Progranulin mutations in clinical and neuropathological Alzheimer's disease

• Published in: Alzheimer's & dementia Vol. 18; no. 12; pp. 2458 - 2467
• Main Authors: Vardarajan, Badri N., Reyes‐Dumeyer, Dolly, Piriz, Angel L., Lantigua, Rafael A., Medrano, Martin, Rivera, Diones, Jiménez‐Velázquez, Ivonne Z., Martin, Eden, Pericak‐Vance, Margaret A., Bush, William, Farrer, Lindsay, Haines, Jonathan L., Wang, Li‐San, Leung, Yuk Yee, Schellenberg, Gerard, Kukull, Walter, De Jager, Philip, Bennett, David A., Schneider, Julie A., Mayeux, Richard
• Format: Journal Article
• Language: English
• Published: United States John Wiley and Sons Inc 01.12.2022
• Subjects: Alzheimer Disease - genetics; Alzheimer Disease - pathology; Alzheimer's disease; DNA-Binding Proteins - genetics; Frontotemporal Lobar Degeneration - genetics; Humans; Intercellular Signaling Peptides and Proteins - genetics; Mutation - genetics; neuropathology; progranulin; Progranulins - genetics; TDP43; TDP43; progranulin; Alzheimer's disease; neuropathology
• ISSN: 1552-5260; 1552-5279; 1552-5279
• DOI: 10.1002/alz.12567

Introduction Progranulin (GRN) mutations occur in frontotemporal lobar degeneration (FTLD) and in Alzheimer's disease (AD), often with TDP‐43 pathology. Methods We determined the frequency of rs5848 and rare, pathogenic GRN mutations in two autopsy and one family cohort. We compared Braak stage, β‐amyloid load, hyperphosphorylated tau (PHFtau) tangle density and TDP‐43 pathology in GRN carriers and non‐carriers. Results Pathogenic GRN mutations were more frequent in all cohorts compared to the Genome Aggregation Database (gnomAD), but there was no evidence for association with AD. Pathogenic GRN carriers had significantly higher PHFtau tangle density adjusting for age, sex and APOE ε4 genotype. AD patients with rs5848 had higher frequencies of hippocampal sclerosis and TDP‐43 deposits. Twenty‐two rare, pathogenic GRN variants were observed in the family cohort. Discussion GRN mutations in clinical and neuropathological AD increase the burden of tau‐related brain pathology but show no specific association with β‐amyloid load or AD.