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家族性和非家族性精神分裂症先证者及其未患病亲属的正常脑不对称性。

Normal cerebral asymmetry in familial and non-familial schizophrenic probands and their unaffected relatives.

作者信息

Chapple Ben, Grech Anton, Sham Pak, Toulopoulou Timothea, Walshe Muriel, Schulze Katja, Morgan Kevin, Murray Robin M, McDonald Colm

机构信息

Division of Psychological Medicine, Institute of Psychiatry, de Crespigny Park, London SE5 8AF, UK.

出版信息

Schizophr Res. 2004 Mar 1;67(1):33-40. doi: 10.1016/s0920-9964(03)00095-1.

Abstract

Loss of normal fronto-occipital cerebral asymmetry has been reported in patients with schizophrenia and also in their well relatives from multiply affected families, suggesting a relationship with susceptibility genes. We sought to confirm this relationship in a family study of patients with schizophrenia and their unaffected relatives of presumed differing genetic risk. MRI scans were carried out on 25 probands from families multiply affected with the disorder, and 36 of their unaffected relatives, 34 probands from families with no other affected members, 42 of their unaffected relatives, and 76 controls. Volumetric measurements of prefrontal, premotor, sensorimotor and occipitoparietal regions were obtained from which a measure of fronto-occipital torque was derived. There were no significant differences in measurements of fronto-occipital torque between the subject groups. Both schizophrenic probands and their relatives displayed the normal pattern of cerebral asymmetry, with larger right than left frontal regions and a larger left than right occipitoparietal region. Our findings failed to confirm an association between loss of fronto-occipital torque and genetic liability for schizophrenia and also failed to replicate the previously reported association between loss/reversal of fronto-occipital asymmetry and schizophrenia.

摘要

据报道,精神分裂症患者及其来自多例患者家庭的健康亲属存在正常的额枕脑不对称性缺失,这表明其与易感基因有关。我们试图在一项针对精神分裂症患者及其假定遗传风险不同的未患病亲属的家庭研究中证实这种关系。对来自多例患者家庭的25名先证者及其36名未患病亲属、来自无其他患病成员家庭的34名先证者及其42名未患病亲属以及76名对照进行了MRI扫描。获得了前额叶、运动前区、感觉运动区和枕顶叶区域的体积测量数据,并由此得出额枕扭矩测量值。各受试者组之间的额枕扭矩测量值无显著差异。精神分裂症先证者及其亲属均表现出正常的脑不对称模式,右侧额叶区域大于左侧,左侧枕顶叶区域大于右侧。我们的研究结果未能证实额枕扭矩缺失与精神分裂症遗传易感性之间的关联,也未能重复先前报道的额枕不对称性缺失/反转与精神分裂症之间的关联。

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