Plasma Oligomer β-Amyloid and White Matter Microstructural Integrity in Cognitively Normal Older Adults According to

Sheng-Min Wang1, Dong Woo Kang, Yoo Hyun Um

  • 1Hyun Kook Lim, MD, PhD, Department of Psychiatry, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 10, 63-ro, Yeongdeungpo-gu, Seoul, Korea, Tel; +82-2-3779-1048, Fax: +82-2-780-6577,

Abstract

Insights

Plasma oligomeric amyloid-β (OAβ) levels measured by MDS-OAβ may indicate earlier Alzheimer's disease pathology than cerebral amyloid-β deposition. Elevated plasma OAβ is linked to brain amyloid burden and white matter integrity changes in cognitively normal adults.

Area of Science:

  • Neuroscience
  • Biomarkers
  • Alzheimer's Disease Research

Background:

  • Plasma oligomeric amyloid-β (OAβ) measured by Multimer Detection System-oligomeric amyloid-β (MDS-OAβ) is associated with early Alzheimer's disease (AD) pathology.
  • Previous research has not examined MDS-OAβ differences in cognitively normal (CN) older adults based on cerebral Aβ burden.
  • The correlation between plasma OAβ, cerebral Aβ deposition, and white matter (WM) integrity in CN individuals requires investigation.

Purpose of the Study:

  • To investigate the associations among cerebral Aβ burden, plasma OAβ levels (MDS-OAβ), and WM integrity in cognitively normal older adults.
  • To compare MDS-OAβ levels and WM integrity between CN individuals with and without cerebral Aβ deposition.

Main Methods:

  • Cross-sectional study utilizing data from the Catholic Aging Brain Imaging (CABI) database.
  • Participants included 34 amyloid-PET negative and 23 amyloid-PET positive cognitively normal individuals.
  • Measurements included plasma OAβ (MDS-OAβ), cerebral Aβ deposition (SUVR), WM integrity (FA, MD), and cortical thickness from structural MRI.

Main Results:

  • Amyloid-PET positive individuals had higher MDS-OAβ levels than amyloid-PET negative individuals (P <0.005).
  • MDS-OAβ positive individuals showed higher cerebral Aβ deposition (P <0.05) and reduced regional WM integrity (FA, P <0.05) and cortical thickness (P <0.05).
  • MDS-OAβ levels positively correlated with cerebral Aβ deposition (r=0.278, P <0.05) and negatively with WM integrity (r = -0.324, P <0.05).

Conclusions:

  • MDS-OAβ levels may reflect earlier or different Alzheimer's disease pathology compared to cerebral Aβ retention identified by amyloid-PET.
  • Longitudinal studies are necessary to understand the causal relationships between plasma OAβ, cerebral Aβ, WM integrity, and cortical atrophy in the AD continuum.