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Serum and cerebrospinal fluid neurofilament light chain and glial fibrillary acid protein levels in early and advanced stages of cerebral amyloid Angiopathy.
Rasing, Ingeborg; Voigt, Sabine; Koemans, Emma A; de Kort, Anna M; van Harten, Thijs W; van Etten, Ellis S; van Zwet, Erik W; Stoops, Erik; Francois, Cindy; Kuiperij, H Bea; Klijn, Catharina J M; Schreuder, Floris H B M; van der Weerd, Louise; van Osch, Matthias J P; van Walderveen, Marianne A A; Verbeek, Marcel M; Terwindt, Gisela M; Wermer, Marieke J H.
Affiliation
  • Rasing I; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands. i.rasing@lumc.nl.
  • Voigt S; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
  • Koemans EA; Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
  • de Kort AM; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
  • van Harten TW; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van Etten ES; Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
  • van Zwet EW; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
  • Stoops E; Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, The Netherlands.
  • Francois C; ADx NeuroSciences, Ghent, Belgium.
  • Kuiperij HB; ADx NeuroSciences, Ghent, Belgium.
  • Klijn CJM; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Schreuder FHBM; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van der Weerd L; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van Osch MJP; Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
  • van Walderveen MAA; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Verbeek MM; Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
  • Terwindt GM; Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
  • Wermer MJH; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Alzheimers Res Ther ; 16(1): 86, 2024 04 23.
Article in En | MEDLINE | ID: mdl-38654326
ABSTRACT

BACKGROUND:

Neurofilament light chain (NFL) is a biomarker for neuroaxonal damage and glial fibrillary acidic protein (GFAP) for reactive astrocytosis. Both processes occur in cerebral amyloid angiopathy (CAA), but studies investigating the potential of NFL and GFAP as markers for CAA are lacking. We aimed to investigate NFL and GFAP as biomarkers for neuroaxonal damage and astrocytosis in CAA.

METHODS:

For this cross-sectional study serum and cerebrospinal fluid (CSF) samples were collected between 2010 and 2020 from controls, (pre)symptomatic Dutch-type hereditary (D-CAA) mutation-carriers and participants with sporadic CAA (sCAA) from two prospective CAA studies at two University hospitals in the Netherlands. NFL and GFAP levels were measured with Simoa-assays. The association between NFL and GFAP levels and age, cognitive performance (MoCA), CAA-related MRI markers (CAA-CSVD-burden) and Aß40 and Aß42 levels in CSF were assessed with linear regression adjusted for confounders. The control group was divided in age < 55 and ≥55 years to match the specific groups.

RESULTS:

We included 187

participants:

28 presymptomatic D-CAA mutation-carriers (mean age 40 years), 29 symptomatic D-CAA participants (mean age 58 years), 59 sCAA participants (mean age 72 years), 33 controls < 55 years (mean age 42 years) and 38 controls ≥ 55 years (mean age 65 years). In presymptomatic D-CAA, only GFAP in CSF (7.7*103pg/mL vs. 4.4*103pg/mL in controls; P<.001) was increased compared to controls. In symptomatic D-CAA, both serum (NFL26.2pg/mL vs. 12.5pg/mL; P=0.008, GFAP130.8pg/mL vs. 123.4pg/mL; P=0.027) and CSF (NFL16.8*102pg/mL vs. 7.8*102pg/mL; P=0.01 and GFAP11.4*103pg/mL vs. 7.5*103pg/mL; P<.001) levels were higher than in controls and serum levels (NFL26.2pg/mL vs. 6.7pg/mL; P=0.05 and GFAP130.8pg/mL vs. 66.0pg/mL; P=0.004) were higher than in pre-symptomatic D-CAA. In sCAA, only NFL levels were increased compared to controls in both serum (25.6pg/mL vs. 12.5pg/mL; P=0.005) and CSF (20.0*102pg/mL vs 7.8*102pg/mL; P=0.008). All levels correlated with age. Serum NFL correlated with MoCA (P=0.008) and CAA-CSVD score (P<.001). NFL and GFAP in CSF correlated with Aß42 levels (P=0.01/0.02).

CONCLUSIONS:

GFAP level in CSF is an early biomarker for CAA and is increased years before symptom onset. NFL and GFAP levels in serum and CSF are biomarkers for advanced CAA.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Neurofilament Proteins / Cerebral Amyloid Angiopathy / Glial Fibrillary Acidic Protein Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Alzheimers Res Ther Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Neurofilament Proteins / Cerebral Amyloid Angiopathy / Glial Fibrillary Acidic Protein Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Alzheimers Res Ther Year: 2024 Document type: Article Affiliation country: