A Human Depression Circuit Derived From Focal Brain Lesions.
A Human Depression Circuit Derived From Focal Brain Lesions.
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DOI:
10.1016/j.biopsych.2019.07.023
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发表时间:
2019-11-15
影响因子:
10.6
通讯作者:
Fox MD
中科院分区:
文献类型:
--
作者:
Padmanabhan JL;Cooke D;Joutsa J;Siddiqi SH;Ferguson M;Darby RR;Soussand L;Horn A;Kim NY;Voss JL;Naidech AM;Brodtmann A;Egorova N;Gozzi S;Phan TG;Corbetta M;Grafman J;Fox MD
Focal brain lesions can lend insight into the causal neuroanatomical substrate of depression in the human brain. However, studies of lesion location have led to inconsistent results. Five independent datasets with different lesion etiologies and measures of post-lesion depression were collated (N = 461). Each 3D lesion location was mapped to a common brain atlas. We used voxel lesion symptom mapping to test for associations between depression and lesion locations. Next, we computed the network of regions functionally connected to each lesion location using a large normative connectome dataset (N = 1000). We used these lesion network maps to test for associations between depression and connected brain circuits. Reproducibility was assessed using a rigorous leave-one-dataset-out validation. Finally, we tested whether lesion locations associated with depression fell within the same circuit as brain stimulation sites effective for improving post-stroke depression. Lesion locations associated with depression were highly heterogeneous, and no single brain region was consistently implicated. However, these same lesion locations mapped to a connected brain circuit, centered on the left dorsolateral prefrontal cortex. Results were robust to leave one-dataset-out cross-validation. Finally, our depression circuit derived from brain lesions aligned with brain stimulation sites effective for improving post-stroke depression. Lesion locations associated with depression fail to map to a specific brain region but do map to a specific brain circuit. This circuit may have prognostic utility in identifying patients at risk for post-stroke depression and therapeutic utility in refining brain stimulation targets.
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影响因子:
9.8
作者:
Holmes, Avram J.;Hollinshead, Marisa O.;O'Keefe, Timothy M.;Petrov, Victor I.;Fariello, Gabriele R.;Wald, Lawrence L.;Fischl, Bruce;Rosen, Bruce R.;Mair, Ross W.;Roffman, Joshua L.;Smoller, Jordan W.;Buckner, Randy L.
通讯作者:
Buckner, Randy L.
DOI:
10.1073/pnas.1706587115
发表时间:
2018-01-16
影响因子:
11.1
作者:
Darby RR;Horn A;Cushman F;Fox MD
通讯作者:
Fox MD
影响因子:
16.2
作者:
Corbetta M;Ramsey L;Callejas A;Baldassarre A;Hacker CD;Siegel JS;Astafiev SV;Rengachary J;Zinn K;Lang CE;Connor LT;Fucetola R;Strube M;Carter AR;Shulman GL
通讯作者:
Shulman GL
影响因子:
5.7
作者:
Fox MD;Liu H;Pascual-Leone A
通讯作者:
Pascual-Leone A
影响因子:
10.6
作者:
George, MS;Nahas, Z;Ballenger, JC
通讯作者:
Ballenger, JC