Department of Psychiatry, CHA Bundang Medical Center, CHA University, Seongnam, Republic of Korea.
J Affect Disord. 2013 May;147(1-3):64-71. doi: 10.1016/j.jad.2012.10.009. Epub 2012 Nov 7.
The catechol-O-methyltransferase (COMT) gene val158met polymorphism (rs4680) has been found to be associated with various psychiatric phenotypes including panic disorder. Considering the probable genetic influence of COMT on the pathogenesis of panic disorder and white matter connectivity, the present study investigated white matter connectivity using diffusion tensor imaging in relation to the COMT genotype in panic disorder.
Twenty-six patients with panic disorder and twenty-six age- and gender-matched healthy controls participated in this study. Brain magnetic resonance scans and genotype analysis for COMT rs4680 were conducted. Panic Disorder Severity Scale, Albany Panic and Phobia Questionnaire, and Anxiety Sensitivity Inventory-Revised were assessed. Tract-based spatial statistics (TBSS) were used for image analysis.
There was no significant difference in white matter analysis between panic disorder and healthy controls. However, TBSS analysis showed increased fractional anisotropy (FA) in posterior thalamic radiation, posterior and superior corona radiata, superior longitudinal fasciculus, and sagittal stratum, all located in the right hemisphere in COMT AA/AG genotype group compared to GG genotype in panic disorder. Voxelwise correlational analysis revealed the symptom severity scores are correlated with the FA in white matter tracts that previously showed significant group differences between AA/AG and GG genotypes in COMT AA/AG genotype group, while no significant correlation was found in GG genotype group.
The sample size in each group was small, hence, further studies with larger numbers of patients are needed to confirm our findings.
These data suggested that COMT rs4680 could affect the white matter connectivity in panic disorder.
儿茶酚氧位甲基转移酶(COMT)基因 val158met 多态性(rs4680)与包括惊恐障碍在内的各种精神表型有关。考虑到 COMT 对惊恐障碍发病机制和白质连通性的可能遗传影响,本研究使用弥散张量成像(DTI)研究了 COMT 基因型与惊恐障碍之间的白质连通性。
本研究纳入 26 例惊恐障碍患者和 26 名年龄和性别匹配的健康对照者。进行脑磁共振扫描和 COMT rs4680 基因型分析。评估惊恐障碍严重程度量表、奥尔巴尼惊恐和恐惧症问卷、焦虑敏感量表修订版。使用基于体素的空间统计学(TBSS)进行图像分析。
惊恐障碍组和健康对照组之间的白质分析没有显著差异。然而,TBSS 分析显示,在 COMT AA/AG 基因型组中,右侧后丘脑辐射、后和上冠状辐射、上纵束和矢状层的分数各向异性(FA)增加,而在惊恐障碍 GG 基因型组中则没有。体素相关性分析显示,症状严重程度评分与白质束的 FA 相关,在 COMT AA/AG 基因型组中,AA/AG 和 GG 基因型之间存在显著的组间差异,而在 GG 基因型组中则没有显著相关性。
每组的样本量较小,因此需要进一步的研究,纳入更多的患者以证实我们的发现。
这些数据表明,COMT rs4680 可能影响惊恐障碍的白质连通性。