A machine learning PROGRAM to identify COVID-19 and other diseases from hematology data

Author:

Gladding Patrick A1ORCID,Ayar Zina2,Smith Kevin3,Patel Prashant3,Pearce Julia3,Puwakdandawa Shalini3,Tarrant Dianne3,Atkinson Jon3,McChlery Elizabeth3,Hanna Merit4,Gow Nick5,Bhally Hasan5,Read Kerry5,Jayathissa Prageeth6,Wallace Jonathan6,Norton Sam7,Kasabov Nick8,Calude Cristian S9,Steel Deborah10,Mckenzie Colin10

Affiliation:

1. Department of Cardiology, Waitematā District Health Board, Auckland, New Zealand

2. Clinical Information Services, Waitematā District Health Board, Auckland, New Zealand

3. Clinical laboratory, Waitematā District Health Board, Auckland, New Zealand

4. Department of Hematology, Waitematā District Health Board, Auckland, New Zealand

5. Department of Infectious diseases, Waitematā District Health Board, Auckland, New Zealand

6. Institute for Innovation & Improvement (i3), Waitematā District Health Board, Auckland, New Zealand

7. Nanix Ltd, Dunedin, New Zealand

8. Knowledge Engineering & Discovery Research Institute (KEDRI), Auckland University of Technology, Auckland, New Zealand

9. School of Computer Science, University of Auckland, Auckland, New Zealand

10. Sysmex New Zealand Ltd, Auckland, New Zealand

Abstract

Aim: We propose a method for screening full blood count metadata for evidence of communicable and noncommunicable diseases using machine learning (ML). Materials & methods: High dimensional hematology metadata was extracted over an 11-month period from Sysmex hematology analyzers from 43,761 patients. Predictive models for age, sex and individuality were developed to demonstrate the personalized nature of hematology data. Both numeric and raw flow cytometry data were used for both supervised and unsupervised ML to predict the presence of pneumonia, urinary tract infection and COVID-19. Heart failure was used as an objective to prove method generalizability. Results: Chronological age was predicted by a deep neural network with R2: 0.59; mean absolute error: 12; sex with AUROC: 0.83, phi: 0.47; individuality with 99.7% accuracy, phi: 0.97; pneumonia with AUROC: 0.74, sensitivity 58%, specificity 79%, 95% CI: 0.73–0.75, p < 0.0001; urinary tract infection AUROC: 0.68, sensitivity 52%, specificity 79%, 95% CI: 0.67–0.68, p < 0.0001; COVID-19 AUROC: 0.8, sensitivity 82%, specificity 75%, 95% CI: 0.79–0.8, p = 0.0006; and heart failure area under the receiver operator curve (AUROC): 0.78, sensitivity 72%, specificity 72%, 95% CI: 0.77–0.78; p < 0.0001. Conclusion: ML applied to hematology data could predict communicable and noncommunicable diseases, both at local and global levels.

Publisher

Future Science Ltd

Subject

Biotechnology

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