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Bone Mineral Density in Sjögren Syndrome Patients with and Without Distal Renal Tubular Acidosis
Primary Sjögren’s syndrome (pSS) can be complicated by distal renal tubular acidosis (dRTA), which may contribute to low bone mineral density (BMD). Our objective was to evaluate BMD in pSS patients with and without dRTA as compared with healthy controls. BMD of lumbar spine (LS) and femoral neck (F...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860192/ https://www.ncbi.nlm.nih.gov/pubmed/26873478 http://dx.doi.org/10.1007/s00223-016-0112-z |
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author | Both, Tim Zillikens, M. Carola Hoorn, Ewout J. Zietse, Robert van Laar, Jan A. M. Dalm, Virgil A. S. H. van Duijn, Cornelia M. Versnel, Marjan A. Maria, Naomi I. van Hagen, P. Martin van Daele, Paul L. A. |
author_facet | Both, Tim Zillikens, M. Carola Hoorn, Ewout J. Zietse, Robert van Laar, Jan A. M. Dalm, Virgil A. S. H. van Duijn, Cornelia M. Versnel, Marjan A. Maria, Naomi I. van Hagen, P. Martin van Daele, Paul L. A. |
author_sort | Both, Tim |
collection | PubMed |
description | Primary Sjögren’s syndrome (pSS) can be complicated by distal renal tubular acidosis (dRTA), which may contribute to low bone mineral density (BMD). Our objective was to evaluate BMD in pSS patients with and without dRTA as compared with healthy controls. BMD of lumbar spine (LS) and femoral neck (FN) was measured in 54 pSS patients and 162 healthy age- and sex-matched controls by dual-energy X-ray absorptiometry (DXA). dRTA was defined as inability to reach urinary pH <5.3 after an ammonium chloride (NH(4)Cl) test. LS- and FN-BMD were significantly higher in pSS patients compared with controls (1.18 ± 0.21 g/cm(2) for patients vs. 1.10 ± 0.18 g/cm(2) for controls, P = 0.008 and 0.9 ± 0.16 g/cm(2) for patients vs. 0.85 ± 0.13 g/cm(2) for controls, P = 0.009, respectively). After adjustment for BMI and smoking, the LS- and FN-BMD remained significantly higher. Patients with dRTA (N = 15) did not have a significantly different LS- and FN-BMD compared with those without dRTA (N = 39) after adjustment for BMI, age, and gender. Thirty-seven (69 %) pSS patients were using hydroxychloroquine (HCQ). Unexpectedly, pSS patients had a significantly higher LS- and FN-BMD compared with healthy controls. Patients with dRTA had similar BMD compared with patients without dRTA. We postulate that an explanation for the higher BMD in pSS patients may be the frequent use of HCQ. |
format | Online Article Text |
id | pubmed-4860192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-48601922016-05-21 Bone Mineral Density in Sjögren Syndrome Patients with and Without Distal Renal Tubular Acidosis Both, Tim Zillikens, M. Carola Hoorn, Ewout J. Zietse, Robert van Laar, Jan A. M. Dalm, Virgil A. S. H. van Duijn, Cornelia M. Versnel, Marjan A. Maria, Naomi I. van Hagen, P. Martin van Daele, Paul L. A. Calcif Tissue Int Original Research Primary Sjögren’s syndrome (pSS) can be complicated by distal renal tubular acidosis (dRTA), which may contribute to low bone mineral density (BMD). Our objective was to evaluate BMD in pSS patients with and without dRTA as compared with healthy controls. BMD of lumbar spine (LS) and femoral neck (FN) was measured in 54 pSS patients and 162 healthy age- and sex-matched controls by dual-energy X-ray absorptiometry (DXA). dRTA was defined as inability to reach urinary pH <5.3 after an ammonium chloride (NH(4)Cl) test. LS- and FN-BMD were significantly higher in pSS patients compared with controls (1.18 ± 0.21 g/cm(2) for patients vs. 1.10 ± 0.18 g/cm(2) for controls, P = 0.008 and 0.9 ± 0.16 g/cm(2) for patients vs. 0.85 ± 0.13 g/cm(2) for controls, P = 0.009, respectively). After adjustment for BMI and smoking, the LS- and FN-BMD remained significantly higher. Patients with dRTA (N = 15) did not have a significantly different LS- and FN-BMD compared with those without dRTA (N = 39) after adjustment for BMI, age, and gender. Thirty-seven (69 %) pSS patients were using hydroxychloroquine (HCQ). Unexpectedly, pSS patients had a significantly higher LS- and FN-BMD compared with healthy controls. Patients with dRTA had similar BMD compared with patients without dRTA. We postulate that an explanation for the higher BMD in pSS patients may be the frequent use of HCQ. Springer US 2016-02-12 2016 /pmc/articles/PMC4860192/ /pubmed/26873478 http://dx.doi.org/10.1007/s00223-016-0112-z Text en © The Author(s) 2016 Open AccessThis 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. |
spellingShingle | Original Research Both, Tim Zillikens, M. Carola Hoorn, Ewout J. Zietse, Robert van Laar, Jan A. M. Dalm, Virgil A. S. H. van Duijn, Cornelia M. Versnel, Marjan A. Maria, Naomi I. van Hagen, P. Martin van Daele, Paul L. A. Bone Mineral Density in Sjögren Syndrome Patients with and Without Distal Renal Tubular Acidosis |
title | Bone Mineral Density in Sjögren Syndrome Patients with and Without Distal Renal Tubular Acidosis |
title_full | Bone Mineral Density in Sjögren Syndrome Patients with and Without Distal Renal Tubular Acidosis |
title_fullStr | Bone Mineral Density in Sjögren Syndrome Patients with and Without Distal Renal Tubular Acidosis |
title_full_unstemmed | Bone Mineral Density in Sjögren Syndrome Patients with and Without Distal Renal Tubular Acidosis |
title_short | Bone Mineral Density in Sjögren Syndrome Patients with and Without Distal Renal Tubular Acidosis |
title_sort | bone mineral density in sjögren syndrome patients with and without distal renal tubular acidosis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860192/ https://www.ncbi.nlm.nih.gov/pubmed/26873478 http://dx.doi.org/10.1007/s00223-016-0112-z |
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