Aguglia E, Onor M L, Saina M, Maso E
Department of Clinical, Morphological and Technological Science, UCO of Clinical Psychiatry, University of Trieste, Trieste, Italy.
Curr Med Res Opin. 2004 Nov;20(11):1747-52. doi: 10.1185/030079904X6273.
We analysed the effects of donepezil, rivastigmine and galantamine, prescribed for the treatment of Alzheimer disease in a real-world setting in Italy.
Outcome measures included the MiniMental State Examination (MMSE), the Alzheimer Disease Assessment Scale cognitive subscale (ADAS-cog), Instrumental Activity of Daily Living (IADL) and ADL scales.
Seventy patients were treated with donepezil, 121 with rivastigmine and 51 with galantamine. At 6 months, rivastigmine-treated patients improved by 1.29 points from baseline on the ADAS-cog, while donepezil- and galantamine-treated patients showed 'no change' (changes of < 0.2 points). On the IADL, patients treated with rivastigmine, donepezil and galantamine showed decreases of 0.42, 0.58 and 0.75 points, respectively. On the ADL, donepezil- and galantamine-treated patients showed decreases of 0.44 and 0.86 points, respectively, while there was 'no change' with rivastigmine. On the MMSE, donepezil- and rivastigmine-treated patients showed 'no change' and galantamine-treated patients showed a mean decrease of 1.19 points. A subgroup analysis of 'pseudo-randomised' patients (rivastigmine, n = 63; donepezil, n = 55; galantamine, n = 51) supported the main findings. Side effects were similar (in type and frequency) in the three treatment groups.
This is the first study to compare the effects of the three most commonly-used cholinesterase inhibitors on the MMSE, ADAS-cog, IADL and ADL. Limitations included its small population size, its open-label design, and the fact that patients were randomised only after the introduction of galantamine. There were no statistically significant differences between the three drugs at 3 months. While numerical trends were observed suggesting the effect of rivastigmine > donepezil > galantamine, larger, longer-term prospective studies are needed to confirm whether there are important differences in the long-term efficacy of the three drugs.
我们分析了多奈哌齐、卡巴拉汀和加兰他敏在意大利实际临床环境中用于治疗阿尔茨海默病的效果。
结果指标包括简易精神状态检查表(MMSE)、阿尔茨海默病评估量表认知分量表(ADAS-cog)、日常生活能力量表(IADL)和日常生活活动量表(ADL)。
70例患者接受多奈哌齐治疗,121例接受卡巴拉汀治疗,51例接受加兰他敏治疗。在6个月时,接受卡巴拉汀治疗的患者ADAS-cog评分较基线提高了1.29分,而接受多奈哌齐和加兰他敏治疗的患者显示“无变化”(变化<0.2分)。在IADL方面,接受卡巴拉汀、多奈哌齐和加兰他敏治疗的患者分别下降了0.42、0.58和0.75分。在ADL方面,接受多奈哌齐和加兰他敏治疗的患者分别下降了0.44和0.86分,而接受卡巴拉汀治疗的患者“无变化”。在MMSE方面,接受多奈哌齐和卡巴拉汀治疗的患者“无变化”,接受加兰他敏治疗的患者平均下降了1.19分。对“伪随机”患者(卡巴拉汀组n = 63;多奈哌齐组n = 55;加兰他敏组n = 51)的亚组分析支持了主要研究结果。三个治疗组的副作用在类型和频率上相似。
这是第一项比较三种最常用的胆碱酯酶抑制剂对MMSE、ADAS-cog、IADL和ADL影响的研究。局限性包括样本量小、开放标签设计以及患者仅在加兰他敏引入后才进行随机分组。三种药物在3个月时无统计学显著差异。虽然观察到数值趋势表明卡巴拉汀>多奈哌齐>加兰他敏的效果,但需要更大规模、更长期的前瞻性研究来证实这三种药物在长期疗效上是否存在重要差异。