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Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and implicates causal proteins for Alzheimer's disease.

Authors :
Western D
Timsina J
Wang L
Wang C
Yang C
Phillips B
Wang Y
Liu M
Ali M
Beric A
Gorijala P
Kohlfeld P
Budde J
Levey AI
Morris JC
Perrin RJ
Ruiz A
Marquié M
Boada M
de Rojas I
Rutledge J
Oh H
Wilson EN
Le Guen Y
Reus LM
Tijms B
Visser PJ
van der Lee SJ
Pijnenburg YAL
Teunissen CE
Del Campo Milan M
Alvarez I
Aguilar M
Greicius MD
Pastor P
Pulford DJ
Ibanez L
Wyss-Coray T
Sung YJ
Cruchaga C
Source :
Nature genetics [Nat Genet] 2024 Dec; Vol. 56 (12), pp. 2672-2684. Date of Electronic Publication: 2024 Nov 11.
Publication Year :
2024

Abstract

The integration of quantitative trait loci (QTLs) with disease genome-wide association studies (GWASs) has proven successful in prioritizing candidate genes at disease-associated loci. QTL mapping has been focused on multi-tissue expression QTLs or plasma protein QTLs (pQTLs). We generated a cerebrospinal fluid (CSF) pQTL atlas by measuring 6,361 proteins in 3,506 samples. We identified 3,885 associations for 1,883 proteins, including 2,885 new pQTLs, demonstrating unique genetic regulation in CSF. We identified CSF-enriched pleiotropic regions on chromosome (chr)3q28 near OSTN and chr19q13.32 near APOE that were enriched for neuron specificity and neurological development. We integrated our associations with Alzheimer's disease (AD) through proteome-wide association study (PWAS), colocalization and Mendelian randomization and identified 38 putative causal proteins, 15 of which have drugs available. Finally, we developed a proteomics-based AD prediction model that outperforms genetics-based models. These findings will be instrumental to further understand the biology and identify causal and druggable proteins for brain and neurological traits.<br />Competing Interests: Competing interests: C.C. has received research support from GSK and Eisai. The funders of the study had no role in the collection, analysis or interpretation of data; in the writing of the report; or in the decision to submit the paper for publication. C.C. is a member of the advisory board of Circular Genomics and owns stocks in this company. D.J.P. is an employee of GSK and holds stock in GSK. M.d.C.M. has been an invited speaker at Eisai. M.d.C.M. is an associate editor at Alzheimer’s Research and Therapy. B.T. and P.J.V. are inventors on a patent (WO2020197399A1, owned by Stichting VUmc). C.E.T. has a collaboration contract with ADx Neurosciences, Quanterix and Eli Lilly and performed contract research or received grants from AC Immune, Axon Neuroscience, BioConnect, Bioorchestra, Brainstorm Therapeutics, Celgene, EIP Pharma, Eisai, Grifols, Novo Nordisk, PeopleBio, Roche, Toyama and Vivoryon. She serves on editorial boards of Medidact Neurologie–Springer, Alzheimer’s Research and Therapy and Neurology: Neuroimmunology and Neuroinflammation and is an editor of the Neuromethods book (Springer). She had speaker contracts for Roche, Grifols and Novo Nordisk. The rest of the authors declare no competing interest.<br /> (© 2024. The Author(s), under exclusive licence to Springer Nature America, Inc.)

Details

Language :
English
ISSN :
1546-1718
Volume :
56
Issue :
12
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
39528825
Full Text :
https://doi.org/10.1038/s41588-024-01972-8