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白细胞介素-1β基因多态性及其与神经调节蛋白-1基因多态性的相互作用与精神分裂症有关。

Interleukin-1 beta gene polymorphism and its interactions with neuregulin-1 gene polymorphism are associated with schizophrenia.

作者信息

Hänninen Kari, Katila Heikki, Saarela Marika, Rontu Riikka, Mattila Kari M, Fan Meng, Hurme Mikko, Lehtimäki Terho

机构信息

Dept. of Psychiatry, South Karelia Central Hospital, Valto Käkelän katu 14 C/6, Lappeenranta 53130, Finland.

出版信息

Eur Arch Psychiatry Clin Neurosci. 2008 Feb;258(1):10-5. doi: 10.1007/s00406-007-0756-9. Epub 2007 Sep 27.

Abstract

Interleukin-1beta (IL-1beta) and neuregulin-1 (NRG-1) have an important role in development of the central nervous system. Several recent studies suggest that their genetic polymorphisms are associated with schizophrenia. We studied the effects of the IL-1beta gene (IL-1B) -511 and NRG-1 SNP8NRG221533 polymorphisms and their interactions on the risk and age of onset of schizophrenia in 113 Finnish schizophrenic patients and 393 healthy controls. The allele and genotype frequencies of IL-1B and NRG-1 did not differ between schizophrenic patients and healthy controls, but the risk of schizophrenia was more than 10 times higher (odds ratio 10.20, 95% CI 2.53-41.09, p = 0.001) among subjects with the IL-1B 2.2, NRG-1 CC genotypes compared to subjects with the IL-1B 2.2, NRG-1 T-allele carriage. There was also a trend for an association between the interaction between IL-1B and NRG-1 polymorphisms and the age at onset of schizophrenia (chi(2) = 2.80; df = 1; p = 0.09, log rank test). IL-1B-511 allele 1 homozygotes had a significantly higher age of onset than allele 2 carriers (mean age of onset 25.9 +/- 7.7 and 22.7 +/- 5.4 years, t-test: t = 2.46; p = 0.032). Our results suggest that there is an interaction between the IL-1B and NRG-1 genes in schizophrenia. In addition, the IL-1B-511 polymorphism seems to be associated with the age at onset of schizophrenia.

摘要

白细胞介素-1β(IL-1β)和神经调节蛋白-1(NRG-1)在中枢神经系统发育中起重要作用。最近的几项研究表明,它们的基因多态性与精神分裂症有关。我们研究了IL-1β基因(IL-1B)-511和NRG-1 SNP8NRG221533多态性及其相互作用对113例芬兰精神分裂症患者和393例健康对照者精神分裂症发病风险和发病年龄的影响。精神分裂症患者与健康对照者之间IL-1B和NRG-1的等位基因和基因型频率没有差异,但与携带IL-1B 2.2、NRG-1 T等位基因的受试者相比,携带IL-1B 2.2、NRG-1 CC基因型的受试者患精神分裂症的风险高出10倍以上(优势比10.20,95%可信区间2.53-41.09,p = 0.001)。IL-1B和NRG-1多态性之间的相互作用与精神分裂症发病年龄之间也存在关联趋势(χ² = 2.80;自由度 = 1;p = 0.09,对数秩检验)。IL-1B -511等位基因1纯合子的发病年龄显著高于等位基因2携带者(平均发病年龄分别为25.9±7.7岁和22.7±5.4岁,t检验:t = 2.46;p = 0.032)。我们的结果表明,IL-1B和NRG-1基因在精神分裂症中存在相互作用。此外,IL-1B -511多态性似乎与精神分裂症的发病年龄有关。

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