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Association study of dopamine receptor genes polymorphism with cognitive functions in bipolar I disorder patients

机译:多巴胺受体基因多态性与I型双相情感障碍患者认知功能的相关性研究

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Objective: To determine the correlation among the polymorphisms of dopamine receptor genes, cognitive function of Bipolar disorder (BD) patients, and BD. Methods: Twenty-three Single Nucleotide Polymorphisms (SNPs) of dopamine receptor genes were genotyped using Illumina GoldenGate genotyping assay in 375 patients with bipolar I disorder (BD-I) (patients group) and 475 healthy controls (control group). Cognitive function tests were performed in 158 patients who were clinically stable and 307 healthy controls who were matched with the patients in age, sex, and education.Results: The allele frequencies of rs3758653 in the promoter region of the DRD4 gene were significantly different between patients group and control group (^=9.386, Corrected P=0.046). This significant difference was also observed between BD-I patients with psychotic symptoms and healthy controls (^=9.27, Corrected P=0.049). Patients with BD-I performed significantly worse than healthy controls in all cognitive domains (p < 0.01) except TMTA errors and illegal time. Significant interactions between polymorphisms of rs5326 in DRD1 gene and phenotype (affected or unaffected with BD-I) were found in non-perseverative errors (/?=3.20 and Corrected P= 0.0034) on the Wisconsin Card Sorting Test (WCST). The allele of this SNP denoted the positive effect on the WCST non-perseverative errors in BD-I patients group (/?=2.80 and Corrected P=0.017). The genotypic association analyses also supported the findings (F=4.24 and P=0.007), but this effect was not found in controls. Limitations: The sample size was relatively small and the SNP coverage was limited, making it very important to be cautious when drawing a conclusion. Conclusions: DRD4 gene may play an important role in psychotic symptomatology rather than in unique diagnosis, BD, for example. A genetic association exists between DRD1 gene and impaired cognition in BD.
机译:目的:确定多巴胺受体基因多态性与躁郁症(BD)患者的认知功能和BD之间的相关性。方法:采用Illumina GoldenGate基因分型法,对375例双相I障碍患者(BD-I)(患者组)和475例健康对照组(对照组)进行多巴胺受体基因的二十三个单核苷酸多态性(SNP)基因分型。在158名临床稳定的患者和307名健康对照者中进行了认知功能测试,这些患者的年龄,性别和教育程度均与该患者相匹配。结果:DRD4基因启动子区域rs3758653的等位基因频率在患者之间存在显着差异组和对照组(^ = 9.386,校正的P = 0.046)。在患有精神病性症状的BD-1患者和健康对照者之间也观察到了这一显着差异(^ = 9.27,校正后的P = 0.049)。在TMTA错误和非法时间以外的所有认知领域,BD-I患者的表现均显着低于健康对照(p <0.01)。在威斯康星卡片分类测试(WCST)的非持久性错误(/?=3.20和校正后的P = 0.0034)中,发现DRD1基因rs5326多态性与表型(受影响或未受BD-I影响)之间存在显着的相互作用。该SNP的等位基因表明对BD-1患者组的WCST非持久性错误有积极作用(/?=2.80,校正后的P = 0.017)。基因型关联分析也支持这一发现(F = 4.24和P = 0.007),但在对照中未发现这种作用。局限性:样本量相对较小,SNP覆盖范围有限,因此得出结论时务必谨慎。结论:DRD4基因可能在精神病症状学中起重要作用,而不是在BD的独特诊断中起重要作用。 DRD1基因与BD认知障碍之间存在遗传关联。

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