McKeith I G, Dickson D W, Lowe J, Emre M, O'Brien J T, Feldman H, Cummings J, Duda J E, Lippa C, Perry E K, Aarsland D, Arai H, Ballard C G, Boeve B, Burn D J, Costa D, Del Ser T, Dubois B, Galasko D, Gauthier S, Goetz C G, Gomez-Tortosa E, Halliday G, Hansen L A, Hardy J, Iwatsubo T, Kalaria R N, Kaufer D, Kenny R A, Korczyn A, Kosaka K, Lee V M Y, Lees A, Litvan I, Londos E, Lopez O L, Minoshima S, Mizuno Y, Molina J A, Mukaetova-Ladinska E B, Pasquier F, Perry R H, Schulz J B, Trojanowski J Q, Yamada M
Institute for Ageing and Health, University of Newcastle upon Tyne, UK.
Neurology. 2005 Dec 27;65(12):1863-72. doi: 10.1212/01.wnl.0000187889.17253.b1. Epub 2005 Oct 19.
The dementia with Lewy bodies (DLB) Consortium has revised criteria for the clinical and pathologic diagnosis of DLB incorporating new information about the core clinical features and suggesting improved methods to assess them. REM sleep behavior disorder, severe neuroleptic sensitivity, and reduced striatal dopamine transporter activity on functional neuroimaging are given greater diagnostic weighting as features suggestive of a DLB diagnosis. The 1-year rule distinguishing between DLB and Parkinson disease with dementia may be difficult to apply in clinical settings and in such cases the term most appropriate to each individual patient should be used. Generic terms such as Lewy body (LB) disease are often helpful. The authors propose a new scheme for the pathologic assessment of LBs and Lewy neurites (LN) using alpha-synuclein immunohistochemistry and semiquantitative grading of lesion density, with the pattern of regional involvement being more important than total LB count. The new criteria take into account both Lewy-related and Alzheimer disease (AD)-type pathology to allocate a probability that these are associated with the clinical DLB syndrome. Finally, the authors suggest patient management guidelines including the need for accurate diagnosis, a target symptom approach, and use of appropriate outcome measures. There is limited evidence about specific interventions but available data suggest only a partial response of motor symptoms to levodopa: severe sensitivity to typical and atypical antipsychotics in approximately 50%, and improvements in attention, visual hallucinations, and sleep disorders with cholinesterase inhibitors.
路易体痴呆(DLB)联盟修订了DLB的临床和病理诊断标准,纳入了有关核心临床特征的新信息,并提出了改进的评估方法。快速眼动睡眠行为障碍、严重的抗精神病药物敏感性以及功能性神经影像学检查显示纹状体多巴胺转运体活性降低,作为提示DLB诊断的特征,在诊断中具有更大的权重。区分DLB和帕金森病痴呆的1年规则在临床环境中可能难以应用,在这种情况下,应使用最适合每个患者的术语。诸如路易体(LB)病等通用术语通常很有帮助。作者提出了一种新的方案,用于使用α-突触核蛋白免疫组织化学和病变密度的半定量分级对LB和路易神经突(LN)进行病理评估,区域受累模式比LB总数更重要。新的标准考虑了路易体相关和阿尔茨海默病(AD)类型的病理,以确定这些病理与临床DLB综合征相关的可能性。最后,作者提出了患者管理指南,包括准确诊断的必要性、目标症状方法以及使用适当的结局指标。关于特定干预措施的证据有限,但现有数据表明运动症状对左旋多巴仅部分有反应:约50%的患者对典型和非典型抗精神病药物严重敏感,胆碱酯酶抑制剂可改善注意力、视幻觉和睡眠障碍。