Cross-Sectional Exploration of Plasma Biomarkers of Alzheimer’s Disease in Down Syndrome: Early Data from the Longitudinal Investigation for Enhancing Down Syndrome Research (LIFE-DSR) Study
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Published:2021-04-28
Issue:9
Volume:10
Page:1907
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ISSN:2077-0383
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Container-title:Journal of Clinical Medicine
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language:en
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Short-container-title:JCM
Author:
Hendrix James A.ORCID, Airey David C., Britton Angela, Burke Anna D., Capone George T., Chavez Ronelyn, Chen Jacqueline, Chicoine Brian, Costa Alberto C. S.ORCID, Dage Jeffrey L.ORCID, Doran Eric, Esbensen Anna, Evans Casey L., Faber Kelley M., Foroud Tatiana M., Hart SarahORCID, Haugen Kelsey, Head Elizabeth, Hendrix Suzanne, Hillerstrom Hampus, Kishnani Priya S., Krell Kavita, Ledesma Duvia Lara, Lai Florence, Lott Ira, Ochoa-Lubinoff Cesar, Mason Jennifer, Nicodemus-Johnson Jessie, Proctor Nicholas Kyle, Pulsifer Margaret B., Revta Carolyn, Rosas H. Diana, Rosser Tracie C., Santoro Stephanie, Schafer Kim, Scheidemantel Thomas, Schmitt FrederickORCID, Skotko Brian G.ORCID, Stasko Melissa R., Talboy Amy, Torres Amy, Wilmes Kristi, Woodward JasonORCID, Zimmer Jennifer A., Feldman Howard H., Mobley William
Abstract
With improved healthcare, the Down syndrome (DS) population is both growing and aging rapidly. However, with longevity comes a very high risk of Alzheimer’s disease (AD). The LIFE-DSR study (NCT04149197) is a longitudinal natural history study recruiting 270 adults with DS over the age of 25. The study is designed to characterize trajectories of change in DS-associated AD (DS-AD). The current study reports its cross-sectional analysis of the first 90 subjects enrolled. Plasma biomarkers phosphorylated tau protein (p-tau), neurofilament light chain (NfL), amyloid β peptides (Aβ1-40, Aβ1-42), and glial fibrillary acidic protein (GFAP) were undertaken with previously published methods. The clinical data from the baseline visit include demographics as well as the cognitive measures under the Severe Impairment Battery (SIB) and Down Syndrome Mental Status Examination (DS-MSE). Biomarker distributions are described with strong statistical associations observed with participant age. The biomarker data contributes to understanding DS-AD across the spectrum of disease. Collectively, the biomarker data show evidence of DS-AD progression beginning at approximately 40 years of age. Exploring these data across the full LIFE-DSR longitudinal study population will be an important resource in understanding the onset, progression, and clinical profiles of DS-AD pathophysiology.
Cited by
16 articles.
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