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UCP4(SLC25A27)单倍型与超高抵抗性精神分裂症的关联。

Association of an UCP4 (SLC25A27) haplotype with ultra-resistant schizophrenia.

机构信息

INSERM, Laboratoire de Physiopathologie des Maladies Psychiatriques, U894 Centre de Psychiatrie et Neurosciences, Paris, France.

出版信息

Pharmacogenomics. 2011 Feb;12(2):185-93. doi: 10.2217/pgs.10.179.

Abstract

AIMS

Neuronal uncoupling proteins are involved in the regulation of reactive oxygen species production and intracellular calcium homeostasis, and thus, play a neuroprotective role. In order to explore the potential consequences of neuronal uncoupling proteins variants we examined their association in a sample of Caucasian patients suffering from schizophrenia and phenotyped them according to antipsychotic response.

MATERIALS & METHODS: Using a case-control design, we compared the frequencies of 15 genetic variants spanning UCP2, UCP4 and UCP5 in 106 French Caucasian patients suffering from schizophrenia and 127 healthy controls. In addition, patients with schizophrenia who responded to antipsychotic treatment were compared with patients with ultra-resistant schizophrenia (URS). This latter population presented no clinical, social and/or occupational remission despite at least two periods of treatment with conventional or atypical antipsychotic drugs and also with clozapine.

RESULTS

There were no differences in the distribution of the respective alleles between URS and responding patients. However, one haplotype spanning UCP4 was found to be significantly under-represented in URS patients. This relationship remained significant after multiple testing corrections.

CONCLUSION

Although our sample is of limited size and not representative of schizophrenia as a whole, the association found between the URS group and the UCP4 haplotype is noteworthy as it may influence treatment outcome in schizophrenia.

摘要

目的

神经元解偶联蛋白参与活性氧产生和细胞内钙稳态的调节,从而发挥神经保护作用。为了探讨神经元解偶联蛋白变异体的潜在后果,我们在一组患有精神分裂症的白种人患者中研究了它们的关联,并根据抗精神病药物反应对它们进行了表型分析。

材料和方法

采用病例对照设计,我们比较了 106 名法国白种人精神分裂症患者和 127 名健康对照者中跨越 UCP2、UCP4 和 UCP5 的 15 个遗传变异的频率。此外,还比较了对抗精神病药物治疗有反应的精神分裂症患者与超抗精神分裂症(URS)患者。尽管接受了至少两个疗程的常规或非典型抗精神病药物治疗,以及氯氮平治疗,该人群仍未出现临床、社会和/或职业缓解。

结果

在 URS 和有反应的患者之间,各自等位基因的分布没有差异。然而,跨越 UCP4 的一个单倍型在 URS 患者中明显缺失。在经过多次测试校正后,这种关系仍然显著。

结论

尽管我们的样本规模有限,不能代表整个精神分裂症,但 URS 组与 UCP4 单倍型之间的关联值得注意,因为它可能会影响精神分裂症的治疗结果。

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