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Nature communications · 2024

Comparative neurofilament light chain trajectories in CSF and plasma in autosomal dominant Alzheimer's disease.

Сравнительное исследованиеСтатьяМногоцентровое исследованиеНаблюдательное исследованиеПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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Hofmann Anna, Häsler Lisa M, Lambert Marius, Kaeser Stephan A, Gräber-Sultan Susanne, Obermüller Ulrike, Kuder-Buletta Elke, la Fougere Christian, Laske Christoph, Vöglein Jonathan, Levin Johannes, Fox Nick C, Ryan Natalie S, Zetterberg Henrik, Llibre-Guerra Jorge J, Perrin Richard J, Ibanez Laura, Schofield Peter R, Brooks William S, Day Gregory S, Farlow Martin R, Allegri Ricardo F, Chrem Mendez Patricio, Ikeuchi Takeshi, Kasuga Kensaku, Lee Jae-Hong, Roh Jee Hoon, Mori Hiroshi, Lopera Francisco, Bateman Randall J, McDade Eric, Gordon Brian A, Chhatwal Jasmeer P, Jucker Mathias, Schultz Stephanie A, Dominantly Inherited Alzheimer Network

Аннотация

Disease-modifying therapies for Alzheimer's disease (AD) are likely to be most beneficial when initiated in the presymptomatic phase. To track the benefit of such interventions, fluid biomarkers are of great importance, with neurofilament light chain protein (NfL) showing promise for monitoring neurodegeneration and predicting cognitive outcomes. Here, we update and complement previous findings from the Dominantly Inherited Alzheimer Network Observational Study by using matched cross-sectional and longitudinal cerebrospinal fluid (CSF) and plasma samples from 567 individuals, allowing timely comparative analyses of CSF and blood trajectories across the entire disease spectrum. CSF and plasma trajectories were similar at presymptomatic stages, discriminating mutation carriers from non-carrier controls 10-20 years before the estimated onset of clinical symptoms, depending on the statistical model used. However, after symptom onset the rate of change in CSF NfL continued to increase steadily, whereas the rate of change in plasma NfL leveled off. Both plasma and CSF NfL changes were associated with grey-matter atrophy, but not with Aβ-PET changes, supporting a temporal decoupling of Aβ deposition and neurodegeneration. These observations support NfL in both CSF and blood as an early marker of neurodegeneration but suggest that NfL measured in the CSF may be better suited for monitoring clinical trial outcomes in symptomatic AD patients.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты