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已有大量证据表明,白细胞介素-1 基因复合体座与白种人群精神分裂症易感性呈正相关。

Convergent evidence shows a positive association of interleukin-1 gene complex locus with susceptibility to schizophrenia in the Caucasian population.

机构信息

School of Public Health, Harvard University, Boston, MA 02115, USA.

出版信息

Schizophr Res. 2010 Jul;120(1-3):131-42. doi: 10.1016/j.schres.2010.02.1031. Epub 2010 Mar 26.

Abstract

Recent genetic studies have revealed that the Interleukin-1 (IL1) gene complex (IL1 alpha, IL1 beta and IL1 receptor antagonist) is associated with schizophrenia, but contradictory findings have also been reported. We investigated the association of the IL1 gene complex locus and schizophrenia using meta-analytic techniques, covering all published data up to January 2010, to restrict to the most commonly reported 4 single nucleotide polymorphisms (SNP). We also explored potential sources of heterogeneity and to investigate whether ancestry and study design moderated any association. The combined allele-wise odds ratio (OR) for schizophrenia of the rs16944 (IL1B gene; T-511C) polymorphism was 0.86 (95% CI: 0.77to 0.96).When applying stratified analysis to this polymorphism, the pooled allele-wise OR was 0.88 (95% CI, 0.79 to 0.97) in 10 population-based studies and 0.85 (95% CI: 0.73 to 0.99) in Caucasian samples. In a stratified analysis of the rs1143634 (IL1B gene; T3953C) polymorphism, the pooled genotype-wise results in a dominant model were also statistically significant both in a population-based study subgroup with summary OR of 0.64 (95% CI: 0.41 to 0.99) and a Caucasian population subgroup with summary OR of 0.62 (95% CI: 0.40 to 0.97). Neither combined nor stratified analyses found any association of the rs1800587 (IL1A gene; T-889C) or rs1794068 (IL1RA Gene; IL1RN_86 bp; T/C) with schizophrenia susceptibility. Our study suggests the IL1B gene or the IL1 gene complex may play a moderate role in the etiology of schizophrenia in the Caucasian population.

摘要

最近的遗传研究表明,白细胞介素-1(IL1)基因复合物(IL1α、IL1β 和 IL1 受体拮抗剂)与精神分裂症有关,但也有报道称存在矛盾的结果。我们使用元分析技术研究了白细胞介素 1 基因复合物基因座与精神分裂症的关联,该技术涵盖了截至 2010 年 1 月发表的所有数据,以限制在最常报道的 4 个单核苷酸多态性(SNP)。我们还探讨了异质性的潜在来源,并研究了祖先和研究设计是否调节任何关联。rs16944(IL1B 基因;T-511C)多态性与精神分裂症的联合等位基因比值比(OR)为 0.86(95%CI:0.77 至 0.96)。当对该多态性进行分层分析时,在 10 项基于人群的研究中,该多态性的合并等位基因比值比为 0.88(95%CI,0.79 至 0.97),在白种人样本中为 0.85(95%CI:0.73 至 0.99)。在 rs1143634(IL1B 基因;T3953C)多态性的分层分析中,在基于人群的研究亚组中,优势模型的合并基因型结果也具有统计学意义,其汇总比值比为 0.64(95%CI:0.41 至 0.99),在白种人亚组中为 0.62(95%CI:0.40 至 0.97)。无论是合并分析还是分层分析,都没有发现 rs1800587(IL1A 基因;T-889C)或 rs1794068(IL1RA 基因;IL1RN_86 bp;T/C)与精神分裂症易感性相关。我们的研究表明,IL1B 基因或白细胞介素 1 基因复合物可能在白种人群体的精神分裂症发病机制中起中等作用。

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