Whyte Marie-Claire, Whalley Heather C, Simonotto Enrico, Flett Susanna, Shillcock Richard, Marshall Ian, Goddard Nigel H, Johnstone Eve C, Lawrie Stephen M
Division of Psychiatry, University of Edinburgh, UK.
Psychol Med. 2006 Oct;36(10):1427-39. doi: 10.1017/S0033291706008178.
Verbal declarative memory is a core deficit in schizophrenia patients, seen to a lesser extent in unaffected biological relatives. Neuroimaging studies suggest volumetric differences and aberrant function in prefrontal and temporal regions in schizophrenia patients compared to controls. These deficits are also reflected in the small number of similar investigations in unaffected biological relatives. However, it is unclear the extent to which dysfunction is genetically mediated or a feature of the established illness.
Event-related blood-oxygen-level-dependent (BOLD) functional magnetic resonance imaging (fMRI) was used to measure brain activation in 68 biological relatives of schizophrenia patients (of whom 27 experienced transient or isolated psychotic symptoms) and 21 controls during verbal classification and recognition.
During word classification, the high-risk group showed a greater response relative to controls in the right inferior frontal gyrus. During correct recognition (relative to correct rejection), the high-risk group showed significantly greater response relative to controls in the right cerebellum. When the high-risk group was split into those with (HR+) and without (HR-) psychotic symptoms, the increased response in the right inferior frontal gyrus was only seen when the HR+ were compared to controls. The greater cerebellar response was seen when both HR groups were compared to controls.
Activation increases in the right inferior frontal gyrus and cerebellum in high-risk subjects compared to controls during a relatively low-load memory task are likely to represent compensation for genetically mediated abnormalities. This is consistent with a leftward shift of the inverted 'U' load-response model of cognitive function in schizophrenia.
言语陈述性记忆是精神分裂症患者的核心缺陷,在未患病的生物学亲属中也有较轻程度的表现。神经影像学研究表明,与对照组相比,精神分裂症患者前额叶和颞叶区域存在体积差异和功能异常。这些缺陷在对未患病生物学亲属进行的少量类似研究中也有体现。然而,尚不清楚功能障碍在多大程度上是由基因介导的,还是既定疾病的特征。
采用事件相关血氧水平依赖(BOLD)功能磁共振成像(fMRI)来测量68名精神分裂症患者的生物学亲属(其中27人经历过短暂或孤立的精神病性症状)和21名对照组在言语分类和识别过程中的大脑激活情况。
在单词分类过程中,高危组相对于对照组在右侧额下回表现出更大的反应。在正确识别(相对于正确拒绝)过程中,高危组相对于对照组在右侧小脑表现出明显更大的反应。当将高危组分为有(HR+)和无(HR-)精神病性症状的两组时,只有将HR+组与对照组比较时,才会在右侧额下回看到反应增加。当将两个HR组与对照组比较时,均会在小脑看到更大的反应。
在相对低负荷记忆任务中,与对照组相比,高危受试者右侧额下回和小脑的激活增加可能代表对基因介导异常的代偿。这与精神分裂症认知功能倒“U”形负荷-反应模型的左移一致。