数据日期 2026-10-29 · 生成时间 2026-10-29 06:03
研究问题
Alzheimer’s disease is increasingly recognized as a complex biological syndrome rather than a disorder driven by a single pathway.
方法
(全文无独立方法节,正文亦未给出可抽取的实验动作句)
核心结论
In addition to amyloid-β and tau pathology, the disease is shaped by inflammation, vascular injury, aging biology, metabolic dysfunction, and host-microbe interactions (Livingston et al., 2024; Kakkar et al., 2025).;It asks how amyloid-β, tau, immune regulation, vascular health, metabolism, aging biology, and environmental exposures interact across scales and over time to produce heterogeneous patterns of vulnerability, compensation, and clinical expression (Jennifer et al., 2023; Khachaturian et al., 2023; Khachaturian and Khachaturian, 2023). ‖ 结论:The test of precision medicine is not only how precisely it classifies disease, but how reliably it changes the trajectory of a person’s life.
局限
全文未设独立 limitations 节;结构上为非 RCT 设计,因果推断强度受限。
对本项目的价值
★★☆☆☆ 脑老化是最大未满足需求,也是终点最难量化的领域;biomarker 与认知读数选择最敏感。设计 多组学。
全文来源
PMC JATS 全文(正文 17,894 字符,已过标题/DOI 逐字归属校验)
原文题录
- 英文标题:Integrating cure and care in Alzheimer's disease: a systems perspective for precision medicine.
- 期刊与标识:Front Mol Med · PMID 42948807 · DOI 10.3389/fmmed.2026.1960763**
C 级证据分级:C 级(预印本 / 观点评论,非原始研究)
本文属观点/评论类文献,不是原始研究。其论点依赖于作者对既有证据的梳理与判断,不构成新的实验证据。本站标注 C 级即为此意——阅读时请把它当作「领域内的思考框架」,而非「研究发现」。
关于本文的文献来源:本站依据 IMA 知识库「五刊监控·深度文献卡片」撰写,依据已获取的期刊全文(方法、样本量与结论已回到原文核对);未能获取全文的同批条目另行标注「摘要级」,全程未做任何数值推算补全。