PSEN1型
早老素
生物标志物
观察研究
疾病
阿尔茨海默病
遗传学
生物
淀粉样蛋白(真菌学)
医学
病理
内科学
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
标识
DOI:10.1016/s1474-4422(24)00236-9
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.
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