Literature DB >> 22941263

Pathogenesis and therapy of inclusion body myositis.

Steven A Greenberg1.   

Abstract

PURPOSE OF REVIEW: Inclusion body myositis (IBM) is a poorly understood progressive muscle disease of middle and later life. Its dual pathologies of autoimmunity and unexplained myofiber degeneration and loss have been enigmatic since its earliest descriptions over 40 years ago. No reliable effective therapy currently exists for IBM. This review provides an update of current issues in the pathogenesis and therapy of IBM. RECENT
FINDINGS: Recent studies have further defined the clinical features of IBM, including natural history, pattern of muscle involvement, and role of MRI imaging. Further potential immune mediators have been identified. An autoantibody directed against a muscle antigen appears to have high specificity for IBM among muscle diseases. Further evidence for myonuclear degeneration has been reported.
SUMMARY: IBM remains a poorly understood muscle disease, although understanding of the pathophysiological mechanisms continues to expand and is supporting new therapeutic approaches.

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Year:  2012        PMID: 22941263     DOI: 10.1097/WCO.0b013e328357f211

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  14 in total

1.  Seropositivity for NT5c1A antibody in sporadic inclusion body myositis predicts more severe motor, bulbar and respiratory involvement.

Authors:  N A Goyal; T M Cash; U Alam; S Enam; P Tierney; N Araujo; F H Mozaffar; A Pestronk; T Mozaffar
Journal:  J Neurol Neurosurg Psychiatry       Date:  2015-04-09       Impact factor: 10.154

2.  Cytosolic 5'-Nucleotidase 1A As a Target of Circulating Autoantibodies in Autoimmune Diseases.

Authors:  Thomas E Lloyd; Lisa Christopher-Stine; Iago Pinal-Fernandez; Eleni Tiniakou; Michelle Petri; Alan Baer; Sonye K Danoff; Katherine Pak; Livia A Casciola-Rosen; Andrew L Mammen
Journal:  Arthritis Care Res (Hoboken)       Date:  2016-01       Impact factor: 4.794

3.  Treatment of sporadic inclusion body myositis with bimagrumab.

Authors:  Anthony A Amato; Kumaraswamy Sivakumar; Namita Goyal; William S David; Mohammad Salajegheh; Jens Praestgaard; Estelle Lach-Trifilieff; Anne-Ulrike Trendelenburg; Didier Laurent; David J Glass; Ronenn Roubenoff; Brian S Tseng; Steven A Greenberg
Journal:  Neurology       Date:  2014-11-07       Impact factor: 9.910

4.  Demographic and clinical features of inclusion body myositis in North America.

Authors:  A David Paltiel; Einar Ingvarsson; Donald K K Lee; Richard L Leff; Richard J Nowak; Kurt D Petschke; Seth Richards-Shubik; Ange Zhou; Martin Shubik; Kevin C O'Connor
Journal:  Muscle Nerve       Date:  2015-02-17       Impact factor: 3.217

5.  [Therapy of myositis].

Authors:  A D Keck; U A Walker
Journal:  Z Rheumatol       Date:  2013-04       Impact factor: 1.372

Review 6.  Cytokines in immune-mediated inflammatory myopathies: cellular sources, multiple actions and therapeutic implications.

Authors:  E M Moran; F L Mastaglia
Journal:  Clin Exp Immunol       Date:  2014-12       Impact factor: 4.330

Review 7.  Idiopathic inflammatory myopathies - a guide to subtypes, diagnostic approach and treatment.

Authors:  Alexander Oldroyd; James Lilleker; Hector Chinoy
Journal:  Clin Med (Lond)       Date:  2017-07       Impact factor: 2.659

Review 8.  Lysosomal storage diseases and the heat shock response: convergences and therapeutic opportunities.

Authors:  Linda Ingemann; Thomas Kirkegaard
Journal:  J Lipid Res       Date:  2014-05-16       Impact factor: 5.922

9.  BACE-1, PS-1 and sAPPβ Levels Are Increased in Plasma from Sporadic Inclusion Body Myositis Patients: Surrogate Biomarkers among Inflammatory Myopathies.

Authors:  Marc Catalán-García; Glòria Garrabou; Constanza Morén; Mariona Guitart-Mampel; Ingrid Gonzalez-Casacuberta; Adriana Hernando; Jose Miquel Gallego-Escuredo; Dèlia Yubero; Francesc Villarroya; Raquel Montero; Albert Selva O-Callaghan; Francesc Cardellach; Josep Maria Grau
Journal:  Mol Med       Date:  2015-11-03       Impact factor: 6.354

10.  Two recurrent mutations are associated with GNE myopathy in the North of Britain.

Authors:  Amina Chaouch; Kathryn M Brennan; Judith Hudson; Cheryl Longman; John McConville; Patrick J Morrison; Maria E Farrugia; Richard Petty; Willie Stewart; Fiona Norwood; Rita Horvath; Patrick F Chinnery; Donald Costigan; John Winer; Tuomo Polvikoski; Estelle Healy; Anna Sarkozy; Teresinha Evangelista; Oksana Pogoryelova; Michelle Eagle; Kate Bushby; Volker Straub; Hanns Lochmüller
Journal:  J Neurol Neurosurg Psychiatry       Date:  2014-04-02       Impact factor: 10.154

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