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Low bone mineral density and the severity of cholestasis in biliary atresia
AIM: To investigate the prevalence of osteopenia and osteoporosis in postoperative biliary atresia (BA) children and the association of bone mineral density (BMD) and biochemical parameters in postKasai BA subjects. METHODS: A total of 70 patients with postKasai BA were enrolled in this prospective...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468343/ https://www.ncbi.nlm.nih.gov/pubmed/28652893 http://dx.doi.org/10.4254/wjh.v9.i16.746 |
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author | Homchan, Krittapak Chaiwatanarat, Tawatchai Udomsinprasert, Wanvisa Chongsrisawat, Voranush Poovorawan, Yong Honsawek, Sittisak |
author_facet | Homchan, Krittapak Chaiwatanarat, Tawatchai Udomsinprasert, Wanvisa Chongsrisawat, Voranush Poovorawan, Yong Honsawek, Sittisak |
author_sort | Homchan, Krittapak |
collection | PubMed |
description | AIM: To investigate the prevalence of osteopenia and osteoporosis in postoperative biliary atresia (BA) children and the association of bone mineral density (BMD) and biochemical parameters in postKasai BA subjects. METHODS: A total of 70 patients with postKasai BA were enrolled in this prospective study. The patients were classified into two groups according to their jaundice status. BMD of the lumbar spine was analyzed using dual energy X-ray absorptiometry. RESULTS: The prevalence of low bone mass (osteopenia and osteoporosis) in BA patients were 51.4% (36 out of 70). Ten patients (35.7%) in the jaundice group and 8 patients (19.0%) in the non-jaundice group had osteopenia. Sixteen patients (57.1%) in the jaundice group and 2 patients (4.8%) in the no jaundice group had osteoporosis. In addition, lumbar spine BMD Z-score was substantially lower in the jaundice BA patients compared with non-jaundice patients. BA subjects with persistent jaundice had significantly lower serum 25-hydroxyvitamin D than those without jaundice. Further analysis revealed that lumbar spine BMD was correlated with age (r = 0.774, P < 0.001), serum albumin (r = 0.333, P = 0.005), total bilirubin (r = -0.476, P < 0.001), aspartate aminotransferase (r = -0.583, P < 0.001), alanine aminotransferase (r = -0.428, P < 0.001), and alkaline phosphatase(r = -0.456, P < 0.001). CONCLUSION: Low BMD was associated with biochemical parameters reflecting the severity of cholestasis in postKasai BA patients. |
format | Online Article Text |
id | pubmed-5468343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-54683432017-06-26 Low bone mineral density and the severity of cholestasis in biliary atresia Homchan, Krittapak Chaiwatanarat, Tawatchai Udomsinprasert, Wanvisa Chongsrisawat, Voranush Poovorawan, Yong Honsawek, Sittisak World J Hepatol Prospective Study AIM: To investigate the prevalence of osteopenia and osteoporosis in postoperative biliary atresia (BA) children and the association of bone mineral density (BMD) and biochemical parameters in postKasai BA subjects. METHODS: A total of 70 patients with postKasai BA were enrolled in this prospective study. The patients were classified into two groups according to their jaundice status. BMD of the lumbar spine was analyzed using dual energy X-ray absorptiometry. RESULTS: The prevalence of low bone mass (osteopenia and osteoporosis) in BA patients were 51.4% (36 out of 70). Ten patients (35.7%) in the jaundice group and 8 patients (19.0%) in the non-jaundice group had osteopenia. Sixteen patients (57.1%) in the jaundice group and 2 patients (4.8%) in the no jaundice group had osteoporosis. In addition, lumbar spine BMD Z-score was substantially lower in the jaundice BA patients compared with non-jaundice patients. BA subjects with persistent jaundice had significantly lower serum 25-hydroxyvitamin D than those without jaundice. Further analysis revealed that lumbar spine BMD was correlated with age (r = 0.774, P < 0.001), serum albumin (r = 0.333, P = 0.005), total bilirubin (r = -0.476, P < 0.001), aspartate aminotransferase (r = -0.583, P < 0.001), alanine aminotransferase (r = -0.428, P < 0.001), and alkaline phosphatase(r = -0.456, P < 0.001). CONCLUSION: Low BMD was associated with biochemical parameters reflecting the severity of cholestasis in postKasai BA patients. Baishideng Publishing Group Inc 2017-06-08 2017-06-08 /pmc/articles/PMC5468343/ /pubmed/28652893 http://dx.doi.org/10.4254/wjh.v9.i16.746 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Prospective Study Homchan, Krittapak Chaiwatanarat, Tawatchai Udomsinprasert, Wanvisa Chongsrisawat, Voranush Poovorawan, Yong Honsawek, Sittisak Low bone mineral density and the severity of cholestasis in biliary atresia |
title | Low bone mineral density and the severity of cholestasis in biliary atresia |
title_full | Low bone mineral density and the severity of cholestasis in biliary atresia |
title_fullStr | Low bone mineral density and the severity of cholestasis in biliary atresia |
title_full_unstemmed | Low bone mineral density and the severity of cholestasis in biliary atresia |
title_short | Low bone mineral density and the severity of cholestasis in biliary atresia |
title_sort | low bone mineral density and the severity of cholestasis in biliary atresia |
topic | Prospective Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468343/ https://www.ncbi.nlm.nih.gov/pubmed/28652893 http://dx.doi.org/10.4254/wjh.v9.i16.746 |
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