Abstract

Background: Only less than 40% of patients with Major depressive disorder (MDD) can achieve remission after several weeks of initial antidepressant treatment. Predicting whether the prescribed treatment is effective in the following course may help clinicians modify the treatment regimen in time, and reduce the staggering burden for patients and society. However, there are not yet reliable markers based on neurobiological change after a treatment regimen steadily applied, for predicting clinical treatment outcome. The striatal circuits often exhibit abnormality for MDD patients, and are implicated in antidepressant treatments.Methods: Nineteen first-episode drug-naive MDD patients (nine females, mean age was 30 years old) were recruited to undergo clinical symptom assessment and resting state fMRI scanning at baseline, after 2 and 8 weeks of treatment with duloxetine. A seed-based analysis was used to obtain functional connectivity (FC) maps of six sub-regions of the stratum, then we explored the relationship of 2-week changes of striatal FC with clinical symptom improvement after 8-week duloxetine treatment.Results: The results revealed that 2-week FC changes of the striatal cognitive and affective subdivisions with the frontoparietal regions positively correlated with 8-week symptom improvement. We also found that early FC changes between the striatal motor subdivision and the motor-related cortical regions negatively correlated with later symptom improvement.Conclusions: These findings suggest that change of the FC of the cortical-striatal circuits at the early stage of treatment is critical for later remission of MDD. Furthermore, the association between the FC change and symptom improvement may have significant implication for clinical practice to regard neural changes as reference for evaluating how antidepressant treatment works.

Highlights

  • Major depressive disorder (MDD) is a common and disabling psychiatric disorder, with multi-dimensional clinical symptoms involving emotion, cognition, psychomotor, and somatic domains [1]

  • The present results revealed that greater DFC of striatal subdivisions with brain regions in the frontoparietal network (FPN) and default mode network (DMN) after 2week treatment was associated with better clinical improvement at 8-week

  • The DFC of the left VSs with right middle frontal gyrus (MFG) and right inferior parietal lobule (IPL) in the FPN was positively related to treatment response at 8-week as well (r = 0.91 for right MFG and r = 0.87 for the right IPL)

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Summary

Introduction

Major depressive disorder (MDD) is a common and disabling psychiatric disorder, with multi-dimensional clinical symptoms involving emotion, cognition, psychomotor, and somatic domains [1]. Though antidepressant medication is used as first-line treatment for MDD, only less than 40% of patients achieve remission with initial treatment [2, 3]. Several lines of clinical evidence have shown that early improvement of clinical symptoms within the first 2 weeks of antidepressant treatment can partly predict later treatment outcome [5, 6], highlighting 2week as a key time frame in determining long-term clinical therapeutic effect. Less than 40% of patients with Major depressive disorder (MDD) can achieve remission after several weeks of initial antidepressant treatment. There are not yet reliable markers based on neurobiological change after a treatment regimen steadily applied, for predicting clinical treatment outcome. The striatal circuits often exhibit abnormality for MDD patients, and are implicated in antidepressant treatments

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