4.7 Article

Distinct alterations of amygdala subregional functional connectivity in early- and late-onset obsessive-compulsive disorder

期刊

JOURNAL OF AFFECTIVE DISORDERS
卷 298, 期 -, 页码 421-430

出版社

ELSEVIER
DOI: 10.1016/j.jad.2021.11.005

关键词

Obsessive-compulsive disorder; Functional MRI; Age of onset; Amygdala; Resting-state functional connectivity

资金

  1. 1.3.5 Project for Disciplines of Excellence, West China Hospital, Sichuan University [ZYJC21041]
  2. Clinical and Translational Research Fund of Chinese Academy of Medical Sciences [2021-I2M-CT-B-097]
  3. Sichuan Science and Technology Program [2021YFS0140]
  4. West China Hospital [2019HXBH022]
  5. Sichuan University [2019HXBH022]

向作者/读者索取更多资源

This study aimed to identify pathophysiological specifics in OCD with different onset times by assessing amygdala subregional functional connectivity alterations. The findings emphasized different patterns of amygdala subregional connectivity alterations associated with EO-OCD and LO-OCD patients, providing unique insights into constructing distinct OCD subtypes based on brain intrinsic connectivity. Specific management for EO-OCD and LO-OCD patients may be needed based on these results.
Background: Age of onset may be an important feature associated with distinct subtypes of obsessive-compulsive disorder (OCD). The amygdala joined neurocircuitry models of OCD for its role in mediating fear and regulating anxiety. The present study aims to identify the underlying pathophysiological specifics in OCD with different onset times by assessing amygdala subregional functional connectivity (FC) alterations in early-onset OCD (EOOCD) and late-onset OCD (LO-OCD). Methods: Resting-state functional magnetic resonance imaging data were acquired from 88 medication-free OCD patients (including 30 EO-OCD and 58 LO-OCD) and age- and sex-matched healthy controls (HC) for each patient group. Onset-by-diagnosis interactions were examined and comparisons between each OCD group and the corresponding HC group were performed regarding the FC of amygdala subregions including the basolateral amygdala (BLA), centromedial amygdala (CMA), superficial amygdala (SFA) and amygdalostriatal transition area (Astr). Results: Significant onset-by-diagnosis interactions were found in FC between bilateral SFA, right CMA, left Astr and the cerebellum. EO-OCD patients showed abnormally increased BLA/SFA-cerebellum, BLA-precuneus and BLA/SFA-fusiform connectivity in addition to decreased BLA/SFA-orbitofrontal cortex connectivity. In contrast, LO-OCD patients exhibited increased CMA/Astr-precentral/postcentral gyrus and CMA-cuneus connectivity as well as decreased CMA/Astr-cerebellum and BLA-striatum connectivity. Limitations: The exclusion of comorbidity may reduce the generalizability of our results. Conclusions: These findings emphasized the different patterns of amygdala subregional connectivity alterations associated with EO-OCD and LO-OCD patients. These results provide unique insights into constructing evidencebased distinct OCD subtypes based on brain intrinsic connectivity and point to the need of specified management for EO-OCD and LO-OCD in clinical setting.

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