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Cerebrospinal Fluid Biomarkers and Amyloid-ß Elimination from the Brain in Cerebral Amyloid Angiopathy-Related Inflammation.
Sakai, Kenji; Noguchi-Shinohara, Moeko; Tanaka, Hidetomo; Ikeda, Tokuhei; Hamaguchi, Tsuyoshi; Kakita, Akiyoshi; Yamada, Masahito; Ono, Kenjiro.
Afiliación
  • Sakai K; Department of Neurology, Joetsu General Hospital, Joetsu, Japan.
  • Noguchi-Shinohara M; Department of Neurology, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
  • Tanaka H; Department of Neurology, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
  • Ikeda T; Department of Preemptive Medicine for Dementia, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
  • Hamaguchi T; Department of Pathology, Brain Research Institute, Niigata University, Niigata, Japan.
  • Kakita A; Department of Neurology, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
  • Yamada M; Department of Neurology, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
  • Ono K; Department of Neurology, Kanazawa Medical University, Uchinada, Japan.
J Alzheimers Dis ; 91(3): 1173-1183, 2023.
Article en En | MEDLINE | ID: mdl-36565118
ABSTRACT

BACKGROUND:

Cerebrospinal fluid (CSF) biomarkers in patients with cerebral amyloid angiopathy-related inflammation (CAA-ri) have demonstrated inconsistent results.

OBJECTIVE:

We investigated the relationship between CSF amyloidprotein (Aß) and vascular pathological findings to elucidate the mechanisms of Aß elimination from the brain in CAA-ri.

METHODS:

We examined Aß40 and Aß42 levels in CSF samples in 15 patients with CAA-ri and 15 patients with Alzheimer's disease and cerebral amyloid angiopathy (AD-CAA) using ELISA as a cross-sectional study. Furthermore, we pathologically examined Aß40 and Aß42 depositions on the leptomeningeal blood vessels (arteries, arterioles, and veins) using brain biopsy samples from six patients with acute CAA-ri and brain tissues of two autopsied patients with CAA-ri.

RESULTS:

The median Aß40 and Aß42 levels in the CSF showed no significant difference between pre-treatment CAA-ri (Aß40, 6837 pg/ml; Aß42, 324 pg/ml) and AD-CAA (Aß40, 7669 pg/ml, p = 0.345; Aß42, 355 pg/ml, p = 0.760). Aß40 and Aß42 levels in patients with post-treatment CAA-ri (Aß40, 1770 pg/ml, p = 0.056; Aß42, 167 pg/ml, p = 0.006) were lower than those in patients with pre-treatment CAA-ri. Regarding Aß40 and Aß42 positive arteries, acute CAA-ri cases showed a higher frequency of partially Aß-deposited blood vessels than postmortem CAA-ri cases (Aß40, 20.8% versus 3.9%, p = 0.0714; Aß42, 27.4% versus 2.0%, p = 0.0714, respectively).

CONCLUSION:

Lower levels of CSF Aß40 and Aß42 could be biomarkers for the cessation of inflammation in CAA-ri reflecting the recovery of the intramural periarterial drainage pathway and vascular function.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Angiopatía Amiloide Cerebral / Enfermedad de Alzheimer Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: J Alzheimers Dis Asunto de la revista: GERIATRIA / NEUROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Angiopatía Amiloide Cerebral / Enfermedad de Alzheimer Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: J Alzheimers Dis Asunto de la revista: GERIATRIA / NEUROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Japón