Pretreatment brain states identify likely nonresponse to standard treatments for depression.

Pretreatment brain states identify likely nonresponse to standard treatments for depression.
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DOI:
10.1016/j.biopsych.2013.12.005
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发表时间:
2014-10-01
影响因子:
10.6
通讯作者:
Mayberg, Helen S.
Mayberg, Helen S.
中科院分区:
医学1区
文献类型:
--
作者:
McGrath, Callie L.;Kelley, Mary E.;Dunlop, Boadie W.;Holtzheimer, Paul E., III;Craighead, W. Edward;Mayberg, Helen S.

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Treatment approaches for major depressive disorder (MDD) result in approximately one-third of patients achieving remission after a first treatment. Added treatment generally improves remission rates, but approximately one-third of all patients fail to respond after several treatments (sequential monotherapies or combined treatment). A pretreatment biomarker could help identify these patients. Over activity of the subcallosal cingulate has been associated with treatment non-response in MDD, and it is a potential candidate for such a biomarker. Eighty-two currently untreated MDD patients were enrolled in a two-phase treatment study. A flurodeoxyglucose positron emission tomography scan was acquired. Following scanning, patients were randomized to 12 weeks of either escitalopram or cognitive behavior therapy (CBT). Patients not achieving remission after 12 weeks of initial treatment were treated with an additional 12 weeks of escitalopram plus CBT. Subcallosal cingulate metabolism was compared between non-responders and remitters to either Phase 1 or Phase 2 treatment. This analysis was followed by a whole brain analysis making the same comparison. After two phases of treatment (24 weeks), 36 patients achieved remission, 6 patients achieved response, and 9 patients were non-responders. Subcallosal cingulate metabolism was significantly higher in non-responders than remitters. In the follow-up whole brain analysis, increased superior temporal sulcus activity was also associated with two-treatment non-response. Depressed patients who fail to remit to CBT or escitalopram, either alone or in combination, have a distinct brain metabolic pattern compared to patients who remit with CBT, escitalopram or their combination. Registered at clinicaltrials.gov (NCT00367341)
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