TY - JOUR
T1 - Large-scale plasma proteomic profiling unveils diagnostic biomarkers and pathways for Alzheimer’s disease
AU - Heo, Gyujin
AU - Xu, Ying
AU - Wang, Erming
AU - Ali, Muhammad
AU - Oh, Hamilton Se Hwee
AU - Moran-Losada, Patricia
AU - Anastasi, Federica
AU - González Escalante, Armand
AU - Puerta, Raquel
AU - Song, Soomin
AU - Timsina, Jigyasha
AU - Liu, Menghan
AU - Western, Daniel
AU - Gong, Katherine
AU - Chen, Yike
AU - Kohlfeld, Pat
AU - Flynn, Allison
AU - Thomas, Alvin G.
AU - Lowery, Joseph
AU - Morris, John C.
AU - Holtzman, David M.
AU - Perlmutter, Joel S.
AU - Schindler, Suzanne E.
AU - Vilor-Tejedor, Natalia
AU - Suárez-Calvet, Marc
AU - García-González, Pablo
AU - Marquié, Marta
AU - Fernández, Maria Victoria
AU - Boada, Mercè
AU - Cano, Amanda
AU - Ruiz, Agustín
AU - Zhang, Bin
AU - Bennett, David A.
AU - Benzinger, Tammie
AU - Wyss-Coray, Tony
AU - Ibanez, Laura
AU - Sung, Yun Ju
AU - Cruchaga, Carlos
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature America, Inc. 2025.
PY - 2025/6
Y1 - 2025/6
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=105005548547&partnerID=8YFLogxK
U2 - 10.1038/s43587-025-00872-8
DO - 10.1038/s43587-025-00872-8
M3 - Article
C2 - 40394224
AN - SCOPUS:105005548547
SN - 2662-8465
VL - 5
SP - 1114
EP - 1131
JO - Nature Aging
JF - Nature Aging
IS - 6
ER -