Cognitive Versus Hemorrhagic Onset in Cerebral Amyloid Angiopathy: Neuroimaging Features

Author:

Perini Giulia12ORCID,Ramusino Matteo Cotta1,Farina Lisa Maria3,Fabbro Beatrice Dal12,Canavero Isabella4,Picascia Marta5,Muzic Shaun6,Ballante Elena7,Cavallini Anna8,Pichiecchio Anna23,Costa Alfredo12

Affiliation:

1. Unit of Behavioral Neurology and Center for Cognitive Disorders and Dementias (CDCD), IRCCS Mondino Foundation, Pavia, Italy

2. Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy

3. Department of Neuroradiology, Advanced Imaging and Radiomics Center, IRCCS Mondino Foundation, Pavia, Italy

4. Cerebrovascular Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy

5. Unit of Neuropsychology, Laboratory of Neuropsychology, IRCCS Mondino Foundation, Pavia, Italy

6. Department of Radiology, Fondazione IRCCS Policlinico San Matteo Foundation, Medical School, University of Pavia, Pavia, Italy

7. Department of Political and Social Sciences, BioData Science Center, IRCCS Mondino Foundation, University of Pavia, Pavia, Italy

8. Department of Emergency Neurology/Stroke Unit, IRCCS Mondino Foundation, Pavia, Italy

Abstract

Background: Intracerebral hemorrhage and cognitive decline are typical clinical presentations of cerebral amyloid angiopathy (CAA). Objective: To determine whether magnetic resonance imaging (MRI) features differ between CAA with hemorrhagic versus cognitive onset. Methods: In this retrospective study, sixty-one patients with CAA were classified by onset presentation of the disease: hemorrhage (n = 31) or cognitive decline (n = 30). The two groups were compared for MRI markers of small vessel disease, namely cerebral microbleeds (CMBs), cortical superficial siderosis, white matter hyperintensities (WMHs), enlarged perivascular spaces, cortical microinfarcts, and visual rating scales for cortical atrophy. In the patients with cognitive onset, further exploratory analyses investigated MRI markers according to cerebrospinal fluid (CSF) and neuropsychological profiles. Results: Patients with cognitive onset showed a higher prevalence of CMBs (p < 0.001), particularly in temporal (p = 0.015) and insular (p = 0.002) lobes, and a higher prevalence of WMHs (p = 0.012). Within the cognitive onset group, 12 out of 16 (75%) patients had an Alzheimer’s disease (AD) CSF profile but did not differ in MRI markers from those without AD pathology. Patients with cognitive onset displayed a multidomain profile in 16 out of 23 (70%) cases; patients with this profile showed increased WMHs and CMBs in parietal lobes compared with the amnestic group (p = 0.002) and dysexecutive group (p = 0.032), respectively. Conclusion: Higher burdens of WMHs and CMBs, especially in temporal and insular lobes, are associated with the cognitive onset of CAA. MRI markers could help to shed light on the clinical heterogeneity of the CAA spectrum and its underlying mechanisms.

Publisher

Bentham Science Publishers Ltd.

Subject

Neurology (clinical),Neurology

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