Cerebral Amyloid Angiopathy-Related Inflammation and Biopsy-Positive Primary Angiitis of the CNS: A Comparative Study.

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Grangeon, Lou | Boulouis, Grégoire | Capron, Jean | Bala, Fouzi | Renard, Dimitri | Raposo, Nicolas | Ozkul-Wermester, Ozlem | Triquenot-Bagan, Aude | Ayrignac, Xavier | Wallon, David | Gerardin, Emmanuel | Kerschen, Philippe | Sablot, Denis | Formaglio, Maïté | Pico, Fernando | Turc, Guillaume | Verny, Marc | Humbertjean, Lisa | Gaudron, Marie | Vannier, Stéphane | Dequatre, Nelly | Guillon, Benoit | Isabel, Clothilde | Arquizan, Caroline | Detante, Olivier | Godard, Sophie | Casolla, Barbara | Levraut, Michael | Gollion, Cédric | Gerfaud-Valentin, Mathieu | Kremer, Laurent | Daelman, Laure | Lambert, Nicolas | Lanthier, Sylvain | Poppe, Alexandre | Régent, Alexis | Weisenburger-Lile, David | Verdure, Pierre | Quesney, Gérald | Vautier, Mathieu | Wacongne, Anne | Thouvenot, Eric | Pariente, Jérémie | Coulette, Sarah | Labauge, Pierre M. | Olivier, Nadège | Allou, Thibaut | Zephir, Helene | Néel, Antoine | Bresch, Saskia | Terrier, Benjamin | Martinaud, Olivier | Schneckenburger, Romain | Papo, Thomas | Comarmond-Ortoli, Chloé | Jouvent, Eric | Subréville, Marie | Poncet-Megemont, Louis | Khatib, Muhammad A. | Lun, François | Henry, Carole | Magnin, Eloi | Thomas, Quentin | Graber, Mathilde | Boukriche, Yassine | Blanchet-Fourcade, Geneviève | Ratiu, Diana | Pagnoux, Christian | Touzé, Emmanuel | de Boysson, Hubert | Alamowitch, Sonia | Nehme, Ahmad

Edité par CCSD ; American Academy of Neurology -

International audience. Background and ObjectivesCerebral amyloid angiopathy-related inflammation (CAA-RI) and biopsy-positive primary angiitis of the CNS (BP-PACNS) have overlapping clinicoradiologic presentations. It is unknown whether clinical and radiologic features can differentiate CAA-RI from BP-PACNS and whether both diseases have different relapse rates. The objectives of this study were to compare clinicoradiologic presentations and relapse rates in patients with CAA-RI vs BP-PACNS.MethodsPatients with CAA-RI and BP-PACNS were enrolled from 2 retrospective multicenter cohorts. Patients with CAA-RI were biopsy-positive or met probable clinicoradiologic criteria. Patients with BP-PACNS had histopathologic confirmation of CNS angiitis, with no secondary etiology. A neuroradiologist read brain MRIs, blinded to the diagnosis of CAA-RI or BP-PACNS. Clinicoradiologic features were compared using univariable logistic regression models. Relapse rates were compared using a univariable Fine-Gray subdistribution hazard model, with death as a competing risk.ResultsThis study enrolled 104 patients with CAA-RI (mean age 73 years, 48% female sex) and 52 patients with BP-PACNS (mean age 45 years, 48% female sex). Patients with CAA-RI more often had white matter hyperintense lesions meeting the probable CAA-RI criteria (93% vs 51%, p < 0.001), acute subarachnoid hemorrhage (15% vs 2%, p = 0.02), cortical superficial siderosis (27% vs 4%, p < 0.001), ≥1 lobar microbleed (94% vs 26%, p < 0.001), past intracerebral hemorrhage (17% vs 4%, p = 0.04), ≥21 visible centrum semiovale perivascular spaces (34% vs 4%, p < 0.01), and leptomeningeal enhancement (70% vs 27%, p < 0.001). Patients with BP-PACNS more often had headaches (56% vs 31%, p < 0.01), motor deficits (56% vs 36%, p = 0.02), and nonischemic parenchymal gadolinium enhancement (82% vs 16%, p < 0.001). The prevalence of acute ischemic lesions was 18% in CAA-RI and 22% in BP-PACNS (p = 0.57). The features with the highest specificity for CAA-RI were acute subarachnoid hemorrhage (98%), cortical superficial siderosis (96%), past intracerebral hemorrhage (96%), and ≥21 visible centrum semiovale perivascular spaces (96%). The probable CAA-RI criteria had a 71% sensitivity (95% CI 44%–90%) and 91% specificity (95% CI 79%–98%) in differentiating biopsy-positive CAA-RI from BP-PACNS. The rate of relapse in the first 2 years after remission was lower in CAA-RI than in BP-PACNS (hazard ratio 0.46, 95% CI 0.22–0.96, p = 0.04).ConclusionClinicoradiologic features differed between patients with CAA-RI and those with BP-PACNS. Specific markers for CAA-RI were hemorrhagic signs of subarachnoid involvement, past intracerebral hemorrhage, ≥21 visible centrum semiovale perivascular spaces, and the probable CAA-RI criteria. A biopsy remains necessary for diagnosis in some cases of CAA-RI. The rate of relapse in the first 2 years after disease remission was lower in CAA-RI than in BP-PACNS.

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