Integrated Multi-Omics Analysis of Cerebrospinal Fluid in Postoperative Delirium

Author:

Tripp Bridget A.1ORCID,Dillon Simon T.23ORCID,Yuan Min4,Asara John M.34ORCID,Vasunilashorn Sarinnapha M.356,Fong Tamara G.378ORCID,Inouye Sharon K.358,Ngo Long H.356,Marcantonio Edward R.35ORCID,Xie Zhongcong39ORCID,Libermann Towia A.235ORCID,Otu Hasan H.1

Affiliation:

1. Department of Electrical and Computer Engineering, University of Nebraska-Lincoln, Lincoln, NE 68588, USA

2. Genomics, Proteomics, Bioinformatics and Systems Biology Center, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA

3. Harvard Medical School, Boston, MA 02215, USA

4. Division of Signal Transduction and Mass Spectrometry Core, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA

5. Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA

6. Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA

7. Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA

8. Aging Brain Center, Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA 02131, USA

9. Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, MA 02114, USA

Abstract

Preoperative risk biomarkers for delirium may aid in identifying high-risk patients and developing intervention therapies, which would minimize the health and economic burden of postoperative delirium. Previous studies have typically used single omics approaches to identify such biomarkers. Preoperative cerebrospinal fluid (CSF) from the Healthier Postoperative Recovery study of adults ≥ 63 years old undergoing elective major orthopedic surgery was used in a matched pair delirium case–no delirium control design. We performed metabolomics and lipidomics, which were combined with our previously reported proteomics results on the same samples. Differential expression, clustering, classification, and systems biology analyses were applied to individual and combined omics datasets. Probabilistic graph models were used to identify an integrated multi-omics interaction network, which included clusters of heterogeneous omics interactions among lipids, metabolites, and proteins. The combined multi-omics signature of 25 molecules attained an AUC of 0.96 [95% CI: 0.85–1.00], showing improvement over individual omics-based classification. We conclude that multi-omics integration of preoperative CSF identifies potential risk markers for delirium and generates new insights into the complex pathways associated with delirium. With future validation, this hypotheses-generating study may serve to build robust biomarkers for delirium and improve our understanding of its pathophysiology.

Funder

National Institute on Aging

Alzheimer’s Association

BIDMC Capital Equipment Fund

NIH

Publisher

MDPI AG

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