纵向基于血液的生物标志物和主观认知衰退的临床进展
Calvin Trieu1,2,3,4, Argonde C van Harten1,2, Mardou S S A van Leeuwenstijn1,2
1Alzheimer Center Amsterdam, Department of Neurology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
JAMA network open
|December 3, 2025
概括
像pTau217和GFAP这样的血液生物标志物对跟踪主观认知衰退 (SCD) 个体的阿尔茨海默病 (AD) 进展和认知衰退充满希望. 它们的纵向变化与疾病进展相关,有助于早期干预.
科学领域:
- 神经科学和神经病学 神经科学和神经病学
- 生物标志物发现发现
- 阿尔茨海默氏症疾病研究研究
背景情况:
- 基于血液的生物标志物对于识别阿尔茨海默病 (AD) 和监测其进展至关重要,即使是在临床前阶段.
- 主观认知衰退 (SCD) 代表了认知障碍的早期阶段,通常是轻度认知障碍 (MCI) 或痴呆症之前.
- 了解SCD的纵向生物标志物变化对于早期检测和干预至关重要.
研究的目的:
- 研究SCD患者血生物标志物的纵向变化.
- 评估这些生物标志物轨迹与认知衰退之间的关联.
- 确定生物标志物变化对MCI或痴呆症临床进展的预测价值.
主要方法:
- 对298名患有SCD的人进行前性队列研究 (主观认知障碍队列).
- 每两年一次的血生物标志物收集:Aβ42/40,pTau217,GFAP和NfL.
- 每年进行认知评估和诊断评估,平均随访时间为4.8年.
- 由PET或CSF确定的粉样状况.
主要成果:
- 与SCD和粉样蛋白阳性 (A+) 个体相比,与粉样蛋白阴性 (A-) 个体相比,SCD和粉样蛋白阳性 (A+) 个体的基线水平较高,pTau217,GFAP和NfL的增加更快.
- 在pTau217和GFAP的纵向增加与所有测量领域的认知衰退有关.
- 对于pTau217,GFAP和NfL的更的斜坡显着与进展到MCI或痴呆症的风险增加有关.
结论:
- 纵向血pTau217和GFAP是监测SCD患者阿尔茨海默病病理学的宝贵生物标志物.
- 这些生物标志物的变化与认知衰退和临床进展相关,支持它们在早期干预策略中的使用.
- 这些发现突出了血液生物标志物的潜力,用于早期发现AD和疾病管理.
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