Inserm-EPHE-Université de Caen/Basse-Normandie, Unité U923, GIP Cyceron, CHU Côte de Nacre, Caen, France.
PLoS One. 2009 Nov 13;4(11):e7748. doi: 10.1371/journal.pone.0007748.
Gray matter volume studies have been limited to few brain regions of interest, and white matter and glucose metabolism have received limited research attention in Korsakoff's syndrome (KS). Because of the lack of brain biomarkers, KS was found to be underdiagnosed in postmortem studies.
METHODOLOGY/PRINCIPAL FINDINGS: Nine consecutively selected patients with KS and 22 matched controls underwent both structural magnetic resonance imaging and (18)F-fluorodeoxyglucose positron emission tomography examinations. Using a whole-brain analysis, the between-group comparisons of gray matter and white matter density and relative glucose uptake between patients with KS and controls showed the involvement of both the frontocerebellar and the Papez circuits, including morphological abnormalities in their nodes and connection tracts and probably resulting hypometabolism. The direct comparison of the regional distribution and degree of gray matter hypodensity and hypometabolism within the KS group indicated very consistent gray matter distribution of both abnormalities, with a single area of significant difference in the middle cingulate cortex showing greater hypometabolism than hypodensity. Finally, the analysis of the variability in the individual patterns of brain abnormalities within our sample of KS patients revealed that the middle cingulate cortex was the only brain region showing significant GM hypodensity and hypometabolism in each of our 9 KS patients.
CONCLUSIONS/SIGNIFICANCE: These results indicate widespread brain abnormalities in KS including both gray and white matter damage mainly involving two brain networks, namely, the fronto-cerebellar circuit and the Papez circuit. Furthermore, our findings suggest that the middle cingulate cortex may play a key role in the pathophysiology of KS and could be considered as a potential in vivo brain biomarker.
灰质体积研究仅限于少数感兴趣的脑区,而克氏综合征 (KS) 的白质和葡萄糖代谢受到的研究关注有限。由于缺乏脑生物标志物,KS 在尸检研究中被发现诊断不足。
方法/主要发现:连续选择了 9 名 KS 患者和 22 名匹配的对照者进行结构磁共振成像和(18)F-氟脱氧葡萄糖正电子发射断层扫描检查。通过全脑分析,KS 患者与对照组之间的灰质和白质密度以及相对葡萄糖摄取的组间比较显示,前脑-小脑和帕佩兹环路均受累,包括其节点和连接束的形态异常,可能导致代谢低下。KS 组内区域性分布和灰质密度低下及代谢低下的直接比较表明,两种异常的灰质分布非常一致,在中扣带回皮层有一个显著差异的区域显示出代谢低下程度大于密度低下。最后,对我们的 KS 患者样本中个体脑异常模式的变异性进行分析,结果显示中扣带回皮层是我们 9 名 KS 患者中唯一显示出灰质明显密度低下和代谢低下的脑区。
结论/意义:这些结果表明 KS 存在广泛的脑异常,包括灰质和白质损伤,主要涉及两个脑网络,即额-小脑回路和帕佩兹回路。此外,我们的发现表明,中扣带回皮层可能在 KS 的病理生理学中起关键作用,并可被视为潜在的活体脑生物标志物。