Thalamic shape and volume abnormalities in female patients with panic disorder

PLoS One. 2018 Dec 19;13(12):e0208152. doi: 10.1371/journal.pone.0208152. eCollection 2018.

Abstract

The thalamus is believed to play crucial role in processing viscero-sensory information, and regulating the activity of amygdala in patients with panic disorder (PD). Previous functional neuroimaging studies have detected abnormal activation in the thalamus in patients with PD compared with healthy control subjects (HC). Very few studies, however, have investigated for volumetric abnormalities in the thalamus in patients with PD. Furthermore, to the best of our knowledge, no previous study has investigated for shape abnormalities in the thalamus in patients with PD. Twenty-five patients with PD and 25 HC participants (all female) were recruited for the study. A voxel-wise volume comparison analysis and a vertex-wise shape analysis were conducted to evaluate structural abnormalities in the PD patients compared to HC. The patients with PD demonstrated significant gray matter volume reductions in the thalamus bilaterally, relative to the HC. The shape analysis detected significant inward deformation in some thalamic regions in the PD patients, including the anterior nucleus, mediodorsal nucleus, and pulvinar nucleus. PD patients showed shape deformations in key thalamic regions that are believed to play a role in regulating emotional and cognitive functions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anterior Thalamic Nuclei / diagnostic imaging
  • Anterior Thalamic Nuclei / pathology*
  • Case-Control Studies
  • Female
  • Healthy Volunteers
  • Humans
  • Image Processing, Computer-Assisted / methods
  • Magnetic Resonance Imaging / methods
  • Male
  • Mediodorsal Thalamic Nucleus / diagnostic imaging
  • Mediodorsal Thalamic Nucleus / pathology*
  • Middle Aged
  • Organ Size
  • Panic Disorder / diagnostic imaging
  • Panic Disorder / pathology*
  • Pulvinar / diagnostic imaging
  • Pulvinar / pathology*
  • Young Adult

Grants and funding

This study was supported by grants from the Ministry of Health, Labor and Welfare (Kokoro 200400762A, 200500806A, and 200632005A, B) (Y.H.), and JSPS KAKENHI Grant Numbers JP25861023 and JP17K10313 (T.A.), and a grant from SENSHIN Medical Research Foundation (T.A.) of Japan. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.