Identifying Depression Through Machine Learning Analysis of Omics Data: A Scoping Review (Preprint)

Author:

Taylor BrittanyORCID,Hobensack MollieORCID,Niño de Rivera StephanieORCID,Zhao YihongORCID,Masterson Creber RuthORCID,Cato KenrickORCID

Abstract

BACKGROUND

Depression is one of the most common mental disorders that affects over 300 million people worldwide. There is a shortage of providers trained in the provision of mental health care, and the nursing workforce is essential in filling this gap. The diagnosis of depression relies heavily on self-reported symptoms and clinical interviews, which is subject to implicit biases. Omics methods, including genomics, transcriptomics, epigenomics, and microbiomics, are novel methods for identifying the biological underpinnings of depression. Machine learning is used to analyze genomic data which includes large, heterogeneous, and multidimensional datasets.

OBJECTIVE

This scoping review will review the existing literature on machine learning methods for omics data analysis to identify individuals with depression, with the goal of providing insight into alternative objective and driven insights into the diagnostic process for depression.

METHODS

This scoping review was reported following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Extension for Scoping Reviews guidelines. Searches were conducted in three databases to identify relevant publications. Three independent researchers performed screening, and discrepancies were resolved by consensus. Critical appraisal was performed using the Joanna Briggs Institute Critical Appraisal Checklist for Analytical Cross Sectional Studies.

RESULTS

The screening process identified 15 relevant papers. Omics methods included genomics, transcriptomics, epigenomics, multi-omics, and microbiomics, and machine learning methods included random forest, support vector machine, k-nearest neighbor, and artificial neural network.

CONCLUSIONS

The findings of this scoping review indicate that the omics methods had similar performance in identifying omics variants associated with depression. All machine learning methods performed well based on their performance metrics. When variants in omics data are associated with an increased risk of depression, the important next step is for clinicians, especially nurses, to assess individuals for symptoms of depression, and provide a diagnosis and any necessary treatment.

Publisher

JMIR Publications Inc.

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