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Cerebrospinal fluid cytokines and metalloproteinases in cerebral amyloid angiopathy-related inflammation.
Sakai, Kenji; Noguchi-Shinohara, Moeko; Ikeda, Tokuhei; Hamaguchi, Tsuyoshi; Ono, Kenjiro; Yamada, Masahito.
Afiliación
  • Sakai K; Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
  • Noguchi-Shinohara M; Department of Neurology and Neurobiology of Aging, 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 Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
  • Ono K; Department of Neurology, Ishikawa Prefectural Central Hospital, Kanazawa, Japan.
  • Yamada M; Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
Acta Neurol Scand ; 143(4): 450-457, 2021 Apr.
Article en En | MEDLINE | ID: mdl-33247941
ABSTRACT

OBJECTIVES:

To clarify pathomechanisms of cerebral amyloid angiopathy-related inflammation/vasculitis (CAA-ri).

METHODS:

We collected cerebrospinal fluid (CSF) samples of nine patients with CAA-ri of before (acute CAA-ri group) and after treatment (post-treatment CAA-ri group) and nine patients with CAA (CAA without inflammation group). We examined anti-amyloid ß protein (Aß) antibody titer by ELISA, and measured 27 Cytokines, nine matrix metalloproteinases (MMPs), and four tissue inhibitors of MMPs (TIMPs) by multiplexed fluorescent bead-based immunoassay.

RESULTS:

We demonstrated TIMP-2 (median) in CSF of the acute CAA-ri group (30,994.49 pg/ml, p = 0.007) and the post-treatment CAA-ri group (36,430.97 pg/ml, p = 0.001) was significantly elevated compared to that of the CAA without inflammation group (22,013.58 pg/ml). TIMP-1 was also higher in the post-treatment CAA-ri group than that in the CAA without inflammation group (58,167.75 pg/ml vs. 45,770.03 pg/ml, p = 0.005). There was a significant positive correlation between TIMP-1 and anti-Aß antibodies in CAA-ri (rs  = 0.900, p = 0.037). Median MMP-2 tended to be higher in the acute and post-treatment CAA-ri groups (10,619.82 pg/ml and 8396.98 pg/ml, respectively) than in the CAA without inflammation group (4436.34 pg/ml). Platelet-derived growth factor (PDGF)-BB levels before treatment were higher than those after treatment (median, 12.66 pg/ml vs. 6.39 pg/ml; p = 0.011) and correlated with the titer of anti-Aß antibodies (rs  =0.900, p = 0.037).

CONCLUSIONS:

Elevated levels of MMP-2, TIMP-1, and TIMP-2 might be related to the development of CAA-ri. Elevation of PDGF-BB could be a useful marker for clinical diagnosis of CAA-ri.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Citocinas / Angiopatía Amiloide Cerebral / Mediadores de Inflamación / Metaloproteasas Tipo de estudio: Observational_studies Idioma: En Revista: Acta Neurol Scand Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Citocinas / Angiopatía Amiloide Cerebral / Mediadores de Inflamación / Metaloproteasas Tipo de estudio: Observational_studies Idioma: En Revista: Acta Neurol Scand Año: 2021 Tipo del documento: Article