Fernandez Hubert H, Wu Chuang-Kuo, Ott Brian R
Division of Neurology, Memorial Hospital of Rhode Island, 111 Brewster Street, Pawtucket, RI 02860, USA.
Expert Opin Pharmacother. 2003 Nov;4(11):2027-37. doi: 10.1517/14656566.4.11.2027.
The syndrome of dementia with Lewy bodies (DLB) is characterised by the clinical triad of fluctuating cognitive impairment, recurrent visual hallucinations and spontaneous motor features of Parkinsonism. In an attempt to define DLB as a distinct clinical syndrome separate from Alzheimer's disease (AD) and Parkinson's disease (PD) with dementia, a consensus workshop in 1995 established a new set of diagnostic criteria. Dementia that precedes or accompanies the onset of spontaneous (i.e., not neuroleptic-induced) Parkinsonism is termed DLB. In addition, fluctuations in alertness, cognition and function and visual hallucinations are emphasised and included as core features of DLB. The degree to which an individual patient exhibits cognitive impairment, behavioural problems and Parkinsonian features is variable. Therefore, treatment must be individualised. Although there are no officially approved drugs for DLB, limited experience from clinical trials, as well as past experience with the treatment of AD and PD patients, provide some basis for making drug choices. The cholinergic deficit seen in DLB makes cholinesterase inhibitor drugs the mainstay of treatment for cognitive impairment. This class of drugs has also shown therapeutic benefit in reducing hallucinations and other neuropsychiatric symptoms of the disease. Because of their relatively greater therapeutic window, cholinesterase inhibitors are also used as first-line therapy for the treatment of psychosis in DLB. Patients with DLB are extremely sensitive to the extrapyramidal side effects of neuroleptic medications. Thus, only atypical antipsychotic agents such as quetiapine, should be considered as alternative treatment for psychosis. Anxiety and depression are best treated with selective serotonin re-uptake inhibitors, whereas REM sleep behaviour disorder may be treated with low dose clonazepam. Parkinsonism responds to dopaminergic agents; however, precipitation or aggravation of hallucinosis may occur. Levodopa is preferred over dopamine agonists due to its lower propensity to cause hallucinations and somnolence. As the diagnostic criteria for DLB become more refined and validated by postmortem studies, it is hoped that rigorous, well-designed trials will be performed, aimed at alleviating the primary target symptoms of dementia, psychosis and Parkinsonism.
路易体痴呆(DLB)综合征的特征为波动性认知障碍、反复出现的视幻觉以及帕金森病的自发运动特征这一临床三联征。为了将DLB定义为一种有别于阿尔茨海默病(AD)和帕金森病(PD)所致痴呆的独特临床综合征,1995年的一次共识研讨会制定了一套新的诊断标准。先于或伴随自发(即非抗精神病药物所致)帕金森病起病的痴呆被称为DLB。此外,警觉性、认知和功能的波动以及视幻觉被强调并纳入DLB的核心特征。个体患者出现认知障碍、行为问题和帕金森病特征的程度各不相同。因此,治疗必须个体化。虽然目前尚无官方批准用于DLB的药物,但临床试验的有限经验以及过去治疗AD和PD患者的经验为药物选择提供了一些依据。DLB中所见的胆碱能缺陷使胆碱酯酶抑制剂药物成为治疗认知障碍的主要药物。这类药物在减少幻觉和该疾病的其他神经精神症状方面也显示出治疗益处。由于其相对更宽的治疗窗,胆碱酯酶抑制剂还被用作DLB中治疗精神病的一线疗法。DLB患者对抗精神病药物的锥体外系副作用极其敏感。因此,仅应考虑使用非典型抗精神病药物如喹硫平作为精神病的替代治疗。焦虑和抑郁最好用选择性5-羟色胺再摄取抑制剂治疗,而快速眼动睡眠行为障碍可用低剂量氯硝西泮治疗。帕金森病对多巴胺能药物有反应;然而,可能会出现幻觉症的诱发或加重。由于左旋多巴引起幻觉和嗜睡的倾向较低,因此比多巴胺激动剂更受青睐。随着DLB的诊断标准通过尸检研究变得更加精确和得到验证,希望能开展严格的、设计良好的试验,旨在减轻痴呆、精神病和帕金森病的主要目标症状。