Association between the severity of Hashimoto's disease and the functional +874A/T polymorphism in the interferon-γ gene

被引:52
|
作者
Ito, Chisato [1 ]
Watanabe, Mikio [1 ]
Okuda, Noriko [1 ]
Watanabe, Chikami [1 ]
Iwatani, Yoshinori [1 ]
机构
[1] Osaka Univ, Div Hlth Sci, Dept Bioned Informat, Suita, Osaka, Japan
关键词
IFN-gamma; single nucleotide polymorphism; disease severity; ethnic difference; type 1 helper T cell;
D O I
10.1507/endocrj.K06-015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CD8(+)CD25(+)-activated cytotoxic T cells and anti-thyroglobulin antibodies (TgAb) are independently involved in the severity of Hashimoto's disease (HD). Interferon gamma (IFN-gamma) activates cytotoxic T cells. To evaluate the hypothesis that the functional +874A/T polymorphism in the gene encoding IFN-gamma is associated with the severity of HD, we examined the frequencies of this polymorphism in 34 HD patients who developed hypothyroidism (severe HD); 22 untreated, euthyroid HD patients (mild HD); 49 patients With intractable Graves' disease (GD); 16 GD patients in remission; and 57 healthy volunteers. Frequency of the +874T allele, which is associated with high IFN-gamma production, was higher in patients with severe HD than in those with mild HD (odds ratio [OR], 3.5; 95% confidence interval [CI], 1.0-12.4; p = 0.047), but there Was no difference in the frequency between GD patients. The difference in the frequency of +874T was observed in the subset of patients with HD negative for TgAb (OR, 8.4; 95% Cl, 1.2-57.3; p = 0.029) but not in the subset of patients With HD positive for TgAb. Our data indicate that the +874A/T polymorphism in the IFN-gamma gene is associated with severity of HD.
引用
收藏
页码:473 / 478
页数:6
相关论文
共 50 条
  • [31] Association of the rs2430561 polymorphism of the interferon-γ gene with cervical cancer susceptibility and prognosis in Han Chinese women
    Wei, Heng
    Zhang, Yang
    Zhang, Qiao
    Lu, Yanming
    Huo, Yunlong
    Wang, Ning
    EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY, 2021, 42 (04) : 788 - 794
  • [32] Association between IFN-γ+874T/A SNP and COVID-19 Severity
    Rezaei, Seyyed Amin Seyyed
    Asgharzadeh, Vahid
    Poor, Behroz Mahdavi
    Asgharzadeh, Mohammad
    Poorghani, Asra
    Ozma, Mahdi Asghari
    Khalili, Ahmad Ali
    Nobari, Hossein Jalaei
    Raeisi, Mortaza
    Rashedi, Jalil
    IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY, 2025, 24 (02) : 254 - 258
  • [33] Interferon-Gamma Gene Polymorphism+874 (A/T) in Chinese Children with Henoch-Schonlein Purpura
    Xu, Hui
    Li, Wei
    Fu, Haidong
    Jiang, Guizheng
    IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY, 2014, 13 (03) : 184 - 189
  • [34] No evidence for association between an MAOA functional polymorphism and susceptibility to Parkinson’s disease
    Caroline Williams-Gray
    An Goris
    Thomas Foltynie
    Alastair Compston
    Stephen Sawcer
    Roger A. Barker
    Journal of Neurology, 2009, 256 : 132 - 133
  • [35] Interferon Gamma Gene Polymorphism (+874 T > A) and Chronic Hepatitis B in the Population of Gorgan, North-Eastern Iran
    Ghasemian, Nadia
    Shahbazi, Majid
    JUNDISHAPUR JOURNAL OF MICROBIOLOGY, 2016, 9 (08)
  • [36] ASSOCIATION BETWEEN IFN-γ+874A/T, TNF-α-308G/A AND IL-12Rβ2-237C/T GENE POLYMORPHISMS AND SUSCEPTIBILITY TO PULMONARY TUBERCULOSIS IN A TURKISH POPULATION
    Caliskan, Tayfun
    Yilmazz, Ismail
    Babalik, Aylin
    Ortakoylu, Mediha Gonenc
    Kaya, Hatice
    Fidan, Ali
    Ciftci, Faruk
    ACTA MEDICA MEDITERRANEA, 2015, 31 (06): : 1291 - 1297
  • [37] Polymorphism of the LMP2 gene and disease phenotype in ankylosing spondylitis: No association with disease severity
    W. P. Maksymowych
    N. Adlam
    D. Lind
    A. S. Russell
    Clinical Rheumatology, 1997, 16 : 461 - 465
  • [38] High levels of plasma interferon gamma and+874T/A gene polymorphism is associated with HIV-TB co-infection
    Gutlapalli, V. R.
    Sykam, Aparna
    Tenali, Sandeep P.
    Suneetha, Sujai
    Suneetha, Lavanya M.
    HUMAN IMMUNOLOGY, 2016, 77 (12) : 1264 - 1270
  • [39] Polymorphism of the LMP2 gene and disease phenotype in ankylosing spondylitis: No association with disease severity.
    Maksymowych, WP
    Adlam, N
    Lind, D
    Russell, AS
    CLINICAL RHEUMATOLOGY, 1997, 16 (05) : 461 - 465
  • [40] Association of a polymorphism in the indoleamine-2,3-dioxygenase gene and interferon-α-induced depression in patients with chronic hepatitis C
    Smith, A. K.
    Simon, J. S.
    Gustafson, E. L.
    Noviello, S.
    Cubells, J. F.
    Epstein, M. P.
    Devlin, D. J.
    Qiu, P.
    Albrecht, J. K.
    Brass, C. A.
    Sulkowski, M. S.
    McHutchinson, J. G.
    Miller, A. H.
    MOLECULAR PSYCHIATRY, 2012, 17 (08) : 781 - 789