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Changes in bone mineral density and bone turnover markers in patients undergoing hematopoietic stem cell transplant

INTRODUCTION: Hematopoietic stem cell transplant (HSCT) is frequently complicated by endocrine abnormalities and loss of bone mass. This prospective study was conducted to evaluate the bone loss post-HSCT. MATERIALS AND METHODS: A total of 50 patients was evaluated pretransplantation, and 25 had HSC...

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Autores principales: Pandit, Aditi, Garg, M. K., Kotwal, N., Brar, K. S., Gundgurthi, Abhay, Sharma, A. K., Sharma, Sanjeevan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366780/
https://www.ncbi.nlm.nih.gov/pubmed/25932397
http://dx.doi.org/10.4103/2230-8210.152785
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author Pandit, Aditi
Garg, M. K.
Kotwal, N.
Brar, K. S.
Gundgurthi, Abhay
Sharma, A. K.
Sharma, Sanjeevan
author_facet Pandit, Aditi
Garg, M. K.
Kotwal, N.
Brar, K. S.
Gundgurthi, Abhay
Sharma, A. K.
Sharma, Sanjeevan
author_sort Pandit, Aditi
collection PubMed
description INTRODUCTION: Hematopoietic stem cell transplant (HSCT) is frequently complicated by endocrine abnormalities and loss of bone mass. This prospective study was conducted to evaluate the bone loss post-HSCT. MATERIALS AND METHODS: A total of 50 patients was evaluated pretransplantation, and 25 had HSCT (17 males, 8 females; 19 allogenic, 6 autologous). Bone mineral density (BMD) and bone markers were measured at baseline, 3–6 months and 12 months. RESULTS: The mean age and body mass index were 25.1 ± 16.3 years and 19.4 ± 4.5 kg/m(2), respectively. There were 15 adults (60%), and 10 adolescents (40%). There was a significant decline in BMD from the baseline at total femur (−8.7%; P < 0.0001), femoral neck (−5.0%; P = 0.003), femoral trochanter (−6.0%; P = 0.001), and Ward's triangle (−9.9%; P < 0.0001) at 6 months posttransplantation. From the 6 months to 12 months, there was a significant improvement in BMD at above sites except at Ward's triangle. The decline in BMD was nonsignificant at the whole body (−0.3%, P = 0.748) and the lumbar spine (−2.7%, P = 0.130) at 6 months posttransplant. Younger patients with allogenic graft and steroid use are more likely to have significant loss of BMD at hip posttransplant. Serum osteocalcin decreased, and N-telopeptide increased at 3–6 months, which return to baseline at 1-year posttransplant. CONCLUSIONS: A significant bone loss is observed at 6 months in patients with post-HSCT. The bone loss occurs predominantly at cortical bone. There is recovery of bone mass at 12 months posttransplant except at Ward's triangle. Bone loss after HSCT is multifactorial.
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spelling pubmed-43667802015-05-01 Changes in bone mineral density and bone turnover markers in patients undergoing hematopoietic stem cell transplant Pandit, Aditi Garg, M. K. Kotwal, N. Brar, K. S. Gundgurthi, Abhay Sharma, A. K. Sharma, Sanjeevan Indian J Endocrinol Metab Original Article INTRODUCTION: Hematopoietic stem cell transplant (HSCT) is frequently complicated by endocrine abnormalities and loss of bone mass. This prospective study was conducted to evaluate the bone loss post-HSCT. MATERIALS AND METHODS: A total of 50 patients was evaluated pretransplantation, and 25 had HSCT (17 males, 8 females; 19 allogenic, 6 autologous). Bone mineral density (BMD) and bone markers were measured at baseline, 3–6 months and 12 months. RESULTS: The mean age and body mass index were 25.1 ± 16.3 years and 19.4 ± 4.5 kg/m(2), respectively. There were 15 adults (60%), and 10 adolescents (40%). There was a significant decline in BMD from the baseline at total femur (−8.7%; P < 0.0001), femoral neck (−5.0%; P = 0.003), femoral trochanter (−6.0%; P = 0.001), and Ward's triangle (−9.9%; P < 0.0001) at 6 months posttransplantation. From the 6 months to 12 months, there was a significant improvement in BMD at above sites except at Ward's triangle. The decline in BMD was nonsignificant at the whole body (−0.3%, P = 0.748) and the lumbar spine (−2.7%, P = 0.130) at 6 months posttransplant. Younger patients with allogenic graft and steroid use are more likely to have significant loss of BMD at hip posttransplant. Serum osteocalcin decreased, and N-telopeptide increased at 3–6 months, which return to baseline at 1-year posttransplant. CONCLUSIONS: A significant bone loss is observed at 6 months in patients with post-HSCT. The bone loss occurs predominantly at cortical bone. There is recovery of bone mass at 12 months posttransplant except at Ward's triangle. Bone loss after HSCT is multifactorial. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4366780/ /pubmed/25932397 http://dx.doi.org/10.4103/2230-8210.152785 Text en Copyright: © Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Pandit, Aditi
Garg, M. K.
Kotwal, N.
Brar, K. S.
Gundgurthi, Abhay
Sharma, A. K.
Sharma, Sanjeevan
Changes in bone mineral density and bone turnover markers in patients undergoing hematopoietic stem cell transplant
title Changes in bone mineral density and bone turnover markers in patients undergoing hematopoietic stem cell transplant
title_full Changes in bone mineral density and bone turnover markers in patients undergoing hematopoietic stem cell transplant
title_fullStr Changes in bone mineral density and bone turnover markers in patients undergoing hematopoietic stem cell transplant
title_full_unstemmed Changes in bone mineral density and bone turnover markers in patients undergoing hematopoietic stem cell transplant
title_short Changes in bone mineral density and bone turnover markers in patients undergoing hematopoietic stem cell transplant
title_sort changes in bone mineral density and bone turnover markers in patients undergoing hematopoietic stem cell transplant
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366780/
https://www.ncbi.nlm.nih.gov/pubmed/25932397
http://dx.doi.org/10.4103/2230-8210.152785
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