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Published Online: 1 July 2011

Duloxetine's Effects in Resting Functional Magnetic Resonance Imaging of First-Episode, Drug-Naïve Major Depressive Disorder With Panic Disorder Patients

Publication: The Journal of Neuropsychiatry and Clinical Neurosciences
To the Editor: Resting functional MRI (RFMRI) represents the default brain activity while subjects are at rest. We present that two cases of first-episode, drug-naïve major depressive disorder (MDD) with panic disorder (PD) who showed increases of activity in several regions after a 6 weeks of duloxetine's therapy.

Case Report

Two cases (1 woman, and 1 man; 28 and 18 years old, respectively) with first-onset, drug naïve MDD with PD were enrolled. They all received clinical rating scales, with scores as follows: Hamilton Rating Scale for Depression (Ham-D): 30, 24; and Panic Disorder Severity Scale (PDSS): 20, 18. The treatment with duloxetine 30 mg/day was started and titrated to 60 mg within 2 weeks without any significant side effects except mild nausea and sedation. After a 6-week therapy, their MDD and PD symptoms responded to duloxetine [Ham-D: 4, 5; PDSS: 2, 1]. RFMRI scans were obtained with a 3T GE version scanner. Echo planar imaging (EPI) sequences were acquired in 20 axial slices (TR=2,000 msec, TE=40 msec, flip angle=90°, FOV=24 cm; 5-mm thickness and 1 mm gap; 400 sec for each subject) at baseline and 6th week visit. RFMRI data were first preprocessed by DPARSF (Data Processing Assistant and Resting-State FMRI, Version 1.4), which included slice timing, realignment, normalization, smoothing by 4 × 4 × 4 kernel, detrend and filter RFMRI, with data within 0.008–0.08 Hz. The preprocessed RFMRI data were then processed by GIFT (Group Independent Component Analysis of FMRI Toolbox, Version 1.3 hour), and subsequently compared analysis between baseline and the 6th week (uncorrected p<0.00005; voxel threshold >50). There were modest increases of RFMRI brain activities after duloxetine treatment (Table 1).
TABLE 1. Changes of RFMRI brain activities after a 6-week duloxethine therapy
(MNI: Montreal Neurological Institute)

Discussion

Limbic and paralimbic activations usually inhibit the activities of dorsal cortical structures (such as middle frontal gyrus) in MDD patients.1 Remitted MDD patients have been reported with increased regional homogeneity in frontal areas.2 Liao et al.3 found that decreased dorsal attentional network in middle frontal gyrus with hyperactive episodic-memory and self-projection network in temporal and parahippocampal gyrus probably contributed to the anxiety and panic attacks. Also, the increased vigilance and autonomic, visceral dysregulations due to abnormal activities of RFMRI in these regions4 should be associated with panic symptoms in these patients.

Acknowledgments

Acknowledgement of assistance: I want to thank Dr. Yuan-Yu Hsu (Department of Medical Imaging, Buddhist Tzu-Chi General Hospital Taipei Branch) for MRI acquisition help and technical assistance.

References

1.
Hamilton JP, Chen G, Thomason ME, et al. Investigating neural primacy in major depressive disorder: multivariate Granger causality analysis of resting-state fMRI time-series data. Mol Psychiatry 2010
2.
Yuan Y, Zhang Z, Bai F, et al.: Abnormal neural activity in the patients with remitted geriatric depression: a resting-state functional magnetic resonance imaging study. J Affect Disord 2008; 111:145–152
3.
Liao W, Chen H, Feng Y, et al.: Selective aberrant functional connectivity of resting-state networks in social anxiety disorder. Neuroimage 2010; 52:1549–1558
4.
Sheline YI, Price JL, Yan Z, et al.: Resting-state functional MRI in depression unmasks increased connectivity between networks via the dorsal nexus. Proc Natl Acad Sci U S A 2010; 107:11020–11025

Information & Authors

Information

Published In

Go to The Journal of Neuropsychiatry and Clinical Neurosciences
Go to The Journal of Neuropsychiatry and Clinical Neurosciences
The Journal of Neuropsychiatry and Clinical Neurosciences
Pages: E10 - E11
PubMed: 21948903

History

Published online: 1 July 2011
Published in print: Summer 2011

Authors

Details

Chien-Han Lai, M.D., M.Sc.
Department of Psychiatry, Buddhist Tzu-Chi General Hospital, Taipei Branch, Taipei, TaiwanInstitute of Brain Science, National Yang Ming University, Taipei City, Taiwan e-mail: [email protected]

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