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

IF 3 Q2 PSYCHIATRY
Diana O Perkins, Clark D Jeffries, Scott R Clark, Rachel Upthegrove, Cassandra M J Wannan, Naomi R Wray, Qingqin S Li, Kim Q Do, Elaine Walker, G Paul Amminger, Alan Anticevic, David Cotter, Lauren M Ellman, David Mongan, Christina Phassouliotis, Jenna Barbee, Sharin Roth, Tashrif Billah, Cheryl Corcoran, Monica E Calkins, Felecia Cerrato, Ines Khadimallah, Paul Klauser, Inge Winter-van Rossum, Angela R Nunez, Rachel S Bleggi, Alicia R Martin, Sylvain Bouix, Ofer Pasternak, Jai L Shah, Catherine Toben, Daniel H Wolf, Rene S Kahn, John M Kane, Patrick D McGorry, Carrie E Bearden, Barnaby Nelson, Martha E Shenton, Scott W Woods
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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 .

加速药物合作伙伴®精神分裂症计划中的体液生物标志物和精神病风险:设计考虑。
蛋白质组分析方法和基因组学的进步显著提高了我们对血液蛋白质组的理解。精神分裂症和精神病风险与精神分裂症和其他精神障碍的多基因评分有关,也与血液和唾液中涉及激素信号、氧化还原平衡和慢性全身性炎症的生物标志物水平的改变有关。加速药物合作伙伴®精神分裂症(AMP®SCZ)旨在确定既能预测临床结果的生物标志物,又能提供对符合CHR标准的人驱动临床结果的生物学过程的见解。AMP®SCZ将对近2000名CHR和640名社区研究参与者进行为期两年的随访,在基线时评估生物标志物,并进行为期两个月的随访,包括收集血液和唾液样本。以下提供了利用精神分裂症和其他疾病的多基因风险评分、唾液皮质醇水平和基于发现的血浆蛋白质组学分析平台的计划的基本原理和方法。我们还详细介绍了用于收集和储存这些生物样品的标准化方法,以及研究参与者的元数据和与可能影响生物标志物值的分析前因素相关的质量控制措施。最后,我们讨论了分析基于血液和唾液的生物标志物结果的计划。观看珀金斯博士讨论他们的工作和这篇文章:https://vimeo.com/1062879582?share=copy#t=0。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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