Association of STAT4, TGFβ1, SH2B3 and PTPN22 polymorphisms with autoimmune hepatitis

被引:15
作者
Chaouali, Marwa [1 ,2 ]
Fernandes, Veronica [3 ,4 ]
Ghazouani, Ezzedine [1 ]
Pereira, Luisa [3 ,4 ,5 ]
Kochkar, Radhia [1 ]
机构
[1] Mil Hosp Tunis, Dept Immunol, Tunis 1008, Tunisia
[2] El Manar Univ, Lab Mycol Pathol & Biomarkers, Tunis 1092, Tunisia
[3] Univ Porto, i3S, P-4200135 Porto, Portugal
[4] Univ Porto IPATIMUP, Inst Patol & Imunol Mol, P-4200135 Porto, Portugal
[5] Univ Porto, Fac Med, Porto, Portugal
关键词
Autoimmune hepatitis; Genetic susceptibility; SH2B3; TGF beta 1; STAT4; PTPN22; GENOME-WIDE ASSOCIATION; RHEUMATOID-ARTHRITIS; RISK; GENE; SUSCEPTIBILITY; IDENTIFICATION; VARIANT;
D O I
10.1016/j.yexmp.2018.10.001
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The physiopathology of autoimmune hepatitis (AIH) is complex and still not fully elucidated. The genes localized outside the histocompatibility complex involved in regulation and signal transduction of the immune system SH2B3, TGF beta 1, STAT4 and PTPN22 could be associated to the susceptibility and hepatocyte lysis mechanism of this lethal autoimmune disorder. Patients and methods: We investigated four polymorphic sites in SH2B3 (rs3184504), TGF beta 1 (rs1800471), STAT4 (rs7574865) and PTPN22 (rs2476601) in 45 AIH patients and 150 healthy controls from Tunisia using real-time PCR. Results: Significant associations were found for SH2B3 T allele (OR = 1.861; p = 0.015, pc = 0.366) and PTPN22 A allele (OR = 7.070; p = 0.026; pc = 1.00) and AIH with opposite homozygous being protective against the disease (CC genotype with OR = 0.420, p = 0.025; GG genotype with OR = 0.136, p = 0.025, respectively). No statistically significant associations were found for the TGF beta 1 and STAT4 polymorphisms with AIH susceptibility. Conclusion: Our work enlarges information on non-HLA genes that are associated with AIH by focusing in a region of the world that was poorly molecularly characterized for this disease.
引用
收藏
页码:279 / 284
页数:6
相关论文
共 32 条
[31]   The clinical phenotypes of autoimmune hepatitis: A comprehensive review [J].
Wang, Qixia ;
Yang, Fan ;
Miao, Qi ;
Krawitt, Edward L. ;
Gershwin, M. Eric ;
Ma, Xiong .
JOURNAL OF AUTOIMMUNITY, 2016, 66 :98-107
[32]   Systematic identification of trans eQTLs as putative drivers of known disease associations [J].
Westra, Harm-Jan ;
Peters, Marjolein J. ;
Esko, Tonu ;
Yaghootkar, Hanieh ;
Schurmann, Claudia ;
Kettunen, Johannes ;
Christiansen, Mark W. ;
Fairfax, Benjamin P. ;
Schramm, Katharina ;
Powell, Joseph E. ;
Zhernakova, Alexandra ;
Zhernakova, Daria V. ;
Veldink, Jan H. ;
Van den Berg, Leonard H. ;
Karjalainen, Juha ;
Withoff, Sebo ;
Uitterlinden, Andre G. ;
Hofman, Albert ;
Rivadeneira, Fernando ;
't Hoen, Peter A. C. ;
Reinmaa, Eva ;
Fischer, Krista ;
Nelis, Mari ;
Milani, Lili ;
Melzer, David ;
Ferrucci, Luigi ;
Singleton, Andrew B. ;
Hernandez, Dena G. ;
Nalls, Michael A. ;
Homuth, Georg ;
Nauck, Matthias ;
Radke, Doerte ;
Voelker, Uwe ;
Perola, Markus ;
Salomaa, Veikko ;
Brody, Jennifer ;
Suchy-Dicey, Astrid ;
Gharib, Sina A. ;
Enquobahrie, Daniel A. ;
Lumley, Thomas ;
Montgomery, Grant W. ;
Makino, Seiko ;
Prokisch, Holger ;
Herder, Christian ;
Roden, Michael ;
Grallert, Harald ;
Meitinger, Thomas ;
Strauch, Konstantin ;
Li, Yang ;
Jansen, Ritsert C. .
NATURE GENETICS, 2013, 45 (10) :1238-U195