Myers John, Xiao Jiayang, Mathura Raissa, Shofty Ben, Pirtle Victoria, Adkinson Joshua, Allawala Anusha B, Anand Adrish, Gadot Ron, Najera Ricardo, Rey Hernan G, Mathew Sanjay J, Bijanki Kelly, Banks Garrett, Watrous Andrew, Bartoli Eleonora, Heilbronner Sarah R, Provenza Nicole, Goodman Wayne K, Pouratian Nader, Hayden Benjamin Y, Sheth Sameer A
Baylor College of Medicine, Department of Neurosurgery.
Brown University, Department of Biomedical Engineering.
medRxiv. 2024 Aug 8:2024.08.07.24311546. doi: 10.1101/2024.08.07.24311546.
Understanding the neural basis of major depressive disorder (MDD) is vital to guiding neuromodulatory treatments. The available evidence supports the hypothesis that MDD is fundamentally a disease of cortical disinhibition, where breakdowns of inhibitory neural systems lead to diminished emotion regulation and intrusive ruminations. Recent research also points towards network changes in the brain, especially within the prefrontal cortex (PFC), as primary sources of MDD etiology. However, due to limitations in spatiotemporal resolution and clinical opportunities for intracranial recordings, this hypothesis has not been directly tested. We recorded intracranial EEG from the dorsolateral (dlPFC), orbitofrontal (OFC), and anterior cingulate cortices (ACC) in neurosurgical patients with MDD. We measured daily fluctuations in self-reported depression severity alongside directed connectivity between these PFC subregions. We focused primarily on delta oscillations (1-3 Hz), which have been linked to GABAergic inhibitory control and intracortical communication. Depression symptoms worsened when connectivity within the left vs. right PFC became imbalanced. In the left hemisphere, all directed connectivity towards the ACC, from the dlPFC and OFC, was positively correlated with depression severity. In the right hemisphere, directed connectivity between the OFC and dlPFC increased with depression severity as well. This is the first evidence that delta oscillations flowing between prefrontal subregions transiently increase intensity when people are experiencing more negative mood. These findings support the overarching hypothesis that MDD worsens with prefrontal disinhibition.
了解重度抑郁症(MDD)的神经基础对于指导神经调节治疗至关重要。现有证据支持这样一种假说,即MDD本质上是一种皮质抑制解除疾病,其中抑制性神经系统的崩溃导致情绪调节能力下降和侵入性沉思。最近的研究还指出,大脑中的网络变化,尤其是前额叶皮质(PFC)内的变化,是MDD病因的主要来源。然而,由于时空分辨率和颅内记录的临床机会有限,这一假说尚未得到直接验证。我们记录了患有MDD的神经外科患者背外侧前额叶皮质(dlPFC)、眶额皮质(OFC)和前扣带回皮质(ACC)的颅内脑电图。我们测量了自我报告的抑郁严重程度的每日波动以及这些PFC子区域之间的定向连接性。我们主要关注δ振荡(1-3赫兹),它与GABA能抑制控制和皮质内通信有关。当左、右PFC内的连接性变得不平衡时,抑郁症状会加重。在左半球,从dlPFC和OFC到ACC的所有定向连接性与抑郁严重程度呈正相关。在右半球,OFC和dlPFC之间的定向连接性也随着抑郁严重程度的增加而增加。这是第一个证据,表明当人们经历更消极的情绪时,前额叶子区域之间流动的δ振荡会短暂增加强度。这些发现支持了总体假说,即MDD会随着前额叶抑制解除而恶化。