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Association of human leukocyte antigen alleles with chronic lung diseases in rheumatoid arthritis.
Oka, Shomi; Furukawa, Hiroshi; Shimada, Kota; Sugii, Shoji; Hashimoto, Atsushi; Komiya, Akiko; Fukui, Naoshi; Suda, Akiko; Tsunoda, Shinichiro; Ito, Satoshi; Katayama, Masao; Nakamura, Tadashi; Saisho, Koichiro; Sano, Hajime; Migita, Kiyoshi; Nagaoka, Shouhei; Tsuchiya, Naoyuki; Tohma, Shigeto.
Afiliación
  • Oka S; Clinical Research Center for Allergy and Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara.
  • Furukawa H; Clinical Research Center for Allergy and Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara Molecular and Genetic Epidemiology Laboratory, Faculty of Medicine, University of Tsukuba, Tsukuba furukawa-tky@umin.org.
  • Shimada K; Department of Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Fuchu.
  • Sugii S; Department of Rheumatology, Yokohama Minami Kyosai Hospital.
  • Hashimoto A; Department of Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara.
  • Komiya A; Clinical Research Center for Allergy and Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara.
  • Fukui N; Clinical Research Center for Allergy and Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara.
  • Suda A; Department of Rheumatology, Yokohama Minami Kyosai Hospital Center for Rheumatic Diseases, Yokohama City University Medical Center, Yokohama.
  • Tsunoda S; Division of Rheumatology, Department of Internal Medicine, Hyogo College of Medicine, Nishinomiya.
  • Ito S; Department of Rheumatology, Niigata Rheumatic Center, Shibata.
  • Katayama M; Department of Internal Medicine, Nagoya Medical Center, National Hospital Organization, Nagoya.
  • Nakamura T; Department of Rheumatology, Kumamoto Shinto General Hospital, Kumamoto.
  • Saisho K; Department of Orthopedics/Rheumatology, Miyakonojo Hospital, National Hospital Organization, Miyakonojo.
  • Sano H; Clinical Research Center for Allergy and Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara.
  • Migita K; Clinical Research Center, Nagasaki Medical Center, National Hospital Organization, Omura, Japan.
  • Nagaoka S; Department of Rheumatology, Yokohama Minami Kyosai Hospital.
  • Tsuchiya N; Molecular and Genetic Epidemiology Laboratory, Faculty of Medicine, University of Tsukuba, Tsukuba.
  • Tohma S; Clinical Research Center for Allergy and Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara.
Rheumatology (Oxford) ; 55(7): 1301-7, 2016 07.
Article en En | MEDLINE | ID: mdl-27048628
OBJECTIVES: Chronic lung diseases including interstitial lung disease and airway disease (AD) occur in RA patients. Interstitial lung disease and AD in RA are extra-articular manifestations that influence the prognosis quoad vitam of RA. Studies on associations of HLA alleles with RA have been carried out, and shared epitopes of several alleles are reported to be associated with RA susceptibility. Few association studies in RA subpopulations with chronic lung diseases have been conducted. The aim of the study was to identify HLA alleles predisposing to RA phenotypes including the presence of AD. METHODS: Associations of HLA-DRB1 and DQB1 alleles with chronic lung diseases in RA were analysed. RESULTS: A positive association was found between the DR4 serological group and resistance to usual interstitial pneumonia [P = 0.0250, odds ratio (OR) 0.62, 95% CI: 0.41, 0.93]. The DR2 serological group was associated with susceptibility to usual interstitial pneumonia (P = 0.0036, OR = 1.86, 95% CI: 1.23, 2.81). An association was found for shared epitopes alleles with bronchiolitic AD (P = 0.0040, OR = 2.06, 95% CI: 1.24, 3.41). DQB1*03:01 was associated with bronchiectatic AD (P = 0.0021, corrected P-value (Pc) = 0.0315, OR = 1.99, 95% CI: 1.30, 3.06), as well as with emphysema (P = 0.0007, Pc = 0.0104, OR = 2.43, 95% CI: 1.49, 3.95). In combined analysis, a predisposing association of DQB1*03:01 (P = 1.94 ×10(-5), Pc = 0.0003, OR = 2.16, 95% CI: 1.53, 3.06) and a negative association of DQB1*03:02 (P = 0.0008, Pc = 0.0117, OR = 0.33, 95% CI: 0.17, 0.67) with bronchiectatic AD or emphysema were observed in RA. CONCLUSION: The present study identified an association of HLA-DQB1*03:01 with predisposition to, and DQB1*03:02 with resistance to, bronchiectatic AD or emphysema in RA.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Artritis Reumatoide / Enfisema Pulmonar / Enfermedades Pulmonares Intersticiales / Cadenas beta de HLA-DQ / Cadenas HLA-DRB1 Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2016 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Artritis Reumatoide / Enfisema Pulmonar / Enfermedades Pulmonares Intersticiales / Cadenas beta de HLA-DQ / Cadenas HLA-DRB1 Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2016 Tipo del documento: Article Pais de publicación: Reino Unido