Association between the IL10 rs1800896 Polymorphism and Tardive Dyskinesia in Schizophrenia
- Authors
- Choi, Kwang-Yeon; Choo, Jeong Min; Lee, Youn-Jung; Lee, Yujin; Cho, Chul-Hyun; Kim, Seung-Hyun; Lee, Heon-Jeong
- Issue Date
- 10월-2020
- Publisher
- KOREAN NEUROPSYCHIATRIC ASSOC
- Keywords
- Tardive dyskinesia; Oxidative stress; Interleukin-10
- Citation
- PSYCHIATRY INVESTIGATION, v.17, no.10, pp.1031 - 1036
- Indexed
- SCIE
SSCI
SCOPUS
KCI
- Journal Title
- PSYCHIATRY INVESTIGATION
- Volume
- 17
- Number
- 10
- Start Page
- 1031
- End Page
- 1036
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/52621
- DOI
- 10.30773/pi.2020.0191
- ISSN
- 1738-3684
- 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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