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Nature aging · 2025

Large-scale plasma proteomic profiling unveils diagnostic biomarkers and pathways for Alzheimer's disease.

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Heo Gyujin, Xu Ying, Wang Erming, Ali Muhammad, Oh Hamilton Se-Hwee, Moran-Losada Patricia, Anastasi Federica, González Escalante Armand, Puerta Raquel, Song Soomin, Timsina Jigyasha, Liu Menghan, Western Daniel, Gong Katherine, Chen Yike, Kohlfeld Pat, Flynn Allison, Thomas Alvin G, Lowery Joseph, Morris John C, Holtzman David M, Perlmutter Joel S, Schindler Suzanne E, Vilor-Tejedor Natalia, Suárez-Calvet Marc, García-González Pablo, Marquié Marta, Fernández Maria Victoria, Boada Mercè, Cano Amanda, Ruiz Agustín, Zhang Bin, Bennett David A, Benzinger Tammie, Wyss-Coray Tony, Ibanez Laura, Sung Yun Ju, Cruchaga Carlos

Аннотация

Proteomic studies have been instrumental in identifying brain, cerebrospinal fluid and plasma proteins associated with Alzheimer's disease (AD). Here, we comprehensively examined 6,905 aptamers corresponding to 6,106 unique proteins in plasma in more than 3,300 well-characterized individuals to identify new proteins, pathways and predictive models for AD. We identified 416 proteins (294 new) associated with clinical AD status and validated the findings in two external datasets representing more than 7,000 samples. AD-related proteins reflected blood-brain barrier disruption and other processes implicated in AD, such as lipid dysregulation or immune responses. A machine learning model was used to identify a set of seven proteins that were highly predictive of both clinical AD (area under the curve (AUC) of >0.72) and biomarker-defined AD status (AUC of >0.88), which were replicated in multiple external cohorts and orthogonal platforms. These findings underscore the potential of using plasma proteins as biomarkers for the early detection and monitoring of AD and for guiding treatment decisions.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты