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Markers of autoimmune liver diseases in postmenopausal women with osteoporosis

INTRODUCTION: Osteoporosis is a common complication of chronic liver diseases. However, there is limited information about autoimmune liver diseases as a factor of secondary osteoporosis. Therefore, we aimed to investigate the autoantibodies of autoimmune liver diseases in patients with osteoporosis...

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Autores principales: Demirdal, Umit Secil, Ciftci, Ihsan Hakkı, Kavuncu, Vural
Formato: Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972595/
https://www.ncbi.nlm.nih.gov/pubmed/21120296
http://dx.doi.org/10.1590/S1807-59322010001000008
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author Demirdal, Umit Secil
Ciftci, Ihsan Hakkı
Kavuncu, Vural
author_facet Demirdal, Umit Secil
Ciftci, Ihsan Hakkı
Kavuncu, Vural
author_sort Demirdal, Umit Secil
collection PubMed
description INTRODUCTION: Osteoporosis is a common complication of chronic liver diseases. However, there is limited information about autoimmune liver diseases as a factor of secondary osteoporosis. Therefore, we aimed to investigate the autoantibodies of autoimmune liver diseases in patients with osteoporosis. METHODS: One hundred fifty female patients with postmenopausal osteoporosis were included. Bone mineral density was measured by dual energy X‐ray absorptiometry. We analysized autoantibodies including antinuclear antibodies, liver membrane antibodies, anti‐liver/kidney microsomal autoantibodies1, liver‐specific protein, anti‐smooth muscle antibodies, and anti‐mitochondrial antibodies by indirect immunofluorescence. Serum was assayed for the levels of aminotransferases. RESULTS: The mean age of the patients was 63,13±8,6 years. The mean values of L1‐L4 T‐scores and femur total T‐scores were ‐3,08±0,58 and ‐1,53±0,81, respectively. Among the 150 patients with osteoporosis, 14 (9.3%) were antinuclear antibodies, four (2.7%) were liver membrane antibodies, three (2.0%) were anti‐liver/kidney microsomal autoantibodies1, and two (1.3%) were liver‐specific protein positive. None of the patients had anti‐mitochondrial antibodies or smooth muscle antibodies positivity. The mean values of levels of aminotransferases were within normal range. CONCLUSIONS: The presence of liver membrane antibodies, liver‐specific protein, and anti‐liver/kidney microsomal autoantibodies1 has permitted us to see that there may be some suspicious clues of autoimmune liver diseases in patients with osteoporosis as a secondary risk factor. On the other hand, there is a need for comprehensive studies with a larger sample size and studies designed to compare the results with a normal population to understand the clinical importance of our findings.
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spelling pubmed-29725952010-11-04 Markers of autoimmune liver diseases in postmenopausal women with osteoporosis Demirdal, Umit Secil Ciftci, Ihsan Hakkı Kavuncu, Vural Clinics (Sao Paulo) Clinical Science INTRODUCTION: Osteoporosis is a common complication of chronic liver diseases. However, there is limited information about autoimmune liver diseases as a factor of secondary osteoporosis. Therefore, we aimed to investigate the autoantibodies of autoimmune liver diseases in patients with osteoporosis. METHODS: One hundred fifty female patients with postmenopausal osteoporosis were included. Bone mineral density was measured by dual energy X‐ray absorptiometry. We analysized autoantibodies including antinuclear antibodies, liver membrane antibodies, anti‐liver/kidney microsomal autoantibodies1, liver‐specific protein, anti‐smooth muscle antibodies, and anti‐mitochondrial antibodies by indirect immunofluorescence. Serum was assayed for the levels of aminotransferases. RESULTS: The mean age of the patients was 63,13±8,6 years. The mean values of L1‐L4 T‐scores and femur total T‐scores were ‐3,08±0,58 and ‐1,53±0,81, respectively. Among the 150 patients with osteoporosis, 14 (9.3%) were antinuclear antibodies, four (2.7%) were liver membrane antibodies, three (2.0%) were anti‐liver/kidney microsomal autoantibodies1, and two (1.3%) were liver‐specific protein positive. None of the patients had anti‐mitochondrial antibodies or smooth muscle antibodies positivity. The mean values of levels of aminotransferases were within normal range. CONCLUSIONS: The presence of liver membrane antibodies, liver‐specific protein, and anti‐liver/kidney microsomal autoantibodies1 has permitted us to see that there may be some suspicious clues of autoimmune liver diseases in patients with osteoporosis as a secondary risk factor. On the other hand, there is a need for comprehensive studies with a larger sample size and studies designed to compare the results with a normal population to understand the clinical importance of our findings. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2010-10 /pmc/articles/PMC2972595/ /pubmed/21120296 http://dx.doi.org/10.1590/S1807-59322010001000008 Text en Copyright © 2010 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Science
Demirdal, Umit Secil
Ciftci, Ihsan Hakkı
Kavuncu, Vural
Markers of autoimmune liver diseases in postmenopausal women with osteoporosis
title Markers of autoimmune liver diseases in postmenopausal women with osteoporosis
title_full Markers of autoimmune liver diseases in postmenopausal women with osteoporosis
title_fullStr Markers of autoimmune liver diseases in postmenopausal women with osteoporosis
title_full_unstemmed Markers of autoimmune liver diseases in postmenopausal women with osteoporosis
title_short Markers of autoimmune liver diseases in postmenopausal women with osteoporosis
title_sort markers of autoimmune liver diseases in postmenopausal women with osteoporosis
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972595/
https://www.ncbi.nlm.nih.gov/pubmed/21120296
http://dx.doi.org/10.1590/S1807-59322010001000008
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