih.gov/pubmed/26311162
http://dx.doi.org/10.1186/s12891-015-0684-1
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