Urvi Desai, PhD, Analysis Group, Inc., 111 Huntington Avenue, 14th Floor, Boston, MA 02199, USA, Phone: +1-617-425-8315, Email:
J Prev Alzheimers Dis. 2024;11(2):310-319. doi: 10.14283/jpad.2024.27.
Emerging therapies have shown promising results for slowing the progression of Alzheimer's disease (AD). However, the potential impact of these therapies on real-world outcomes remains to be explored.
To examine the impact of slowing AD progression on functional abilities and behavioral symptoms.
Retrospective observational study.
Data from the National Alzheimer's Coordinating Center (NACC) Uniform Data Set (UDS) in the United States (06/2005-11/2021, primary analysis) and the Alzheimer's Disease Neuroimaging Initiative (ADNI) database (09/2005-03/2022, sensitivity analysis) were used.
Individuals with mild cognitive impairment (MCI) or mild dementia, Clinical Dementia Rating Scale Sum of Boxes (CDR-SB) score 0.5-9.0 (inclusive; first visit defined as the index date), and confirmed amyloid positivity were identified in NACC. In ADNI, individuals with at least one clinical center visit with a clinical assessment of MCI or mild dementia and confirmed amyloid positivity were identified.
Hypothetical effects of slowing disease progression as assessed by CDR-SB on functional and behavioral outcomes including the Functional Activities Questionnaire (FAQ) score, Neuropsychiatric Inventory Questionnaire (NPI-Q) score, and the probability of complete dependence over five years were evaluated using multivariable regression among NACC participants, separately for the subgroups with MCI and mild dementia at baseline, respectively. For the ADNI sensitivity analysis, the hypothetical effects of slowing disease progression were evaluated for FAQ score using multivariable regression among the MCI participants only.
Compared with natural disease progression, slowing progression by 20% over five years for NACC participants with MCI and mild dementia, respectively, would result in 1.7-point (10.8%) and 1.6-point (12.9%) less deterioration based on FAQ; 0.5-point (20.3%) and 0.5-point (19.3%) less deterioration based on NPI-Q; 4.7 percentage-point (22.2%) and 10.1 percentage-point (21.6%) lower probability of complete dependence. Among ADNI participants, delaying disease progression by 20% or 30% over 4 years would avert deterioration based on FAQ of 1.1 points (20.4%) and 1.6 points (29.6%), respectively, compared to natural disease progression.
Slowing early AD progression could result in preservation of functional and behavioral attributes and functional autonomy for longer.
新兴疗法已显示出延缓阿尔茨海默病(AD)进展的有前景的结果。然而,这些疗法对真实世界结果的潜在影响仍有待探索。
检查减缓 AD 进展对功能能力和行为症状的影响。
回顾性观察研究。
美国国家阿尔茨海默病协调中心(NACC)统一数据集(UDS)的数据(2005 年 6 月至 2021 年 11 月,主要分析)和阿尔茨海默病神经影像学倡议(ADNI)数据库(2005 年 9 月至 2022 年 3 月,敏感性分析)。
轻度认知障碍(MCI)或轻度痴呆,临床痴呆评定量表总分(CDR-SB)评分 0.5-9.0(含),首次就诊定义为指数日期,在 NACC 中确认淀粉样蛋白阳性。在 ADNI 中,在至少有一次临床中心就诊的临床评估为 MCI 或轻度痴呆且确认淀粉样蛋白阳性的个体中进行了识别。
使用多变量回归分别评估 NACC 参与者中 CDR-SB 评估的疾病进展减缓对功能和行为结果(包括功能活动问卷(FAQ)评分、神经精神病学问卷(NPI-Q)评分和五年内完全依赖的概率)的假设影响,分别针对基线时 MCI 和轻度痴呆的亚组。对于 ADNI 敏感性分析,仅在 MCI 参与者中使用多变量回归评估减缓疾病进展的假设效果。
与自然疾病进展相比,NACC 中 MCI 和轻度痴呆患者分别在五年内减缓 20%的疾病进展,FAQ 恶化分别减少 1.7 分(10.8%)和 1.6 分(12.9%);NPI-Q 恶化分别减少 0.5 分(20.3%)和 0.5 分(19.3%);完全依赖的概率分别降低 4.7 个百分点(22.2%)和 10.1 个百分点(21.6%)。在 ADNI 参与者中,与自然疾病进展相比,在 4 年内减缓 20%或 30%的疾病进展,FAQ 恶化分别减少 1.1 分(20.4%)和 1.6 分(29.6%)。
减缓早期 AD 进展可延长功能和行为特征以及功能自主性的保持时间。