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Catechol-o-methyl transferase (COMT) val(158)met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls

机译:儿童期精神分裂症,其非精神病兄弟姐妹和健康对照者的儿茶酚-邻甲基转移酶(COMT)val(158)met多态性和青春期皮质发育

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摘要

Non-psychotic individuals at increased risk for schizophrenia show alterations in fronto-striatal dopamine signaling and cortical gray matter maturation reminiscent of those seen in schizophrenia. It remains unclear however if variations in dopamine signaling influence rates of structural cortical maturation in typically developing individuals, and whether such influences are disrupted in patients with schizophrenia and their non-psychotic siblings. We sought to address these issues by relating a functional Val -> Met polymorphism within the gene encoding catechol-o-methyltransferase (COMT)-a key enzymatic regulator of cortical dopamine levels-to longitudinal structural neuroimaging measures of cortical gray matter thickness. We included a total of 792 magnetic resonance imaging brain scans, acquired between ages 9 and 22 years from patients with childhood-onset schizophrenia (COS), their non-psychotic full siblings, and matched healthy controls. Whereas greater Val allele dose (which confers enhanced dopamine catabolism and is proposed to aggravate cortical deficits in schizophrenia) accelerated adolescent cortical thinning in both schizophrenia probands and their siblings, it attenuated cortical thinning in healthy controls. This similarity between COS patients and their siblings was accompanied by differences between the two groups in the timing and spatial distribution of disrupted COMT influences on cortical maturation. Consequently, whereas greater Val "dose" conferred persistent dorsolateral prefrontal cortical deficits amongst affected probands by adulthood, cortical thickness differences associated with varying Val dose in non-psychotic siblings resolved over the age-range studied. These findings suggest that cortical abnormalities in pedigrees affected by schizophrenia may be contributed to by a disruption of dopaminergic infleunces on cortical maturation. (C) 2011 Published by Elsevier Inc.
机译:精神分裂症风险增加的非精神病患者表现出额纹状体多巴胺信号传导和皮质灰质成熟的改变,使人联想到精神分裂症。然而,目前尚不清楚多巴胺信号传导的变化是否会影响典型发育个体的结构皮质成熟率,以及这种影响是否会在精神分裂症患者及其非精神病性兄弟姐妹中被破坏。我们试图通过将编码儿茶酚-o-甲基转移酶(COMT)的基因(皮质多巴胺水平的关键酶调节剂)内的功能性Val-> Met多态性与皮质灰质厚度的纵向结构神经影像学测量联系起来来解决这些问题。我们纳入了792例磁共振成像脑扫描,这些扫描是在9岁至22岁之间从儿童期精神分裂症(COS),其非精神病性全兄弟姐妹以及相匹配的健康对照组中获得的。尽管较高的Val等位基因剂量(可增强多巴胺分解代谢,并建议加剧精神分裂症的皮质功能障碍)可加速精神分裂症先证者及其兄弟姐妹的青春期皮质变薄,但在健康对照者中可减弱其皮质变薄。 COS患者及其兄弟姐妹之间的这种相似性伴随着两组间在COMT对皮质成熟的影响受到影响的时间和空间分布上的差异。因此,尽管成年期较大的Val“剂量”使受影响的先证者持续存在背外侧前额叶皮质缺陷,但随着年龄的增长,非精神病性兄弟姐妹中与不同Val剂量相关的皮质厚度差异得以解决。这些发现表明,受精神分裂症影响的血统谱系中的皮质异常可能是由于皮质成熟过程中的多巴胺能不足引起的。 (C)2011由Elsevier Inc.出版

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