TY - JOUR
T1 - Intrinsic functional connectivity of the central extended amygdala
AU - Tillman, Rachael M.
AU - Stockbridge, Melissa D.
AU - Nacewicz, Brendon M.
AU - Torrisi, Salvatore
AU - Fox, Andrew S.
AU - Smith, Jason F.
AU - Shackman, Alexander J.
N1 - Funding Information:
Authors acknowledge assistance from J. Blackford, K. DeYoung, L. Friedman, M. Milham, and D. Tromp and critical feedback from N. Fox, L. Pessoa, and E. Redcay. They also wish to thank Drs R. Poldrack and A. Holmes for guidance on the signal quality analyses. This work was supported by the University of California, Davis; University of Maryland, College Park; University of Wisconsin—Madison; and National Institutes of Health (DA040717 and MH107444)
Funding Information:
Authors acknowledge assistance from J. Blackford, K. DeYoung, L. Friedman, M. Milham, and D. Tromp and critical feedback from N. Fox, L. Pessoa, and E. Redcay. They also wish to thank Drs R. Pol-drack and A. Holmes for guidance on the signal quality analyses. This work was supported by the University of California, Davis; University of Maryland, College Park; University of Wisconsin—
Publisher Copyright:
© 2017 Wiley Periodicals, Inc.
PY - 2018/3
Y1 - 2018/3
N2 - The central extended amygdala (EAc)—including the bed nucleus of the stria terminalis (BST) and central nucleus of the amygdala (Ce)—plays a critical role in triggering fear and anxiety and is implicated in the development of a range of debilitating neuropsychiatric disorders. Although it is widely believed that these disorders reflect the coordinated activity of distributed neural circuits, the functional architecture of the EAc network and the degree to which the BST and the Ce show distinct patterns of functional connectivity is unclear. Here, we used a novel combination of imaging approaches to trace the connectivity of the BST and the Ce in 130 healthy, racially diverse, community-dwelling adults. Multiband imaging, high-precision registration techniques, and spatially unsmoothed data maximized anatomical specificity. Using newly developed seed regions, whole-brain regression analyses revealed robust functional connectivity between the BST and Ce via the sublenticular extended amygdala, the ribbon of subcortical gray matter encompassing the ventral amygdalofugal pathway. Both regions displayed coupling with the ventromedial prefrontal cortex (vmPFC), midcingulate cortex (MCC), insula, and anterior hippocampus. The BST showed stronger connectivity with the thalamus, striatum, periaqueductal gray, and several prefrontal territories. The only regions showing stronger functional connectivity with the Ce were neighboring regions of the dorsal amygdala, amygdalohippocampal area, and anterior hippocampus. These observations provide a baseline against which to compare a range of special populations, inform our understanding of the role of the EAc in normal and pathological fear and anxiety, and showcase image registration techniques that are likely to be useful for researchers working with “deidentified” neuroimaging data.
AB - The central extended amygdala (EAc)—including the bed nucleus of the stria terminalis (BST) and central nucleus of the amygdala (Ce)—plays a critical role in triggering fear and anxiety and is implicated in the development of a range of debilitating neuropsychiatric disorders. Although it is widely believed that these disorders reflect the coordinated activity of distributed neural circuits, the functional architecture of the EAc network and the degree to which the BST and the Ce show distinct patterns of functional connectivity is unclear. Here, we used a novel combination of imaging approaches to trace the connectivity of the BST and the Ce in 130 healthy, racially diverse, community-dwelling adults. Multiband imaging, high-precision registration techniques, and spatially unsmoothed data maximized anatomical specificity. Using newly developed seed regions, whole-brain regression analyses revealed robust functional connectivity between the BST and Ce via the sublenticular extended amygdala, the ribbon of subcortical gray matter encompassing the ventral amygdalofugal pathway. Both regions displayed coupling with the ventromedial prefrontal cortex (vmPFC), midcingulate cortex (MCC), insula, and anterior hippocampus. The BST showed stronger connectivity with the thalamus, striatum, periaqueductal gray, and several prefrontal territories. The only regions showing stronger functional connectivity with the Ce were neighboring regions of the dorsal amygdala, amygdalohippocampal area, and anterior hippocampus. These observations provide a baseline against which to compare a range of special populations, inform our understanding of the role of the EAc in normal and pathological fear and anxiety, and showcase image registration techniques that are likely to be useful for researchers working with “deidentified” neuroimaging data.
KW - affective neuroscience
KW - amygdala
KW - anxiety
KW - bed nucleus of the stria terminalis (BST/BNST)
KW - central extended amygdala
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U2 - 10.1002/hbm.23917
DO - 10.1002/hbm.23917
M3 - Article
C2 - 29235190
AN - SCOPUS:85041714686
SN - 1065-9471
VL - 39
SP - 1291
EP - 1312
JO - Human Brain Mapping
JF - Human Brain Mapping
IS - 3
ER -