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Article: Body fluid biomarkers and psychosis risk in The Accelerating Medicines Partnership® Schizophrenia Program: design considerations

TitleBody fluid biomarkers and psychosis risk in The Accelerating Medicines Partnership® Schizophrenia Program: design considerations
Authors
Issue Date21-May-2025
PublisherNature Publishing Group UK
Citation
Schizophrenia, 2025, v. 11 How to Cite?
Abstract

Advances in proteomic assay methodologies and genomics have significantly improved our understanding of the blood proteome. Schizophrenia and psychosis risk are linked to polygenic scores for schizophrenia and other mental disorders, as well as to altered blood and saliva levels of biomarkers involved in hormonal signaling, redox balance, and chronic systemic inflammation. The Accelerating Medicines Partnership® Schizophrenia (AMP®SCZ) aims to ascertain biomarkers that both predict clinical outcomes and provide insights into the biological processes driving clinical outcomes in persons meeting CHR criteria. AMP®SCZ will follow almost 2000 CHR and 640 community study participants for two years, assessing biomarkers at baseline and two-month follow-up including the collection of blood and saliva samples. The following provides the rationale and methods for plans to utilize polygenic risk scores for schizophrenia and other disorders, salivary cortisol levels, and a discovery-based proteomic platform for plasma analyses. We also provide details about the standardized methods used to collect and store these biological samples, as well as the study participant metadata and quality control measures related to preanalytical factors that could influence the values of the biomarkers. Finally, we discuss our plans for analyzing the results of blood- and saliva-based biomarkers. Watch Dr. Perkins discuss their work and this article: https://vimeo.com/1062879582?share=copy#t=0.


Persistent Identifierhttp://hdl.handle.net/10722/357957
ISSN
2023 Impact Factor: 3.0
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorPerkins, Diana O-
dc.contributor.authorJeffries, Clark D-
dc.contributor.authorClark, Scott R-
dc.contributor.authorUpthegrove, Rachel-
dc.contributor.authorWannan, Cassandra M J-
dc.contributor.authorWray, Naomi R-
dc.contributor.authorLi, Qingqin S-
dc.contributor.authorDo, Kim Q-
dc.contributor.authorWalker, Elaine-
dc.contributor.authorPaul, Amminger G-
dc.contributor.authorAnticevic, Alan-
dc.contributor.authorCotter, David-
dc.contributor.authorEllman, Lauren M-
dc.contributor.authorMongan, David-
dc.contributor.authorPhassouliotis, Christina-
dc.contributor.authorBarbee, Jenna-
dc.contributor.authorRoth, Sharin-
dc.contributor.authorBillah, Tashrif-
dc.contributor.authorCorcoran, Cheryl-
dc.contributor.authorCalkins, Monica E-
dc.contributor.authorCerrato, Felecia-
dc.contributor.authorKhadimallah, Ines-
dc.contributor.authorKlauser, Paul-
dc.contributor.authorWinter-van, Rossum Inge-
dc.contributor.authorNunez, Angela R-
dc.contributor.authorBleggi, Rachel S-
dc.contributor.authorMartin, Alicia R-
dc.contributor.authorBouix, Sylvain-
dc.contributor.authorPasternak, Ofer-
dc.contributor.authorShah, Jai L-
dc.contributor.authorToben, Catherine-
dc.contributor.authorWolf, Daniel H-
dc.contributor.authorKahn, Rene S-
dc.contributor.authorKane, John M-
dc.contributor.authorMcGorry, Patrick D-
dc.contributor.authorBearden, Carrie E-
dc.contributor.authorNelson, Barnaby-
dc.contributor.authorShenton, Martha E-
dc.contributor.authorWoods, Scott W-
dc.contributor.authorSuen, Yi Nam-
dc.contributor.authorAccelerating Medicines Partnership® Schizophrenia-
dc.date.accessioned2025-07-23T00:30:57Z-
dc.date.available2025-07-23T00:30:57Z-
dc.date.issued2025-05-21-
dc.identifier.citationSchizophrenia, 2025, v. 11-
dc.identifier.issn2754-6993-
dc.identifier.urihttp://hdl.handle.net/10722/357957-
dc.description.abstract<p>Advances in proteomic assay methodologies and genomics have significantly improved our understanding of the blood proteome. Schizophrenia and psychosis risk are linked to polygenic scores for schizophrenia and other mental disorders, as well as to altered blood and saliva levels of biomarkers involved in hormonal signaling, redox balance, and chronic systemic inflammation. The Accelerating Medicines Partnership® Schizophrenia (AMP®SCZ) aims to ascertain biomarkers that both predict clinical outcomes and provide insights into the biological processes driving clinical outcomes in persons meeting CHR criteria. AMP®SCZ will follow almost 2000 CHR and 640 community study participants for two years, assessing biomarkers at baseline and two-month follow-up including the collection of blood and saliva samples. The following provides the rationale and methods for plans to utilize polygenic risk scores for schizophrenia and other disorders, salivary cortisol levels, and a discovery-based proteomic platform for plasma analyses. We also provide details about the standardized methods used to collect and store these biological samples, as well as the study participant metadata and quality control measures related to preanalytical factors that could influence the values of the biomarkers. Finally, we discuss our plans for analyzing the results of blood- and saliva-based biomarkers. Watch Dr. Perkins discuss their work and this article: <a href="https://vimeo.com/1062879582?share=copy#t=0">https://vimeo.com/1062879582?share=copy#t=0</a>.<br></p>-
dc.languageeng-
dc.publisherNature Publishing Group UK-
dc.relation.ispartofSchizophrenia-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleBody fluid biomarkers and psychosis risk in The Accelerating Medicines Partnership® Schizophrenia Program: design considerations-
dc.typeArticle-
dc.identifier.doi10.1038/s41537-025-00610-4-
dc.identifier.volume11-
dc.identifier.eissn2754-6993-
dc.identifier.isiWOS:001493761500001-

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