A longitudinal functional neuroimaging study in medication-naïve depression after antidepressant treatment

PLoS One. 2015 Mar 18;10(3):e0120828. doi: 10.1371/journal.pone.0120828. eCollection 2015.

Abstract

Recent studies have indicated the potential clinical use of near infrared spectroscopy (NIRS) as a tool in assisting the diagnosis of major depressive disorder (MDD); however, it is still unclear whether NIRS signal changes during cognitive task are state- or trait-dependent, and whether NIRS could be a neural predictor of treatment response. Therefore, we conducted a longitudinal study to explore frontal haemodynamic changes following antidepressant treatment in medication-naïve MDD using 52-channel NIRS. This study included 25 medication-naïve individuals with MDD and 62 healthy controls (HC). We performed NIRS scans before and after antidepressant treatment and measured changes of [oxy-Hb] activation during a verbal fluency task (VFT) following treatment. Individuals with MDD showed significantly decreased [oxy-Hb] values during a VFT compared with HC in the bilateral frontal and temporal cortices at baseline. There were no [oxy-Hb] changes between pre- and post-antidepressant treatment time points in the MDD cohort despite significant improvement in depressive symptoms. There was a significant association between mean [oxy-Hb] values during a VFT at baseline and improvement in depressive symptoms following treatment in the bilateral inferior frontal and middle temporal gyri in MDD. These findings suggest that hypofrontality response to a VFT may represent a potential trait marker for depression rather than a state marker. Moreover, the correlation analysis indicates that the NIRS signals before the initiation of treatment may be a biological marker to predict patient's clinical response to antidepressant treatment. The present study provides further evidence to support a potential application of NIRS for the diagnosis and treatment of depression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antidepressive Agents / therapeutic use
  • Biomarkers / blood
  • Brain Mapping
  • Case-Control Studies
  • Depressive Disorder, Major / blood*
  • Depressive Disorder, Major / diagnosis*
  • Depressive Disorder, Major / drug therapy
  • Depressive Disorder, Major / physiopathology
  • Female
  • Functional Neuroimaging
  • Humans
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Neuropsychological Tests
  • Oxyhemoglobins / metabolism*
  • Prefrontal Cortex / drug effects
  • Prefrontal Cortex / physiopathology
  • Psychiatric Status Rating Scales
  • Spectroscopy, Near-Infrared
  • Temporal Lobe / drug effects
  • Temporal Lobe / physiopathology

Substances

  • Antidepressive Agents
  • Biomarkers
  • Oxyhemoglobins

Grants and funding

This study was supported by the Intramural Research Grant (23-10) for Neurological and Psychiatric Disorders of NCNP (National Center of Neurology and Psychiatry). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Hitachi Medical Corporation provided support in the form of a salary for author SK, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific role of this author is articulated in the ‘author contributions’ section.