A Critical Appraisal of Neuroimaging Studies of Bipolar Disorder: Toward a New Conceptualization of Underlying Neural Circuitry and a Road Map for Future Research

被引:416
作者
Phillips, Mary L. [1 ]
Swartz, Holly A.
机构
[1] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA 15260 USA
关键词
WHITE-MATTER ABNORMALITIES; ANTERIOR CINGULATE CORTEX; MEDIAL PREFRONTAL CORTEX; FUNCTIONAL CONNECTIVITY; RESTING-STATE; AMYGDALA ACTIVATION; I DISORDER; ORBITOFRONTAL CORTEX; MICROSTRUCTURAL ABNORMALITIES; FACIAL EXPRESSIONS;
D O I
10.1176/appi.ajp.2014.13081008
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: In this critical review, the authors appraise neuroimaging findings in bipolar disorder in emotion-processing, emotion-regulation, and reward-processing neural circuitry in order to synthesize the current knowledge of the neural underpinnings of bipolar disorder and provide a neuroimaging research road map for future studies. Method: The authors examined findings from all major studies in bipolar disorder that used functional MRI, volumetric analysis, diffusion imaging, and resting-state techniques, integrating findings to provide a better understanding of larger-scale neural circuitry abnormalities in bipolar disorder. Results: Bipolar disorder can be conceptualized, in neural circuitry terms, as parallel dysfunction in prefrontal cortical (especially ventrolateral prefrontal cortical)hippocampal-amygdala emotion-processing and emotion-regulation circuits bilaterally, together with an "overactive" left-sided ventral. striatal-ventrolateral and orbitofrontal cortical reward-processing circuitry, resulting in characteristic behavioral abnormalities associated with bipolar disorder: emotional lability, emotional dysregulation, and heightened reward sensitivity. A potential structural basis for these functional abnormalities is gray matter volume decreases in the prefrontal and temporal cortices, the amygdala, and the hippocampus and fractional anisotropy decreases in white matter tracts connecting prefrontal and subcortical regions. Conclusions: Neuroimaging studies of bipolar disorder clearly demonstrate abnormalities in neural circuits supporting emotion processing, emotion regulation, and reward processing, although there are several limitations to these studies. Future neuroimaging research in bipolar disorder should include studies adopting dimensional approaches; larger studies examining neurodevelopmental trajectories in youths with bipolar disorder or at risk for bipolar disorder; multimodal neuroimaging studies using integrated systems approaches; and studies using pattern recognition approaches to provide clinically useful individual-level data. Such studies will help identify clinically relevant biomarkers to guide diagnosis and treatment decision making for individuals with bipolar disorder.
引用
收藏
页码:829 / 843
页数:15
相关论文
共 153 条
[1]   Abnormal reward system activation in mania [J].
Abler, Birgit ;
Greenhouse, Ian ;
Ongur, Dost ;
Walter, Henrik ;
Heckers, Stephan .
NEUROPSYCHOPHARMACOLOGY, 2008, 33 (09) :2217-2227
[2]   Abnormal frontal white matter tracts in bipolar disorder: a diffusion tensor imaging study [J].
Adler, CM ;
Holland, SK ;
Schmithorst, V ;
Wilke, M ;
Weiss, KL ;
Pan, H ;
Strakowski, SM .
BIPOLAR DISORDERS, 2004, 6 (03) :197-203
[3]   High Behavioral Approach System (BAS) Sensitivity, Reward Responsiveness, and Goal-Striving Predict First Onset of Bipolar Spectrum Disorders: A Prospective Behavioral High-Risk Design [J].
Alloy, Lauren B. ;
Bender, Rachel E. ;
Whitehouse, Wayne G. ;
Wagner, Clara A. ;
Liu, Richard T. ;
Grant, David A. ;
Jager-Hyman, Shari ;
Molz, Ashleigh ;
Choi, James Y. ;
Harmon-Jones, Eddie ;
Abramson, Lyn Y. .
JOURNAL OF ABNORMAL PSYCHOLOGY, 2012, 121 (02) :339-351
[4]   Pattern recognition analysis of anterior cingulate cortex blood flow to classify depression polarity [J].
Almeida, J. R. C. ;
Mourao-Miranda, J. ;
Aizenstein, H. J. ;
Versace, A. ;
Kozel, F. A. ;
Lu, H. ;
Marquand, A. ;
LaBarbara, E. J. ;
Brammer, M. ;
Trivedi, M. ;
Kupfer, D. J. ;
Phillips, M. L. .
BRITISH JOURNAL OF PSYCHIATRY, 2013, 203 (04) :310-311
[5]   Reduced gray matter volume in ventral prefrontal cortex but not amygdala in bipolar disorder: Significant effects of gender and trait anxiety [J].
Almeida, Jorge R. C. ;
Akkal, Dalila ;
Hassel, Stefanie ;
Travis, Michael J. ;
Banihashemi, Layla ;
Kerr, Natalie ;
Kupfer, David J. ;
Phillips, Mary L. .
PSYCHIATRY RESEARCH-NEUROIMAGING, 2009, 171 (01) :54-68
[6]   Amygdala enlargement in bipolar disorder and hippocampal reduction in schizophrenia: An MRI study demonstrating neuroanatomic specificity [J].
Altshuler, LL ;
Bartzokis, G ;
Grieder, T ;
Curran, J ;
Mintz, J .
ARCHIVES OF GENERAL PSYCHIATRY, 1998, 55 (07) :663-664
[7]   Regional brain changes in bipolar I depression: a functional magnetic resonance imaging study [J].
Altshuler, Lori ;
Bookheimer, Susan ;
Townsend, Jennifer ;
Proenza, Manuel A. ;
Sabb, Fred ;
Mintz, Jim ;
Cohen, Mark S. .
BIPOLAR DISORDERS, 2008, 10 (06) :708-717
[8]   Resting state corticolimbic connectivity abnormalities in unmedicated bipolar disorder and unipolar depression [J].
Anand, Amit ;
Li, Yu ;
Wang, Yang ;
Lowe, Mark J. ;
Dzemidzic, Mario .
PSYCHIATRY RESEARCH-NEUROIMAGING, 2009, 171 (03) :189-198
[9]  
Anticevic A., 2013, CEREB CORTEX
[10]   Global Prefrontal and Fronto-Amygdala Dysconnectivity in Bipolar I Disorder with Psychosis History [J].
Anticevic, Alan ;
Brumbaugh, Margaret S. ;
Winkler, Anderson M. ;
Lombardo, Lauren E. ;
Barrett, Jennifer ;
Corlett, Phillip R. ;
Kober, Hedy ;
Gruber, June ;
Repovs, Grega ;
Cole, Michael W. ;
Krystal, John H. ;
Pearlson, Godfrey D. ;
Glahn, David C. .
BIOLOGICAL PSYCHIATRY, 2013, 73 (06) :565-573