Prof. Dr. Anja Schneider
Department of Cognitive Disorders and Old Age Psychiatry
anja.schneider@ukbonn.de View member: Prof. Dr. Anja Schneider
Nature communications
Cerebrospinal fluid amyloid beta 42, total tau, and phosphorylated tau 181 are well accepted markers of Alzheimer's disease. These biomarkers better reflect disease pathogenesis compared to clinical diagnosis. Here, we perform a genome wide association study meta-analysis including 18,948 individuals of European ancestry and identify 12 genome-wide significant loci across all three biomarkers, eight of them novel. We replicate the association of biomarkers with APOE, CR1, GMNC/CCDC50 and C16orf95/MAP1LC3B. Novel loci include BIN1 for amyloid beta and GNA12, MS4A6A, SLCO1A2 with both total tau and phosphorylated tau 181, as well as additional loci on chr. 8, near ANGPT1 and chr. 9 near SMARCA2. We also demonstrate that these variants have significant association with Alzheimer's disease risk, disease progression and/or brain amyloidosis. The associated genes are implicated in lipid metabolism independent of APOE, coupled with autophagy and brain volume regulation driven by total tau and phosphorylated tau 181 dysregulation.
© 2026. The Author(s).
PMID: 42014397
Department of Cognitive Disorders and Old Age Psychiatry
anja.schneider@ukbonn.de View member: Prof. Dr. Anja SchneiderInstitute of medical Biometry, Computer Science and Epidemiology
sekretariat@imbie.uni-bonn.de View member: Prof. Dr. Matthias SchmidInstitute of Human Genetics
markus.noethen@uni-bonn.de View member: Prof. Dr. med. Markus M. NöthenDepartment of Psychiatry and Psychotherapy, University of Cologne
alfredo.ramirez@uk-koeln.de View member: Prof. Dr. Alfredo Ramirez