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Bone resorption predicts for skeletal complications in metastatic bone disease
Relationships between the rate of bone resorption (measured by urinary N-telopeptide (Ntx) excretion) and a range of skeletal complications have been evaluated in patients with metastatic bone disease. A total of 121 patients had monthly measurements of Ntx during treatment with bisphosphonates. All...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376859/ https://www.ncbi.nlm.nih.gov/pubmed/14647134 http://dx.doi.org/10.1038/sj.bjc.6601437 |
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author | Brown, J E Thomson, C S Ellis, S P Gutcher, S A Purohit, O P Coleman, R E |
author_facet | Brown, J E Thomson, C S Ellis, S P Gutcher, S A Purohit, O P Coleman, R E |
author_sort | Brown, J E |
collection | PubMed |
description | Relationships between the rate of bone resorption (measured by urinary N-telopeptide (Ntx) excretion) and a range of skeletal complications have been evaluated in patients with metastatic bone disease. A total of 121 patients had monthly measurements of Ntx during treatment with bisphosphonates. All skeletal-related events, plus hospital admissions for bone pain and death during the period of observation, were recorded. Data were available for 121 patients over the first 3-month period of monitoring (0–3 months) and 95 patients over the second 3-month period (4–6 months). N-telopeptide levels were correlated with the number of skeletal-related events and/or death (r=0.62, P<0.001 for 0–3 months and r=0.46, P<0.001 for 4–6 months, respectively). Patients with baseline Ntx values ⩾100 nmol mmol(−1) creatinine (representing clearly accelerated bone resorption) were 19.48 times (95% CI 7.55, 50.22) more likely to experience a skeletal-related event/death during the first 3 months than those with Ntx <100 (P<0.001). In a multivariate logistic regression model, Ntx was highly predictive for events/death. This study is the first to indicate a strong correlation between the rate of bone resorption and the frequency of skeletal complications in metastatic bone disease. N-telopeptide appears useful in the prediction of patients most likely to experience skeletal complications and thus benefit from bisphosphonate treatment. |
format | Text |
id | pubmed-2376859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23768592009-09-10 Bone resorption predicts for skeletal complications in metastatic bone disease Brown, J E Thomson, C S Ellis, S P Gutcher, S A Purohit, O P Coleman, R E Br J Cancer Clinical Relationships between the rate of bone resorption (measured by urinary N-telopeptide (Ntx) excretion) and a range of skeletal complications have been evaluated in patients with metastatic bone disease. A total of 121 patients had monthly measurements of Ntx during treatment with bisphosphonates. All skeletal-related events, plus hospital admissions for bone pain and death during the period of observation, were recorded. Data were available for 121 patients over the first 3-month period of monitoring (0–3 months) and 95 patients over the second 3-month period (4–6 months). N-telopeptide levels were correlated with the number of skeletal-related events and/or death (r=0.62, P<0.001 for 0–3 months and r=0.46, P<0.001 for 4–6 months, respectively). Patients with baseline Ntx values ⩾100 nmol mmol(−1) creatinine (representing clearly accelerated bone resorption) were 19.48 times (95% CI 7.55, 50.22) more likely to experience a skeletal-related event/death during the first 3 months than those with Ntx <100 (P<0.001). In a multivariate logistic regression model, Ntx was highly predictive for events/death. This study is the first to indicate a strong correlation between the rate of bone resorption and the frequency of skeletal complications in metastatic bone disease. N-telopeptide appears useful in the prediction of patients most likely to experience skeletal complications and thus benefit from bisphosphonate treatment. Nature Publishing Group 2003-12-01 2003-11-25 /pmc/articles/PMC2376859/ /pubmed/14647134 http://dx.doi.org/10.1038/sj.bjc.6601437 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Brown, J E Thomson, C S Ellis, S P Gutcher, S A Purohit, O P Coleman, R E Bone resorption predicts for skeletal complications in metastatic bone disease |
title | Bone resorption predicts for skeletal complications in metastatic bone disease |
title_full | Bone resorption predicts for skeletal complications in metastatic bone disease |
title_fullStr | Bone resorption predicts for skeletal complications in metastatic bone disease |
title_full_unstemmed | Bone resorption predicts for skeletal complications in metastatic bone disease |
title_short | Bone resorption predicts for skeletal complications in metastatic bone disease |
title_sort | bone resorption predicts for skeletal complications in metastatic bone disease |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376859/ https://www.ncbi.nlm.nih.gov/pubmed/14647134 http://dx.doi.org/10.1038/sj.bjc.6601437 |
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