重度抑郁症、创伤后应激障碍及其并发症的共同和不同神经影像特征。

Psychoradiology Pub Date : 2024-11-04 eCollection Date: 2024-01-01 DOI:10.1093/psyrad/kkae022
Jing Jiang, Stefania Ferraro, Youjin Zhao, Baolin Wu, Jinping Lin, Taolin Chen, Jin Gao, Lei Li
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引用次数: 0

摘要

创伤后应激障碍(PTSD)和重度抑郁障碍(MDD)是常见的应激相关精神疾病。遗传学和神经生物学研究支持这样一种观点,即创伤后应激障碍和重性抑郁障碍可能具有共同的和特定的潜在机制。在这篇系统性综述中,我们总结了 MDD、创伤后应激障碍及其合并症的大脑功能和结构特征的异同证据,以及在创伤后应激障碍和 MDD(创伤后应激障碍 + MDD)合并症患者中广泛使用的疗法的效果。这些功能性磁共振成像(MRI)研究强调了:(i) MDD 和创伤后应激障碍患者在认知和情绪处理过程中前额叶皮层的低激活性;(ii) 与 MDD 患者相比,创伤后应激障碍患者的恐惧处理区域(包括杏仁核、海马和岛叶)的激活性更高;(iii) 与单纯创伤后应激障碍患者相比,创伤后应激障碍 + MDD 患者参与恐惧和奖赏处理的脑区存在明显的功能缺陷。这些结构性核磁共振成像研究表明,创伤后应激障碍和多发性硬化症的共同特征是局灶性额叶区体积缩小。PTSD + MDD 患者的治疗效果可能与结构改变的正常化趋势相关。创伤后应激障碍+ MDD 患者重复经颅磁刺激反应的神经影像学预测因素可能与单一诊断组不同。总之,迄今为止的神经影像学研究只提供了有关 MDD 和创伤后应激障碍的共同特征和疾病特异性特征的有限信息。为了针对 MDD 和创伤后应激障碍患者共同和不同的脑部改变,开发出更好的诊断标记,并最终提供有针对性的治疗方法,进一步的研究是必不可少的。
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Common and divergent neuroimaging features in major depression, posttraumatic stress disorder, and their comorbidity.

Posttraumatic stress disorder (PTSD) and major depressive disorder (MDD) are common stress-related psychiatric disorders. Genetic and neurobiology research has supported the viewpoint that PTSD and MDD may possess common and disorder-specific underlying mechanisms. In this systematic review, we summarize evidence for the similarities and differences in brain functional and structural features of MDD, PTSD, and their comorbidity, as well as the effects of extensively used therapies in patients with comorbid PTSD and MDD (PTSD + MDD). These functional magnetic resonance imaging (MRI) studies highlight the (i) shared hypoactivation in the prefrontal cortex during cognitive and emotional processing in MDD and PTSD; (ii) higher activation in fear processing regions including amygdala, hippocampus, and insula in PTSD compared to MDD; and (iii) distinct functional deficits in brain regions involved in fear and reward processing in patients with PTSD + MDD relative to those with PTSD alone. These structural MRI studies suggested that PTSD and MDD share features of reduced volume in focal frontal areas. The treatment effects in patients with PTSD + MDD may correlate with the normalization trend of structural alterations. Neuroimaging predictors of repetitive transcranial magnetic stimulation response in patients with PTSD + MDD may differ from the mono-diagnostic groups. In summary, neuroimaging studies to date have provided limited information about the shared and disorder-specific features in MDD and PTSD. Further research is essential to pave the way for developing improved diagnostic markers and eventually targeted treatment approaches for the shared and distinct brain alterations presented in patients with MDD and PTSD.

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