首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Gender-specific association of a functional coding polymorphism in the Neuropeptide S receptor gene with panic disorder but not with schizophrenia or attention-deficit/hyperactivity disorder
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Gender-specific association of a functional coding polymorphism in the Neuropeptide S receptor gene with panic disorder but not with schizophrenia or attention-deficit/hyperactivity disorder

机译:神经肽S受体基因中功能编码多态性与恐慌症而非精神分裂症或注意力不足/多动症的性别特异性关联

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摘要

Panic disorder is a common anxiety disorder characterized by sudden and recurrent panic attacks. Previous studies have indicated significant genetic contributions and a susceptibility locus for panic disorder has been mapped to human chromosome 7p15. The receptor for Neuropeptide S (NPS) is located in the same genomic region while NPS is known to produce arousal and anxiolytic-like effects in rodents. Here we report that a coding polymorphism in the Neuropeptide S receptor (NPSR) is associated with panic disorder in male patients of Japanese ancestry. The polymorphism (Asn~(107)Ile) results in a gain-of-function of the receptor protein by increasing the agonist sensitivity about tenfold. The allele representing the less active isoform (NPSR Asn~(107)) was found under-represented in male panic disorder patients, indicating a potential protective function of the protein. Two unrelated groups of patients diagnosed with schizophrenia or attention-deficit/hyperactivity disorder (ADHD) showed no association of particular NPSR alleles with the disorders. These results provide evidence for a gender-specific effect of NPSR in the pathogenesis of panic disorder.
机译:恐慌症是一种常见的焦虑症,其特征是突发性和反复发作的惊恐发作。先前的研究已经表明了重要的遗传学贡献,并且已将恐慌症的易感基因座定位于人类7p15号染色体。 Neuropeptide S(NPS)的受体位于同一基因组区域,而已知NPS在啮齿动物中会产生唤醒和抗焦虑作用。在这里,我们报道在日本血统的男性患者中,神经肽S受体(NPSR)的编码多态性与恐慌症相关。多态性(Asn〜(107)Ile)通过使激动剂敏感性增加约十倍而导致受体蛋白的功能获得。发现在男性恐慌症患者中代表较低活性同工型(NPSR Asn〜(107))的等位基因代表性不足,表明该蛋白具有潜在的保护功能。两组不相关的被诊断为精神分裂症或注意力缺陷/多动障碍(ADHD)的患者没有显示特定的NPSR等位基因与疾病相关。这些结果提供了NPSR在恐慌症发病机理中的性别特异性作用的证据。

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