The use of missing values in proteomic data-independent acquisition mass spectrometry to enable disease activity discrimination

Author:

McGurk Kathryn A123ORCID,Dagliati Arianna4,Chiasserini Davide2,Lee Dave2,Plant Darren5ORCID,Baricevic-Jones Ivona2,Kelsall Janet2,Eineman Rachael2,Reed Rachel2,Geary Bethany2,Unwin Richard D12,Nicolaou Anna3ORCID,Keavney Bernard D1,Barton Anne56ORCID,Whetton Anthony D2,Geifman Nophar4

Affiliation:

1. Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester, UK

2. Stoller Biomarker Discovery Centre, Division of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK

3. Laboratory for Lipidomics and Lipid Biology, Division of Pharmacy and Optometry, UK

4. Division of Informatics, Imaging and Data Sciences, School of Health Sciences, Faculty of Biology, Medicine and Health, University of Manchester, UK

5. NIHR Manchester Biomedical Research Centre, Manchester Academic Health Science Centre, Manchester University NHS Foundation Trust, Manchester, UK

6. Arthritis Research UK Centre for Genetics and Genomics, Centre for Musculoskeletal Research, University of Manchester, Manchester, UK

Abstract

Abstract Motivation Data-independent acquisition mass spectrometry allows for comprehensive peptide detection and relative quantification than standard data-dependent approaches. While less prone to missing values, these still exist. Current approaches for handling the so-called missingness have challenges. We hypothesized that non-random missingness is a useful biological measure and demonstrate the importance of analysing missingness for proteomic discovery within a longitudinal study of disease activity. Results The magnitude of missingness did not correlate with mean peptide concentration. The magnitude of missingness for each protein strongly correlated between collection time points (baseline, 3 months, 6 months; R = 0.95–0.97, confidence interval = 0.94–0.97) indicating little time-dependent effect. This allowed for the identification of proteins with outlier levels of missingness that differentiate between the patient groups characterized by different patterns of disease activity. The association of these proteins with disease activity was confirmed by machine learning techniques. Our novel approach complements analyses on complete observations and other missing value strategies in biomarker prediction of disease activity. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

Medical Research Council

MRC Flexible Training Supplement

University of Manchester President’s Doctoral Scholarship

Engineering and Physical Sciences Research Council

Manchester Molecular Pathology Innovation Centre

National Institute for Health Research Manchester Biomedical Research Centre

Versus Arthritis

Cancer Research UK Manchester Centre

British Heart Foundation Personal Chair

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

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