Plasma and neuroimaging biomarkers of small vessel disease and Alzheimer's disease in a diverse cohort: MESA.

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Tác giả: Nicholas J Ashton, Kaj Blennow, Suzanne Craft, Fernando Gonzalez-Ortiz, Mohamad Habes, Kathleen M Hayden, Susan R Heckbert, Kevin D Hiatt, Timothy M Hughes, Przemysław R Kac, Thomas K Karikari, Robert Koeppe, Samuel N Lockhart, Michelle M Mielke, Stephen R Rapp, Thomas C Register, Marc D Rudolph, Bonnie C Sachs, Courtney L Sutphen, Jordan Tanley, Christopher T Whitlow, Henrik Zetterberg

Ngôn ngữ: eng

Ký hiệu phân loại: 635.931 Groupings by life duration

Thông tin xuất bản: United States : medRxiv : the preprint server for health sciences , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 675669

INTRODUCTION: Little is known about how Alzheimer's disease (AD) plasma biomarkers relate to cerebral small vessel disease (cSVD) neuroimaging biomarkers. METHODS: The study involved 251 Wake Forest Multi-Ethnic Study of Atherosclerosis (MESA) Exam 6 participants with plasma AD biomarkers, MRI, amyloid PET, and adjudicated cognitive status. Multivariable models examined cross-sectional relationships between plasma and neuroimaging biomarkers, considering comorbidities. RESULTS: Lower Aβ42/Aβ40, and higher GFAP, NfL, and p-tau217 were associated with greater neurodegeneration. Lower plasma Aβ42/Aβ40 and higher p-tau217 and p-tau231 were associated with greater Aβ PET deposition. NfL was positively associated with WMH and WM Free Water. P-tau measures were positively associated with WM Free Water. Lower Aβ42/Aβ40 was associated with presence of microbleeds. GFAP was positively associated with WMH. DISCUSSION: We observed expected associations of plasma biomarkers with cognitive status and imaging biomarkers. GFAP, NfL, p-tau181, p-tau217, and p-tau231 are associated with cSVD in addition to AD-related pathology.
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