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Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data
Colchicine is a medication most commonly used in the treatment of gout and familial mediterannean fever. A rare complication of therapy is toxicity causing proximal myopathy and polyneuropathy. Colchicine myopathy has been associated with the coadministration of other medications with colchicine, su...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542945/ https://www.ncbi.nlm.nih.gov/pubmed/31178824 http://dx.doi.org/10.3389/fneur.2019.00553 |
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author | Gupta, Mehul Nikolic, Ana Ng, Denise Martens, Kristina Ebadi, Hamid Chhibber, Sameer Pfeffer, Gerald |
author_facet | Gupta, Mehul Nikolic, Ana Ng, Denise Martens, Kristina Ebadi, Hamid Chhibber, Sameer Pfeffer, Gerald |
author_sort | Gupta, Mehul |
collection | PubMed |
description | Colchicine is a medication most commonly used in the treatment of gout and familial mediterannean fever. A rare complication of therapy is toxicity causing proximal myopathy and polyneuropathy. Colchicine myopathy has been associated with the coadministration of other medications with colchicine, such as statins or tacrolimus, and is more common in patients with renal impairment. Otherwise, it is unclear which patients are at greatest risk of developing this adverse drug reaction. ABCB1 is important to the metabolism of colchicine, so we speculated that it was possible that colchicine myopathy patients may have a particular genotype that is associated with this side effect. We describe two cases of colchicine myopathy which occurred with co-administration of rosuvastatin. From one case, we present the first published data on muscle MRI in this condition. We additionally present an analysis of four genetic polymorphisms in ABCB1 and transcript levels in muscle tissue, and demonstrate the descriptive finding of reduced ABCB1 transcript levels in the colchicine myopathy patients. |
format | Online Article Text |
id | pubmed-6542945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65429452019-06-07 Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data Gupta, Mehul Nikolic, Ana Ng, Denise Martens, Kristina Ebadi, Hamid Chhibber, Sameer Pfeffer, Gerald Front Neurol Neurology Colchicine is a medication most commonly used in the treatment of gout and familial mediterannean fever. A rare complication of therapy is toxicity causing proximal myopathy and polyneuropathy. Colchicine myopathy has been associated with the coadministration of other medications with colchicine, such as statins or tacrolimus, and is more common in patients with renal impairment. Otherwise, it is unclear which patients are at greatest risk of developing this adverse drug reaction. ABCB1 is important to the metabolism of colchicine, so we speculated that it was possible that colchicine myopathy patients may have a particular genotype that is associated with this side effect. We describe two cases of colchicine myopathy which occurred with co-administration of rosuvastatin. From one case, we present the first published data on muscle MRI in this condition. We additionally present an analysis of four genetic polymorphisms in ABCB1 and transcript levels in muscle tissue, and demonstrate the descriptive finding of reduced ABCB1 transcript levels in the colchicine myopathy patients. Frontiers Media S.A. 2019-05-24 /pmc/articles/PMC6542945/ /pubmed/31178824 http://dx.doi.org/10.3389/fneur.2019.00553 Text en Copyright © 2019 Gupta, Nikolic, Ng, Martens, Ebadi, Chhibber and Pfeffer. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Gupta, Mehul Nikolic, Ana Ng, Denise Martens, Kristina Ebadi, Hamid Chhibber, Sameer Pfeffer, Gerald Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data |
title | Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data |
title_full | Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data |
title_fullStr | Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data |
title_full_unstemmed | Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data |
title_short | Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data |
title_sort | colchicine myopathy: a case series including muscle mri and abcb1 polymorphism data |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542945/ https://www.ncbi.nlm.nih.gov/pubmed/31178824 http://dx.doi.org/10.3389/fneur.2019.00553 |
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