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Inflammatory cytokines and aromatase inhibitor-associated musculoskeletal syndrome: a case–control study
BACKGROUND: The aromatase inhibitor (AI)-associated musculoskeletal syndrome (AIMSS) occurs in approximately 50% of AI-treated patients. Inflammatory mediators are associated with oestrogen signalling and may change with oestrogen depletion. We hypothesised that AIMSS may be associated with changes...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2920022/ https://www.ncbi.nlm.nih.gov/pubmed/20606683 http://dx.doi.org/10.1038/sj.bjc.6605768 |
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author | Henry, N L Pchejetski, D A'Hern, R Nguyen, A T Charles, P Waxman, J Li, L Storniolo, A M Hayes, D F Flockhart, D A Stearns, V Stebbing, J |
author_facet | Henry, N L Pchejetski, D A'Hern, R Nguyen, A T Charles, P Waxman, J Li, L Storniolo, A M Hayes, D F Flockhart, D A Stearns, V Stebbing, J |
author_sort | Henry, N L |
collection | PubMed |
description | BACKGROUND: The aromatase inhibitor (AI)-associated musculoskeletal syndrome (AIMSS) occurs in approximately 50% of AI-treated patients. Inflammatory mediators are associated with oestrogen signalling and may change with oestrogen depletion. We hypothesised that AIMSS may be associated with changes in circulating inflammatory markers. METHODS: Patients with breast cancer were enroled in a trial of adjuvant AI therapy. Changes in pain and function during therapy were assessed prospectively. We selected 30 cases with AIMSS and 22 controls without AIMSS, matched for demographics and prior therapy. Serum samples collected at baseline and during treatment were assayed for multiple inflammatory cytokines and lipid mediators using multiplex assays. RESULTS: Before AI therapy, mean serum concentrations of 6 of 36 assayed factors were statistically significantly lower in cases than controls (all P<0.003). No statistically significant changes during AI therapy relative to pre-treatment were observed between cases and controls for any of the inflammatory markers tested. CONCLUSION: AIMSS is probably not associated with a systemic inflammatory response. Pre-treatment cytokine levels may predict for development of AIMSS. |
format | Text |
id | pubmed-2920022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-29200222011-07-27 Inflammatory cytokines and aromatase inhibitor-associated musculoskeletal syndrome: a case–control study Henry, N L Pchejetski, D A'Hern, R Nguyen, A T Charles, P Waxman, J Li, L Storniolo, A M Hayes, D F Flockhart, D A Stearns, V Stebbing, J Br J Cancer Clinical Study BACKGROUND: The aromatase inhibitor (AI)-associated musculoskeletal syndrome (AIMSS) occurs in approximately 50% of AI-treated patients. Inflammatory mediators are associated with oestrogen signalling and may change with oestrogen depletion. We hypothesised that AIMSS may be associated with changes in circulating inflammatory markers. METHODS: Patients with breast cancer were enroled in a trial of adjuvant AI therapy. Changes in pain and function during therapy were assessed prospectively. We selected 30 cases with AIMSS and 22 controls without AIMSS, matched for demographics and prior therapy. Serum samples collected at baseline and during treatment were assayed for multiple inflammatory cytokines and lipid mediators using multiplex assays. RESULTS: Before AI therapy, mean serum concentrations of 6 of 36 assayed factors were statistically significantly lower in cases than controls (all P<0.003). No statistically significant changes during AI therapy relative to pre-treatment were observed between cases and controls for any of the inflammatory markers tested. CONCLUSION: AIMSS is probably not associated with a systemic inflammatory response. Pre-treatment cytokine levels may predict for development of AIMSS. Nature Publishing Group 2010-07-27 2010-07-06 /pmc/articles/PMC2920022/ /pubmed/20606683 http://dx.doi.org/10.1038/sj.bjc.6605768 Text en Copyright © 2010 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 Study Henry, N L Pchejetski, D A'Hern, R Nguyen, A T Charles, P Waxman, J Li, L Storniolo, A M Hayes, D F Flockhart, D A Stearns, V Stebbing, J Inflammatory cytokines and aromatase inhibitor-associated musculoskeletal syndrome: a case–control study |
title | Inflammatory cytokines and aromatase inhibitor-associated musculoskeletal syndrome: a case–control study |
title_full | Inflammatory cytokines and aromatase inhibitor-associated musculoskeletal syndrome: a case–control study |
title_fullStr | Inflammatory cytokines and aromatase inhibitor-associated musculoskeletal syndrome: a case–control study |
title_full_unstemmed | Inflammatory cytokines and aromatase inhibitor-associated musculoskeletal syndrome: a case–control study |
title_short | Inflammatory cytokines and aromatase inhibitor-associated musculoskeletal syndrome: a case–control study |
title_sort | inflammatory cytokines and aromatase inhibitor-associated musculoskeletal syndrome: a case–control study |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2920022/ https://www.ncbi.nlm.nih.gov/pubmed/20606683 http://dx.doi.org/10.1038/sj.bjc.6605768 |
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