Brown Alpert Medical School, Providence, RI 02906, USA.
Am J Alzheimers Dis Other Demen. 2012 Sep;27(6):421-32. doi: 10.1177/1533317512454708.
To better understand responses in the large number of US-based patients included in a global trial of donepezil 23 mg/d versus 10 mg/d for moderate-to-severe Alzheimer's disease (AD), post hoc exploratory analyses were performed to assess the efficacy and safety in US and non-US (rest of the world [RoW]) patient subgroups. In both subgroups, donepezil 23 mg/d was associated with significantly greater cognitive benefits than donepezil 10 mg/d. Significant global function benefits of donepezil 23 mg/d over 10 mg/d were also observed in the US subgroup only. Compared with RoW patients, US patients had relatively more severe AD, had been treated with donepezil 10 mg/d for longer periods prior to the start of the study, and a higher proportion took concomitant memantine. In both subgroups, donepezil had acceptable tolerability; overall incidence of treatment-emergent adverse events was higher in patients receiving donepezil 23 mg/d compared with donepezil 10 mg/d.
为了更好地理解在一项全球多奈哌齐 23mg/d 与 10mg/d 治疗中重度阿尔茨海默病(AD)的试验中纳入的大量美国患者的反应,进行了事后探索性分析,以评估美国和非美国(世界其他地区[RoW])患者亚组中的疗效和安全性。在这两个亚组中,多奈哌齐 23mg/d 与多奈哌齐 10mg/d 相比,认知功能获益显著更大。仅在美国亚组中观察到多奈哌齐 23mg/d 相对于 10mg/d 的全球功能显著获益。与 RoW 患者相比,美国患者的 AD 相对更严重,在研究开始前接受多奈哌齐 10mg/d 治疗的时间更长,且比例更高的患者同时使用美金刚。在这两个亚组中,多奈哌齐均具有可接受的耐受性;与接受多奈哌齐 10mg/d 治疗的患者相比,接受多奈哌齐 23mg/d 治疗的患者出现治疗后不良事件的总体发生率更高。