Impact of hs-CRP concentration on brain structure alterations and cognitive trajectory in Alzheimer’s disease
Present study was to investigate hs-CRP concentration, brain structural alterations, and cognitive function in the context of AD (Subjective cognitive decline [SCD], mild cognitive impairment [MCI], and AD). We retrospectively included 313 patients (Mean age= 76.40 years, 59 SCD, 101 MCI, 153 AD) in...
Gespeichert in:
Veröffentlicht in: | Frontiers in aging neuroscience 2023-08, Vol.15, p.1227325-1227325 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Present study was to investigate hs-CRP concentration, brain structural alterations, and cognitive function in the context of AD (Subjective cognitive decline [SCD], mild cognitive impairment [MCI], and AD). We retrospectively included 313 patients (Mean age= 76.40 years, 59 SCD, 101 MCI, 153 AD) in a cross-sectional analysis and 91 patients (Mean age= 75.83 years, 12 SCD, 43 MCI, 36 AD) in a longitudinal analysis. Multivariable linear regression was conducted to investigate the relationship between hs-CRP concentration and brain structural alterations, and cognitive function, respectively. Hs-CRP was positively associated with gray matter volume in the left fusiform (??= 0.16, pFDR= 0.023) and the left parahippocampal gyrus (??= 0.16, pFDR= 0.029). Posthoc analysis revealed that these associations were mainly driven by patients with MCI and AD. The interaction of diagnosis and CRP was significantly associated with annual cognitive changes (??= 0.43, p= 0.008). Among these patients with AD, lower baseline CRP was correlated with greater future cognitive decline (r= -0.41, p= 0.013). Our study suggests that increased hs-CRP level may exert protective effect on brain structure alterations and future cognitive changes among patients already with cognitive impairment. |
---|---|
ISSN: | 1663-4365 1663-4365 |
DOI: | 10.3389/fnagi.2023.1227325 |