Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.
Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Mov Disord. 2019 Mar;34(3):344-352. doi: 10.1002/mds.27603. Epub 2019 Jan 7.
Posterior cortical atrophy and dementia with Lewy bodies are 2 distinct clinical syndromes, yet they can overlap in symptoms and occipital hypometabolism. Patients with dementia with Lewy bodies often have overlapping Alzheimer's disease pathology. Similarly, Lewy bodies can be found in patients with posterior cortical atrophy. We investigated differences in the distribution and magnitude of F18-AV-1451 uptake in patients with these 2 syndromes.
Consecutive patients with probable dementia with Lewy bodies (n = 33), posterior cortical atrophy (n = 18), and cognitively unimpaired controls (n = 100) underwent F-AV-1451 positron emission tomography. Regional differences in AV-1451 uptake were assessed using voxel-wise and an atlas-based approach. The greatest differences in AV-1451 uptake between patient groups were identified using area under receiver operating curve statistics, and a composite region was derived.
AV-1451 uptake in both patient groups was predominantly localized to the lateral occipital regions, but the magnitude of uptake was markedly greater in posterior cortical atrophy compared with dementia with Lewy bodies. The posterior cortical atrophy group showed the greatest AV-1451 uptake throughout all the gray matter compared with that in other groups. The occipital composite region, consisting of superior, middle, and inferior occipital cortices, distinguished posterior cortical atrophy from dementia with Lewy bodies (area under the curve >0.97; P < 0.001, Bonferroni-corrected) with excellent sensitivity (88%) and specificity (100%).
Posterior cortical atrophy and dementia with Lewy bodies can share clinical features, and although the pattern of AV-1451 uptake in occipital cortices overlaps between these 2 syndromes, its magnitude is significantly higher in posterior cortical atrophy. © 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
后部皮质萎缩和路易体痴呆是 2 种不同的临床综合征,但它们在症状和枕叶代谢低下方面可能重叠。路易体痴呆患者常有重叠的阿尔茨海默病病理学。同样,路易体也可以在后部皮质萎缩患者中发现。我们研究了这 2 种综合征患者 F18-AV-1451 摄取的分布和程度的差异。
连续纳入可能患有路易体痴呆的患者(n=33)、后部皮质萎缩(n=18)和认知正常对照(n=100)进行 F-AV-1451 正电子发射断层扫描。使用体素和基于图谱的方法评估 AV-1451 摄取的区域差异。使用接收者操作特征曲线下面积的统计学方法确定患者组之间 AV-1451 摄取的最大差异,并得出一个复合区域。
两组患者的 AV-1451 摄取主要局限于外侧枕叶区域,但后部皮质萎缩患者的摄取量明显大于路易体痴呆患者。与其他组相比,后部皮质萎缩组在整个灰质中显示出最大的 AV-1451 摄取。由上、中、下枕叶皮质组成的枕部复合区将后部皮质萎缩与路易体痴呆区分开来(曲线下面积>0.97;P<0.001,Bonferroni 校正),具有良好的敏感性(88%)和特异性(100%)。
后部皮质萎缩和路易体痴呆可能具有共同的临床特征,尽管枕叶皮质中 AV-1451 摄取的模式在这两种综合征之间重叠,但后部皮质萎缩的程度要高得多。©2019 作者。运动障碍由 Wiley 期刊出版公司代表国际帕金森和运动障碍协会出版。