Association between promoter variants of interleukin-18 and schizophrenia in a han Chinese population

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Abstract

An increasing amount of evidence suggests that interleukin-18 (IL-18) plays a pivotal role in the pathophysiology of schizophrenia. However, association between single nucleotide polymorphism of IL-18 and the risk of schizophrenia has not been clarified. This study examined whether two promoter polymorphisms-137 G/C (rs187238) and-607 C/A (rs1946518) of IL-18 were associated with schizophrenia and six clinical symptoms (disorder of perception, thought disorder, disturbance of emotion, disorder of behavior and volition, suicide action, and aggressive action) to provide data for screening high-risk Han Chinese individuals. Three hundred seventy-two schizophrenic patients and 353 healthy controls from a Han Chinese population were examined to assess their genotype and allele frequencies of the two promoter polymorphisms of IL-18. The genotype distributions in both patients and controls were within Hardy-Weinberg equilibrium. No significant differences were observed in the genotype or the allele frequencies of the two single-nucleotide polymorphisms between patients and controls. However, genotype frequencies of-607 C/A showed significant differences between patients and controls in the appearance of perception disorder (χ 2=6.153, p=0.046). A significant difference was detected in-137 G/C between patients and controls in the appearance of aggressive action (χ 2=3.909, p=0.048). In conclusion, IL-18 gene promoter polymorphisms may not contribute to the susceptibility of schizophrenia in a Han Chinese population, but two single-nucleotide polymorphisms,-137 G/C and-607 C/A, may play a role in the development of perception disorder and aggressive action, respectively. © 2011, Mary Ann Liebert, Inc.

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Liu, J., Liu, J., Zhou, Y., Li, S., Li, Y., Song, X., … Ying, B. (2011). Association between promoter variants of interleukin-18 and schizophrenia in a han Chinese population. DNA and Cell Biology, 30(11), 913–917. https://doi.org/10.1089/dna.2011.1221

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