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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
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.
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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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