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. 2023 May 23;16(1):113.
doi: 10.1186/s12920-023-01546-3.

Association of ZC3HAV1 single nucleotide polymorphisms with the susceptibility of Vogt-Koyanagi-Harada Disease

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Association of ZC3HAV1 single nucleotide polymorphisms with the susceptibility of Vogt-Koyanagi-Harada Disease

Qiuying Wu et al. BMC Med Genomics. .

Abstract

Background: Polymorphisms of genes related to the immune response have been reported to confer susceptibility to Vogt-Koyanagi-Harada (VKH) disease. This study was carried out to determine whether zinc finger CCCH-type containing antiviral 1 (ZC3HAV1) and tripartite motif-containing protein 25 (TRIM25) genetic polymorphisms are associated with this disease.

Methods: A total of 766 VKH patients and 909 healthy individuals were enrolled in this two-stage case-control study. Thirty-one tag single nucleotide polymorphisms (SNPs) of ZC3HAV1 and TRIM25 were genotyped by MassARRAY System and iPLEX Gold Genotyping Assay. Allele and genotype frequencies were analyzed by the χ2 test or Fisher's exact test. Cochran-Mantel-Haenszel test was used to assess the pooled odds ratio (OR) in the combined study. A stratified analysis was performed in terms of the major clinical features of VKH disease.

Results: We found a statistically significant increased frequency of the minor A allele of ZC3HAV1 rs7779972 (P = 1.50 × 10- 4, pooled OR = 1.332, 95%CI = 1.149-1.545) in VKH disease as compared with controls by using the Cochran-Mantel-Haenszel test. The GG genotype of rs7779972 showed a protective association with VKH disease (P = 1.88 × 10- 3, OR = 0.733, 95%CI = 0.602-0.892). There was no difference regarding the frequency of the remaining SNPs between VKH cases and controls (all P > 2.08 × 10- 3). The stratified analysis showed no significant association of rs7779972 with the major clinical characteristics of VKH disease.

Conclusion: Our study indicated that the ZC3HAV1 variant rs7779972 might confer susceptibility to VKH disease in Han Chinese.

Keywords: Autoimmune; Genetic susceptibility; Single nucleotide polymorphisms; Vogt-Koyanagi-Harada disease; ZC3HAV1.

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Conflict of interest statement

The authors declare that they have no competing interests.

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References

    1. Du L, Kijlstra A, Yang P. Vogt-Koyanagi-Harada disease: novel insights into pathophysiology, diagnosis and treatment. PROG RETIN EYE RES. 2016;52:84–111. doi: 10.1016/j.preteyeres.2016.02.002. - DOI - PubMed
    1. Yang P, Ren Y, Li B, Fang W, Meng Q, Kijlstra A. Clinical characteristics of Vogt-Koyanagi-Harada syndrome in chinese patients. Ophthalmology. 2007;114(3):606–14. doi: 10.1016/j.ophtha.2006.07.040. - DOI - PubMed
    1. Yang P, Zhong Z, Du L, Li F, Chen Z, Zhu Y, et al. Prevalence and clinical features of systemic diseases in chinese patients with uveitis. Br J Ophthalmol. 2021;105(1):75–82. doi: 10.1136/bjophthalmol-2020-315960. - DOI - PubMed
    1. Hou S, Kijlstra A, Yang P. Molecular genetic advances in Uveitis. Prog Mol Biol Transl Sci. 2015;134:283–98. doi: 10.1016/bs.pmbts.2015.04.009. - DOI - PubMed
    1. Zhong Z, Su G, Kijlstra A, Yang P. Activation of the interleukin-23/interleukin-17 signalling pathway in autoinflammatory and autoimmune uveitis. PROG RETIN EYE RES. 2021;80:100866. doi: 10.1016/j.preteyeres.2020.100866. - DOI - PubMed

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