Analysis of rs1864182 and rs1864183 variants in ATG10 gene and antineutrophil cytoplasmic autoantibody-associated vasculitis in Chinese Guangxi population

被引:0
作者
Huang, Shanshan [1 ]
Rao, Jinlan [1 ]
Wei, Jingsi [1 ]
Huang, Qunshen [1 ]
Zhu, Yan [1 ,2 ]
Li, Wei [3 ]
Xue, Chao [3 ]
机构
[1] Guangxi Med Univ, Clin Med Coll 2, Nanning, Peoples R China
[2] Univ South China, Affiliated Hosp 1, Hengyang, Peoples R China
[3] Guangxi Med Univ, Affiliated Hosp 2, Dept Nephrol, Nanning 530000, Guangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
antineutrophil cytoplasmic antibody-associated vasculitis; autophagy-related protein 10; GMDR; interaction; polymorphism; AUTOPHAGY; PATHOGENESIS; DISEASE;
D O I
10.1002/jcla.24193
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives To investigate the association of autophagy-associated gene 10 (ATG10) gene polymorphisms (rs1864182 and rs1864183) with antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) in Chinese Guangxi population. Methods The single nucleotide polymorphisms (SNPs) of ATG10 rs1864182 and rs1864183 in 395 participants (195 AAVs and 200 healthy controls) were genotyped. Generalized multiple dimensionality reduction (GMDR) was used to analyze the SNP-SNP interactions among two SNPs of ATG10 gene and other SNPs of autophagy gene previously studied by our research team. Results In this study, we found that the two ATG10 SNPs were not associated with AAV risk in Chinese Guangxi population. However, there were statistically significant differences in the incidence of hemoptysis, hematuria, and proteinuria among the three genotypes of ATG10 rs1864182 and rs1864183 (p < 0.05). Moreover, permutation test of GMDR suggested that immunity-related GTPase M(IRGM) rs4958847, autophagy-associated gene 7 (ATG7) rs6442260, ATG7 rs2594966, ATG10 rs1864183, protein kinase B(AKT2) rs3730051, and AKT2 rs11552192 might interact with each other in the process of developing AAV (p < 0.05). Conclusions Our results indicated that there existed no association between ATG10 SNPs and AAV, and SNP-SNP interactions among IRGM rs4958847, ATG7 rs6442260, ATG7 rs2594966, ATG10 rs1864183, AKT2 rs3730051, and AKT2 rs11552192 may confer AAV risk in the Chinese Guangxi population.
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页数:7
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共 24 条
[1]   Genetic aspects of anti-neutrophil cytoplasmic antibody-associated vasculitis [J].
Alberici, Federico ;
Martorana, Davide ;
Vaglio, Augusto .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2015, 30 :i37-i45
[2]   Vasculitis update: pathogenesis and biomarkers [J].
Brogan, Paul ;
Eleftheriou, Despina .
PEDIATRIC NEPHROLOGY, 2018, 33 (02) :187-198
[3]   Interleukin-8: A pathogenetic role in antineutrophil cytoplasmic autoantibody-associated glomerulonephritis [J].
Cockwell, P ;
Brooks, CJ ;
Adu, D ;
Savage, COS .
KIDNEY INTERNATIONAL, 1999, 55 (03) :852-863
[4]   Association of ANCA associated vasculitis and rheumatoid arthritis: a lesser recognized overlap syndrome [J].
Draibe, Juliana ;
Salama, Alan D. .
SPRINGERPLUS, 2015, 4
[5]   Macrophage migration inhibitory factor contributes to anti-neutrophil cytoplasmic antibody-induced neutrophils activation [J].
Hao, Jian ;
Lv, Tie-Gang ;
Wang, Chen ;
Xu, Li-Ping ;
Zhao, Jian-Rong .
HUMAN IMMUNOLOGY, 2016, 77 (12) :1209-1214
[6]   Overview of the 2012 revised International Chapel Hill Consensus Conference nomenclature of vasculitides [J].
Jennette, J. Charles .
CLINICAL AND EXPERIMENTAL NEPHROLOGY, 2013, 17 (05) :603-606
[7]   Pathogenesis of Antineutrophil Cytoplasmic Autoantibody-Associated Small-Vessel Vasculitis [J].
Jennette, J. Charles ;
Falk, Ronald J. ;
Hu, Peiqi ;
Xiao, Hong .
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 8, 2013, 8 :139-160
[8]   Autophagy and Autoimmune Diseases [J].
Jin, Min ;
Zhang, Yanyun .
AUTOPHAGY: BIOLOGY AND DISEASES: CLINICAL SCIENCE, 2020, 1207 :405-408
[9]   The interplay between autophagy and ROS in tumorigenesis [J].
Kongara, Sameera ;
Karantza, Vassiliki .
FRONTIERS IN ONCOLOGY, 2012, 2
[10]   Immunoglobulins G from patients with ANCA-associated vasculitis are atypically glycosylated in both the Fc and Fab regions and the relation to disease activity [J].
Lardinois, Olivier M. ;
Deterding, Leesa J. ;
Hess, Jacob J. ;
Poulton, Caroline J. ;
Henderson, Candace D. ;
Jennette, J. Charles ;
Nachman, Patrick H. ;
Falk, Ronald J. .
PLOS ONE, 2019, 14 (02)