纤维蛋白原
纵向研究
脑脊液
内科学
医学
置信区间
心脏病学
基线(sea)
内分泌学
疾病
退行性疾病
中枢神经系统疾病
前瞻性队列研究
炎症
病理生理学
线性回归
试验预测值
心理学
血小板
回归
肿瘤科
中枢神经系统
阿尔茨海默病
纵向数据
作者
Christos Panagiotis Lisgaras,Tovia Jacobs,Luisa Figueredo,Elizabeth Pirraglia,Caleb H. Radtke,Jonah N Keller,Nikolaos Karvelas,Jennifer Bernal,Joaquin Ruiz,Henrik Zetterberg,Lidia Glodzik,Mony J de Leon,Laura Beth McIntire,Allal Boutajangout,Thomas Wisniewski,Jaime Ramos‐Cejudo,Daniel Alcolea,Sandra Giménez,Juan Fortea,Katerina Akassoglou
摘要
INTRODUCTION: Blood-brain barrier (BBB) dysfunction is an early feature of Alzheimer's disease (AD). Fibrinogen represents a sensitive marker of BBB leakage, but whether it modifies longitudinal tau progression in cognitively unimpaired (CU) individuals remains unknown. METHODS: CU older adults underwent clinical evaluation and cerebrospinal fluid (CSF) assessment of fibrinogen, Aβ42, total tau (tTau), phosphorylated tau 181 (pTau181), and YKL-40. Linear regression tested baseline associations. Linear mixed-effects models tested whether baseline fibrinogen predicted longitudinal pTau181 change. RESULTS: Among 169 CU participants with baseline fibrinogen, 87 had longitudinal pTau181 measurements (mean follow-up 2.5-years). Higher fibrinogen was associated with elevated YKL-40 (β = 0.28, 95% confidence interval [CI] [0.11, 0.45]) but not Aβ42, tTau, or pTau181 at baseline. Baseline fibrinogen modified longitudinal pTau181 trajectories (interaction β = 0.11, 95% CI [0.04, 0.19]), with only participants above the median showing significant pTau181 increases (β = 0.13, 95% CI [0.08, 0.18]). DISCUSSION: CSF fibrinogen associates cross-sectionally with glial inflammation and predicts accelerated tau accumulation in preclinical AD.
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