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Journal of Alzheimer's disease : JAD · 2020

Validation of Plasma Proteomic Biomarkers Relating to Brain Amyloid Burden in the EMIF-Alzheimer's Disease Multimodal Biomarker Discovery Cohort.

СтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАВалидационное исследованиеНазвание и аннотация: Перевод пока не подготовлен
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Westwood Sarah, Baird Alison L, Anand Sneha N, Nevado-Holgado Alejo J, Kormilitzin Andrey, Shi Liu, Hye Abdul, Ashton Nicholas J, Morgan Angharad R, Bos Isabelle, Vos Stephanie J B, Baker Susan, Buckley Noel J, Ten Kate Mara, Scheltens Philip, Teunissen Charlotte E, Vandenberghe Rik, Gabel Silvy, Meersmans Karen, Engelborghs Sebastiaan, De Roeck Ellen E, Sleegers Kristel, Frisoni Giovanni B, Blin Olivier, Richardson Jill C, Bordet Régis, Molinuevo José L, Rami Lorena, Wallin Anders, Kettunen Petronella, Tsolaki Magda, Verhey Frans, Lléo Alberto, Sala Isabel, Popp Julius, Peyratout Gwendoline, Martinez-Lage Pablo, Tainta Mikel, Johannsen Peter, Freund-Levi Yvonne, Frölich Lutz, Dobricic Valerija, Legido-Quigley Cristina, Bertram Lars, Barkhof Frederik, Zetterberg Henrik, Morgan B Paul, Streffer Johannes, Visser Pieter Jelle, Lovestone Simon

Аннотация

We have previously investigated, discovered, and replicated plasma protein biomarkers for use to triage potential trials participants for PET or cerebrospinal fluid measures of Alzheimer's disease (AD) pathology. This study sought to undertake validation of these candidate plasma biomarkers in a large, multi-center sample collection. Targeted plasma analyses of 34 proteins with prior evidence for prediction of in vivo pathology were conducted in up to 1,000 samples from cognitively healthy elderly individuals, people with mild cognitive impairment, and in patients with AD-type dementia, selected from the EMIF-AD catalogue. Proteins were measured using Luminex xMAP, ELISA, and Meso Scale Discovery assays. Seven proteins replicated in their ability to predict in vivo amyloid pathology. These proteins form a biomarker panel that, along with age, could significantly discriminate between individuals with high and low amyloid pathology with an area under the curve of 0.74. The performance of this biomarker panel remained consistent when tested in apolipoprotein E ɛ4 non-carrier individuals only. This blood-based panel is biologically relevant, measurable using practical immunocapture arrays, and could significantly reduce the cost incurred to clinical trials through screen failure.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты