Literature DB >> 26429707

Idiopathic Inflammatory Myopathies: an Update on Classification and Treatment with Special Focus on Juvenile Forms.

Ilaria Pagnini1, Antonio Vitale2, Carlo Selmi3,4, Rolando Cimaz1, Luca Cantarini5.   

Abstract

Juvenile inflammatory myopathies represent a heterogeneous group of rare and potentially fatal disorders of unknown aetiology, characterised by inflammation and proximal and symmetric muscle weakness. Beyond many similarities, specific clinical, laboratoristic and histopathologic features underlie different subsets with distinguishing demographic, prognostic and therapeutic peculiarities. Over time, several forms of inflammatory idiopathic myopathies have been described, including macrophagic myofascitis, immune-mediated necrozing myopathy and the spectrum of amyopathic dermatomyositis that include hypomyopathic dermatomyositis, inclusion body myositis and cancer-associated myositis occurring almost exclusively in adults. However, juvenile dermatomyositis is the most frequent in childhood, whereas polymyositis is relatively more frequent in adults. The aetiology is nowadays widely unclear; however, current theories contemplate a combination of environmental triggers, immune dysfunction and specific tissue responses involving muscle, skin and small vessels endothelium in genetically susceptible individuals. Myositis-specific autoantibodies, found almost exclusively in patients with myositis and myositis-associated autoantibodies, detectable both among patients with myositis and in subjects suffering from other autoimmune diseases, have an important clinical role because of their relation to specific clinical features, response to therapy and prognosis. The gold standard treatment for juvenile dermatomyositis is represented by corticosteroids, along with adjunctive steroid-sparing immunosuppressive therapies, which are used to counteract disease activity, prevent mortality, and reduce long-term disability. Further treatment approach such as biologic agents and autologous stem cell transplantation are emerging during the last years, in particular in patients difficult to treat and with poor prognosis. Therefore, a highly medical specialised approach is required for diagnosis and management of these conditions. This review comprehensively examines juvenile inflammatory myopathies focusing on clinical and laboratory classifications as well as on the current treatment approaches, referring in particular on biologic agents and latest therapeutic opportunities.

Entities:  

Keywords:  Autoantibodies; Autoimmune disorders; Dermatomyositis; Myopathies; Polymyositis

Mesh:

Year:  2017        PMID: 26429707     DOI: 10.1007/s12016-015-8512-9

Source DB:  PubMed          Journal:  Clin Rev Allergy Immunol        ISSN: 1080-0549            Impact factor:   10.817


  95 in total

1.  Consensus treatments for moderate juvenile dermatomyositis: beyond the first two months. Results of the second Childhood Arthritis and Rheumatology Research Alliance consensus conference.

Authors:  Adam M Huber; Angela B Robinson; Ann M Reed; Leslie Abramson; Sharon Bout-Tabaku; Ruy Carrasco; Megan Curran; Brian M Feldman; Harry Gewanter; Thomas Griffin; Kathleen Haines; Mark F Hoeltzel; Josephine Isgro; Philip Kahn; Bianca Lang; Patti Lawler; Bracha Shaham; Heinrike Schmeling; Rosie Scuccimarri; Michael Shishov; Elizabeth Stringer; Julie Wohrley; Norman T Ilowite; Carol Wallace
Journal:  Arthritis Care Res (Hoboken)       Date:  2012-04       Impact factor: 4.794

2.  Antisignal recognition particle-positive polymyositis successfully treated with myeloablative autologous stem cell transplantation.

Authors:  J C Henes; F Heinzelmann; A Wacker; H P Seelig; R Klein; A Bornemann; C Faul; L Kanz; I Koetter
Journal:  Ann Rheum Dis       Date:  2009-03       Impact factor: 19.103

3.  Use of etanercept in the treatment of dermatomyositis: a case series.

Authors:  Florenzo Iannone; Crescenzio Scioscia; Paola C F Falappone; Michele Covelli; Giovanni Lapadula
Journal:  J Rheumatol       Date:  2006-09       Impact factor: 4.666

4.  Protocols for the initial treatment of moderately severe juvenile dermatomyositis: results of a Children's Arthritis and Rheumatology Research Alliance Consensus Conference.

Authors:  Adam M Huber; Edward H Giannini; Suzanne L Bowyer; Susan Kim; Bianca Lang; Carol B Lindsley; Lauren M Pachman; Clarissa Pilkington; Ann M Reed; Robert M Rennebohm; Lisa G Rider; Carol A Wallace; Brian M Feldman
Journal:  Arthritis Care Res (Hoboken)       Date:  2010-02       Impact factor: 4.794

Review 5.  Soft tissue and subcutaneous calcification in connective tissue diseases.

Authors:  Sumeet Chander; Patrick Gordon
Journal:  Curr Opin Rheumatol       Date:  2012-03       Impact factor: 5.006

6.  Distribution and severity of weakness among patients with polymyositis, dermatomyositis and juvenile dermatomyositis.

Authors:  M O Harris-Love; J A Shrader; D Koziol; N Pahlajani; M Jain; M Smith; H L Cintas; C L McGarvey; L James-Newton; A Pokrovnichka; B Moini; I Cabalar; D J Lovell; R Wesley; P H Plotz; F W Miller; J E Hicks; L G Rider
Journal:  Rheumatology (Oxford)       Date:  2008-12-11       Impact factor: 7.580

7.  HLA class II haplotype and autoantibody associations in children with juvenile dermatomyositis and juvenile dermatomyositis-scleroderma overlap.

Authors:  L R Wedderburn; N J McHugh; H Chinoy; R G Cooper; F Salway; W E R Ollier; L J McCann; H Varsani; J Dunphy; J North; J E Davidson
Journal:  Rheumatology (Oxford)       Date:  2007-11-14       Impact factor: 7.580

8.  Open-label trial of anti-TNF-alpha in dermato- and polymyositis treated concomitantly with methotrexate.

Authors:  G J D Hengstman; J L De Bleecker; E Feist; J Vissing; C P Denton; M N Manoussakis; H Slott Jensen; B G M van Engelen; F H J van den Hoogen
Journal:  Eur Neurol       Date:  2008-01-29       Impact factor: 1.710

9.  Dermatomyositis induced by anti-tumor necrosis factor in a patient with juvenile idiopathic arthritis.

Authors:  Stephanie W Liu; Nicole F Velez; Christina Lam; Alisa Femia; Scott R Granter; Henry B Townsend; Ruth Ann Vleugels
Journal:  JAMA Dermatol       Date:  2013-10       Impact factor: 10.282

10.  Autoantibodies to a 140-kd protein in juvenile dermatomyositis are associated with calcinosis.

Authors:  H Gunawardena; L R Wedderburn; H Chinoy; Z E Betteridge; J North; W E R Ollier; R G Cooper; C V Oddis; A V Ramanan; J E Davidson; N J McHugh
Journal:  Arthritis Rheum       Date:  2009-06
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  5 in total

Review 1.  The role of exosome in autoimmune connective tissue disease.

Authors:  Tian Zhu; Yiman Wang; Hongzhong Jin; Li Li
Journal:  Ann Med       Date:  2019-04-22       Impact factor: 4.709

Review 2.  Autoimmunity in 2017.

Authors:  Carlo Selmi
Journal:  Clin Rev Allergy Immunol       Date:  2018-12       Impact factor: 8.667

Review 3.  Cutaneous Manifestations of Dermatomyositis: a Comprehensive Review.

Authors:  Carlo Mainetti; Benedetta Terziroli Beretta-Piccoli; Carlo Selmi
Journal:  Clin Rev Allergy Immunol       Date:  2017-12       Impact factor: 8.667

4.  Pervasive inflammatory activation in patients with deficiency in very-long-chain acyl-coA dehydrogenase (VLCADD).

Authors:  Abbe N Vallejo; Henry J Mroczkowski; Joshua J Michel; Michael Woolford; Harry C Blair; Patricia Griffin; Elizabeth McCracken; Stephanie J Mihalik; Miguel Reyes-Mugica; Jerry Vockley
Journal:  Clin Transl Immunology       Date:  2021-06-27

5.  Long-term follow-up of autologous hematopoietic stem cell transplantation for refractory juvenile dermatomyositis: a case-series study.

Authors:  Jia Zhu; Gaixiu Su; Jianming Lai; Boya Dong; Min Kang; Shengnan Li; Zhixuan Zhou; Fengqi Wu
Journal:  Pediatr Rheumatol Online J       Date:  2018-11-20       Impact factor: 3.054

  5 in total

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