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Personality in Relation to Genetic Liability for Schizophrenia and Bipolar Disorder: Differential Associations with the COMT Val108/158Met Polymorphism

机译:人格与精神分裂症和双相情感障碍的遗传责任有关:与COMT Val108 / 158Met多态性的差异关联。

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摘要

Schizophrenia and bipolar disorder may share aspects of genetic etiology. Evidence supports the Val108/158Met polymorphism of the Catechol-o-Methyltransferase (COMT) gene as potentially contributing to the etiology of both disorders. To determine whether the COMT gene is associated with personality traits related to genetic risk for either schizophrenia or bipolar disorder, we examined dimensions of personality psychopathology in biological relatives of individuals with the disorders. Specifically, we contrasted personality characteristics of first-degree relatives of people with schizophrenia, first-degree relatives of people with bipolar-I disorder, and nonpsychiatric control participants using scores from the Dimensional Assessment of Personality Pathology – Brief Questionnaire (DAPP-BQ). We also characterized the COMT Val108/158Met polymorphism of subjects. Compared to controls, relatives of schizophrenia patients scored lower on stimulus seeking and higher on restrictive expression and social avoidance. Compared to relatives of bipolar patients, relatives of schizophrenia patients had lower scores on narcissism, rejectionality (i.e., rejection of ideas of others), stimulus seeking, passive-aggressive oppositionality, and self-harm. The subset of relatives of schizophrenia patients who were COMT val homozygotes exhibited lower scores on narcissism, rejectionality, and stimulus seeking than met homozygote relatives of schizophrenia patients and control participants. Although relatives of bipolar patients showed scale elevations consistent with emotional dysregulation, the scores failed to be associated with the Val108/158Met polymorphism. Abnormally low narcissism and rejectionality in val homozygote relatives of schizophrenia patients suggests that the val allele of the COMT polymorphism may be associated with an underdeveloped self-concept phenomenologically similar to made volition and passivity experiences comprising first-rank symptoms of schizophrenia.
机译:精神分裂症和躁郁症可能在遗传病因学方面有共同之处。证据支持儿茶酚-邻-甲基转移酶(COMT)基因的Val 108/158 Met多态性可能是两种疾病的病因。为了确定COMT基因是否与精神分裂症或双相情感障碍的遗传风险相关的人格特质相关,我们检查了患有该疾病的个体的生物学亲属中人格心理病理学的维度。具体来说,我们使用“人格病理学维度评估-简短问卷”(DAPP-BQ)中的得分,对比了精神分裂症患者一级亲属,双相I型障碍患者一级亲属和非精神病学控制参与者的人格特征。我们还表征了受试者的COMT Val 108/158 Met多态性。与对照组相比,精神分裂症患者的亲属在寻求刺激方面得分较低,在限制性表达和社交回避方面得分较高。与双相情感障碍患者的亲属相比,精神分裂症患者的亲属在自恋,拒绝(即拒绝他人的想法),寻求刺激,被动攻击性对立和自残方面得分较低。 COMT val纯合子的精神分裂症患者的亲属在自恋,排斥和刺激寻求方面的得分低于精神分裂症患者和对照参与者的纯合子亲戚。尽管双相情感障碍患者的亲属表现出与情绪失调相一致的量表升高,但得分与Val 108/158 Met多态性没有关联。精神分裂症患者的val纯合子亲属的异常自恋和排斥反应异常低,表明COMT多态性的val等位基因可能与不成熟的自我概念有关,该现象在精神上类似于精神分裂症的首发症状。

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