Pharmaceutical Outcomes Research and Policy Program, University of Washington, Seattle, WA 98195-7630, USA.
J Alzheimers Dis. 2011;24(3):599-607. doi: 10.3233/JAD-2011-101758.
Cholinesterase inhibitors and memantine are medications used in the treatment of Alzheimer's disease (AD). These agents have been shown to reduce the rate of AD progression in randomized trials. The objective of this study is to evaluate the association between treatment with cholinesterase inhibitors or memantine and the probability of transitioning to a more severe Clinical Dementia Rating (CDR) state. Analysis was limited to possible or probable AD patients from NACC-UDS with three or more observations, baseline CDR score of 0.5 or 1, and without reported use AD drugs at enrollment. Use of an AD drug at any observation after baseline was classified as treatment. Odds of CDR stage were calculated by multinomial logistic regression controlling for baseline age, baseline MMSE score, education, marital status, race, gender, place of residence, and time since last measure. The resulting coefficients from logistic regression were used to calculate transitional probabilities. A total of 1,114 patients were included. No differences were observed in the probability of transitioning to more severe CDR states based on treatment, but treated patients had lower odds of death, OR 0.49 (95% CI 0.31 to 0.79) compared to untreated. Ultimately, this study failed to detect a difference in the probability of progressing to a more severe AD state as a result of treatment in an observational cohort of AD patients, but is limited by non-randomized treatment selection and small dataset. The NACC-UDS dataset is ongoing and this analysis may be improved if repeated when more data is available.
胆碱酯酶抑制剂和美金刚是用于治疗阿尔茨海默病(AD)的药物。随机试验表明,这些药物可降低 AD 进展的速度。本研究的目的是评估使用胆碱酯酶抑制剂或美金刚治疗与向更严重的临床痴呆评定量表(CDR)状态转变的可能性之间的关系。分析仅限于 NACC-UDS 中具有三个或更多观察结果、基线 CDR 评分为 0.5 或 1 且在入组时未报告使用 AD 药物的可能或可能的 AD 患者。将基线后任何观察点使用 AD 药物归类为治疗。通过多变量逻辑回归控制基线年龄、基线 MMSE 评分、教育程度、婚姻状况、种族、性别、居住地和上次测量后的时间,计算 CDR 阶段的几率。从逻辑回归中得到的系数用于计算过渡概率。共纳入 1114 例患者。基于治疗,未观察到向更严重 CDR 状态转变的概率存在差异,但与未治疗患者相比,治疗患者的死亡几率较低,OR 为 0.49(95%CI 0.31 至 0.79)。最终,由于观察性 AD 患者队列中的治疗选择非随机且数据集较小,本研究未能检测到治疗对进展为更严重 AD 状态的可能性产生差异。NACC-UDS 数据集仍在进行中,如果有更多数据可用,当重复此分析时,可能会有所改进。