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A hospital based study of biochemical markers of bone turnovers & bone mineral density in north Indian women

BACKGROUND & OBJECTIVES: The osteoporotic risk for women increases soon after menopause. Bone turnover markers are known to be associated with bone loss and fracture risk. This study was aimed to assess bone turnover using bone markers and their correlation with bone mineral density (BMD) in pre...

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Autores principales: Kumar, Ashok, Devi, Salam Gyaneshwori, Mittal, Soniya, Shukla, Deepak Kumar, Sharma, Shashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657898/
https://www.ncbi.nlm.nih.gov/pubmed/23481051
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author Kumar, Ashok
Devi, Salam Gyaneshwori
Mittal, Soniya
Shukla, Deepak Kumar
Sharma, Shashi
author_facet Kumar, Ashok
Devi, Salam Gyaneshwori
Mittal, Soniya
Shukla, Deepak Kumar
Sharma, Shashi
author_sort Kumar, Ashok
collection PubMed
description BACKGROUND & OBJECTIVES: The osteoporotic risk for women increases soon after menopause. Bone turnover markers are known to be associated with bone loss and fracture risk. This study was aimed to assess bone turnover using bone markers and their correlation with bone mineral density (BMD) in pre- and post-menopausal women. METHODS: A total of 255 healthy women (160 pre- and 95 post-menopausal) were enrolled. Serum bone alkaline phosphatase (sBAP) and serum N-terminal telopeptide of type I collagen (NTX) were measured to evaluate the bone formation and resorption, respectively. Bone mineral density was determined at lumbar spine (L2-L4) anteroposteriorly, femoral neck and Ward's triangle using Prodigy dual-energy X-ray absorptiometry (DXA) system. The comparison of years since menopause with respect to BMD and bone markers was also evaluated. RESULTS: NTX and sBAP showed significant negative correlation with BMD of femur neck and Ward's triangle in postmenopausal women. BMD of all three sides were significant variables for NTX and BMD of femur neck and Ward's triangle for sBAP in postmenopausal women. BMD lumbar spine was a significant variable for sBAP in premenopausal women. The mean values of NTX increased significantly with increase in the duration of years since menopause. The BMD of all three sides decreased significantly with increase in the duration of years since menopause. INTERPRETATION & CONCLUSIONS: Serum NTX and sBAP were inversely correlated to BMD of femur neck and Ward's triangle in post-menopausal women. Simultaneous measurements of NTX and BMD in the north Indian women, suggest that bone resorption in women with low BMD remains high after menopause.
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spelling pubmed-36578982013-05-28 A hospital based study of biochemical markers of bone turnovers & bone mineral density in north Indian women Kumar, Ashok Devi, Salam Gyaneshwori Mittal, Soniya Shukla, Deepak Kumar Sharma, Shashi Indian J Med Res Original Article BACKGROUND & OBJECTIVES: The osteoporotic risk for women increases soon after menopause. Bone turnover markers are known to be associated with bone loss and fracture risk. This study was aimed to assess bone turnover using bone markers and their correlation with bone mineral density (BMD) in pre- and post-menopausal women. METHODS: A total of 255 healthy women (160 pre- and 95 post-menopausal) were enrolled. Serum bone alkaline phosphatase (sBAP) and serum N-terminal telopeptide of type I collagen (NTX) were measured to evaluate the bone formation and resorption, respectively. Bone mineral density was determined at lumbar spine (L2-L4) anteroposteriorly, femoral neck and Ward's triangle using Prodigy dual-energy X-ray absorptiometry (DXA) system. The comparison of years since menopause with respect to BMD and bone markers was also evaluated. RESULTS: NTX and sBAP showed significant negative correlation with BMD of femur neck and Ward's triangle in postmenopausal women. BMD of all three sides were significant variables for NTX and BMD of femur neck and Ward's triangle for sBAP in postmenopausal women. BMD lumbar spine was a significant variable for sBAP in premenopausal women. The mean values of NTX increased significantly with increase in the duration of years since menopause. The BMD of all three sides decreased significantly with increase in the duration of years since menopause. INTERPRETATION & CONCLUSIONS: Serum NTX and sBAP were inversely correlated to BMD of femur neck and Ward's triangle in post-menopausal women. Simultaneous measurements of NTX and BMD in the north Indian women, suggest that bone resorption in women with low BMD remains high after menopause. Medknow Publications & Media Pvt Ltd 2013-01 /pmc/articles/PMC3657898/ /pubmed/23481051 Text en Copyright: © The Indian Journal of Medical Research 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
Kumar, Ashok
Devi, Salam Gyaneshwori
Mittal, Soniya
Shukla, Deepak Kumar
Sharma, Shashi
A hospital based study of biochemical markers of bone turnovers & bone mineral density in north Indian women
title A hospital based study of biochemical markers of bone turnovers & bone mineral density in north Indian women
title_full A hospital based study of biochemical markers of bone turnovers & bone mineral density in north Indian women
title_fullStr A hospital based study of biochemical markers of bone turnovers & bone mineral density in north Indian women
title_full_unstemmed A hospital based study of biochemical markers of bone turnovers & bone mineral density in north Indian women
title_short A hospital based study of biochemical markers of bone turnovers & bone mineral density in north Indian women
title_sort hospital based study of biochemical markers of bone turnovers & bone mineral density in north indian women
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657898/
https://www.ncbi.nlm.nih.gov/pubmed/23481051
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