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Cerebral Amyloid Angiopathy in Patients with Cognitive Impairment: Cerebrospinal Fluid Biomarkers.
Rothenberg, Kasia Gustaw; Bekris, Lynn; Leverenz, James B; Wu, Jenny; Lee, Jonathan; Statsevych, Volodymyr; Ruggieri, Paul; Jones, Stephen E.
Afiliación
  • Rothenberg KG; Lou Ruvo Center for Brain Health, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.
  • Bekris L; Genomic Medicine Institute Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.
  • Leverenz JB; Lou Ruvo Center for Brain Health, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.
  • Wu J; Department of Radiology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Lee J; Department of Radiology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Statsevych V; Department of Radiology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Ruggieri P; Department of Radiology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Jones SE; Department of Radiology, Cleveland Clinic, Cleveland, Ohio, USA.
Dement Geriatr Cogn Disord ; : 1-7, 2024 Jun 18.
Article en En | MEDLINE | ID: mdl-38889704
ABSTRACT

INTRODUCTION:

Cerebral amyloid angiopathy (CAA) is characterized by amyloid ß (Aß) deposition in brain vessels, leading to hemorrhagic phenomena and cognitive impairment. Magnetic resonance imaging (MRI)-based criteria allow a diagnosis of probable CAA in vivo, but such a diagnosis cannot predict the eventual development of CAA.

METHODS:

We conducted a retrospective cohort study of 464 patients with cognitive disorders whose data were included in a brain health biobank. De-identified parameters including sex, age, cognitive score, APOE status, and cerebrospinal fluid (CSF) levels of Aß 1-40, Aß 1-42, phosphorylated tau, and total tau were assessed in those with and without CAA. Odds ratios (ORs) and 95% confidence intervals (CIs) were determined.

RESULTS:

CAA was present in 53 of 464 (11.5%) patients. P-tau level was significantly higher in those with CAA (115 vs. 84.3 pg/mL p = 0.038). In univariate analyses, the risk of developing CAA was higher with increased age (OR, 1.036; 95% CI 1.008, 1.064; p = 0.011) and decreased CSF level of Aß 1-40 (OR, 0.685; 95% CI 0.534, 0.878; p = 0.003). In multivariate analyses, the risk of CAA remained higher with a decreased CSF level of Aß 1-40 (OR, 0.681; 95% CI 0.531, 0.874; p = 0.003).

CONCLUSION:

These findings suggest that Aß 1-40 levels in the CSF might be a useful molecular biomarker of CAA in patients with dementia.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Dement Geriatr Cogn Disord Asunto de la revista: GERIATRIA / NEUROLOGIA / PSIQUIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Dement Geriatr Cogn Disord Asunto de la revista: GERIATRIA / NEUROLOGIA / PSIQUIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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