Claus Jacqueline J, Vom Hofe Ilse, van Ijlzinga Veenstra Annekee, Licher Silvan, Seelaar Harro, de Jong Frank J, Neitzel Julia, Vernooij Meike W, Ikram M Arfan, Wolters Frank J
Department of Epidemiology, Erasmus MC, Rotterdam, The Netherlands.
Department of Radiology & Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands.
Eur J Epidemiol. 2025 Mar 23. doi: 10.1007/s10654-025-01220-1.
Treatment with anti-amyloid-β monoclonal antibodies slowed cognitive decline in recent RCTs in patients with mild cognitive impairment (MCI) and early dementia due to Alzheimer's disease (AD). However, stringent trial eligibility criteria may affect generalisability to clinical practice. We extracted eligibility criteria for trials of aducanumab, lecanemab and donanemab, and applied these to participants with MCI and early clinical AD dementia from the population-based Rotterdam Study. Participants underwent questionnaires, genotyping, brain-MRI, cognitive testing, and cardiovascular assessment. We determined amyloid status using a validated prediction model based on age and APOE-genotype. Of 968 participants (mean age: 75 years, 56% women), 779 had MCI and 189 dementia. Across trials, around 40% of participants would be ineligible because of predicted amyloid negativity. At least one clinical exclusion criterion was present in 76.3% of participants for aducanumab, 75.8% for lecanemab, and 59.8% for donanemab. Common criteria were cardiovascular disease (35.2%), anticoagulant (31.2%), psychotropic or immunological medication use (20.4%), anxiety or depression (15.9%), or lack of social support (15.6%). One-third were ineligible based on brain-MRI findings alone, similar across trials and predominantly due to cerebral small-vessel disease. Combining amyloid, clinical, and imaging criteria, eligibility ranged from 9% (95% CI:7.0-11.1) for aducanumab, 8% (6.2-9.9) lecanemab to 15% (12.4-17.5) for donanemab. Findings from recent RCTs reporting protective effects of monoclonal antibodies against amyloid-β are applicable to less than 15% of community-dwelling individuals with MCI or early AD. These findings underline that evidence for drug efficacy and safety is lacking for the vast majority of patients with MCI/AD in routine clinical practice.
在近期针对轻度认知障碍(MCI)和阿尔茨海默病(AD)所致早期痴呆患者的随机对照试验(RCT)中,使用抗淀粉样蛋白-β单克隆抗体进行治疗减缓了认知能力下降。然而,严格的试验纳入标准可能会影响其在临床实践中的推广性。我们提取了阿杜卡努单抗、莱卡奈单抗和多奈单抗试验的纳入标准,并将其应用于基于人群的鹿特丹研究中患有MCI和临床早期AD痴呆的参与者。参与者接受了问卷调查、基因分型、脑部磁共振成像(MRI)、认知测试和心血管评估。我们使用基于年龄和载脂蛋白E(APOE)基因型的经过验证的预测模型来确定淀粉样蛋白状态。在968名参与者(平均年龄:75岁,56%为女性)中,779人患有MCI,189人患有痴呆。在各项试验中,约40%的参与者由于预测淀粉样蛋白呈阴性而不符合纳入标准。对于阿杜卡努单抗,76.3%的参与者至少存在一项临床排除标准;对于莱卡奈单抗,这一比例为75.8%;对于多奈单抗,为59.8%。常见标准包括心血管疾病(35.2%)、使用抗凝剂(31.2%)、使用精神类或免疫类药物(20.4%)、焦虑或抑郁(15.9%)或缺乏社会支持(15.6%)。仅基于脑部MRI检查结果,三分之一的参与者不符合纳入标准,在各项试验中情况相似,主要原因是脑小血管疾病。综合考虑淀粉样蛋白、临床和影像学标准,阿杜卡努单抗的符合纳入标准率为9%(95%置信区间:7.0 - 11.1),莱卡奈单抗为8%(6.2 - 9.9),多奈单抗为15%(12.4 - 17.5)。近期报告单克隆抗体对淀粉样蛋白-β有保护作用的RCT结果适用于不到15%的社区居住的MCI或早期AD患者。这些发现强调,在常规临床实践中,绝大多数MCI/AD患者缺乏药物疗效和安全性的证据。