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Current classification criteria underestimate the incidence of idiopathic inflammatory myopathies by ignoring subgroups.

作者信息

Giannini Margherita, Debrut Léa, Nespola Benoit, Velten Michel, Geny Bernard, Sibilia Jean, Meyer Alain

机构信息

Physiologie et Explorations Fonctionnelles Musculaires, University Hospital of Strasbourg, Strasbourg, France.

Centre de Recherche en Biomédecine, University of Strasbourg, UR3072, Strasbourg, France.

出版信息

Nat Rev Rheumatol. 2024 May;20(5):311-312. doi: 10.1038/s41584-024-01105-9.

DOI:10.1038/s41584-024-01105-9
PMID:38514811
Abstract
摘要

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Current classification criteria underestimate the incidence of idiopathic inflammatory myopathies by ignoring subgroups.当前的分类标准通过忽略亚组而低估了特发性炎性肌病的发病率。
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Reply to: Current classification criteria underestimate the incidence of idiopathic inflammatory myopathies by ignoring subgroups.回复:当前的分类标准因忽略亚组而低估了特发性炎性肌病的发病率。
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引用本文的文献

1
Reply to: Current classification criteria underestimate the incidence of idiopathic inflammatory myopathies by ignoring subgroups.回复:当前的分类标准因忽略亚组而低估了特发性炎性肌病的发病率。
Nat Rev Rheumatol. 2024 May;20(5):313-314. doi: 10.1038/s41584-024-01106-8.

本文引用的文献

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Epidemiology of the idiopathic inflammatory myopathies.特发性炎症性肌病的流行病学
Nat Rev Rheumatol. 2023 Nov;19(11):695-712. doi: 10.1038/s41584-023-01033-0. Epub 2023 Oct 6.
2
Refining Incidence and Characteristics of Inflammatory Myopathies: A Quadruple-Source Capture-Recapture Survey Using the 2017 European League Against Rheumatism/American College of Rheumatology Classification Criteria.细化炎症性肌病的发病情况和特征:采用 2017 年欧洲抗风湿病联盟/美国风湿病学会分类标准的四重源捕获-再捕获调查。
Arthritis Rheumatol. 2023 Oct;75(10):1850-1855. doi: 10.1002/art.42561. Epub 2023 Aug 4.
3
Scleromyositis: A distinct novel entity within the systemic sclerosis and autoimmune myositis spectrum. Implications for care and pathogenesis.
硬皮病性肌炎:系统性硬化症和自身免疫性肌炎谱中的一种独特新型实体。对护理和发病机制的影响。
Front Immunol. 2023 Jan 26;13:974078. doi: 10.3389/fimmu.2022.974078. eCollection 2022.
4
Defining anti-synthetase syndrome: a systematic literature review.抗合成酶综合征的定义:系统文献回顾。
Clin Exp Rheumatol. 2022 Feb;40(2):309-319. doi: 10.55563/clinexprheumatol/8xj0b9. Epub 2022 Feb 25.
5
Performance of the 2017 European Alliance of Associations for Rheumatology/American College of Rheumatology Classification Criteria for Idiopathic Inflammatory Myopathies in Patients With Myositis-Specific Autoantibodies.2017 年欧洲风湿病学会联盟/美国风湿病学会特发性炎性肌病分类标准在肌炎特异性自身抗体患者中的性能。
Arthritis Rheumatol. 2022 Mar;74(3):508-517. doi: 10.1002/art.41964. Epub 2022 Feb 1.
6
Anti-Ku syndrome with elevated CK and anti-Ku syndrome with anti-dsDNA are two distinct entities with different outcomes.抗-Ku 综合征伴 CK 升高和抗-Ku 综合征伴抗 dsDNA 是两种不同的实体,具有不同的结局。
Ann Rheum Dis. 2019 Aug;78(8):1101-1106. doi: 10.1136/annrheumdis-2018-214439. Epub 2019 May 24.
7
Muscular and extramuscular clinical features of patients with anti-PM/Scl autoantibodies.抗 PM/Scl 自身抗体患者的肌肉和肌肉外临床特征。
Neurology. 2018 Jun 5;90(23):e2068-e2076. doi: 10.1212/WNL.0000000000005638. Epub 2018 May 4.
8
Clinical Spectrum Time Course in Anti Jo-1 Positive Antisynthetase Syndrome: Results From an International Retrospective Multicenter Study.抗 Jo-1 阳性抗合成酶综合征的临床谱随时间变化:一项国际回顾性多中心研究的结果
Medicine (Baltimore). 2015 Aug;94(32):e1144. doi: 10.1097/MD.0000000000001144.
9
Incidence and prevalence of inflammatory myopathies: a systematic review.炎性肌病的发病率和患病率:系统评价。
Rheumatology (Oxford). 2015 Jan;54(1):50-63. doi: 10.1093/rheumatology/keu289. Epub 2014 Jul 26.