Spontaneous ARIA-like Events in Cerebral Amyloid Angiopathy–Related Inflammation

Author:

Antolini LauraORCID,DiFrancesco Jacopo C.ORCID,Zedde Marialuisa,Basso GianpaoloORCID,Arighi AndreaORCID,Shima AtsushiORCID,Cagnin AnnachiaraORCID,Caulo MassimoORCID,Carare Roxana O.ORCID,Charidimou AndreasORCID,Cirillo MarioORCID,Di Lazzaro Vincenzo,Ferrarese Carlo,Giossi Alessia,Inzitari Domenico,Marcon Michela,Marconi Roberto,Ihara MasafumiORCID,Nitrini RicardoORCID,Orlandi BerardinoORCID,Padovani AlessandroORCID,Pascarella Rosario,Perini Francesco,Perini Giulia,Sessa Maria,Scarpini ElioORCID,Tagliavini FabrizioORCID,Valenti RaffaellaORCID,Vázquez-Costa Juan FranciscoORCID,Villarejo-Galende AlbertoORCID,Hagiwara YutaORCID,Ziliotto NicoleORCID,Piazza Fabrizio

Abstract

Background and ObjectivesThe goal of this work was to investigate the natural history and outcomes after treatment for spontaneous amyloid-related imaging abnormalities (ARIA)-like in cerebral amyloid angiopathy–related inflammation (CAA-ri).MethodsThis was a multicenter, hospital-based, longitudinal, prospective observational study of inpatients meeting CAA-ri diagnostic criteria recruited through the Inflammatory Cerebral Amyloid Angiopathy and Alzheimer's Disease βiomarkers International Network from January 2013 to March 2017. A protocol for systematic data collection at first-ever presentation and at subsequent in-person visits, including T1-weighted, gradient recalled echo–T2*, fluid-suppressed T2-weighted (fluid-attenuated inversion recovery), and T1 postgadolinium contrast-enhanced images acquired on 1.5T MRI, was used at the 3-, 6-, 12-, and 24-month follow-up. Centralized reads of MRIs were performed by investigators blinded to clinical, therapeutic, and time-point information. Main outcomes were survival, clinical and radiologic recovery, intracerebral hemorrhage (ICH), and recurrence of CAA-ri.ResultsThe study enrolled 113 participants (10.6% definite, 71.7% probable, and 17.7% possible CAA-ri). Their mean age was 72.9 years; 43.4% were female; 37.1% were APOEε4 carriers; 36.3% had a history of Alzheimer disease; and 33.6% had a history of ICH. A history of ICH and the occurrence of new ICH at follow-up were more common in patients with cortical superficial siderosis at baseline (52.6% vs 14.3%, p < 0.0001 and 19.3% vs 3.6%, p < 0.009, respectively). After the first-ever presentation of CAA-ri, 70.3% (95% confidence interval [CI] 61.6%–78.5%) and 84.1% (95% CI 76.2%–90.6%) clinically recovered within 3 and 12 months, followed by radiologic recovery in 45.1% (95% CI 36.4%–54.8%) and 77.4% (95% CI 67.7%–85.9%), respectively. After clinicoradiologic resolution of the first-ever episode, 38.3% (95% CI 22.9%–59.2%) had at least 1 recurrence within the following 24 months. Recurrence was more likely if IV high-dose corticosteroid pulse therapy was suddenly stopped compared to slow oral tapering off (hazard ratio 4.68, 95% CI 1.57–13.93; p = 0.006).DiscussionThese results from the largest longitudinal cohort registry of patients with CAA-ri support the transient and potentially relapsing inflammatory nature of the clinical-radiologic acute manifestations of the disease and the effectiveness of slow oral tapering off after IV corticosteroid pulse therapy in preventing recurrences. Our results highlight the importance of differential diagnosis for spontaneous ARIA-like events in β-amyloid–driven diseases, including treatment-related ARIA in patients with Alzheimer disease exposed to immunotherapy drugs.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

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