4.7 Article

Heterogeneity in Blood Biomarker Trajectories After Mild TBI Revealed by Unsupervised Learning

Publisher

IEEE COMPUTER SOC
DOI: 10.1109/TCBB.2021.3091972

Keywords

Trajectory; Sports; Blood; Injuries; Proteins; Precision medicine; Biological system modeling; Unsupervised learning; statistical analysis; concussions; predictive modeling; GFAP; NF-L; tau; UCH-L1

Funding

  1. Leonard Wood Institute
  2. U.S. Army Research Laboratory
  3. [W911NF-14-2-0034]

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Concussions, or mild traumatic brain injuries (mTBI), pose a growing health challenge. This study applies data-driven decision support to cluster blood biomarker trajectories in mTBI patients, providing improved tools for assessment and prediction. The ability to cluster these trajectories enhances the possibilities for precision medicine approaches to mTBI.
Concussions, also known as mild traumatic brain injury (mTBI), are a growing health challenge. Approximately four million concussions are diagnosed annually in the United States. Concussion is a heterogeneous disorder in causation, symptoms, and outcome making precision medicine approaches to this disorder important. Persistent disabling symptoms sometimes delay recovery in a difficult to predict subset of mTBI patients. Despite abundant data, clinicians need better tools to assess and predict recovery. Data-driven decision support holds promise for accurate clinical prediction tools for mTBI due to its ability to identify hidden correlations in complex datasets. We apply a Locality-Sensitive Hashing model enhanced by varied statistical methods to cluster blood biomarker level trajectories acquired over multiple time points. Additional features derived from demographics, injury context, neurocognitive assessment, and postural stability assessment are extracted using an autoencoder to augment the model. The data, obtained from FITBIR, consisted of 301 concussed subjects (athletes and cadets). Clustering identified 11 different biomarker trajectories. Two of the trajectories (rising GFAP and rising NF-L) were associated with a greater risk of loss of consciousness or post-traumatic amnesia at onset. The ability to cluster blood biomarker trajectories enhances the possibilities for precision medicine approaches to mTBI.

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