Major Histocompatibility Complex Class I-Related Chain A Alleles and Histology of Nonalcoholic Fatty Liver Disease

被引:4
|
作者
Karrar, Azza [1 ]
Rajput, Bijal [1 ]
Hariharan, Siddharth [1 ]
Abdelatif, Dinan [2 ]
Houry, Mohamad [1 ]
Moosvi, Ali [1 ]
Ali, Irfan [2 ]
Tan, Daisong [2 ]
Noor, Sohailla [1 ]
Esmaeili, Donna [1 ]
Felix, Sean [1 ]
Alaparthi, Lakshmi [2 ]
Otgonsuren, Munkhzul [1 ]
Lam, Brian [1 ,2 ]
Goodman, Zachary D. [2 ]
Younossi, Zobair M. [1 ,2 ]
机构
[1] Inova Fairfax Med Campus, Betty & Guy Beatty Ctr Integrated Res, Falls Church, VA USA
[2] Inova Fairfax Hosp, Ctr Liver Dis, Dept Med, Falls Church, VA USA
关键词
SERUM-LEVELS; HEPATITIS; MICA; CELLS; EXPRESSION; HLA;
D O I
10.1002/hep4.1610
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Major histocompatibility complex class I-related chain A (MICA) is a highly polymorphic gene that modulates immune surveillance by binding to its receptor on natural killer cells, and its genetic polymorphisms have been associated with chronic immune-mediated diseases. The progressive form of nonalcoholic fatty liver disease (NAFLD), nonalcoholic steatohepatitis (NASH), is characterized by accumulation of fat and inflammatory cells in the hepatic parenchyma, potentially leading to liver cell injury and fibrosis. To date, there are no data describing the potential role of MICA in the pathogenesis of NAFLD. Therefore, our aim was to assess the association between MICA polymorphism and NASH and its histologic features. A total of 134 subjects were included. DNA from patients with biopsy-proven NAFLD were genotyped using polymerase chain reaction-sequence-specific oligonucleotide for MICA alleles. Liver biopsies were assessed for histologic diagnosis of NASH and specific pathologic features, including stage of fibrosis and grade of inflammation. Multivariate analysis was performed to draw associations between MICA alleles and the different variables;P <= 0.05 was considered significant. Univariate analysis showed that MICA*011 (odds ratio [OR], 7.14; 95% confidence interval [CI], 1.24-41.0;P = 0.04) was associated with a higher risk for histologic NASH. Multivariate analysis showed that MICA*002 was independently associated with a lower risk for focal hepatocyte necrosis (OR, 0.24; 95% CI, 0.08-0.74;P = 0.013) and advanced fibrosis (OR, 0.11; 95% CI, 0.02-0.70;P = 0.019). MICA*017 was independently associated with a higher risk for lymphocyte-mediated inflammation (OR, 5.12; 95% CI, 1.12-23.5;P = 0.035).Conclusion:MICA alleles may be associated with NASH and its histologic features of inflammation and fibrosis. Additional research is required to investigate the potential role of MICA in increased risk or protection against NAFLD.
引用
收藏
页码:63 / 73
页数:11
相关论文
共 50 条
  • [31] Detection of Antibodies Against Major Histocompatibility Complex Class I-Related Chain A in Long-term Renal Graft Recipients
    Li, Zuowei
    Luo, Ming
    Qiu, Jianxin
    Liu, Yong
    Fan, Yu
    Jahr, Fay M.
    Cai, Junchao
    Terasaki, Paul I.
    EXPERIMENTAL AND CLINICAL TRANSPLANTATION, 2012, 10 (03) : 239 - 242
  • [32] Expression characteristics of major histocompatibility complex class I-related chain A antibodies and immunoadsorption effect in sensitized recipients of kidney transplantation
    YAO Qing-chun
    WANG Wei
    LI Xiao-bei
    YIN Hang
    ZHANG Xiao-dong
    中华医学杂志(英文版), 2011, (05) : 669 - 673
  • [33] Expression characteristics of major histocompatibility complex class I-related chain A antibodies and immunoadsorption effect in sensitized recipients of kidney transplantation
    Yao Qing-chun
    Wang Wei
    Li Xiao-bei
    Yin Hang
    Zhang Xiao-dong
    CHINESE MEDICAL JOURNAL, 2011, 124 (05) : 669 - 673
  • [34] Association between soluble major histocompatibility complex class I-related chain A levels and a severity of nasopharyngeal cancer in Tunisian patients
    Ben Chaaben, Arij
    Bpuckouaci, Wahid
    Douik, Hayet
    Ghanem, Abderraouf
    Mamoghli, Tesnim
    Chaouch, Leila
    Harzallah, Latifa
    Bouassida, Jihene
    Saihi, Dorra
    Fortier, Catherine
    Kishnamoorthy, Ragagopal
    Charron, Dominique
    Guemira, Fethi
    Tamouza, Ryad
    TISSUE ANTIGENS, 2010, 75 (05): : 613 - 614
  • [35] Expression and clinical value of the soluble major histocompatibility complex class I-related chain A molecule in the serum of patients with renal tumors
    Zhao, Y. -K.
    Jia, C. -M.
    Yuan, G. -J.
    Liu, W.
    Qiu, Y.
    Zhu, Q. -G.
    GENETICS AND MOLECULAR RESEARCH, 2015, 14 (02) : 7233 - 7240
  • [36] Major Histocompatibility Class II Pathway Is Not Required for the Development of Nonalcoholic Fatty Liver Disease in Mice
    Willemin, Gilles
    Roger, Catherine
    Bauduret, Armelle
    Minehira, Kaori
    INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2013, 2013
  • [37] Serum major-histocompatibility-complex class I-related chain A antibody detection for the evaluation of graft dysfunction in renal allograft recipients
    Zhang Ming
    Lu Fu-ming
    Qu Lian-xi
    He Jun
    Yuan Xiao-niao
    Gu Yong
    CHINESE MEDICAL JOURNAL, 2011, 124 (14) : 2127 - 2131
  • [38] Association of major histocompatibility complex class I chain-related gene A and HLA-B alleles with Behcet's disease in Turkey
    Mizuki, Nobuko
    Meguro, Akira
    Tohnai, Iwai
    Guel, Ahmet
    Ohno, Shigeaki
    Mizuki, Nobuhisa
    JAPANESE JOURNAL OF OPHTHALMOLOGY, 2007, 51 (06) : 431 - 436
  • [39] Major Histocompatibility Complex Class I-Related Chain A and Macrophage Migration Inhibitory Factor Gene Polymorphisms in a Turkish Patient Population with Vitiligo
    Aydingoz, Ikbal E.
    Bingul, Ilknur
    Vural, Pervin
    Dogru-Abbasoglu, Semra
    TURK DERMATOLOJI DERGISI-TURKISH JOURNAL OF DERMATOLOGY, 2023, 17 (01): : 11 - 15
  • [40] Gemcitabine Induces Major Histocompatibility Complex Class I-Related Chain A/B Expression, Activating γδ T Cell Function in Pancreatic Cancer
    Miyashita, Tomoharu
    Miki, Kenji
    Harmon, John W.
    Ahmed, Ali K.
    Tajima, Hidehiro
    Fushida, Sachio
    Ohta, Tetsuo
    GASTROENTEROLOGY, 2015, 148 (04) : S1172 - S1172