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Association between the IL10 rs1800896 Polymorphism and Tardive Dyskinesia in Schizophreniaopen accessAssociation between the <i>IL10</i> rs1800896 Polymorphism and Tardive Dyskinesia in Schizophrenia

Other Titles
Association between the <i>IL10</i> rs1800896 Polymorphism and Tardive Dyskinesia in Schizophrenia
Authors
Choi, Kwang-YeonChoo, Jeong MinLee, Youn-JungLee, YujinCho, Chul-HyunKim, Seung-HyunLee, Heon-Jeong
Issue Date
Oct-2020
Publisher
대한신경정신의학회
Keywords
Tardive dyskinesia; Oxidative stress; Interleukin-10
Citation
Psychiatry Investigation, v.17, no.10, pp 1031 - 1036
Pages
6
Indexed
SCIE
SSCI
SCOPUS
KCI
Journal Title
Psychiatry Investigation
Volume
17
Number
10
Start Page
1031
End Page
1036
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/72119
DOI
10.30773/pi.2020.0191
ISSN
1738-3684
1976-3026
Abstract
Objective Interieuldn-10 (IL-10) is a major immunoregutatorycytokine and its gene plays a fundamental role in anti inflammatory and immunosuppressive activity. This study aimed to examine the association between the IL10 gene promoter -1082G/A polymorphism (rs1800896) and tardive dyskinesia (TD) in schizophrenia. Methods Two hundred and eighty unrelated Korean schizophrenic patients participated in this study (105 TD and 175 non-TD patients). TD was diagnosed using the Research Diagnostic Criteria kw TD and Abnormal Involuntary Movement Scale (AIMS). Genotyping was per-limited by RT-PCR and high-resolution melting curve analysis. Results The distributions of genotypic frequencies did not differ between patients with and without TD (chi(2) =4.33, p=0.115). However, allelic frequencies of the two groups were different (chi(2) =4.45, p=0.035); the A allele frequency was higher in TD. The total AIMS scores of the three genotypes were not different (F=133, p=0.266). However, the total AIMS scores of the A allele carrier and the A allele non-carrier were significantly different (t=5.79, p<0.001). Logistic regression analaysis showed that IL10 -1082G/A genotype significantly predicts presence of TD (p=0.045) after adjusting for covariates such as age and treatment duration. Conclusion This finding suggests that the A allele of rs1800896 may be associated with TD development following a low IL-10 function.
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