作者
Stephanie A. Schultz,Lei Liu,Aaron P. Schultz,Colleen Fitzpatrick,Raina Levin,Jean‐Pierre Bellier,Zahra Shirzadi,Nelly Joseph‐Mathurin,Charles D. Chen,Tammie L.S. Benzinger,Gregory S. Day,Martin R. Farlow,Brian A. Gordon,Jason J. Hassenstab,Clifford R. Jack,Mathias Jucker,Celeste M. Karch,Jae Hong Lee,Johannes Levin,Richard J. Perrin,Peter R. Schofield,Chengjie Xiong,Keith A. Johnson,Eric McDade,Randall J. Bateman,Reisa Sperling,Dennis J. Selkoe,Jasmeer P. Chhatwal
摘要
Genetic variants that cause autosomal dominant Alzheimer's disease are highly penetrant but vary substantially regarding age at symptom onset (AAO), rates of cognitive decline, and biomarker changes. Most pathogenic variants that cause autosomal dominant Alzheimer's disease are in presenilin 1 (PSEN1), which encodes the catalytic core of γ-secretase, an enzyme complex that is crucial in production of amyloid β. We aimed to investigate whether the heterogeneity in AAO and biomarker trajectories in carriers of PSEN1 pathogenic variants could be predicted on the basis of the effects of individual PSEN1 variants on γ-secretase activity and amyloid β production.