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A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease.
Aeschlimann, Florence A; Batu, Ezgi D; Canna, Scott W; Go, Ellen; Gül, Ahmet; Hoffmann, Patrycja; Leavis, Helen L; Ozen, Seza; Schwartz, Daniella M; Stone, Deborah L; van Royen-Kerkof, Annet; Kastner, Daniel L; Aksentijevich, Ivona; Laxer, Ronald M.
Afiliação
  • Aeschlimann FA; Division of Rheumatology, The Hospital for Sick Children, Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.
  • Batu ED; Department of Pediatric Rheumatology, Hacettepe University, Ankara, Turkey.
  • Canna SW; Department of Pediatric Rheumatology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
  • Go E; Division of Pediatric Rheumatology, Riley Hospital for Children, Indiana University, Indianapolis, Indiana, USA.
  • Gül A; Department of Internal Medicine, Istanbul University, Istanbul, Turkey.
  • Hoffmann P; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA.
  • Leavis HL; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Ozen S; Department of Pediatric Rheumatology, Hacettepe University, Ankara, Turkey.
  • Schwartz DM; Molecular Immunology and Inflammation Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland, USA.
  • Stone DL; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA.
  • van Royen-Kerkof A; Department of Pediatric Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Kastner DL; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA.
  • Aksentijevich I; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA.
  • Laxer RM; Division of Rheumatology, The Hospital for Sick Children, Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.
Ann Rheum Dis ; 77(5): 728-735, 2018 05.
Article em En | MEDLINE | ID: mdl-29317407
OBJECTIVES: The association between mutations in TNFAIP3, encoding the NF-kB regulatory protein A20, and a new autoinflammatory disease has recently been recognised. This study aims at describing the clinical phenotypes and disease course of patients with A20 haploinsufficiency (HA20). METHODS: Data for all cases from the initial publication, and additional cases identified through collaborations since, were collected using standardised data collection forms. RESULTS: A total of 16 patients (13 female) from seven families with a genetic diagnosis of HA20 were included. The disease commonly manifested in early childhood (range: first week of life to 29 years of age). The main clinical symptoms were recurrent oral, genital and/or gastrointestinal ulcers (16/16), musculoskeletal (9/16) and gastrointestinal complaints (9/16), cutaneous lesions (8/16), episodic fever (7/16), and recurrent infections (7/16). Clinical phenotypes varied considerably, even within families. Relapsing-remitting disease course was most common, and one patient died. Laboratory abnormalities included elevated acute-phase reactants and fluctuating presence of various autoantibodies such as antinuclear antibodies (4/10 patients tested) and anti-dsDNA (2/5). Tissue biopsy of different sites revealed non-specific chronic inflammation (6/12 patients tested), findings consistent with class V lupus nephritis in one patient, and pustules and normal results in two patients each. All patients were treated: 4/16 received colchicine and 12/16 various immunosuppressive agents. Cytokine inhibitors effectively suppressed systemic inflammation in 7/9 patients. CONCLUSIONS: Early-onset recurrent oral, genital and/or gastrointestinal ulcers are the hallmark feature of HA20. Frequency and intensity of other clinical manifestations varied highly. Treatment regimens should be based on disease severity, and cytokine inhibitors are often required to control relapses.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Fenótipo / NF-kappa B / Doenças Hereditárias Autoinflamatórias / Haploinsuficiência / Proteína 3 Induzida por Fator de Necrose Tumoral alfa Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Ann Rheum Dis Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Fenótipo / NF-kappa B / Doenças Hereditárias Autoinflamatórias / Haploinsuficiência / Proteína 3 Induzida por Fator de Necrose Tumoral alfa Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Ann Rheum Dis Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá