Author
Listed:
- Chengjie Xiong
(Washington University
Washington University School of Medicine)
- Jingqin Luo
(Washington University School of Medicine
Washington University School of Medicine)
- David A. Wolk
(University of Pennsylvania)
- Leslie M. Shaw
(University of Pennsylvania
University of Pennsylvania)
- Erik D. Roberson
(University of Alabama at Birmingham)
- Charles F. Murchison
(University of Alabama at Birmingham)
- Rachel L. Henson
(Washington University School of Medicine)
- Tammie L. S. Benzinger
(Washington University School of Medicine
Washington University)
- Quoc Bui
(Washington University)
- Folasade Agboola
(Washington University)
- Elizabeth Grant
(Washington University)
- Emily N. Gremminger
(Washington University)
- Krista L. Moulder
(Washington University School of Medicine)
- David S. Geldmacher
(University of Alabama at Birmingham)
- Olivio J. Clay
(University of Alabama at Birmingham
University of Alabama at Birmingham)
- Ganesh Babulal
(Washington University School of Medicine)
- Carlos Cruchaga
(Washington University School of Medicine)
- David M. Holtzman
(Washington University School of Medicine)
- Randall J. Bateman
(Washington University School of Medicine)
- John C. Morris
(Washington University School of Medicine)
- Suzanne E. Schindler
(Washington University School of Medicine)
Abstract
Blood-based biomarkers of Alzheimer disease (AD) may facilitate testing of historically under-represented groups. The Study of Race to Understand Alzheimer Biomarkers (SORTOUT-AB) is a multi-center longitudinal study to compare AD biomarkers in participants who identify their race as either Black or white. Plasma samples from 324 Black and 1,547 white participants underwent analysis with C2N Diagnostics’ PrecivityAD test for Aβ42 and Aβ40. Compared to white individuals, Black individuals had higher average plasma Aβ42/40 levels at baseline, consistent with a lower average level of amyloid pathology. Interestingly, this difference resulted from lower average levels of plasma Aβ40 in Black participants. Despite the differences, Black and white individuals had similar longitudinal rates of change in Aβ42/40, consistent with a similar rate of amyloid accumulation. Our results agree with multiple recent studies demonstrating a lower prevalence of amyloid pathology in Black individuals, and additionally suggest that amyloid accumulates consistently across both groups.
Suggested Citation
Chengjie Xiong & Jingqin Luo & David A. Wolk & Leslie M. Shaw & Erik D. Roberson & Charles F. Murchison & Rachel L. Henson & Tammie L. S. Benzinger & Quoc Bui & Folasade Agboola & Elizabeth Grant & Em, 2024.
"Baseline levels and longitudinal changes in plasma Aβ42/40 among Black and white individuals,"
Nature Communications, Nature, vol. 15(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-49859-w
DOI: 10.1038/s41467-024-49859-w
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