Literature DB >> 33067611

Corticosteroid discontinuation, complete clinical response and remission in juvenile dermatomyositis.

Takayuki Kishi1, William Warren-Hicks2,3, Nastaran Bayat1, Ira N Targoff4,5, Adam M Huber6, Michael M Ward7, Lisa G Rider1.   

Abstract

OBJECTIVE: A North American registry of JDM patients was examined for frequency of and factors associated with corticosteroid discontinuation, complete clinical response and remission.
METHODS: We evaluated probability of achieving final corticosteroid discontinuation, complete clinical response and remission in 307 JDM patients by Weibull time-to-event modelling; conditional probability of complete clinical response and remission using Bayesian network modelling; and significant predictors with multivariable Markov chain Monte-Carlo Weibull extension models.
RESULTS: The probability of corticosteroid discontinuation was 56%, complete clinical response 38% and remission 30% by 60 months after initial treatment in 105 patients. The probability of remission was conditional on corticosteroid discontinuation and complete clinical response. Photosensitivity, contractures and a longer time to complete clinical response were predictive of the time to final corticosteroid discontinuation. Anti-MJ (NXP2) autoantibodies and a Northwest residential geoclimatic zone were predictive of shorter time to complete clinical response, while dysphonia, contractures, an increase in medications within 24 months and a longer time to corticosteroid discontinuation were associated with longer time to complete clinical response. Anti-p155/140 (TIF1) autoantibodies, an increase in medications within 12-24 months, or longer times to corticosteroid discontinuation and complete clinical response were associated with longer time to remission.
CONCLUSION: JDM patients achieve favourable outcomes, including corticosteroid discontinuation, complete clinical response and remission, although timelines for these may be several years based on time-dependent analyses. These outcomes are inter-related and strong predictors of each other. Selected clinical features and myositis autoantibodies are additionally associated with these outcomes. Published by Oxford University Press on behalf of the British Society for Rheumatology 2020. This work is written by US Government employees and is in the public domain in the US.

Entities:  

Keywords:  complete clinical response; corticosteroid discontinuation; juvenile dermatomyositis; myositis autoantibodies; outcomes; remission

Year:  2021        PMID: 33067611      PMCID: PMC8121446          DOI: 10.1093/rheumatology/keaa371

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  40 in total

1.  Brief Report: Association of Myositis Autoantibodies, Clinical Features, and Environmental Exposures at Illness Onset With Disease Course in Juvenile Myositis.

Authors:  G Esther A Habers; Adam M Huber; Gulnara Mamyrova; Ira N Targoff; Terrance P O'Hanlon; Sharon Adams; Janardan P Pandey; Chantal Boonacker; Marco van Brussel; Frederick W Miller; Annet van Royen-Kerkhof; Lisa G Rider
Journal:  Arthritis Rheumatol       Date:  2016-03       Impact factor: 10.995

2.  Immunoprecipitation-western blot for proteins of low abundance.

Authors:  Edward P Trieu; Joanne K Gross; Ira N Targoff
Journal:  Methods Mol Biol       Date:  2009

3.  Early illness features associated with mortality in the juvenile idiopathic inflammatory myopathies.

Authors:  Adam M Huber; Gulnara Mamyrova; Peter A Lachenbruch; Julia A Lee; James D Katz; Ira N Targoff; Frederick W Miller; Lisa G Rider
Journal:  Arthritis Care Res (Hoboken)       Date:  2014-05       Impact factor: 4.794

4.  Medium- and long-term functional outcomes in a multicenter cohort of children with juvenile dermatomyositis.

Authors:  A M Huber; B Lang; C M LeBlanc; N Birdi; R K Bolaria; P Malleson; I MacNeil; J A Momy; G Avery; B M Feldman
Journal:  Arthritis Rheum       Date:  2000-03

5.  Race, Income, and Disease Outcomes in Juvenile Dermatomyositis.

Authors:  Kathryn Phillippi; Mark Hoeltzel; Angela Byun Robinson; Susan Kim
Journal:  J Pediatr       Date:  2017-03-03       Impact factor: 4.406

6.  A novel autoantibody to a 155-kd protein is associated with dermatomyositis.

Authors:  Ira N Targoff; Gulnara Mamyrova; Edward P Trieu; Osvaldo Perurena; Bhanu Koneru; Terrance P O'Hanlon; Frederick W Miller; Lisa G Rider
Journal:  Arthritis Rheum       Date:  2006-11

7.  Cumulative organ damage and prognostic factors in juvenile dermatomyositis: a cross-sectional study median 16.8 years after symptom onset.

Authors:  Helga Sanner; Jan-Tore Gran; Ivar Sjaastad; Berit Flatø
Journal:  Rheumatology (Oxford)       Date:  2009-09-23       Impact factor: 7.580

8.  Predicting the course of juvenile dermatomyositis: significance of early clinical and laboratory features.

Authors:  Elizabeth Stringer; Davinder Singh-Grewal; Brian M Feldman
Journal:  Arthritis Rheum       Date:  2008-11

9.  Environmental factors preceding illness onset differ in phenotypes of the juvenile idiopathic inflammatory myopathies.

Authors:  Lisa G Rider; Lan Wu; Gulnara Mamyrova; Ira N Targoff; Frederick W Miller
Journal:  Rheumatology (Oxford)       Date:  2010-08-27       Impact factor: 7.580

10.  Autoantibodies in juvenile-onset myositis: Their diagnostic value and associated clinical phenotype in a large UK cohort.

Authors:  Sarah L Tansley; Stefania Simou; Gavin Shaddick; Zoe E Betteridge; Beverley Almeida; Harsha Gunawardena; Wendy Thomson; Michael W Beresford; Angela Midgley; Francesco Muntoni; Lucy R Wedderburn; Neil J McHugh
Journal:  J Autoimmun       Date:  2017-06-26       Impact factor: 7.094

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