Polymorphisms in the Human Aquaporin 4 Gene Are Associated With Schizophrenia in the Southern Chinese Han Population: A Case-Control Study

被引:13
|
作者
Wu, Yung-Fu [1 ,2 ]
Sytwu, Huey-Kang [3 ]
Lung, For-Wey [2 ,4 ]
机构
[1] Natl Def Med Ctr, Triserv Gen Hosp, Beitou Branch, Dept Psychiat, Taipei, Taiwan
[2] Natl Def Med Ctr, Grad Inst Med Sci, Taipei, Taiwan
[3] Natl Def Med Ctr, Dept Microbiol & Immunol, Taipei, Taiwan
[4] Calo Psychiat Ctr, Dept Psychiat, Xinpi Township, Pingtung County, Taiwan
来源
FRONTIERS IN PSYCHIATRY | 2020年 / 11卷
关键词
schizophrenia (SCZ); single-nucleotide polymorphisms (SNPs); aquaporin 4 (AQP4); haplotype; astrocyte; ENVIRONMENTAL RISK; SYSTEM;
D O I
10.3389/fpsyt.2020.00596
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background In psychiatric illness, pathogenic role of neuroinflammation has been supported by multiple lines of evidence. Astrocytes contribute to the blood-brain barrier (BBB) with formation of the "glymphatic" drainage system of the central nervous system (CNS) through perivascular processes. Found primarily at the end-feet of astrocytes, the aquaporin 4 (AQP4) gene has been suspected to play putative roles in the development of psychiatric disorders as well as the clearance of the glymphatic system. However, there remain many uncertainties because of the limited research on AQP4. The present study is focused on the association between AQP4 gene polymorphisms and schizophrenia (SCZ) in the Southern Chinese Han population. Methods Two hundred ninety-two patients and 100 healthy controls were enrolled in this study. To study the relationship of AQP4 gene polymorphisms and SCZ, genetic information was drawn from a cohort of 100 healthy controls and 100 matched patients with SCZ of Southern Han Chinese descent. Comparisons of the allele and genotype distributions between control and case groups were made using the chi 2 test. Two-group comparisons were made to assess the linkage equilibrium and haplotype. Results Three SNPs were found. In comparison to healthy controls, patients had higher T-allele frequencies at rs1058424 and G-allele frequencies at rs3763043 (p = 0.043 and p = 0.045, respectively). Furthermore, there is an association between the decreased risk of SCZ and the AA genotype at both rs1058424 (p = 0.021, OR = 2.04) and rs3763043 (p = 0.018, OR = 2.25) The TCG haplotype (p = 0.036) was associated with a potential risk of SCZ, while the ACA haplotype (p = 0.0007) was associated with a decreased risk of SCZ and retained statistical significance after Bonferroni correction (p = 0.006). Conclusions An etiological reference for SCZ is provided by the association between AQP4 gene polymorphisms and SCZ in Southern Han Chinese population.
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页数:7
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