Prospective associations of blood-based biomarkers of neurodegenerative diseases with cognitive performance in a cohort of patients with chronic coronary syndrome

In a cohort of persons with chronic coronary syndrome, we investigated associations of blood-based biomarkers of neurodegenerative diseases with cognitive scores and mild cognitive impairment (MCI) after ten years. Biomarker levels were measured in baseline samples of serum (glial fibrillary acid pr...

Full description

Saved in:
Bibliographic Details
Main Authors: Lohner, Valerie (Author) , Perna, Laura (Author) , Schöttker, Ben (Author) , Perneczky, Robert (Author) , Kliegel, Matthias (Author) , Brenner, Hermann (Author) , Mons, Ute (Author)
Format: Article (Journal)
Language:English
Published: Dec 2025
In: Journal of Alzheimer's disease
Year: 2025, Volume: 108, Issue: 4, Pages: 1507-1513
ISSN:1875-8908
DOI:10.1177/13872877251389147
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1177/13872877251389147
Get full text
Author Notes:Valerie Lohner, Laura Perna, Ben Schottker, Robert Perneczky, Matthias Kliegel, Hermann Brenner and Ute Mons
Description
Summary:In a cohort of persons with chronic coronary syndrome, we investigated associations of blood-based biomarkers of neurodegenerative diseases with cognitive scores and mild cognitive impairment (MCI) after ten years. Biomarker levels were measured in baseline samples of serum (glial fibrillary acid protein, neurofilament light chain (NfL), phosphorylated tau181; n = 363) or plasma (amyloid-beta(42/40)-ratio, total-tau; n = 232). Cognitive scores and MCI were measured at ten-year follow-up using the Cognitive Telephone Screening Instrument. At follow-up, 14.7% had MCI. The amyloid-beta(42/40)-ratio was predictive of cognitive scores, while NfL was associated with increased risk of MCI, suggesting that these biomarkers might be utilized for risk stratification.
Item Description:Zuerst online veröffentlicht: November 18, 2025
Gesehen am 09.03.2026
Physical Description:Online Resource
ISSN:1875-8908
DOI:10.1177/13872877251389147