Researching the pathophysiology of pediatric bipolar disorder

被引:93
作者
Leibenluft, E [1 ]
Charney, DS [1 ]
Pine, DS [1 ]
机构
[1] NIMH, Mood & Anxiety Program, Dept Hlth & Human Serv, NIH, Bldg 10,Room 4N-208,10 Ctr Dr,MSC 1255, Bethesda, MD 20892 USA
关键词
child; bipolar disorder; attention; emotion; mania;
D O I
10.1016/S0006-3223(03)00069-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We suggest that the core feature of bipolar disorder (BPD) is marked state fluctuations. The pathophysiology of switches into depressed, irritable, and extreme positive valence states requires study, with the latter deserving particular focus because it represents a pathognomonic feature of BPD in both adults and children. Hypotheses regarding the pathophysiology of pediatric BPD must account for these marked state fluctuations as well as for specific developmental aspects of the illness. These developmental aspects include marked irritability (in addition to euphoria and depression) and very rapid cycles, along with high rates of attention-deficit/hyperactivity disorder. We review research on neural mechanisms underlying positive valence states and state regulation, focusing on those data relevant to BPD and to development. Researchers are beginning to explore the response of manic patients and control subjects to positive affective stimuli, and considerable research in both nonhuman primates and humans has focused on the cortico-limbic-striatal circuits mediating responses to rewarding stimuli. In control subjects, positive affect affects cognition, and data indicate that prefrontal electroencephalogram asymmetry may differ between control subjects with consistently positive affect and those with more negative affect; however, this latter generalization may not apply to adolescents. With regard to the pathophysiology of state switching in pediatric BPD, data in control subjects indicating that attention regulation plays a role in emotion regulation may be germane. In addition, research detailing physiologic and psychological responses to negative emotional stimuli in bipolar patients and control subjects may increase our understanding of the mechanisms underlying both irritability and rapid cycling seen in children with BPD. Potential foci for research on the pathophysiology of pediatric BPD include reactivity to standardized positive and negative emotional stimuli, and the interaction between emotion regulation and attentional processes. (C) 2003 Society of Biological Psychiatry.
引用
收藏
页码:1009 / 1020
页数:12
相关论文
共 50 条
[41]   Cellular plasticity cascades in the pathophysiology and treatment of bipolar disorder [J].
Schloesser, Robert J. ;
Huang, Jian ;
Klein, Peter S. ;
Manji, Husseini K. .
NEUROPSYCHOPHARMACOLOGY, 2008, 33 (01) :110-133
[42]   Mitochondrially mediated plasticity in the pathophysiology and treatment of bipolar disorder [J].
Quiroz, Jorge A. ;
Gray, Neil A. ;
Kato, Tadafumi ;
Manji, Husseini K. .
NEUROPSYCHOPHARMACOLOGY, 2008, 33 (11) :2551-2565
[43]   Cellular Plasticity Cascades in the Pathophysiology and Treatment of Bipolar Disorder [J].
Robert J Schloesser ;
Jian Huang ;
Peter S Klein ;
Husseini K Manji .
Neuropsychopharmacology, 2008, 33 :110-133
[44]   Neurochemical alteration in the caudate: Implications for the pathophysiology of bipolar disorder [J].
Shahana, Nasrin ;
DelBello, Melissa ;
Chu, Wen-Jang ;
Jarvis, Kelly ;
Fleck, David ;
Welge, Jeffrey ;
Strakowski, Stephen ;
Adler, Caleb .
PSYCHIATRY RESEARCH-NEUROIMAGING, 2011, 193 (02) :107-112
[45]   Mitochondrially Mediated Plasticity in the Pathophysiology and Treatment of Bipolar Disorder [J].
Jorge A Quiroz ;
Neil A Gray ;
Tadafumi Kato ;
Husseini K Manji .
Neuropsychopharmacology, 2008, 33 :2551-2565
[46]   The Role of the UPR Pathway in the Pathophysiology and Treatment of Bipolar Disorder [J].
Suliman, Mahmoud ;
Schmidtke, Michael W. ;
Greenberg, Miriam L. .
FRONTIERS IN CELLULAR NEUROSCIENCE, 2021, 15
[47]   ASSOCIATION OF OXIDATIVE STRESS WITH THE PATHOPHYSIOLOGY OF DEPRESSION AND BIPOLAR DISORDER [J].
Lackovic, Maja ;
Rovcanin, B. ;
Pantovic, Maja ;
Ivkovic, Maja ;
Petronijevic, Natasa ;
Damjanovic, A. .
ARCHIVES OF BIOLOGICAL SCIENCES, 2013, 65 (01) :369-373
[48]   A role for white matter abnormalities in the pathophysiology of bipolar disorder [J].
Mahon, Katie ;
Burdick, Katherine E. ;
Szeszko, Philip R. .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2010, 34 (04) :533-554
[49]   The role of DNA methylation in the pathophysiology and treatment of bipolar disorder [J].
Fries, Gabriel R. ;
Li, Qiongzhen ;
McAlpin, Blake ;
Rein, Theo ;
Walss-Bass, Consuelo ;
Soares, Jair C. ;
Quevedo, Joao .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2016, 68 :474-488
[50]   Mitochondrial Dysfunction in the Pathophysiology of Bipolar Disorder: Effects of Pharmacotherapy [J].
Callaly, Edward ;
Walder, Ken ;
Morris, Gerwyn ;
Maes, Michael ;
Debnath, Monojit ;
Berk, Michael .
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2015, 15 (05) :355-365