Increased prefrontal cortex activity during negative emotion regulation as a predictor of depression symptom severity trajectory over 6 months.

Increased prefrontal cortex activity during negative emotion regulation as a predictor of depression symptom severity trajectory over 6 months.
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负面情绪调节期间额叶皮层活性增加,这是6个月内抑郁症状严重程度轨迹的预测指标。

DOI:
10.1001/jamapsychiatry.2013.2430
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发表时间:
2013-11
期刊:
影响因子:
25.8
通讯作者:
Davidson, Richard J.
Davidson, Richard J.
中科院分区:
医学1区
文献类型:
--
作者:
Heller, Aaron S.;Johnstone, Tom;Peterson, Michael J.;Kolden, Gregory G.;Kalin, Ned H.;Davidson, Richard J.

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Emotion regulation is critically disrupted in depression and use of paradigms tapping these processes may uncover essential changes in neurobiology during treatment. In addition, as neuroimaging outcome studies of depression commonly utilize solely baseline and endpoint data – which is more prone to week-to week noise in symptomatology – we sought to use all data points over the course of a six month trial. To examine changes in neurobiology resulting from successful treatment. Double-blind trial examining changes in the neural circuits involved in emotion regulation resulting from one of two antidepressant treatments over a six month trial. Participants were scanned pretreatment, at 2 months and 6 months posttreatment. University functional magnetic resonance imaging facility. 21 patients with Major Depressive Disorder and without other Axis I or Axis II diagnoses. Venlafaxine XR (doses up to 300mg) or Fluoxetine (doses up to 80mg). Neural activity, as measured using functional magnetic resonance imaging during performance of an emotion regulation paradigm as well as regular assessments of symptom severity by the Hamilton Rating Scale for Depression. To utilize all data points, slope trajectories were calculated for rate of change in depression severity as well as rate of change of neural engagement. Those depressed individuals showing the steepest decrease in depression severity over the six months were those individuals showing the most rapid increases in BA10 and right DLPFC activity when regulating negative affect over the same time frame. This relationship was more robust than when using solely the baseline and endpoint data. Changes in PFC engagement when regulating negative affect correlate with changes in depression severity over six months. These results are buttressed by calculating these statistics which are more reliable and robust to week-to-week variation than difference scores.
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