Elizabeth M Haris, Richard A Bryant, Kim L Felmingham, Leanne M Williams, Mayuresh S Korgaonkar
{"title":"Functional connectivity profiles of amygdala subregions in posttraumatic stress disorder.","authors":"Elizabeth M Haris, Richard A Bryant, Kim L Felmingham, Leanne M Williams, Mayuresh S Korgaonkar","doi":"10.1038/s41398-025-03508-y","DOIUrl":null,"url":null,"abstract":"<p><p>The amygdala is crucial to understanding posttraumatic stress disorder (PTSD), yet knowledge of the connectivity of its substructures and their contribution to the functional heterogeneity characteristic of the disorder remains limited. This study sought to delineate the functional profiles of amygdala substructures to advance a more nuanced understanding of their contribution to the neural circuitry underlying PTSD in a large sample. Task-derived intrinsic functional magnetic resonance imaging (rs-fMRI) data for 64 non-trauma-exposed controls (NEC) and 65 individuals with PTSD were analyzed. Amygdala subnuclei were segmented using FreeSurfer and combined into three major substructures for each hemisphere: the basolateral (BLA), centromedial (CMA), and superficial (SFA) nuclei. Seed-to-voxel functional connectivity analyses for the whole brain were performed to investigate group differences in subnuclei connectivity profiles. A significant group by subnuclei interaction was found for four clusters, driven by group differences in connectivity related to the BLA. There was lower connectivity in the PTSD group for the left BLA and precuneus, posterior cingulate, right superior parietal lobe, right postcentral gyrus, and bilateral precentral gyri. Higher connectivity was found in the PTSD group for the left BLA and brainstem, and for the right BLA and cerebellum, and brainstem and right pallidum. No group differences were found for the CMA or SFA. These results illustrate the importance of the BLA in driving task-derived intrinsic functional connectivity between NEC and PTSD groups. Findings suggest that group differences lie in lower connectivity with cortical areas involved in self-referential and sensorimotor processing, but higher connectivity with subcortical areas involved in arousal, salience, sensory, and reward processing.</p>","PeriodicalId":23278,"journal":{"name":"Translational Psychiatry","volume":"15 1","pages":"280"},"PeriodicalIF":6.2000,"publicationDate":"2025-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12350740/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41398-025-03508-y","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0
Abstract
The amygdala is crucial to understanding posttraumatic stress disorder (PTSD), yet knowledge of the connectivity of its substructures and their contribution to the functional heterogeneity characteristic of the disorder remains limited. This study sought to delineate the functional profiles of amygdala substructures to advance a more nuanced understanding of their contribution to the neural circuitry underlying PTSD in a large sample. Task-derived intrinsic functional magnetic resonance imaging (rs-fMRI) data for 64 non-trauma-exposed controls (NEC) and 65 individuals with PTSD were analyzed. Amygdala subnuclei were segmented using FreeSurfer and combined into three major substructures for each hemisphere: the basolateral (BLA), centromedial (CMA), and superficial (SFA) nuclei. Seed-to-voxel functional connectivity analyses for the whole brain were performed to investigate group differences in subnuclei connectivity profiles. A significant group by subnuclei interaction was found for four clusters, driven by group differences in connectivity related to the BLA. There was lower connectivity in the PTSD group for the left BLA and precuneus, posterior cingulate, right superior parietal lobe, right postcentral gyrus, and bilateral precentral gyri. Higher connectivity was found in the PTSD group for the left BLA and brainstem, and for the right BLA and cerebellum, and brainstem and right pallidum. No group differences were found for the CMA or SFA. These results illustrate the importance of the BLA in driving task-derived intrinsic functional connectivity between NEC and PTSD groups. Findings suggest that group differences lie in lower connectivity with cortical areas involved in self-referential and sensorimotor processing, but higher connectivity with subcortical areas involved in arousal, salience, sensory, and reward processing.
期刊介绍:
Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.