萎缩
神经退行性变
脑脊液
早发性阿尔茨海默病
后皮质萎缩
生物标志物
病理
疾病
医学
认知功能衰退
退行性疾病
内科学
神经科学
阿尔茨海默病
高强度
脑萎缩
痴呆
淀粉样蛋白(真菌学)
血管周围间隙
作者
Alexandra Touroutoglou,Yuta Katsumi,Jennifer Hensel,Suzanne E. Schindler,Laura Ibanez,Michael Brickhouse,Ani Eloyan,Ryan Eckbo,Alexander Zaitsev,Renaud La Joie,Maryanne Thangarajah,Alexander Taurone,Prashanthi Vemuri,Clifford R. Jack,Dustin B. Hammers,Tatiana Foroud,P Aisen,Beckett Ls,Robert Koeppe,Walter A. Kukull
摘要
INTRODUCTION: Although cerebrospinal fluid (CSF) biomarkers reflect neurodegeneration in Alzheimer's disease (AD), it remains unclear whether these biomarkers track neurodegeneration in early-onset Alzheimer's disease (EOAD). METHODS: In 80 EOAD patients, we examined correlations between eight CSF biomarker levels and cortical thickness decreases within the EOAD cortical atrophy signature. Significant correlations were then entered into a multiple regression analysis. We also examined contributions of EOAD atrophy and CSF biomarkers to cognitive impairment. RESULTS: The levels of four CSF biomarkers correlated to EOAD signature atrophy. Stepwise regression analyses revealed that CSF neurofilament light chain (NfL) levels best predicted EOAD signature atrophy. Multiple regression showed EOAD signature atrophy combined with CSF NfL levels explained more variance in cognitive impairment than either factor alone. DISCUSSION: Within EOAD patients, CSF NfL levels relate to the magnitude of cortical atrophy, and a combination of EOAD signature atrophy and CSF NfL levels most robustly predict cognitive impairment.
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