Withington Charles G, Turner R Scott
Department of Neurology, Georgetown University, Washington, DC, United States.
Front Neurol. 2022 Mar 23;13:862369. doi: 10.3389/fneur.2022.862369. eCollection 2022.
Second-generation anti-amyloid monoclonal antibodies are emerging as a viable therapeutic option for individuals with prodromal and mild dementia due to Alzheimer's disease (AD). Passive immunotherapy with aducanumab (Aduhelm), lecanemab, donanemab, and gantenerumab all lower CNS amyloid (Aβ) burden but come with a significant risk of amyloid-related imaging abnormality (ARIA)-the most common side effect of this class of drugs. While usually asymptomatic and detected only on brain MRI, ARIA may lead to new signs and symptoms including headache, worsening confusion, dizziness, visual disturbances, nausea, and seizures. In addition, one fatality related to ARIA-E (edema) with aducanumab and one fatality due to ARIA-H (hemorrhage) with donanemab are reported to date. ARIA-E may be associated with excessive neuroinflammation and saturation of perivascular clearance pathways, while ARIA-H may be related to vascular amyloid clearance with weakening and rupture of small blood vessels. The risk of ARIA-E is higher at treatment initiation, in ApoE4 carriers, with higher dosage, and with >4 of microhemorrhages on a baseline MRI. The risk of ARIA-H increases with age and cerebrovascular disease. Dose titration mitigates the risk of ARIA, and contraindications include individuals with >4 microhemorrhages and those prescribed anti-platelet or anti-coagulant drugs. A brain MRI is required before aducanumab is initiated, before each scheduled dose escalation, and with any new neurologic sign or symptom. Management of ARIA ranges from continued antibody treatment with monthly MRI monitoring for asymptomatic individuals to temporary or permanent suspension for symptomatic individuals or those with moderate to severe ARIA on MRI. Controlled studies regarding prevention and treatment of ARIA are lacking, but anecdotal evidence suggests that a pulse of intravenous corticosteroids may be of benefit, as well as a course of anticonvulsant for seizures.
第二代抗淀粉样蛋白单克隆抗体正在成为患有前驱期和轻度阿尔茨海默病(AD)痴呆症患者的一种可行治疗选择。使用阿杜卡单抗(Aduhelm)、来卡奈单抗、多奈单抗和甘特奈单抗进行被动免疫治疗均能降低中枢神经系统淀粉样蛋白(Aβ)负荷,但会带来显著的淀粉样蛋白相关成像异常(ARIA)风险,这是这类药物最常见的副作用。虽然ARIA通常无症状,仅在脑部MRI检查时被发现,但它可能导致新的体征和症状,包括头痛、意识混乱加重、头晕、视觉障碍、恶心和癫痫发作。此外,迄今为止,已报告1例与阿杜卡单抗相关的ARIA-E(水肿)死亡病例和1例与多奈单抗相关的ARIA-H(出血)死亡病例。ARIA-E可能与过度的神经炎症和血管周围清除途径饱和有关,而ARIA-H可能与血管淀粉样蛋白清除以及小血管减弱和破裂有关。在治疗开始时、ApoE4携带者、高剂量以及基线MRI上有>4处微出血的情况下,ARIA-E的风险更高。ARIA-H的风险随年龄和脑血管疾病增加。剂量滴定可降低ARIA风险,禁忌证包括有>4处微出血的个体以及正在服用抗血小板或抗凝药物的个体。在开始使用阿杜卡单抗之前、每次计划的剂量递增之前以及出现任何新的神经系统体征或症状时,都需要进行脑部MRI检查。ARIA的管理范围从对无症状个体进行每月MRI监测的持续抗体治疗到对有症状个体或MRI上有中度至重度ARIA的个体进行临时或永久停药。目前缺乏关于ARIA预防和治疗的对照研究,但轶事证据表明,静脉注射皮质类固醇脉冲治疗可能有益,以及针对癫痫发作的抗惊厥疗程也可能有益。