Literature DB >> 30100561

Consensus proposal for taxonomy and definition of the autoinflammatory diseases (AIDs): a Delphi study.

Eldad Ben-Chetrit1, Marco Gattorno2, Ahmet Gul3, Daniel L Kastner4, Helen J Lachmann5, Isabelle Touitou6, Nicolino Ruperto7.   

Abstract

Autoinflammatory diseases (AIDs) are a relatively new family of disorders, defined about 19 years ago. Some of them are hereditary and some are not. The names given to these diseases do not follow any systematic guidelines, and sometimes the same disorder carries several names. The aim of this study is to refine the definition of AIDs and to provide some conventions for their naming. We focused mainly on monogenetic AIDs. Delphi technique, which enables consensus among a group of experts through internet and mail communication and questionnaires, was employed. After achieving 100% consensus among six members of a steering committee, the questionnaire containing AID definitions and the agreed-upon conventions were sent to 26 physicians and researchers working in the field of AIDs in order to gain broader support for the committee's proposals. The committee proposed the following definition for AIDs: "Autoinflammatory diseases are clinical disorders caused by defect(s) or dysregulation of the innate immune system, characterized by recurrent or continuous inflammation (elevated acute phase reactants-APR) and the lack of a primary pathogenic role for the adaptive immune system (autoreactive T-cells or autoantibody production)." Several rules were defined for guiding the naming of these diseases among which are: abandoning eponyms and preferring the name of the gene over its encoded protein. The new definition for AIDs allows inclusion of clinical disorders mainly associated with defects in the innate immune system. The new conventions propose names with clinical meaning and in some cases even clues for treatment. © Author(s) (or their employer(s)) 2018. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  autoimmune diseases; familial mediterranean fever; fever syndromes; inflammation

Mesh:

Year:  2018        PMID: 30100561     DOI: 10.1136/annrheumdis-2017-212515

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  36 in total

1.  β-Glucan-induced reprogramming of human macrophages inhibits NLRP3 inflammasome activation in cryopyrinopathies.

Authors:  Giorgio Camilli; Mathieu Bohm; Alícia Corbellini Piffer; Rachel Lavenir; David L Williams; Benedicte Neven; Gilles Grateau; Sophie Georgin-Lavialle; Jessica Quintin
Journal:  J Clin Invest       Date:  2020-09-01       Impact factor: 14.808

Review 2.  Toward a better understanding of type I interferonopathies: a brief summary, update and beyond.

Authors:  Zhong-Xun Yu; Hong-Mei Song
Journal:  World J Pediatr       Date:  2019-08-03       Impact factor: 2.764

3.  Comments on Tașdemir et al.: A rare cause of AA amyloidosis and end-stage kidney failure.

Authors:  Joris Galland; Léa Savey
Journal:  Pediatr Nephrol       Date:  2019-05-27       Impact factor: 3.714

Review 4.  Moving towards a systems-based classification of innate immune-mediated diseases.

Authors:  Sinisa Savic; Emily A Caseley; Michael F McDermott
Journal:  Nat Rev Rheumatol       Date:  2020-02-27       Impact factor: 20.543

5.  Pattern and diagnostic evaluation of systemic autoinflammatory diseases other than familial Mediterranean fever among Arab children: a multicenter study from the Pediatric Rheumatology Arab Group (PRAG).

Authors:  Sulaiman M Al-Mayouf; Abdulaziz Almutairi; Safiya Albrawi; Basil M Fathalla; Raed Alzyoud; Abdullatif AlEnazi; Mohammed Abu-Shukair; Adel Alwahadneh; Abdullah Alsonbul; Mabruka Zlenti; Ebtisam Khawaja; Awatif Abushhaiwia; Khulood Khawaja; Zakiya AlMosawi; Wafa Madan; Muna Almuatiri; Nora Almuatiri
Journal:  Rheumatol Int       Date:  2019-11-18       Impact factor: 2.631

6.  Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study.

Authors:  İlker Karacan; Ayşe Balamir; Serdal Uğurlu; Aslı Kireçtepe Aydın; Elif Everest; Seyit Zor; Merve Özkılınç Önen; Selçuk Daşdemir; Ozan Özkaya; Betül Sözeri; Abdurrahman Tufan; Deniz Gezgin Yıldırım; Selçuk Yüksel; Nuray Aktay Ayaz; Rukiye Eker Ömeroğlu; Kübra Öztürk; Mustafa Çakan; Oğuz Söylemezoğlu; Sezgin Şahin; Kenan Barut; Amra Adroviç; Emire Seyahi; Huri Özdoğan; Özgür Kasapçopur; Eda Tahir Turanlı
Journal:  Rheumatol Int       Date:  2019-02-19       Impact factor: 2.631

Review 7.  Efficacy of canakinumab on AA amyloidosis in late-onset NLRP3-associated autoinflammatory disease with an I574F somatic mosaic mutation.

Authors:  Takahiro Itamiya; Toshihiko Komai; Hiroko Kanda; Yasuo Nagafuchi; Hyangri Chang; Shota Shibata; Hiroyuki Ishiura; Hirofumi Shoda; Tatsushi Toda; Keishi Fujio
Journal:  Clin Rheumatol       Date:  2022-03-22       Impact factor: 2.980

8.  Genetic Landscape of Rare Autoinflammatory Disease Variants in Qatar and Middle Eastern Populations Through the Integration of Whole-Genome and Exome Datasets.

Authors:  Parul Sharma; Abhinav Jain; Vinod Scaria
Journal:  Front Genet       Date:  2021-05-13       Impact factor: 4.599

Review 9.  Monogenic Autoinflammatory Diseases: State of the Art and Future Perspectives.

Authors:  Giulia Di Donato; Debora Mariarita d'Angelo; Luciana Breda; Francesco Chiarelli
Journal:  Int J Mol Sci       Date:  2021-06-14       Impact factor: 5.923

Review 10.  A Role for Folate in Microbiome-Linked Control of Autoimmunity.

Authors:  Christine Mölzer; Heather M Wilson; Lucia Kuffova; John V Forrester
Journal:  J Immunol Res       Date:  2021-05-19       Impact factor: 4.818

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