The association of circulating sclerostin level with markers of bone metabolism in patients with thyroid dysfunction
The aim of this study was to compare serum sclerostin concentrations in patients with thyroid dysfunction with euthyroid control subjects and to assess the relationship between sclerostin and markers of bone metabolism (osteocalcin and beta-cross-laps). The study included 30 patients with thyroid dy...
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| Published in | Journal of medical biochemistry Vol. 39; no. 4; pp. 436 - 443 |
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| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Serbia
Society of Medical Biochemists of Serbia, Belgrade
01.01.2020
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| Subjects | |
| Online Access | Get full text |
| ISSN | 1452-8258 1452-8266 1452-8266 |
| DOI | 10.5937/jomb0-24943 |
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| Abstract | The aim of this study was to compare serum sclerostin concentrations in patients with thyroid dysfunction with euthyroid control subjects and to assess the relationship between sclerostin and markers of bone metabolism (osteocalcin and beta-cross-laps).
The study included 30 patients with thyroid dysfunction (hypothyroidism, hyperthyroidism and subclinical hyperthyroidism) and ten euthyroid controls. Free thyroxine (FT4) was measured by radioimmunoassay, while thyroid stimulating hormone (TSH) concentration was determined immunoradiometrically. We used an ELISA kit to determine the sclerostin level. The electrochemiluminescence method was applied for measuring the bone markers.
Sclerostin levels were significantly lower in hypothyroid patients (p=0.009) and significantly elevated in hyperthyroid patients (p=0.008) compared to control values. Hyperthyroid patients also had higher sclerostin than patients with subclinical hyperthyroidism (p=0.013). Sclerostin concentrations were negatively correlated with TSH levels (r=-0.746, p<0.001), but positively with FT4 (r=0.696, p < 0.001). Moreover, sclerostin was positively associated with osteocalcin (r=0.605, p=0.005) and beta-cross-laps levels (r=0.573, p=0.008) in all thyroid patients.
Serum sclerostin is significantly affected in subjects with thyroid dysfunction. Both sclerostin and thyroid status affect bone homeostasis, which is reflected through the significant correlations with osteocalcin and beta-cross-laps. |
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| AbstractList | Background: The aim of this study was to compare serum sclerostin concentrations in patients with thyroid dysfunction with euthyroid control subjects and to assess the relationship between sclerostin and markers of bone metabolism (osteocalcin and beta-cross-laps). Methods: The study included 30 patients with thyroid dysfunction (hypothyroidism, hyperthyroidism and subclinical hyperthyroidism) and ten euthyroid controls. Free thyroxine (FT4) was measured by radioimmunoassay, while thyroid stimulating hormone (TSH) concentration was determined immunoradiometrically. We used an ELISA kit to determine the sclerostin level. The electrochemiluminescence method was applied for measuring the bone markers. Results: Sclerostin levels were significantly lower in hypothyroid patients (p=0.009) and significantly elevated in hyperthyroid patients (p=0.008) compared to control values. Hyperthyroid patients also had higher sclerostin than patients with subclinical hyperthyroidism (p=0.013). Sclerostin concentrations were negatively correlated with TSH levels (r=-0.746, p<0.001), but positively with FT4 (r=0.696, p < 0.001). Moreover, sclerostin was positively associated with osteocalcin (r=0.605, p=0.005) and beta-cross-laps levels (r=0.573, p=0.008) in all thyroid patients. Conclusions: Serum sclerostin is significantly affected in subjects with thyroid dysfunction. Both sclerostin and thyroid status affect bone homeostasis, which is reflected through the significant correlations with osteocalcin and beta-cross-laps. The aim of this study was to compare serum sclerostin concentrations in patients with thyroid dysfunction with euthyroid control subjects and to assess the relationship between sclerostin and markers of bone metabolism (osteocalcin and beta-cross-laps).BACKGROUNDThe aim of this study was to compare serum sclerostin concentrations in patients with thyroid dysfunction with euthyroid control subjects and to assess the relationship between sclerostin and markers of bone metabolism (osteocalcin and beta-cross-laps).The study included 30 patients with thyroid dysfunction (hypothyroidism, hyperthyroidism and subclinical hyperthyroidism) and ten euthyroid controls. Free thyroxine (FT4) was measured by radioimmunoassay, while thyroid stimulating hormone (TSH) concentration was determined immunoradiometrically. We used an ELISA kit to determine the sclerostin level. The electrochemiluminescence method was applied for measuring the bone markers.METHODSThe study included 30 patients with thyroid dysfunction (hypothyroidism, hyperthyroidism and subclinical hyperthyroidism) and ten euthyroid controls. Free thyroxine (FT4) was measured by radioimmunoassay, while thyroid stimulating hormone (TSH) concentration was determined immunoradiometrically. We used an ELISA kit to determine the sclerostin level. The electrochemiluminescence method was applied for measuring the bone markers.Sclerostin levels were significantly lower in hypothyroid patients (p=0.009) and significantly elevated in hyperthyroid patients (p=0.008) compared to control values. Hyperthyroid patients also had higher sclerostin than patients with subclinical hyperthyroidism (p=0.013). Sclerostin concentrations were negatively correlated with TSH levels (r=-0.746, p<0.001), but positively with FT4 (r=0.696, p < 0.001). Moreover, sclerostin was positively associated with osteocalcin (r=0.605, p=0.005) and beta-cross-laps levels (r=0.573, p=0.008) in all thyroid patients.RESULTSSclerostin levels were significantly lower in hypothyroid patients (p=0.009) and significantly elevated in hyperthyroid patients (p=0.008) compared to control values. Hyperthyroid patients also had higher sclerostin than patients with subclinical hyperthyroidism (p=0.013). Sclerostin concentrations were negatively correlated with TSH levels (r=-0.746, p<0.001), but positively with FT4 (r=0.696, p < 0.001). Moreover, sclerostin was positively associated with osteocalcin (r=0.605, p=0.005) and beta-cross-laps levels (r=0.573, p=0.008) in all thyroid patients.Serum sclerostin is significantly affected in subjects with thyroid dysfunction. Both sclerostin and thyroid status affect bone homeostasis, which is reflected through the significant correlations with osteocalcin and beta-cross-laps.CONCLUSIONSSerum sclerostin is significantly affected in subjects with thyroid dysfunction. Both sclerostin and thyroid status affect bone homeostasis, which is reflected through the significant correlations with osteocalcin and beta-cross-laps. The aim of this study was to compare serum sclerostin concentrations in patients with thyroid dysfunction with euthyroid control subjects and to assess the relationship between sclerostin and markers of bone metabolism (osteocalcin and beta-cross-laps). The study included 30 patients with thyroid dysfunction (hypothyroidism, hyperthyroidism and subclinical hyperthyroidism) and ten euthyroid controls. Free thyroxine (FT4) was measured by radioimmunoassay, while thyroid stimulating hormone (TSH) concentration was determined immunoradiometrically. We used an ELISA kit to determine the sclerostin level. The electrochemiluminescence method was applied for measuring the bone markers. Sclerostin levels were significantly lower in hypothyroid patients (p=0.009) and significantly elevated in hyperthyroid patients (p=0.008) compared to control values. Hyperthyroid patients also had higher sclerostin than patients with subclinical hyperthyroidism (p=0.013). Sclerostin concentrations were negatively correlated with TSH levels (r=-0.746, p<0.001), but positively with FT4 (r=0.696, p < 0.001). Moreover, sclerostin was positively associated with osteocalcin (r=0.605, p=0.005) and beta-cross-laps levels (r=0.573, p=0.008) in all thyroid patients. Serum sclerostin is significantly affected in subjects with thyroid dysfunction. Both sclerostin and thyroid status affect bone homeostasis, which is reflected through the significant correlations with osteocalcin and beta-cross-laps. |
| Author | Jovanović, Zorica Živančević-Simonović, Snežana Minić, Rajna Lučić-Tomić, Aleksandra Mijatović-Teodorović, Ljiljana Stanojević-Pirković, Marijana Mihaljević, Olgica Anđelković, Marija Živković, Irena |
| AuthorAffiliation | 1 University of Kragujevac, Faculty of Medical Sciences, Department of Pathophysiology, Kragujevac 3 Institute of Virology, Vaccines and Sera, Torlak, Department of Scientific Research, Belgrade 2 University of Kragujevac, Faculty of Medical Sciences, Department of Internal Medicine, Kragujevac 5 University of Kragujevac, Faculty of Medical Sciences, Department of Biochemistry, Kragujevac 4 University of Kragujevac, Faculty of Medical Sciences, Department of Nuclear Medicine, Kragujevac |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33312059$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_3389_fendo_2022_996157 crossref_primary_10_3389_fendo_2024_1475214 crossref_primary_10_3390_metabo13020241 crossref_primary_10_3390_metabo12080711 crossref_primary_10_3389_fendo_2023_1115834 crossref_primary_10_3390_biomedicines12040758 |
| Cites_doi | 10.1210/jc.2011-2958 10.1016/S0092-8674(03)00771-2 10.1016/S0009-8981(99)00173-4 10.1007/BF03348786 10.1620/tjem.203.183 10.1359/jbmr.2002.17.11.1961 10.1590/0004-2730000003311 10.1155/2013/638727 10.1210/jc.2011-0566 10.4174/astr.2014.86.2.55 10.1186/1756-6614-5-14 10.1210/jc.2012-2218 10.1016/j.bone.2004.05.023 10.1210/jc.2010-0067 10.1210/jc.2011-2280 10.1056/NEJMra053077 10.1210/jc.2013-2786 10.1016/S1043-2760(03)00144-9 10.1016/j.bone.2010.02.018 10.1210/jc.2013-2113 10.15407/ubj87.01.021 10.1074/jbc.M111.311464 10.1007/s00259-008-0883-1 10.1007/s00774-013-0524-z 10.18388/abp.2016_1303 10.1007/s00198-013-2462-y 10.1210/jc.2013-2106 10.1210/en.2015-1073 10.1186/s13044-014-0012-0 10.1016/j.arcmed.2005.09.009 10.1007/s11154-015-9311-6 10.1359/jbmr.070302 10.1007/s00774-003-0460-4 |
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| Copyright | 2020 Olgica Mihaljević, Snežana Živančević-Simonović, Aleksandra Lučić-Tomić, Irena Živković, Rajna Minić, Ljiljana Mijatović-Teodorović, Zorica Jovanović, Marija Anđelković, Marijana Stanojević-Pirković, published by CEON/CEES. 2020 Olgica Mihaljević, Snežana Živančević-Simonović, Aleksandra Lučić-Tomić, Irena Živković, Rajna Minić, Ljiljana Mijatović-Teodorović, Zorica Jovanović, Marija Anđelković, Marijana Stanojević-Pirković, published by CEON/CEES 2020 Society of Medical Biochemists of Serbia, Belgrade |
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| Keywords | beta-cross-laps osteocalcin bone metabolism thyroid dysfunction sclerostin |
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| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Correspondence to: Marijana Stanojevic-Pirkovic, University of Kragujevac, Faculty of Medical Sciences, 69 Svetozara Markovica Street, 34 000 Kragujevac, Serbia marijanas14@gmail.com |
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| SubjectTerms | beta-cross-laps bone metabolism Original Paper osteocalcin sclerostin thyroid dysfunction |
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| Title | The association of circulating sclerostin level with markers of bone metabolism in patients with thyroid dysfunction |
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