Minger S L, Esiri M M, McDonald B, Keene J, Carter J, Hope T, Francis P T
Dementia Research Laboratory, Centre for Neuroscience Research, GKT School of Biomedical Sciences, King's College London, UK.
Neurology. 2000 Nov 28;55(10):1460-7. doi: 10.1212/wnl.55.10.1460.
Noncognitive behavioral changes such as depression, aggressive behavior, psychosis, and overactivity occur frequently in patients with dementia, in addition to cognitive impairment, and often determine the need for institutionalization. The biochemical basis of such changes is poorly understood. Clinical trial data indicate that cholinomimetics improve noncognitive behaviors. This study investigated the relationship between markers of the cholinergic and dopaminergic neurotransmitter systems and noncognitive behavioral symptoms assessed during the course of dementing illness.
Brains from 46 patients with dementia (36 with AD and 10 with mixed or other dementias using Consortium to Establish a Registry for AD criteria) were examined together with 32 normal controls. The patients with dementia had been evaluated every 4 months, often over several years, for cognitive performance (Mini-Mental State Examination) and behavior (Present Behavioral Examination). Concentrations of dopamine (DA) and major metabolites, choline acetyltransferase activity (ChAT), and density (Bmax) of DA D1 receptors in frontal and temporal cortex were studied by radioligand binding protocols. None of the patients was receiving cholinomimetic drugs.
ChAT activity, but no other neurochemical markers, was reduced in AD compared with controls. Loss of ChAT activity correlated with cognitive impairment. Lowered ChAT activity also correlated with increasing overactivity in patients with dementia in both frontal and temporal cortex whereas ChAT:DA and ChAT:D1 ratios in temporal cortex correlated negatively with aggressive behavior.
Disturbance of the cholinergic system may underlie both cognitive and some noncognitive behavioral changes in dementia, providing a basis for rational therapy.-1467
除认知障碍外,痴呆患者还经常出现抑郁、攻击行为、精神病和多动等非认知行为变化,这些变化常常决定了患者是否需要入住养老院。人们对这些变化的生化基础了解甚少。临床试验数据表明,拟胆碱药物可改善非认知行为。本研究调查了胆碱能和多巴胺能神经递质系统标志物与痴呆病程中评估的非认知行为症状之间的关系。
对46例痴呆患者(36例阿尔茨海默病患者和10例符合阿尔茨海默病注册协会标准的混合性或其他痴呆患者)的大脑与32例正常对照者的大脑进行了检查。痴呆患者每4个月接受一次评估,通常持续数年,评估内容包括认知表现(简易精神状态检查表)和行为(当前行为检查表)。通过放射性配体结合实验研究了额叶和颞叶皮质中多巴胺(DA)及其主要代谢产物的浓度、胆碱乙酰转移酶活性(ChAT)以及DA D1受体的密度(Bmax)。所有患者均未服用拟胆碱药物。
与对照组相比,阿尔茨海默病患者的ChAT活性降低,但其他神经化学标志物无变化。ChAT活性的丧失与认知障碍相关。ChAT活性降低还与痴呆患者额叶和颞叶皮质多动的增加相关,而颞叶皮质中ChAT:DA和ChAT:D1比值与攻击行为呈负相关。
胆碱能系统紊乱可能是痴呆患者认知和一些非认知行为变化的基础,为合理治疗提供了依据。-1467