Discriminating head trauma outcomes using machine learning and genomics

, , , Nasrallah, Fatima, , , , & (2022) Discriminating head trauma outcomes using machine learning and genomics. Journal of Molecular Medicine, 100(2), pp. 303-312.

Free-to-read version at publisher website

Description

Abstract: A percentage of the population suffers prolonged and persistent post-concussion symptoms (PCS) following average head injuries or develops severe neurological dysfunction following minor head trauma. Genetic variants that may contribute to individual response to head trauma have been investigated in some studies, but to date none have explored the use of machine learning (ML) methods with genomic data to specifically explore outcomes of head trauma. Whole exome sequencing (WES) was completed for three groups of individuals (N = 60): (a) 16 individuals with severe neurological responses to minor head trauma, (b) 26 individuals with persistent PCS and (c) 18 individuals with normal recovery from concussion or mTBI. Gradient boosted tree algorithms were applied to the data using XGBoost. By using variants with CADD scores above 15 in the training set (randomly sampled 70%), we identified signatures that accurately distinguish to accurately distinguish the test groups with an average area under the curve (AUC) of 0.8 (SE = 0.019). Metrics including positive and negative prediction values, as well as kappa were all within acceptable range to support the prediction accuracy. This study illustrates how ML methods in combination with WES data have the potential to predict severe or prolonged responses to head trauma from healthy recovery. Key messages: Linear association analysis has been inconclusive in concussion genetics. Non-linear methods as boosted trees can offer better insights in small samples. Strong discrimination trends can be achieved from exome data of cases and controls.

Impact and interest:

0 citations in Scopus
Search Google Scholar™

Citation counts are sourced monthly from Scopus and Web of Science® citation databases.

These databases contain citations from different subsets of available publications and different time periods and thus the citation count from each is usually different. Some works are not in either database and no count is displayed. Scopus includes citations from articles published in 1996 onwards, and Web of Science® generally from 1980 onwards.

Citations counts from the Google Scholar™ indexing service can be viewed at the linked Google Scholar™ search.

ID Code: 227099
Item Type: Contribution to Journal (Journal Article)
Refereed: Yes
ORCID iD:
Ibrahim, Omarorcid.org/0000-0003-2495-9286
Sutherland, Heidi G.orcid.org/0000-0002-8512-1498
Maksemous, Nevenorcid.org/0000-0002-4891-4333
Smith, Robert A.orcid.org/0000-0003-4825-2461
Haupt, Larisa M.orcid.org/0000-0002-7735-8110
Griffiths, Lyn R.orcid.org/0000-0002-6774-5475
Additional Information: Funding Information: This work was supported by The Assistant Secretary of Defence for Health Affairs endorsed by the Department of Defence, through FY 2018 Peer Reviewed Medical Research Program Discovery Award, under Award No. W81XWH1910098. Opinions, interpretations, conclusions and recommendations are those of the author and are not necessarily endorsed by the Department of Defense. This work was supported by the National Health and Medical Research Council through grant GNT1122387—Identifying novel gene mutations for molecular diagnosis of familial hemiplegic migraine.
Measurements or Duration: 10 pages
Keywords: Concussion, Genomics, Head trauma, Machine learning, Neurotrauma
DOI: 10.1007/s00109-021-02158-z
ISSN: 0946-2716
Pure ID: 103351110
Divisions: Current > Research Centres > Centre for Biomedical Technologies
Current > Research Centres > Centre for Genomics and Personalised Health
Current > QUT Faculties and Divisions > Academic Division
Current > QUT Faculties and Divisions > Faculty of Engineering
Current > QUT Faculties and Divisions > Faculty of Health
Current > Schools > School of Biomedical Sciences
Funding Information: This work was supported by The Assistant Secretary of Defence for Health Affairs endorsed by the Department of Defence, through FY 2018 Peer Reviewed Medical Research Program Discovery Award, under Award No. W81XWH1910098. Opinions, interpretations, conclusions and recommendations are those of the author and are not necessarily endorsed by the Department of Defense. This work was supported by the National Health and Medical Research Council through grant GNT1122387—Identifying novel gene mutations for molecular diagnosis of familial hemiplegic migraine.
Funding:
Copyright Owner: The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021<br/>
Copyright Statement: This work is covered by copyright. Unless the document is being made available under a Creative Commons Licence, you must assume that re-use is limited to personal use and that permission from the copyright owner must be obtained for all other uses. If the document is available under a Creative Commons License (or other specified license) then refer to the Licence for details of permitted re-use. It is a condition of access that users recognise and abide by the legal requirements associated with these rights. If you believe that this work infringes copyright please provide details by email to qut.copyright@qut.edu.au
Deposited On: 15 Dec 2021 22:34
Last Modified: 29 Feb 2024 11:51