Abnormal Cerebral Benzodiazepine Receptors Binding Measured with (123)I-Iomazenil SPECT in Panic Disorder.
- Author:
Daeyoung ROH
1
;
Kyoung Min PARK
;
Young Kee KIM
;
Sang Min LEE
;
Young Hoon RYU
;
Chan Hyung KIM
Author Information
1. Department of Psychiatry, Yonsei University College of Medicine, Seoul, Korea. spr88@yumc.ac
- Publication Type:Original Article
- Keywords:
Panic disorder;
[(123)I]-Iomazenil SPECT;
Benzodiazepine receptor
- MeSH:
Benzodiazepines;
Brain;
Gyrus Cinguli;
Humans;
Neuroimaging;
Occipital Lobe;
Panic;
Panic Disorder;
Parahippocampal Gyrus;
Receptors, GABA-A;
Temporal Lobe;
Tomography, Emission-Computed;
Tomography, Emission-Computed, Single-Photon
- From:Journal of Korean Neuropsychiatric Association
2010;49(2):235-240
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVES: Researchers have long hypothesized that the benzodiazepine-GABA system plays a role in the pathophysiology of panic disorder (PD). However, previous neuroimaging studies have been inconclusive, possibly due to matching discrepancies between patients and controls, confounding medication factors, and/or image analyzing methods. This study aimed to compare benzodiazepine receptor binding between PD patients and healthy controls. METHODS: Via (123)I-iomazenil single-photon emission computed tomography (IMZ-SPECT), we obtained regional brain patterns of benzodiazepine receptor binding for 12 unmedicated PD patients and 8 healthy age-and sex-matched volunteer controls. To analyze the image data, we used statistical parametric mapping (SPM). RESULTS: Benzodiazepine receptor binding showed a decrease in both the parietal and occipital lobes in PD patients as compared to controls. The anterior cingulate cortex, left parahippocampal gyrus, and both temporal lobes showed increased binding in PD patients. CONCLUSION: Our findings provide evidence of an abnormal BZD-GABA system in PD patients, suggesting that basal and/or compensatory changes in inhibitory neurotransmissions contribute to the pathogenesis of human PD.