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首页> 外文期刊>European journal of human genetics: EJHG >Genetic variants in the BDNF gene and therapeutic response to risperidone in schizophrenia patients: a pharmacogenetic study.
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Genetic variants in the BDNF gene and therapeutic response to risperidone in schizophrenia patients: a pharmacogenetic study.

机译:BDNF基因的遗传变异和精神分裂症患者对利培酮的治疗反应:药物遗传学研究。

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摘要

Risperidone is a widely used atypical antipsychotic agent that produces considerable interindividual differences in patient response. We investigated the pharmacogenetic relationship between the brain-derived neurotrophic factor (BDNF) gene and response to risperidone in 127 Han Chinese schizophrenic patients. Three functional polymorphisms, (GT)(n) dinucleotide repeat polymorphism, C-270T, and the rs6265G/A single-nucleotide polymorphism (SNP), were genotyped and analyzed for association, with reduction of Brief Psychiatric Rating Scale (BPRS) scores following an 8-week period of risperidone monotherapy. For individual polymorphic analysis, we found that the frequency of the 230-bp allele of the (GT)(n) polymorphism was much higher in responders (47.95%) than in nonresponders (32.41%) and the difference was statistically significant even after Bonferroni's adjustment (for the 230-bp allele: adjusted P=0.039). For haplotype-based analyses of the three polymorphisms, no positive finding was observed in the global test, but in specific haplotype tests, two haplotypes were also significantly related to response to risperidone (for haplotype 230-bp/C-270/rs6265G: P=0.0009; for haplotype 234-bp/C-270/rs6265A: P=0.043), indicating that patients with the 230-bp allele of the (GT)(n) polymorphism or the 230-bp/C-270/rs6265G haplotype responded better to risperidone than those with other alleles or haplotypes, and that the positive effect of the individual haplotype 230-bp/C-270/rs6265G was mainly driven by the 230-bp allele. These findings demonstrate that the individual and combinatorial genetic variants in the BDNF gene might have a role in the therapeutic response to risperidone in the Han Chinese population.
机译:利培酮是一种广泛使用的非典型抗精神病药,可在患者反应中产生明显的个体差异。我们调查了127名汉族精神分裂症患者的脑源性神经营养因子(BDNF)基因与对利培酮的反应之间的药理关系。对三种功能性多态性(GT)(n)二核苷酸重复多态性C-270T和rs6265G / A单核苷酸多态性(SNP)进行基因分型并进行关联分析,并通过减少简短的精神病评定量表(BPRS)评分利培酮单药治疗为期8周。对于个体多态性分析,我们发现(GT)(n)多态性的230 bp等位基因的频率在应答者(47.95%)中比无应答者(32.41%)高得多,即使在Bonferroni's攻击后,差异也具有统计学意义。调整(对于230 bp等位基因:调整后的P = 0.039)。对于三种多态性的基于单倍型的分析,在整体测试中未观察到阳性发现,但在特定的单倍型测试中,两种单倍型也与对利培酮的反应显着相关(对于单倍型230-bp / C-270 / rs6265G:P = 0.0009;对于234-bp / C-270 / rs6265A单倍型:P = 0.043),表明具有(GT)(n)多态性的230-bp等位基因或230-bp / C-270 / rs6265G单倍型的患者对利培酮的反应优于具有其他等位基因或单倍型的患者,并且单个单倍型230 bp / C-270 / rs6265G的阳性作用主要由230 bp等位基因驱动。这些发现表明,BDNF基因中的个体和组合遗传变异可能在汉族人群中对利培酮的治疗反应中起作用。

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