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New and emerging therapeutic agents for the treatment of fibromyalgia: an update

Fibromyalgia (FM) is a chronic widespread pain condition that is estimated to affect 5 million US adults. Several molecular pathophysiologies are thought to contribute to the symptoms of FM, complicating the development of effective clinical management techniques. It is now known that abnormalities...

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Detalles Bibliográficos
Autor principal: Recla, Jill M
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004640/
https://www.ncbi.nlm.nih.gov/pubmed/21197313
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author Recla, Jill M
author_facet Recla, Jill M
author_sort Recla, Jill M
collection PubMed
description Fibromyalgia (FM) is a chronic widespread pain condition that is estimated to affect 5 million US adults. Several molecular pathophysiologies are thought to contribute to the symptoms of FM, complicating the development of effective clinical management techniques. It is now known that abnormalities in both nociceptive and central pain processing systems are necessary (but perhaps not sufficient) to condition the onset and maintenance of FM, producing associated neuropsychologic symptoms such as pronounced fatigue, sleep abnormalities, cognitive difficulties, stress sensitivity, anxiety, and depression. Current treatment strategies are focused primarily on correcting the pathophysiologic mechanisms underlying these nervous system abnormalities. Clinical studies demonstrate the safety and efficacy of three drugs recently approved for the treatment of FM: pregabalin (an alpha-2-delta ligand), and duloxetine and milnacipran (serotonin/norepinephrine reuptake inhibitors). This review describes these pharmaceuticals in detail and discusses their current roles in FM management.
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spelling pubmed-30046402010-12-30 New and emerging therapeutic agents for the treatment of fibromyalgia: an update Recla, Jill M J Pain Res Review Fibromyalgia (FM) is a chronic widespread pain condition that is estimated to affect 5 million US adults. Several molecular pathophysiologies are thought to contribute to the symptoms of FM, complicating the development of effective clinical management techniques. It is now known that abnormalities in both nociceptive and central pain processing systems are necessary (but perhaps not sufficient) to condition the onset and maintenance of FM, producing associated neuropsychologic symptoms such as pronounced fatigue, sleep abnormalities, cognitive difficulties, stress sensitivity, anxiety, and depression. Current treatment strategies are focused primarily on correcting the pathophysiologic mechanisms underlying these nervous system abnormalities. Clinical studies demonstrate the safety and efficacy of three drugs recently approved for the treatment of FM: pregabalin (an alpha-2-delta ligand), and duloxetine and milnacipran (serotonin/norepinephrine reuptake inhibitors). This review describes these pharmaceuticals in detail and discusses their current roles in FM management. Dove Medical Press 2010-07-22 /pmc/articles/PMC3004640/ /pubmed/21197313 Text en © 2010 Recla, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Recla, Jill M
New and emerging therapeutic agents for the treatment of fibromyalgia: an update
title New and emerging therapeutic agents for the treatment of fibromyalgia: an update
title_full New and emerging therapeutic agents for the treatment of fibromyalgia: an update
title_fullStr New and emerging therapeutic agents for the treatment of fibromyalgia: an update
title_full_unstemmed New and emerging therapeutic agents for the treatment of fibromyalgia: an update
title_short New and emerging therapeutic agents for the treatment of fibromyalgia: an update
title_sort new and emerging therapeutic agents for the treatment of fibromyalgia: an update
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004640/
https://www.ncbi.nlm.nih.gov/pubmed/21197313
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