
Vol. 52, No. 2, 2005
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Article (PDF 191 KB)
Original Paper
Promoter Polymorphisms of the Interferon- Receptor Gene and Development of Interferon-Induced Depressive Symptoms in Patients with Chronic Hepatitis C: Preliminary Findings
Keizo Yoshidaa, b, Oyetunde Alagbea, Xiaohong Wanga, , Bobbi Woolwinea, Marie Thornburya, Charles L. Raisona, Andrew H. Millera
aDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Ga., USA; bDepartment of Psychiatry, Akita University School of Medicine, Akita, Japan
Address of Corresponding Author
Neuropsychobiology 2005;52:55-61 (DOI: 10.1159/000086605)
Key Words
- Depression
- Interferon-
 - Genetic polymorphism
- Microsatellite
Abstract
Background: Interferon (IFN)- treatment frequently induces depression, which can impair quality of life and reduce treatment adherence. Defining relevant risk factors for IFN- -induced depression is essential for designing preventative treatment strategies. Objective: The purpose of the present study was to determine whether promoter polymorphisms of -408C/T, -3C/T and GT repeat dinucleotide microsatellite in the IFN- / receptor 1 (IFNAR1) gene are associated with the development of IFN-induced depression. Method: Fifty patients with chronic hepatitis C were treated with pegylated IFN -2b plus a standard or weight-based dose of ribavirin. Severity of depression was assessed using the Zung Self-Rating Depression Scale (SDS) at baseline and at 4, 8, 12 and 24 weeks of treatment. Result: The baseline to maximum difference in the SDS index score of neurovegetative/somatic symptoms was higher in patients with the 5/14 genotype of the GT repeat dinucleotide microsatellite polymorphism than in those patients with other genotypes (p = 0.0084). Conclusion: This preliminary result suggests that the promoter GT repeat dinucleotide microsatellite polymorphism of the IFNAR1 gene may represent a risk factor for the development of depressive symptoms during IFN- therapy for hepatitis C and other conditions. Copyright © 2005 S. Karger AG, Basel
Author Contacts
Keizo Yoshida, MD, PhD Department of Psychiatry Akita University School of Medicine, 1-1-1 Hondo Akita 010-8543 (Japan) Tel. +81 18 884 6122, Fax +81 18 884 6445, E-Mail cxw01076@nifty.com
Article Information
Published online: June 29, 2005
Number of Print Pages : 7
Number of Figures : 6, Number of Tables : 3, Number of References : 21 |
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