Fronto-limbic dysfunction in mania pre-treatment and persistent amygdala over-activity post-treatment in pediatric bipolar disorder.
Fronto-limbic dysfunction in mania pre-treatment and persistent amygdala over-activity post-treatment in pediatric bipolar disorder.
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DOI:
10.1007/s00213-011-2243-2
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发表时间:
2011-08
影响因子:
3.4
通讯作者:
Pavuluri, Mani N.
中科院分区:
文献类型:
--
作者:
Passarotti, Alessandra M.;Sweeney, John A.;Pavuluri, Mani N.
关键词:
Neural deficits at the interface of affect and cognition may improve with pharmacotherapy in pediatric bipolar disorder (PBD). We examined lamotrigine treatment impact on the neural interface of working memory and affect in PBD. Un-medicated, acutely ill, patients with mania and hypomania (n=17), and healthy controls (HC; n=13; mean age=13.36±2.55) performed an affective two-back functional magnetic resonance imaging task with blocks of angry vs neutral faces (i.e., angry face condition) or happy vs neutral faces (i.e., happy face condition) before treatment and at follow-up, after 8-week treatment with second-generation antipsychotics followed by 6 weeks of lamotrigine monotherapy. At baseline, for the angry face condition, PBD, relative to HC, showed reduced activation in the left ventrolateral prefrontal cortex (VLPFC) and right caudate; for the happy face condition, PBD showed increased activation in bilateral PFC and right amygdala and middle temporal gyrus. Post-treatment, PBD showed greater activation in right amygdala relative to HC for both conditions. Patients, relative to HC, exhibited greater changes over time in the right VLPFC and amygdala, left subgenual anterior cingulate cortex and left caudate for the angry face condition, and in right middle temporal gyrus for the happy face condition. Pharmacotherapy resulted in symptom improvement and normalization of higher cortical emotional and cognitive regions in patients relative to HC, suggesting that the VLPFC dysfunction may be state-specific in PBD. Amygdala was overactive in PBD, relative to HC, regardless of reduction in manic symptoms, and may be a trait marker of PBD.
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影响因子:
5.7
作者:
Hart, Sarah J.;Green, Steven R.;Casp, Michael;Belger, Aysenil
通讯作者:
Belger, Aysenil
影响因子:
10.6
作者:
Frangou, S;Haldane, M;Kumari, V
通讯作者:
Kumari, V
影响因子:
4.8
作者:
Gruber, Oliver;Tost, Heike;Rietschel, Marcella
通讯作者:
Rietschel, Marcella
影响因子:
5.7
作者:
CASEY, BJ;COHEN, JD;RAPOPORT, JL
通讯作者:
RAPOPORT, JL
DOI:
10.1176/appi.ajp.2009.09010043
发表时间:
2010-01
期刊:
The American journal of psychiatry
影响因子:
--
作者:
Brotman MA;Rich BA;Guyer AE;Lunsford JR;Horsey SE;Reising MM;Thomas LA;Fromm SJ;Towbin K;Pine DS;Leibenluft E
通讯作者:
Leibenluft E