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精神分裂症和双相情感障碍在基质金属蛋白酶3(MMP3)基因上是否存在共同的疾病易感性变异?

Do schizophrenia and bipolar disorders share a common disease susceptibility variant at the MMP3 gene?

作者信息

Kucukali Cem Ismail, Aydin Makbule, Ozkok Elif, Bilge Emine, Orhan Nurcan, Zengin Asli, Kara Ihsan

机构信息

Department of Neurology, Istanbul Erenkoy Psychiatric and Neurological Disorders Hospital, Istanbul, Turkey.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2009 Apr 30;33(3):557-61. doi: 10.1016/j.pnpbp.2009.02.012. Epub 2009 Feb 23.

Abstract

There is growing evidence of partial etiological overlap between schizophrenia (SZ) and bipolar I disorder (BD-I) from linkage analysis, genetic epidemiology and molecular genetics studies. SZ and BD-I are neurodevelopmental disorders with genetic and environmental etiologies. Recent studies have demonstrated that matrix metalloproteinase 3 (MMP3) is a key event in associative memory formation, learning and synaptic plasticity, which are important in psychiatric disorders. In the light of these findings, we analyzed the genetic variations in the MMP3-1171 5A/6A in patients with SZ, patients with BD-I and healthy controls. To the best of our knowledge, this is the first study to report an association of variation in gene encoding MMP3 with SZ. Our study group consisted of 111 unrelated patients with SZ, 141 unrelated patients with BD-I, and 121 unrelated healthy controls. The frequencies of 6A6A genotype and 6A allele distributions of MMP3 in patients with SZ were significantly decreased when compared with controls. In contrast, in patients with SZ, the distributions of 5A5A genotype and 5A allele of MMP3 gene were significantly increased as compared with healthy controls. When the frequencies of genotypes or alleles in schizophrenic patients and bipolar patients were compared, 6A6A genotype and 6A allele in patients with BD-I were significantly higher than patients with SZ. In contrast, 5A5A genotype and 5A allele distributions of MMP3 gene were significantly frequent in patients with SZ. On the other hand, no significant differences were found in the allele or genotype distribution in patients with BD-I compared with controls. In conclusion, our data have supported the hypothesis that there is a possible relationship between -1171 5A/6A polymorphism of MMP3 gene and SZ. A larger sample group is needed to confirm the potential role of this gene in the pathophysiology of psychiatric disorders.

摘要

来自连锁分析、遗传流行病学和分子遗传学研究的证据越来越多地表明,精神分裂症(SZ)和双相I型障碍(BD-I)之间存在部分病因重叠。SZ和BD-I是具有遗传和环境病因的神经发育障碍。最近的研究表明,基质金属蛋白酶3(MMP3)是联想记忆形成、学习和突触可塑性中的关键事件,而这些在精神疾病中很重要。鉴于这些发现,我们分析了SZ患者、BD-I患者和健康对照者中MMP3 - 1171 5A/6A的基因变异。据我们所知,这是第一项报道编码MMP3的基因变异与SZ相关的研究。我们的研究组由111名无亲缘关系的SZ患者、141名无亲缘关系的BD-I患者和121名无亲缘关系的健康对照者组成。与对照组相比,SZ患者中MMP3的6A6A基因型和6A等位基因分布频率显著降低。相反,与健康对照者相比,SZ患者中MMP3基因的5A5A基因型和5A等位基因分布显著增加。当比较精神分裂症患者和双相情感障碍患者的基因型或等位基因频率时, BD-I患者的6A6A基因型和6A等位基因显著高于SZ患者。相反,MMP3基因的5A5A基因型和5A等位基因分布在SZ患者中显著更常见。另一方面,与对照组相比,BD-I患者的等位基因或基因型分布没有发现显著差异。总之,我们的数据支持了MMP3基因的 - 1171 5A/6A多态性与SZ之间可能存在关系的假设。需要更大的样本组来证实该基因在精神疾病病理生理学中的潜在作用。

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