Complex assessment of bone mineral density, fracture risk, vitamin D status, and bone metabolism in Hungarian systemic sclerosis patients

Abstract Objective We wished to determine bone alterations in systemic sclerosis (SSc) patients by conventional densitometry (DXA), peripheral quantitative computed tomography (pQCT), and bone biomarkers. Methods We included 44 SSc patients and 33 age-matched healthy controls. Lumbar spine and femor...

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Main Authors: Ágnes Horváth, Edit Végh, Anita Pusztai, Zsófia Pethő, Attila Hamar, Monika Czókolyová, Harjit Pal Bhattoa, Gábor Nagy, Balázs Juhász, Katalin Hodosi, Andrea Domján, Zoltán Szekanecz, Gabriella Szücs, Szilvia Szamosi
Format: Article
Language:English
Published: BMC 2019-12-01
Series:Arthritis Research & Therapy
Subjects:
DXA
Online Access:https://doi.org/10.1186/s13075-019-2072-y
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spelling doaj-73dc4cfb35db4d0abfd55541c1c275602020-12-13T12:40:48ZengBMCArthritis Research & Therapy1478-63622019-12-0121111010.1186/s13075-019-2072-yComplex assessment of bone mineral density, fracture risk, vitamin D status, and bone metabolism in Hungarian systemic sclerosis patientsÁgnes Horváth0Edit Végh1Anita Pusztai2Zsófia Pethő3Attila Hamar4Monika Czókolyová5Harjit Pal Bhattoa6Gábor Nagy7Balázs Juhász8Katalin Hodosi9Andrea Domján10Zoltán Szekanecz11Gabriella Szücs12Szilvia Szamosi13Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenDepartment of Laboratory Medicine, Faculty of Medicine, University of DebrecenDepartment of Laboratory Medicine, Faculty of Medicine, University of DebrecenDepartment of Oncology, Faculty of Medicine, University of DebrecenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, University of DebrecenAbstract Objective We wished to determine bone alterations in systemic sclerosis (SSc) patients by conventional densitometry (DXA), peripheral quantitative computed tomography (pQCT), and bone biomarkers. Methods We included 44 SSc patients and 33 age-matched healthy controls. Lumbar spine and femoral neck bone mineral density (BMD) was assessed by DXA. Volumetric BMD was measured by pQCT at the radius. FRAX, 25-hydroxyvitamin-D3 (25-OH-D3), parathyroid hormone, osteocalcin, C-terminal collagen telopeptide, and procollagen type I amino-terminal propeptide were also assessed. Results SSc patients had lower L2–4 BMD (0.880 ± 0.108 vs. 0.996 ± 0.181 g/cm2; p = 0.019) and femoral neck (FN) BMD (0.786 ± 0.134 vs. 0.910 ± 0.090 g/cm2; p = 0.007) by DXA. In SSc vs. controls, pQCT indicated lower mean cortical (328.03 ± 103.32 vs. 487.06 ± 42.45 mg/cm3; p < 0.001) and trabecular density (150.93 ± 61.91 vs. 184.76 ± 33.03 mg/cm3; p = 0.037). Vitamin D3 deficiency was more common in SSc vs. controls (60.0% vs. 39.3%; p = 0.003). L2–4 (p = 0.002) and FN BMD (p = 0.015) positively correlated with BMI. pQCT assessments confirmed an inverse correlation between pulmonary manifestation and total (p = 0.024), trabecular (p = 0.035), and cortical density (p = 0.015). Anti-Scl70 positivity inversely correlated with pQCT total density (p = 0.015) and the presence of digital ulcers with cortical density (p = 0.001). We also found that vertebral and FN BMD as determined by DXA significantly correlated with pQCT total, trabecular, and cortical density (p < 0.05). Conclusion The results of our study suggest that bone loss in SSc patients may be associated with lower BMI, anti-Scl70 positivity, and the presence of pulmonary manifestations and digital ulcers. Both DXA and pQCT are appropriate tools to evaluate the bone alterations in SSc patients.https://doi.org/10.1186/s13075-019-2072-ySystemic sclerosisBone lossOsteoporosisDXApQCTPulmonary manifestations
collection DOAJ
language English
format Article
sources DOAJ
author Ágnes Horváth
Edit Végh
Anita Pusztai
Zsófia Pethő
Attila Hamar
Monika Czókolyová
Harjit Pal Bhattoa
Gábor Nagy
Balázs Juhász
Katalin Hodosi
Andrea Domján
Zoltán Szekanecz
Gabriella Szücs
Szilvia Szamosi
spellingShingle Ágnes Horváth
Edit Végh
Anita Pusztai
Zsófia Pethő
Attila Hamar
Monika Czókolyová
Harjit Pal Bhattoa
Gábor Nagy
Balázs Juhász
Katalin Hodosi
Andrea Domján
Zoltán Szekanecz
Gabriella Szücs
Szilvia Szamosi
Complex assessment of bone mineral density, fracture risk, vitamin D status, and bone metabolism in Hungarian systemic sclerosis patients
Arthritis Research & Therapy
Systemic sclerosis
Bone loss
Osteoporosis
DXA
pQCT
Pulmonary manifestations
author_facet Ágnes Horváth
Edit Végh
Anita Pusztai
Zsófia Pethő
Attila Hamar
Monika Czókolyová
Harjit Pal Bhattoa
Gábor Nagy
Balázs Juhász
Katalin Hodosi
Andrea Domján
Zoltán Szekanecz
Gabriella Szücs
Szilvia Szamosi
author_sort Ágnes Horváth
title Complex assessment of bone mineral density, fracture risk, vitamin D status, and bone metabolism in Hungarian systemic sclerosis patients
title_short Complex assessment of bone mineral density, fracture risk, vitamin D status, and bone metabolism in Hungarian systemic sclerosis patients
title_full Complex assessment of bone mineral density, fracture risk, vitamin D status, and bone metabolism in Hungarian systemic sclerosis patients
title_fullStr Complex assessment of bone mineral density, fracture risk, vitamin D status, and bone metabolism in Hungarian systemic sclerosis patients
title_full_unstemmed Complex assessment of bone mineral density, fracture risk, vitamin D status, and bone metabolism in Hungarian systemic sclerosis patients
title_sort complex assessment of bone mineral density, fracture risk, vitamin d status, and bone metabolism in hungarian systemic sclerosis patients
publisher BMC
series Arthritis Research & Therapy
issn 1478-6362
publishDate 2019-12-01
description Abstract Objective We wished to determine bone alterations in systemic sclerosis (SSc) patients by conventional densitometry (DXA), peripheral quantitative computed tomography (pQCT), and bone biomarkers. Methods We included 44 SSc patients and 33 age-matched healthy controls. Lumbar spine and femoral neck bone mineral density (BMD) was assessed by DXA. Volumetric BMD was measured by pQCT at the radius. FRAX, 25-hydroxyvitamin-D3 (25-OH-D3), parathyroid hormone, osteocalcin, C-terminal collagen telopeptide, and procollagen type I amino-terminal propeptide were also assessed. Results SSc patients had lower L2–4 BMD (0.880 ± 0.108 vs. 0.996 ± 0.181 g/cm2; p = 0.019) and femoral neck (FN) BMD (0.786 ± 0.134 vs. 0.910 ± 0.090 g/cm2; p = 0.007) by DXA. In SSc vs. controls, pQCT indicated lower mean cortical (328.03 ± 103.32 vs. 487.06 ± 42.45 mg/cm3; p < 0.001) and trabecular density (150.93 ± 61.91 vs. 184.76 ± 33.03 mg/cm3; p = 0.037). Vitamin D3 deficiency was more common in SSc vs. controls (60.0% vs. 39.3%; p = 0.003). L2–4 (p = 0.002) and FN BMD (p = 0.015) positively correlated with BMI. pQCT assessments confirmed an inverse correlation between pulmonary manifestation and total (p = 0.024), trabecular (p = 0.035), and cortical density (p = 0.015). Anti-Scl70 positivity inversely correlated with pQCT total density (p = 0.015) and the presence of digital ulcers with cortical density (p = 0.001). We also found that vertebral and FN BMD as determined by DXA significantly correlated with pQCT total, trabecular, and cortical density (p < 0.05). Conclusion The results of our study suggest that bone loss in SSc patients may be associated with lower BMI, anti-Scl70 positivity, and the presence of pulmonary manifestations and digital ulcers. Both DXA and pQCT are appropriate tools to evaluate the bone alterations in SSc patients.
topic Systemic sclerosis
Bone loss
Osteoporosis
DXA
pQCT
Pulmonary manifestations
url https://doi.org/10.1186/s13075-019-2072-y
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