Midlife cumulative deficit frailty predicts Alzheimer’s disease-related plasma biomarkers in older adults

Abstract Background The study explores whether frailty at midlife predicts mortality and levels of biomarkers associated with Alzheimer’s disease and related dementias (ADRD) and neurodegeneration by early old age. We also examine the heritability of frailty across this age period. Methods Participa...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Age and ageing 2024-03, Vol.53 (3)
Hauptverfasser: Buchholz, Erik, Gillespie, Nathan A, Hunt, Jack F, Reynolds, Chandra A, Rissman, Robert A, Schroeder, Angelica, Cortes, Isaac, Bell, Tyler, Lyons, Michael J, Kremen, William S, Franz, Carol E
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Abstract Background The study explores whether frailty at midlife predicts mortality and levels of biomarkers associated with Alzheimer’s disease and related dementias (ADRD) and neurodegeneration by early old age. We also examine the heritability of frailty across this age period. Methods Participants were 1,286 community-dwelling men from the Vietnam Era Twin Study of Aging at average ages 56, 62 and 68, all without ADRD at baseline. The cumulative deficit frailty index (FI) comprised 37 items assessing multiple physiological systems. Plasma biomarkers at age 68 included beta-amyloid (Aβ40, Aβ42), total tau (t-tau) and neurofilament light chain (NfL). Results Being frail doubled the risk of all-cause mortality by age 68 (OR = 2.44). Age 56 FI significantly predicted age 68 NfL (P = 0.014), Aβ40 (P = 0.001) and Aβ42 (P = 0.023), but not t-tau. Age 62 FI predicted all biomarkers at age 68: NfL (P = 0.023), Aβ40 (P = 0.002), Aβ42 (P = 0.001) and t-tau (P = 0.001). Age 68 FI scores were associated with age 68 levels of NfL (P = 0.027), Aβ40 (P 
ISSN:0002-0729
1468-2834
1468-2834
DOI:10.1093/ageing/afae028