Multimodal structural neuroimaging markers of risk and recovery from posttrauma anhedonia: A prospective investigation.
Multimodal structural neuroimaging markers of risk and recovery from posttrauma anhedonia: A prospective investigation.
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DOI:
10.1002/da.23104
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发表时间:
2021-01
影响因子:
7.4
通讯作者:
Fani N
中科院分区:
文献类型:
--
作者:
Harnett NG;Stevens JS;van Rooij SJH;Ely TD;Michopoulos V;Hudak L;Jovanovic T;Rothbaum BO;Ressler KJ;Fani N
Anhedonic symptoms of posttraumatic stress disorder (PTSD) reflect deficits in reward processing that have significant functional consequences. Although recent evidence suggests that disrupted integrity of fronto-limbic circuitry is related to PTSD development, including anhedonic PTSD symptoms (post-trauma anhedonia; PTA), little is known about potential structural biomarkers of long-term PTA as well as structural changes in fronto-limbic pathways associated with recovery from PTA over time. We investigated associations between white matter microstructure, gray matter volume, and PTA in 75 recently traumatized individuals, with a subset of participants (n = 35) completing follow-up assessment 12 months after trauma exposure. Deterministic tractography and voxel-based morphometry were used to assess changes in white and gray matter structure associated with changes in PTA. Reduced fractional anisotropy (FA) of the uncinate fasciculus at around the time of trauma predicted greater PTA at 12 months post-trauma. Further, increased FA of the fornix over time was associated with lower PTA between 1- and 12-months post-trauma. Increased gray matter volume of the ventromedial PFC and precuneus over time was also associated with reduced PTA. Microstructure of the uncinate fasciculus, an amygdala-prefrontal white matter connection, may represent a biomarker of vulnerability for later PTA. Conversely, development and recovery from PTA appears to be facilitated by white and gray matter structural changes in a major hippocampal pathway, the fornix. The present findings shed new light on neuroanatomical substrates of recovery from PTA and characterize white matter biomarkers of risk for posttraumatic dysfunction.
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影响因子:
4.2
作者:
Coloigner, Julie;Batail, Jean-Marie;Drapier, Dominique
通讯作者:
Drapier, Dominique
DOI:
10.1038/s41583-018-0039-7
发表时间:
2018-09
期刊:
Nature reviews. Neuroscience
影响因子:
--
作者:
Fenster RJ;Lebois LAM;Ressler KJ;Suh J
通讯作者:
Suh J
影响因子:
5
作者:
Armour C
通讯作者:
Armour C
影响因子:
4.8
作者:
Fani, Negar;Michopoulos, Vasiliki;Stevens, Jennifer S.
通讯作者:
Stevens, Jennifer S.
影响因子:
3.3
作者:
Feeny, NC;Zoellner, LA;Foa, EB
通讯作者:
Foa, EB