Hippocampal subregions and networks linked with antidepressant response to electroconvulsive therapy

被引:39
作者
Leaver, Amber M. [1 ,2 ]
Vasavada, Megha [1 ]
Kubicki, Antoni [1 ]
Wade, Benjamin [1 ]
Loureiro, Joana [1 ]
Hellemann, Gerhard [3 ]
Joshi, Shantanu H. [1 ]
Woods, Roger P. [1 ,3 ]
Espinoza, Randall [3 ]
Narr, Katherine L. [1 ,3 ]
机构
[1] Univ Calif Los Angeles, Ahmanson Lovelace Brain Mapping Ctr, Dept Neurol, Los Angeles, CA 90095 USA
[2] Northwestern Univ, Dept Radiol, Chicago, IL 60611 USA
[3] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA
关键词
TONIC-CLONIC SEIZURES; CEREBRAL-BLOOD-FLOW; GENERALIZED SEIZURES; CLINICAL-RESPONSE; MAJOR DEPRESSION; VOLUME; MODEL; NEUROGENESIS; MORPHOMETRY; INDUCTION;
D O I
10.1038/s41380-020-0666-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Electroconvulsive therapy (ECT) has been repeatedly linked to hippocampal plasticity. However, it remains unclear what role hippocampal plasticity plays in the antidepressant response to ECT. This magnetic resonance imaging (MRI) study tracks changes in separate hippocampal subregions and hippocampal networks in patients with depression (n = 44, 23 female) to determine their relationship, if any, with improvement after ECT. Voxelwise analyses were restricted to the hippocampus, amygdala, and parahippocampal cortex, and applied separately for responders and nonresponders to ECT. In analyses of arterial spin-labeled (ASL) MRI, nonresponders exhibited increased cerebral blood flow (CBF) in bilateral anterior hippocampus, while responders showed CBF increases in right middle and left posterior hippocampus. In analyses of gray matter volume (GMV) using T1-weighted MRI, GMV increased throughout bilateral hippocampus and surrounding tissue in nonresponders, while responders showed increased GMV in right anterior hippocampus only. Using CBF loci as seed regions, BOLD-fMRI data from healthy controls (n = 36, 19 female) identified spatially separable neurofunctional networks comprised of different brain regions. In graph theory analyses of these networks, functional connectivity within a hippocampus-thalamus-striatum network decreased only in responders after two treatments and after index. In sum, our results suggest that the location of ECT-related plasticity within the hippocampus may differ according to antidepressant outcome, and that larger amounts of hippocampal plasticity may not be conducive to positive antidepressant response. More focused targeting of hippocampal subregions and/or circuits may be a way to improve ECT outcome.
引用
收藏
页码:4288 / 4299
页数:12
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