Jelic V, Kivipelto M, Winblad B
Karolinska Institutet, Neurotec Department, Division of Geriatric Medicine, Karolinska University Hospital-Huddinge, Stockholm, Sweden.
J Neurol Neurosurg Psychiatry. 2006 Apr;77(4):429-38. doi: 10.1136/jnnp.2005.072926. Epub 2005 Nov 23.
Mild cognitive impairment (MCI) is an operational definition for a cognitive decline in individuals with a greater risk of developing dementia. The amnestic subtype of MCI is of particular interest because these individuals most likely progress to Alzheimer's disease (AD). Currently hypothesised therapeutic approaches in MCI are mainly based on AD treatment strategies. Long term secondary prevention randomised clinical trials have been completed in amnestic MCI populations, encompassing agents with various mechanisms of action: acetylcholinesterase inhibitors (donepezil, rivastigmine, galantamine), antioxidants (vitamin E), anti-inflammatories (rofecoxib), and nootropics (piracetam). The design of clinical trials in MCI is influenced by study objectives and definition of primary end points: time to clinical diagnosis of dementia, and AD in particular, or symptom progression. As none of the drugs previously shown to have clinical efficacy in AD trials or benefit in everyday practice have met the primary objectives of the respective trials, design of future clinical trials in MCI should be further developed particularly as regards the selection of more homogeneous samples at entry, optimal treatment duration, and multidimensional and reliable outcomes.
轻度认知障碍(MCI)是对患痴呆症风险较高个体认知功能衰退的一种操作性定义。MCI的遗忘型亚型尤其令人关注,因为这些个体最有可能发展为阿尔茨海默病(AD)。目前针对MCI的治疗方法假设主要基于AD的治疗策略。针对遗忘型MCI人群已经完成了长期二级预防随机临床试验,试验涉及具有各种作用机制的药物:乙酰胆碱酯酶抑制剂(多奈哌齐、卡巴拉汀、加兰他敏)、抗氧化剂(维生素E)、抗炎药(罗非昔布)和促智药(吡拉西坦)。MCI临床试验的设计受研究目标和主要终点定义的影响:痴呆症临床诊断的时间,尤其是AD的临床诊断时间,或症状进展情况。由于之前在AD试验中显示具有临床疗效或在日常实践中有益处的药物均未达到各自试验的主要目标,未来MCI临床试验的设计应进一步改进,特别是在入组时选择更同质的样本、确定最佳治疗持续时间以及采用多维且可靠的结果方面。