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Clinical utility of cerebrospinal fluid biomarkers measured by LUMIPULSE® system.
Nojima, Hisashi; Ito, Satoshi; Kushida, Akira; Abe, Aki; Motsuchi, Wataru; Verbel, David; Vandijck, Manu; Jannes, Geert; Vandenbroucke, Ina; Aoyagi, Katsumi.
Afiliação
  • Nojima H; FUJIREBIO Inc., 2-1-1, Nishishinjuku, Shinjuku-ku, Tokyo, 163-0410, Japan.
  • Ito S; Eisai Co., Ltd. 4-6-10 Koishikawa, Bunkyo-ku, Tokyo, 112-8088, Japan.
  • Kushida A; Eisai Inc., 200 Metro Boulevard, Nutley, New Jersey, 07110, USA.
  • Abe A; FUJIREBIO Inc., 2-1-1, Nishishinjuku, Shinjuku-ku, Tokyo, 163-0410, Japan.
  • Motsuchi W; FUJIREBIO Inc., 2-1-1, Nishishinjuku, Shinjuku-ku, Tokyo, 163-0410, Japan.
  • Verbel D; FUJIREBIO Inc., 2-1-1, Nishishinjuku, Shinjuku-ku, Tokyo, 163-0410, Japan.
  • Vandijck M; Eisai Inc., 200 Metro Boulevard, Nutley, New Jersey, 07110, USA.
  • Jannes G; Fujirebio-Europe N.V., Technologiepark 6, 9052, Ghent, Belgium.
  • Vandenbroucke I; Fujirebio-Europe N.V., Technologiepark 6, 9052, Ghent, Belgium.
  • Aoyagi K; Fujirebio-Europe N.V., Technologiepark 6, 9052, Ghent, Belgium.
Ann Clin Transl Neurol ; 9(12): 1898-1909, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36321325
OBJECTIVES: Cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease (AD) are well-established in research settings, but their use in routine clinical practice remains a largely unexploited potential. Here, we examined the relationship between CSF biomarkers, measured by a fully automated immunoassay platform, and brain ß-amyloid (Aß) deposition status confirmed by amyloid positron emission tomography (PET). METHODS: One hundred ninety-nine CSF samples from clinically diagnosed AD patients enrolled in a clinical study and who underwent amyloid PET were used for the measurement of CSF biomarkers Aß 1-40 (Aß40), Aß 1-42 (Aß42), total tau (t-Tau), and phosphorylated tau-181 (p-Tau181) using the LUMIPULSE system. These biomarkers and their combinations were compared to amyloid PET classification (negative or positive) using visual read assessments. Several combinations were also analyzed with a multivariable logistic regression model. RESULTS: Aß42, t-Tau, and p-Tau181, and the ratios of Aß42 with other biomarkers had a good diagnostic agreement with amyloid PET imaging. The multivariable logistic regression analysis showed that amyloid PET status was associated with Aß40 and Aß42, but other factors, such as MMSE, sex, t-Tau, and p-Tau181, did not significantly add information to the model. CONCLUSIONS: CSF biomarkers measured with the LUMIPULSE system showed good agreement with amyloid PET imaging. The ratio of Aß42 with the other analyzed biomarkers showed a higher correlation with amyloid PET than Aß42 alone, suggesting that the combinations of biomarkers could be useful in the diagnostic assessment in clinical research and potentially in routine clinical practice.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Alzheimer Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Alzheimer Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article