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儿茶酚-O-甲基转移酶Val158Met基因型变异与分裂型人格障碍患者及对照组中前额叶依赖的任务表现相关。

Catechol-O-methyltransferase Val158Met genotype variation is associated with prefrontal-dependent task performance in schizotypal personality disorder patients and comparison groups.

作者信息

Minzenberg Michael J, Xu Ke, Mitropoulou Vivian, Harvey Philip D, Finch Thembi, Flory Janine D, New Antonia S, Goldman David, Siever Larry J

机构信息

Bronx Veterans Affairs Medical Center, Bronx, New York, 14068, USA.

出版信息

Psychiatr Genet. 2006 Jun;16(3):117-24. doi: 10.1097/01.ypg.0000199448.00163.e6.

Abstract

OBJECTIVE

A single-nucleotide polymorphism of the gene coding for catechol-O-methyltransferase (COMT Val(158)Met) is associated with prefrontal-dependent task performance in schizophrenia. We evaluated the relationship of the COMT genotype with diagnostic status and cognitive performance in schizotypal personality disorder.

METHODS

Unmedicated outpatients with schizotypal personality disorder (SPD; n = 67) and non-schizotypal personality disorder (NSPD; n = 154) by DSM-III-R, and normal control (NC; n = 60) participants were genotyped at the COMT Val(158)Met locus. Of these, 98 Caucasians (23 SPD, 52 NSPD and 23 NC) performed a brief neurocognitive battery: Wisconsin Card Sorting Test (WCST), Paced Auditory Serial Addition Test (PASAT), California Verbal Learning Test (CVLT), Visuospatial Working Memory (DOT) and Visual Delayed Recall (Wechsler Memory Scale Visual Reproduction, WMS-VR).

RESULTS

Allele distribution was not significantly different in the full sample (by chi(2)) for the SPD group compared with either the NC or combined NC/NSPD groups. In analyses of variance of Caucasian individuals, the SPD group performance met or approached significantly worse performance than NC, NSPD or both groups, on the PASAT, CVLT and WMS-VR. In regression analyses of cognitive performance, the COMT genotype was significantly associated with performance on WCST and PASAT, independent of diagnosis, with the Val/Val genotype associated with the worse performance.

CONCLUSIONS

(1) Allelic variation in COMT activity is unrelated to the diagnosis of SPD in this sample. (2) Individuals with SPD exhibit multiple deficits in prefrontal and temporal lobe-dependent tasks. (3) The COMT genotype is related to performance on prefrontal cortex-dependent tasks and may contribute to the deficit in prefrontal-dependent memory processes in SPD as it does in schizophrenia.

摘要

目的

儿茶酚-O-甲基转移酶(COMT Val(158)Met)编码基因的单核苷酸多态性与精神分裂症中前额叶依赖的任务表现相关。我们评估了COMT基因型与分裂型人格障碍的诊断状态及认知表现之间的关系。

方法

根据《精神疾病诊断与统计手册》第三版修订版(DSM-III-R)诊断为分裂型人格障碍(SPD;n = 67)和非分裂型人格障碍(NSPD;n = 154)的未用药门诊患者以及正常对照(NC;n = 60)参与者在COMT Val(158)Met位点进行基因分型。其中,98名高加索人(23名SPD、52名NSPD和23名NC)进行了一项简短的神经认知测试组合:威斯康星卡片分类测验(WCST)、听觉连续加法测验(PASAT)、加利福尼亚言语学习测验(CVLT)、视觉空间工作记忆(DOT)和视觉延迟回忆(韦氏记忆量表视觉再现,WMS-VR)。

结果

在整个样本中(通过卡方检验),SPD组的等位基因分布与NC组或NC/NSPD合并组相比无显著差异。在对高加索个体的方差分析中,SPD组在PASAT、CVLT和WMS-VR上的表现显著达到或接近比NC组、NSPD组或两组更差的水平。在认知表现的回归分析中,COMT基因型与WCST和PASAT的表现显著相关,与诊断无关,Val/Val基因型与较差的表现相关。

结论

(1)该样本中COMT活性的等位基因变异与SPD的诊断无关。(2)SPD个体在前额叶和颞叶依赖的任务中表现出多种缺陷。(3)COMT基因型与前额叶皮质依赖任务的表现相关,可能如在精神分裂症中一样,导致SPD前额叶依赖记忆过程的缺陷。

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