Personalized prediction of transcranial magnetic stimulation clinical response in patients with treatment-refractory depression using neuroimaging biomarkers and machine learning

J Affect Disord. 2021 Jul 1:290:261-271. doi: 10.1016/j.jad.2021.04.081. Epub 2021 May 16.

Abstract

Background: Functional connectivity between the left dorsolateral prefrontal cortex (DLPFC) and subgenual cingulate (sgACC) may serve as a biomarker for transcranial magnetic stimulation (rTMS) treatment response. The first aim was to establish whether this finding is veridical or artifactually induced by the pre-processing method. Furthermore, alternative biomarkers were identified and the clinical utility for personalized medicine was examined.

Methods: Resting-state fMRI data were collected in medication-refractory depressed patients (n = 70, 16 males) before undergoing neuronavigated left DLPFC rTMS. Seed-based analyses were performed with and without global signal regression pre-processing to identify biomarkers of short-term and long-term treatment response. Receiver Operating Characteristic curve and supervised machine learning analyses were applied to assess the clinical utility of these biomarkers for the classification of categorical rTMS response.

Results: Regardless of the pre-processing method, DLPFC-sgACC connectivity was not associated with treatment outcome. Instead, poorer connectivity between the sgACC and three clusters (peak locations: frontal pole, superior parietal lobule, occipital cortex) and DLPFC-central opercular cortex were observed in long-term nonresponders. The identified connections could serve as acceptable to excellent markers. Combining the features using supervised machine learning reached accuracy rates of 95.35% (CI=82.94-100.00) and 88.89% (CI=63.96-100.00) in the cross-validation and test dataset, respectively.

Limitations: The sample size was moderate, and features for machine learning were based on group differences.

Conclusions: Long-term nonresponders showed greater disrupted connectivity in regions involving the central executive network. Our findings may aid the development of personalized medicine for medication-refractory depression.

Keywords: Biomarkers; Depression; Dorsolateral prefrontal cortex; Subgenual anterior cingulate cortex; Transcranial magnetic stimulation; Treatment response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers
  • Depressive Disorder, Major* / diagnostic imaging
  • Depressive Disorder, Major* / therapy
  • Depressive Disorder, Treatment-Resistant* / diagnostic imaging
  • Depressive Disorder, Treatment-Resistant* / therapy
  • Gyrus Cinguli
  • Humans
  • Machine Learning
  • Magnetic Resonance Imaging
  • Male
  • Neuroimaging
  • Prefrontal Cortex / diagnostic imaging
  • Transcranial Magnetic Stimulation

Substances

  • Biomarkers