Literature DB >> 20497129

Detection of the membrane attack complex as a diagnostic tool in dermatomyositis.

A Jain1, M C Sharma, C Sarkar, R Bhatia, S Singh, S Gulati, R Handa.   

Abstract

BACKGROUND: Currently there is no reliable diagnostic marker to distinguish between the subgroups of idiopathic inflammatory myopathies (IIMs), i.e. dermatomyositis (DM), polymyositis (PM) and inclusion body myositis (IBM). Membrane attack complex (MAC) has been shown to be involved in the pathogenesis of dermatomyositis but its role as a diagnostic marker has not been evaluated. AIM: To assess the diagnostic utility of MAC deposition in distinguishing dermatomyositis from other neuromuscular disorders.
MATERIAL AND METHODS: Immunohistochemical detection of MAC deposition on endomysial microvessels was carried out on 127 muscle biopsies comprising of 21 cases of dermatomyositis, 42 other IIMs and 64 non-IIM neuromuscular diseases.
RESULTS: MAC deposition showed a high sensitivity (80.9%) and specificity (85%) to differentiate DM from other IIMs. Its specificity was higher (98.4%) in discriminating DM from non-IIM muscular diseases and IIM from non-IIMs.
CONCLUSION: MAC deposition can serve as a reliable marker to distinguish DM from other IIMs (i.e. PM and IBM) as well as from non-IIM diseases. It can also serve as a useful adjunct in diagnosis of IIMs when there is diagnostic dilemma with their morphologic similarities. These results provide further credence to the long-standing view that MAC-mediated capillary destruction is involved in the immunopathogenesis of DM.
© 2010 John Wiley & Sons A/S.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 20497129     DOI: 10.1111/j.1600-0404.2010.01353.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  7 in total

1.  Anti-MDA5-Positive Dermatomyositis Presenting as Fever of Unknown Origin.

Authors:  Lori W Lee; Neera S Narang; Anna Postolova; Nicole Seminara; Molly A Kantor
Journal:  J Gen Intern Med       Date:  2016-12       Impact factor: 5.128

Review 2.  Clinical features, pathogenesis and treatment of juvenile and adult dermatomyositis.

Authors:  Angela B Robinson; Ann M Reed
Journal:  Nat Rev Rheumatol       Date:  2011-09-27       Impact factor: 20.543

3.  Polymyositis as a manifestation of chronic graft-versus-host disease after allo-HSCT.

Authors:  Lijuan Meng; Suqiong Ji; Qiong Wang; Bitao Bu
Journal:  Clin Case Rep       Date:  2018-07-12

4.  Proteome study of cutaneous lupus erythematosus (CLE) and dermatomyositis skin lesions reveals IL-16 is differentially upregulated in CLE.

Authors:  Timothy B Niewold; Alexander Meves; Julia S Lehman; Karin Popovic-Silwerfeldt; Aliisa Häyry; Therese Söderlund-Matell; Cristine M Charlesworth; Benjamin Madden; Ingrid E Lundberg; Marie Wahren-Herlenius; Elisabet Svenungsson; Vilija Oke
Journal:  Arthritis Res Ther       Date:  2021-04-30       Impact factor: 5.156

Review 5.  Beyond Systemic Lupus Erythematosus and Anti-Phospholipid Syndrome: The Relevance of Complement From Pathogenesis to Pregnancy Outcome in Other Systemic Rheumatologic Diseases.

Authors:  Silvia Cavalli; Paola Adele Lonati; Maria Gerosa; Roberto Caporali; Rolando Cimaz; Cecilia Beatrice Chighizola
Journal:  Front Pharmacol       Date:  2022-02-15       Impact factor: 5.810

Review 6.  Pathophysiological Mechanisms and Treatment of Dermatomyositis and Immune Mediated Necrotizing Myopathies: A Focused Review.

Authors:  Renske G Kamperman; Anneke J van der Kooi; Marianne de Visser; Eleonora Aronica; Joost Raaphorst
Journal:  Int J Mol Sci       Date:  2022-04-13       Impact factor: 6.208

7.  Scleroderma-polymyositis overlap syndrome versus idiopathic polymyositis and systemic sclerosis: a descriptive study on clinical features and myopathology.

Authors:  Kavish J Bhansing; Martin Lammens; Hanneke K A Knaapen; Piet L C M van Riel; Baziel G M van Engelen; Madelon C Vonk
Journal:  Arthritis Res Ther       Date:  2014-05-13       Impact factor: 5.156

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.