Segobin Shailendra, Ritz Ludivine, Lannuzel Coralie, Boudehent Céline, Vabret François, Eustache Francis, Beaunieux Hélène, Pitel Anne-Lise
INSERM, Caen, France.
Université De Caen Basse-Normandie, Caen, France.
Hum Brain Mapp. 2015 Jul;36(7):2795-808. doi: 10.1002/hbm.22808. Epub 2015 Apr 14.
Alcohol dependence results in two different clinical forms: "uncomplicated" alcoholism (UA) and Korsakoff's syndrome (KS). Certain brain networks are especially affected in UA and KS: the frontocerebellar circuit (FCC) and the Papez circuit (PC). Our aims were (1) to describe the profile of white matter (WM) microstructure in FCC and PC in the two clinical forms, (2) to identify those UA patients at risk of developing KS using their WM microstructural integrity as a biomarker. Tract-based spatial statistics and nonparametric voxel-based permutation tests were used to compare diffusion tensor imaging (DTI) data in 7 KS, 20 UA, and 14 healthy controls. The two patient groups were also pooled together and compared to controls. k-means classifications were then performed on mean fractional anisotropy values of significant clusters across all subjects for two fiber tracts from the FCC (the middle cerebellar peduncle and superior cerebellar peduncle) and two tracts from the PC (fornix and cingulum). We found graded effects of WM microstructural abnormalities in the PC of UA and KS. UA patients classified at risk of developing KS using fiber tracts of the PC from DTI data also had the lowest scores of episodic memory. That finding suggests that WM microstructure could be used as a biomarker for early detection of UA patients at risk of developing KS.
“单纯性”酒精中毒(UA)和科萨科夫综合征(KS)。某些脑网络在UA和KS中受到特别影响:额小脑回路(FCC)和帕佩兹回路(PC)。我们的目的是:(1)描述这两种临床形式下FCC和PC中白质(WM)微观结构的特征,(2)以WM微观结构完整性作为生物标志物,识别有发展为KS风险的UA患者。基于体素的空间统计学和基于体素的非参数置换检验被用于比较7例KS患者、20例UA患者和14名健康对照者的扩散张量成像(DTI)数据。两个患者组也合并在一起与对照组进行比较。然后,对所有受试者中来自FCC的两条纤维束(小脑中脚和小脑上脚)以及来自PC的两条纤维束(穹窿和扣带)的显著簇的平均分数各向异性值进行k均值分类。我们发现UA和KS患者PC中WM微观结构异常存在分级效应。利用DTI数据中PC的纤维束将UA患者分类为有发展为KS风险的,其情景记忆得分也最低。这一发现表明,WM微观结构可作为早期检测有发展为KS风险的UA患者的生物标志物。