α-Synuclein Seed Amplification in CSF and Brain from Patients with Different Brain Distributions of Pathological α-Synuclein in the Context of Co-Pathology and Non-LBD Diagnoses

Objective The purpose of this study was to determine the sensitivity and specificity of alpha-synuclein seed amplification assay (alpha Syn-SAA) in antemortem and postmortem cerebrospinal fluid (CSF) of autopsy-confirmed patients with different distributions of pathological alpha Syn, co-pathologies, and clinical diagnoses. Methods The alpha Syn-SAA was used to test antemortem CSF samples from 119 subjects with a variety of clinical syndromes and standardized neuropathological examinations from Oregon Health and Science University (OHSU) and University of California San Diego (UCSD; 56 additional postmortem CSF samples available). The alpha Syn-SAA was also applied to frontal cortex and amygdala homogenates. Sensitivity and specificity were compared across distributions of alpha Syn pathology. Clinical data and co-pathologies were compared across alpha Syn-SAA positive and negative groups. Results Fifty-three individuals without and 66 with alpha Syn-pathology (neocortical [n = 38], limbic [n = 7], and amygdala-predominant [n = 21]) were included. There was a sensitivity of 97.8% and specificity of 98.1% of the alpha Syn-SAA to identify patients with limbic/neocortical pathology from antemortem CSF. Sensitivity to detect amygdala-predominant pathology was only 14.3%. Postmortem CSF and brain tissue alpha Syn-SAA analyses also showed higher assay positivity in samples from limbic/neocortical cases. Interpretation CSF alpha Syn-SAA reliably identifies alpha Syn seeds in patients with diffuse alpha Syn pathology in the context of co-pathology and non-Lewy body disease (LBD) diagnoses. The analysis of brain homogenates suggests that pathological alpha Syn in the amygdala might differ from pathological alpha Syn in the frontal cortex. The alpha Syn-SAA might facilitate the differential diagnosis of dementias with mixed pathologies. ANN NEUROL 2022