Functional neuroanatomy of bipolar disorder: structure, function, and connectivity in an amygdala–anterior paralimbic neural system
Hilary P Blumberg
Department of Psychiatry
Department of Diagnostic Radiology
The Child Study Center, Yale School of Medicine, New Haven
Research Enhancement Award Program Depression Center, Veterans Affairs Connecticut Healthcare System, West Haven, CT, USA
Search for more papers by this authorHilary P Blumberg
Department of Psychiatry
Department of Diagnostic Radiology
The Child Study Center, Yale School of Medicine, New Haven
Research Enhancement Award Program Depression Center, Veterans Affairs Connecticut Healthcare System, West Haven, CT, USA
Search for more papers by this authorAbstract
Blond BN, Fredericks CA, Blumberg HP. Functional neuroanatomy of bipolar disorder: structure, function, and connectivity in an amygdala–anterior paralimbic neural system. Bipolar Disord 2012: 14: 340–355. © 2012 The Authors. Journal compilation © 2012 John Wiley & Sons A/S.
Objectives: In past decades, neuroimaging research in bipolar disorder has demonstrated a convergence of findings in an amygdala–anterior paralimbic cortex neural system. This paper reviews behavioral neurology literature that first suggested a central role for this neural system in the disorder and the neuroimaging evidence that supports it.
Methods: Relevant articles are reviewed to provide an amygdala–anterior paralimbic cortex neural system model of bipolar disorder, including articles from the fields of behavioral neurology and neuroanatomy, and neuroimaging.
Results: The literature is highly supportive of key roles for the amygdala, anterior paralimbic cortices, and connections among these structures in the emotional dysregulation of bipolar disorder. The functions subserved by their more widely distributed connection sites suggest that broader system dysfunction could account for the range of functions—from neurovegetative to cognitive—disrupted in the disorder. Abnormalities in some components of this neural system are apparent by adolescence, while others, such as those in rostral prefrontal regions, appear to progress over adolescence and young adulthood, suggesting a neurodevelopmental model of the disorder. However, some findings conflict, which may reflect the small sample sizes of some studies, and clinical heterogeneity and methodological differences across studies.
Conclusions: Consistent with models derived from early behavioral neurology studies, neuroimaging studies support a central role for an amygdala–anterior paralimbic neural system in bipolar disorder, and implicate abnormalities in the development of this system in the disorder. This system will be an important focus of future studies on the developmental pathophysiology, detection, treatment, and prevention of the disorder.
References
- 1 Amaral DG, Price JL. Amygdalo-cortical projections in the monkey (Macaca fascicularis). J Comp Neurol 1984; 230: 465–496.
- 2 Devinsky O, Morrell MJ, Vogt BA. Contributions of anterior cingulate cortex to behaviour. Brain 1995; 118: 279–306.
- 3 Mesulam MM, Mufson EJ. Insula of the old world monkey. I. Architectonics in the insulo-orbito-temporal component of the paralimbic brain. J Comp Neurol 1982; 212: 1–22.
- 4 Morecraft RJ, Geula C, Mesulam MM. Cytoarchitecture and neural afferents of orbitofrontal cortex in the brain of the monkey. J Comp Neurol 1992; 323: 341–358.
- 5 Vogt BA, Nimchinsky EA, Vogt LJ, Hof PR. Human cingulate cortex: surface features, flat maps, and cytoarchitecture. J Comp Neurol 1995; 359: 490–506.
- 6 Bechara A, Damasio H, Damasio AR, Lee GP. Different contributions of the human amygdala and ventromedial prefrontal cortex to decision-making. J Neurosci 1999; 19: 5473–5481.
- 7 Blumer D, Benson DF. Psychiatric Aspects of Neurologic Disease. New York: Grune and Stratton, 1975.
- 8 Cummings JL, Mendez MF. Secondary mania with focal cerebrovascular lesions. Am J Psychiatry 1984; 141: 1084–1087.
- 9 Cummings JL. Clinical Neuropsychiatry. Orlando: Grune and Stratton, 1986.
- 10 Damasio AR, Anderson SW. The Frontal Lobes. In: KM Heilman, E Valentstein eds. Clinical Neuropsychology, 3rd ed. Oxford: Oxford University Press, 1993: 409–460.
- 11 Damasio H, Grabowski T, Frank R, Galaburda AM, Damasio AR. The return of Phineas Gage: clues about the brain from the skull of a famous patient. Science 1994; 264: 1102–1105.
- 12
Jastrowitz M.
Beitrage zur localisation im grosshirn and uber deren praktische verwerthung.
Dtsch Med Wochenshr.
1888; 14: 81–83.
10.1055/s-0029-1207725 Google Scholar
- 13
Oppenheim H.
Zur pathologie der grosshirngeschwulste.
Arch Psychiatry
1889; 21: 560–578.
10.1007/BF02229727 Google Scholar
- 14 Rolls ET, Hornak J, Wade D, McGrath J. Emotion-related learning in patients with social and emotional changes associated with frontal lobe damage. J Neurol Neurosurg Psychiatry 1994; 57: 1518–1524.
- 15 Damasio AR. The somatic marker hypothesis and the possible functions of the prefrontal cortex. Philos Trans R Soc Lond B Biol Sci 1996; 351: 1413–1420.
- 16 Schoenbaum G, Chiba AA, Gallagher M. Orbitofrontal cortex and basolateral amygdala encode expected outcomes during learning. Nat Neurosci 1998; 1: 155–159.
- 17 Nauta WJ. The problem of the frontal lobe: a reinterpretation. J Psychiatr Res 1971; 8: 167–187.
- 18 Rolls ET. The Brain and Emotion. Oxford: Oxford University Press, 1999.
- 19 Addington J, Addington D. Facial affect recognition and information processing in schizophrenia and bipolar disorder. Schizophr Res 1998; 32: 171–181.
- 20 Lembke A, Ketter TA. Impaired recognition of facial emotion in mania. Am J Psychiatry 2002; 159: 302–304.
- 21 McClure EB, Pope K, Hoberman AJ, Pine DS, Leibenluft E. Facial expression recognition in adolescents with mood and anxiety disorders. Am J Psychiatry 2003; 160: 1172–1174.
- 22 Rich BA, Grimley ME, Schmajuk M, Blair KS, Blair RJ, Leibenluft E. Face emotion labeling deficits in children with bipolar disorder and severe mood dysregulation. Dev Psychopathol 2008; 20: 529–546.
- 23 Schenkel LS, Pavuluri MN, Herbener ES, Harral EM, Sweeney JA. Facial emotion processing in acutely ill and euthymic patients with pediatric bipolar disorder. J Am Acad Child Adolesc Psychiatry 2007; 46: 1070–1079.
- 24 Adolphs R, Tranel D, Damasio AR. The human amygdala in social judgment. Nature 1998; 393: 470–474.
- 25 Sackeim HA, Greenberg MS, Weiman AL, Gur RC, Hungerbuhler JP, Geschwind N. Hemispheric asymmetry in the expression of positive and negative emotions. Neurologic evidence. Arch Neurol 1982; 39: 210–218.
- 26 Starkstein SE, Fedoroff P, Berthier ML, Robinson RG. Manic-depressive and pure manic states after brain lesions. Biol Psychiatry 1991; 29: 149–158.
- 27 Wexler BE. Cerebral laterality and psychiatry: a review of the literature. Am J Psychiatry 1980; 137: 279–291.
- 28 Bear DM, Fedio P. Quantitative analysis of interictal behavior in temporal lobe epilepsy. Arch Neurol 1977; 34: 454–467.
- 29 Flor-Henry P. Schizophrenic-like reactions and affective psychoses associated with temporal lobe epilepsy: etiological factors. Am J Psychiatry 1969; 126: 400–404.
- 30 Post RM, Rubinow DR, Ballenger JC. Conditioning and sensitisation in the longitudinal course of affective illness. Br J Psychiatry 1986; 149: 191–201.
- 31 Blumberg HP, Donegan NH, Sanislow CA et al. Preliminary evidence for medication effects on functional abnormalities in the amygdala and anterior cingulate in bipolar disorder. Psychopharmacol 2005; 183: 308–313.
- 32 Mega MS, Cummings JL. Frontal-subcortical circuits and neuropsychiatric disorders. J Neuropsychiatry Clin Neurosci 1994; 6: 358–370.
- 33 Lauterbach EC. Bipolar disorders, dystonia, and compulsion after dysfunction of the cerebellum, dentatorubrothalamic tract, and substantia nigra. Biol Psychiatry 1996; 40: 726–730.
- 34 Mayberg HS, Starkstein SE, Sadzot B et al. Selective hypometabolism in the inferior frontal lobe in depressed patients with Parkinson’s disease. Ann Neurol 1990; 28: 57–64.
- 35 Mayberg HS, Starkstein SE, Peyser CE, Brandt J, Dannals RF, Folstein SE. Paralimbic frontal lobe hypometabolism in depression associated with Huntington’s disease. Neurology 1992; 42: 1791–1797.
- 36 Mayberg HS. Frontal lobe dysfunction in secondary depression. J Neuropsychiatry Clin Neurosci 1994; 6: 428–442.
- 37 Starr MA. Organic Nervous Diseases. New York: Lea Brothers & Co., 1903.
- 38 Moniz E. Prefrontal leucotomy in the treatment of mental disorders. 1937. Am J Psychiatry 1994; 151: 236–239.
- 39 Green EK, Raybould R, Macgregor S et al. Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder. Arch Gen Psychiatry 2005; 62: 642–648.
- 40 Kim S, Webster MJ. Correlation analysis between genome-wide expression profiles and cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders. Mol Psychiatry 2010; 15: 326–336.
- 41 Ongur D, Drevets WC, Price JL. Glial reduction in the subgenual prefrontal cortex in mood disorders. Proc Natl Acad Sci USA 1998; 95: 13290–13295.
- 42 Rajkowska G. Cell pathology in mood disorders. Semin Clin Neuropsychiatry 2002; 7: 281–292.
- 43 Tkachev D, Mimmack ML, Ryan MM et al. Oligodendrocyte dysfunction in schizophrenia and bipolar disorder. Lancet 2003; 362: 798–805.
- 44 Uranova NA, Vostrikov VM, Orlovskaya DD, Rachmanova VI. Oligodendroglial density in the prefrontal cortex in schizophrenia and mood disorders: a study from the Stanley Neuropathology Consortium. Schizophr Res 2004; 67: 269–275.
- 45 Vostrikov VM, Uranova NA, Orlovskaya DD. Deficit of perineuronal oligodendrocytes in the prefrontal cortex in schizophrenia and mood disorders. Schizophr Res 2007; 94: 273–280.
- 46 Machado CJ, Bachevalier J. Non-human primate models of childhood psychopathology: the promise and the limitations. J Child Psychol Psychiatry 2003; 44: 64–87.
- 47 Schumann CM, Bauman MD, Amaral DG. Abnormal structure or function of the amygdala is a common component of neurodevelopmental disorders. Neuropsychologia 2011; 49: 745–759.
- 48 Adolphs R, Tranel D, Damasio H, Damasio A. Impaired recognition of emotion in facial expressions following bilateral damage to the human amygdala. Nature 1994; 372: 669–672.
- 49 Shaw P, Lawrence EJ, Radbourne C, Bramham J, Polkey CE, David AS. The impact of early and late damage to the human amygdala on ‘theory of mind’ reasoning. Brain 2004; 127: 1535–1548.
- 50 Hamann SB, Adolphs R. Normal recognition of emotional similarity between facial expressions following bilateral amygdala damage. Neuropsychologia 1999; 37: 1135–1141.
- 51 Liao D, Scannevin RH, Huganir R. Activation of silent synapses by rapid activity-dependent synaptic recruitment of AMPA receptors. J Neurosci 2001; 21: 6008–6017.
- 52 Maletic-Savatic M, Malinow R, Svoboda K. Rapid dendritic morphogenesis in CA1 hippocampal dendrites induced by synaptic activity. Science 1999; 283: 1923–1927.
- 53 Spitzer NC. Electrical activity in early neuronal development. Nature 2006; 444: 707–712.
- 54 Bertolino A, Saunders RC, Mattay VS, Bachevalier J, Frank JA, Weinberger DR. Altered development of prefrontal neurons in rhesus monkeys with neonatal mesial temporo-limbic lesions: a proton magnetic resonance spectroscopic imaging study. Cereb Cortex 1997; 7: 740–748.
- 55 Saunders RC, Kolachana BS, Bachevalier J, Weinberger DR. Neonatal lesions of the medial temporal lobe disrupt prefrontal cortical regulation of striatal dopamine. Nature 1998; 393: 169–171.
- 56
Heinz A,
Saunders RC,
Kolachana BS
et al.
Striatal dopamine receptors and transporters in monkeys with neonatal temporal limbic damage.
Synapse
1999; 32: 71–79.
10.1002/(SICI)1098-2396(199905)32:2<71::AID-SYN1>3.0.CO;2-Q CAS PubMed Web of Science® Google Scholar
- 57 Bunney WE Jr, Goodwin FK, Murphy DL, House KM, Gordon EK. The “switch process” in manic-depressive illness. II. Relationship to catecholamines, REM sleep, and drugs. Arch Gen Psychiatry 1972; 27: 304–309.
- 58 Flor-Henry P. Lateralized temporal-limbic dysfunction and psychopathology. Ann NY Acad Sci 1976; 280: 777–797.
- 59 Altshuler LL, Bartzokis G, Grieder T, Curran J, Mintz J. Amygdala enlargement in bipolar disorder and hippocampal reduction in schizophrenia: an MRI study demonstrating neuroanatomic specificity. Arch Gen Psychiatry 1998; 55: 663–664.
- 60 Blumberg HP, Kaufman J, Martin A et al. Amygdala and hippocampal volumes in adolescents and adults with bipolar disorder. Arch Gen Psychiatry 2003; 60: 1201–1208.
- 61 Pearlson GD, Barta PE, Powers RE et al. Ziskind-Somerfeld Research Award 1996. Medial and superior temporal gyral volumes and cerebral asymmetry in schizophrenia versus bipolar disorder. Biol Psychiatry 1997; 41: 1–14.
- 62 Strakowski SM, DelBello MP, Sax KW et al. Brain magnetic resonance imaging of structural abnormalities in bipolar disorder. Arch Gen Psychiatry 1999; 56: 254–260.
- 63 Chang K, Karchemskiy A, Barnea-Goraly N, Garrett A, Simeonova DI, Reiss A. Reduced amygdalar gray matter volume in familial pediatric bipolar disorder. J Am Acad Child Adolesc Psychiatry 2005; 44: 565–573.
- 64 Chen BK, Sassi R, Axelson D et al. Cross-sectional study of abnormal amygdala development in adolescents and young adults with bipolar disorder. Biol Psychiatry 2004; 56: 399–405.
- 65 DelBello MP, Zimmerman ME, Mills NP, Getz GE, Strakowski SM. Magnetic resonance imaging analysis of amygdala and other subcortical brain regions in adolescents with bipolar disorder. Bipolar Disord 2004; 6: 43–52.
- 66 Dickstein DP, Milham MP, Nugent AC et al. Frontotemporal alterations in pediatric bipolar disorder: results of a voxel-based morphometry study. Arch Gen Psychiatry 2005; 62: 734–741.
- 67 Rosso IM, Killgore WD, Cintron CM, Gruber SA, Tohen M, Yurgelun-Todd DA. Reduced amygdala volumes in first-episode bipolar disorder and correlation with cerebral white matter. Biol Psychiatry 2007; 61: 743–749.
- 68 Wilke M, Kowatch RA, DelBello MP, Mills NP, Holland SK. Voxel-based morphometry in adolescents with bipolar disorder: first results. Psychiatry Res 2004; 131: 57–69.
- 69 Bitter SM, Mills NP, Adler CM, Strakowski SM, DelBello MP. Progression of amygdala volumetric abnormalities in adolescents after their first manic episode. J Am Acad Child Adolesc Psychiatry 2011; 50: 1017–1026.
- 70 Bowley MP, Drevets WC, Ongur D, Price JL. Low glial numbers in the amygdala in major depressive disorder. Biol Psychiatry 2002; 52: 404–412.
- 71 Foland LC, Altshuler LL, Sugar CA et al. Increased volume of the amygdala and hippocampus in bipolar patients treated with lithium. NeuroReport 2008; 19: 221–224.
- 72 Scherk H, Gruber O, Menzel P et al. 5-HTTLPR genotype influences amygdala volume. Eur Arch Psychiatry Clin Neurosci 2009; 259: 212–217.
- 73 McEwen BS. Physiology and neurobiology of stress and adaptation: central role of the brain. Physiol Rev 2007; 87: 873–904.
- 74 Drevets WC, Price JL, Simpson JR Jr et al. Subgenual prefrontal cortex abnormalities in mood disorders. Nature 1997; 386: 824–827.
- 75 Adler CM, DelBello MP, Jarvis K, Levine A, Adams J, Strakowski SM. Voxel-based study of structural changes in first-episode patients with bipolar disorder. Biol Psychiatry 2007; 61: 776–781.
- 76 Blumberg HP, Krystal JH, Bansal R et al. Age, rapid-cycling, and pharmacotherapy effects on ventral prefrontal cortex in bipolar disorder: a cross-sectional study. Biol Psychiatry 2006; 59: 611–618.
- 77 Doris A, Belton E, Ebmeier KP, Glabus MF, Marshall I. Reduction of cingulate gray matter density in poor outcome bipolar illness. Psychiatry Res 2004; 130: 153–159.
- 78 Foland-Ross LC, Thompson PM, Sugar CA et al. Investigation of cortical thickness abnormalities in lithium-free adults with bipolar I disorder using cortical pattern matching. Am J Psychiatry 2011; 168: 530–539.
- 79 Fornito A, Malhi GS, Lagopoulos J et al. Anatomical abnormalities of the anterior cingulate and paracingulate cortex in patients with bipolar I disorder. Psychiatry Res 2008; 162: 123–132.
- 80 Frazier JA, Breeze JL, Makris N et al. Cortical gray matter differences identified by structural magnetic resonance imaging in pediatric bipolar disorder. Bipolar Disord 2005; 7: 555–569.
- 81 Kalmar JH, Wang F, Spencer L et al. Preliminary evidence for progressive prefrontal abnormalities in adolescents and young adults with bipolar disorder. J Int Neuropsychol Soc 2009; 15: 476–481.
- 82 Kaur S, Sassi RB, Axelson D et al. Cingulate cortex anatomical abnormalities in children and adolescents with bipolar disorder. Am J Psychiatry 2005; 162: 1637–1643.
- 83 Lopez-Larson MP, DelBello MP, Zimmerman ME, Schwiers ML, Strakowski SM. Regional prefrontal gray and white matter abnormalities in bipolar disorder. Biol Psychiatry 2002; 52: 93–100.
- 84 Lyoo IK, Kim MJ, Stoll AL et al. Frontal lobe gray matter density decreases in bipolar I disorder. Biol Psychiatry 2004; 55: 648–651.
- 85 Lyoo IK, Sung YH, Dager SR et al. Regional cerebral cortical thinning in bipolar disorder. Bipolar Disord 2006; 8: 65–74.
- 86 Najt P, Nicoletti M, Chen HH et al. Anatomical measurements of the orbitofrontal cortex in child and adolescent patients with bipolar disorder. Neurosci Lett 2007; 413: 183–186.
- 87 Nugent AC, Milham MP, Bain EE et al. Cortical abnormalities in bipolar disorder investigated with MRI and voxel-based morphometry. Neuroimage 2006; 30: 485–497.
- 88 Baloch HA, Hatch JP, Olvera RL et al. Morphology of the subgenual prefrontal cortex in pediatric bipolar disorder. J Psychiatr Res 2010; 44: 1106–1110.
- 89 Sanches M, Sassi RB, Axelson D et al. Subgenual prefrontal cortex of child and adolescent bipolar patients: a morphometric magnetic resonance imaging study. Psychiatry Res 2005; 138: 43–49.
- 90 Raznahan A, Lerch JP, Lee N et al. Patterns of coordinated anatomical change in human cortical development: a longitudinal neuroimaging study of maturational coupling. Neuron 2011; 72: 873–884.
- 91 Wang F, Kalmar JH, Womer FY et al. Olfactocentric paralimbic cortex morphology in adolescents with bipolar disorder. Brain 2011; 134: 2005–2012.
- 92 Gogtay N, Ordonez A, Herman DH et al. Dynamic mapping of cortical development before and after the onset of pediatric bipolar illness. J Child Psychol Psychiatry 2007; 48: 852–862.
- 93 Blumberg HP, Kaufman J, Martin A, Charney DS, Krystal JH, Peterson BS. Significance of adolescent neurodevelopment for the neural circuitry of bipolar disorder. Ann NY Acad Sci 2004; 1021: 376–383.
- 94 Stanfield AC, Moorhead TWJ, Job DE et al. Structural abnormalities of ventrolateral and orbitofrontal cortex in patients with familial bipolar disorder. Bipolar Disord 2009; 11: 135–144.
- 95 Altshuler LL, Bartzokis G, Grieder T et al. An MRI study of temporal lobe structures in men with bipolar disorder or schizophrenia. Biol Psychiatry 2000; 48: 147–162.
- 96 Bearden CE, Soares JC, Klunder AD et al. Three-dimensional mapping of hippocampal anatomy in adolescents with bipolar disorder. J Am Acad Child Adolesc Psychiatry 2008; 47: 515–525.
- 97 Frazier JA, Chiu S, Breeze JL et al. Structural brain magnetic resonance imaging of limbic and thalamic volumes in pediatric bipolar disorder. Am J Psychiatry 2005; 162: 1256–1265.
- 98 Hauser P, Matochik J, Altshuler LL et al. MRI-based measurements of temporal lobe and ventricular structures in patients with bipolar I and bipolar II disorders. J Affect Disord 2000; 60: 25–32.
- 99 Hirayasu Y, Shenton ME, Salisbury DF et al. Lower left temporal lobe MRI volumes in patients with first-episode schizophrenia compared with psychotic patients with first-episode affective disorder and normal subjects. Am J Psychiatry 1998; 155: 1384–1391.
- 100 Moore GJ, Bebchuk JM, Wilds IB, Chen G, Manji HK. Lithium-induced increase in human brain grey matter. Lancet 2000; 356: 1241–1242.
- 101 Noga JT, Vladar K, Torrey EF. A volumetric magnetic resonance imaging study of monozygotic twins discordant for bipolar disorder. Psychiatry Res 2001; 106: 25–34.
- 102 Swayze VW, 2nd, Andreasen NC, Alliger RJ, Yuh WT, Ehrhardt JC. Subcortical and temporal structures in affective disorder and schizophrenia: a magnetic resonance imaging study. Biol Psychiatry 1992; 31: 221–240.
- 103 Velakoulis D, Pantelis C, McGorry PD et al. Hippocampal volume in first-episode psychoses and chronic schizophrenia: a high-resolution magnetic resonance imaging study. Arch Gen Psychiatry 1999; 56: 133–141.
- 104 Chepenik LG, Fredericks C, Papademetris X et al. Effects of the brain-derived neurotrophic growth factor val66met variation on hippocampus morphology in bipolar disorder. Neuropsychopharmacol 2009; 34: 944–951.
- 105 McIntosh AM, Moorhead TW, McKirdy J et al. Temporal grey matter reductions in bipolar disorder are associated with the BDNF Val66Met polymorphism. Mol Psychiatry 2007; 12: 902–903.
- 106 Duman RS, Monteggia LM. A neurotrophic model for stress-related mood disorders. Biol Psychiatry 2006; 59: 1116–1127.
- 107 Geller B, Williams M, Zimerman B, Frazier J, Beringer L, Warner KL. Prepubertal and early adolescent bipolarity differentiate from ADHD by manic symptoms, grandiose delusions, ultra-rapid or ultradian cycling. J Affect Disord 1998; 51: 81–91.
- 108 Muller DJ, de Luca V, Sicard T, King N, Strauss J, Kennedy JL. Brain-derived neurotrophic factor (BDNF) gene and rapid-cycling bipolar disorder: family-based association study. Br J Psychiatry 2006; 189: 317–323.
- 109 Hwang J, Lyoo IK, Dager SR et al. Basal ganglia shape alterations in bipolar disorder. Am J Psychiatry 2006; 163: 276–285.
- 110 Strakowski SM, Adler CM, DelBello MP. Volumetric MRI studies of mood disorders: do they distinguish unipolar and bipolar disorder? Bipolar Disord 2002; 4: 80–88.
- 111 Anand BK, Malhotra CL, Singh B, Dua S. Cerebellar projections to limbic system. J Neurophysiol 1959; 22: 451–457.
- 112 Heath RG, Dempesy CW, Fontana CJ, Myers WA. Cerebellar stimulation: effects on septal region, hippocampus, and amygdala of cats and rats. Biol Psychiatry 1978; 13: 501–529.
- 113 Ramnani N. The primate cortico-cerebellar system: anatomy and function. Nat Rev Neurosci 2006; 7: 511–522.
- 114 Snider RS, Maiti A. Cerebellar contributions to the Papez circuit. J Neurosci Res 1976; 2: 133–146.
- 115 Schmahmann JD, Sherman JC. The cerebellar cognitive affective syndrome. Brain 1998; 121: 561–579.
- 116 Supple WF Jr, Leaton RN, Fanselow MS. Effects of cerebellar vermal lesions on species-specific fear responses, neophobia, and taste-aversion learning in rats. Physiol Behav 1987; 39: 579–586.
- 117 Supple WF Jr, Cranney J, Leaton RN. Effects of lesions of the cerebellar vermis on VMH lesion-induced hyperdefensiveness, spontaneous mouse killing, and freezing in rats. Physiol Behav 1988; 42: 145–153.
- 118 Tavano A, Grasso R, Gagliardi C et al. Disorders of cognitive and affective development in cerebellar malformations. Brain 2007; 130: 2646–2660.
- 119 Yadalam KG, Jain AK, Simpson GM. Mania in two sisters with similar cerebellar disturbance. Am J Psychiatry 1985; 142: 1067–1069.
- 120 DelBello MP, Strakowski SM, Zimmerman ME, Hawkins JM, Sax KW. MRI analysis of the cerebellum in bipolar disorder: a pilot study. Neuropsychopharmacol 1999; 21: 63–68.
- 121 Mills NP, Delbello MP, Adler CM, Strakowski SM. MRI analysis of cerebellar vermal abnormalities in bipolar disorder. Am J Psychiatry 2005; 162: 1530–1532.
- 122 Monkul ES, Hatch JP, Sassi RB et al. MRI study of the cerebellum in young bipolar patients. Prog Neuropsychopharmacol Biol Psychiatry 2008; 32: 613–619.
- 123 Brambilla P, Harenski K, Nicoletti M et al. MRI study of posterior fossa structures and brain ventricles in bipolar patients. J Psychiatr Res 2001; 35: 313–322.
- 124 Womer FY, Wang F, Chepenik LG et al. Sexually dimorphic features of vermis morphology in bipolar disorder. Bipolar Disord 2009; 11: 753–758.
- 125 Almeida JR, Versace A, Hassel S, Kupfer DJ, Phillips ML. Elevated amygdala activity to sad facial expressions: a state marker of bipolar but not unipolar depression. Biol Psychiatry 2010; 67: 414–421.
- 126 Altshuler L, Bookheimer S, Proenza MA et al. Increased amygdala activation during mania: a functional magnetic resonance imaging study. Am J Psychiatry 2005; 162: 1211–1213.
- 127 Chang KD, Wagner C, Garrett A, Howe M, Reiss A. A preliminary functional magnetic resonance imaging study of prefrontal-amygdalar activation changes in adolescents with bipolar depression treated with lamotrigine. Bipolar Disord 2008; 10: 426–431.
- 128 Drevets WC, Price JL, Bardgett ME, Reich T, Todd RD, Raichle ME. Glucose metabolism in the amygdala in depression: relationship to diagnostic subtype and plasma cortisol levels. Pharmacol Biochem Behav 2002; 71: 431–447.
- 129 Jogia J, Haldane M, Cobb A, Kumari V, Frangou S. Pilot investigation of the changes in cortical activation during facial affect recognition with lamotrigine monotherapy in bipolar disorder. Br J Psychiatry 2008; 192: 197–201.
- 130 Kalmar JH, Wang F, Chepenik LG et al. Relation between amygdala structure and function in adolescents with bipolar disorder. J Am Acad Child Adolesc Psychiatry 2009; 48: 636–642.
- 131 Ketter TA, Kimbrell TA, George MS et al. Effects of mood and subtype on cerebral glucose metabolism in treatment-resistant bipolar disorder. Biol Psychiatry 2001; 49: 97–109.
- 132 Lawrence NS, Williams AM, Surguladze S et al. Subcortical and ventral prefrontal cortical neural responses to facial expressions distinguish patients with bipolar disorder and major depression. Biol Psychiatry 2004; 55: 578–587.
- 133 Mah L, Zarate CA Jr, Singh J et al. Regional cerebral glucose metabolic abnormalities in bipolar II depression. Biol Psychiatry 2007; 61: 765–775.
- 134 Malhi GS, Lagopoulos J, Ward PB et al. Cognitive generation of affect in bipolar depression: an fMRI study. Eur J Neurosci 2004; 19: 741–754.
- 135 Pavuluri MN, O’Connor MM, Harral E, Sweeney JA. Affective neural circuitry during facial emotion processing in pediatric bipolar disorder. Biol Psychiatry 2007; 62: 158–167.
- 136 Rich BA, Vinton DT, Roberson-Nay R et al. Limbic hyperactivation during processing of neutral facial expressions in children with bipolar disorder. Proc Natl Acad Sci USA 2006; 103: 8900–8905.
- 137 Yurgelun-Todd DA, Gruber SA, Kanayama G, Killgore WDS, Baird AA, Young AD. fMRI during affect discrimination in bipolar affective disorder. Bipolar Disord 2000; 2: 237–248.
- 138 Shah MP, Wang F, Kalmar JH et al. Role of variation in the serotonin transporter protein gene (SLC6A4) in trait disturbances in the ventral anterior cingulate in bipolar disorder. Neuropsychopharmacol 2009; 34: 1301–1310.
- 139 Foland-Ross LC, Bookheimer SY, Lieberman MD et al. Normal amygdala activation but deficient ventrolateral prefrontal activation in adults with bipolar disorder during euthymia. Neuroimage 2012; 59: 738–744.
- 140 Braga MF, Aroniadou-Anderjaska V, Post RM, Li H. Lamotrigine reduces spontaneous and evoked GABAA receptor-mediated synaptic transmission in the basolateral amygdala: implications for its effects in seizure and affective disorders. Neuropharmacol 2002; 42: 522–529.
- 141 Krystal JH, Sanacora G, Blumberg H et al. Glutamate and GABA systems as targets for novel antidepressant and mood-stabilizing treatments. Mol Psychiatry 2002; 7(Suppl. 1): S71–80.
- 142 Tian LM, Alkadhi KA. Valproic acid inhibits the depolarizing rectification in neurons of rat amygdala. Neuropharmacol 1994; 33: 1131–1138.
- 143 Berretta S, Pantazopoulos H, Lange N. Neuron numbers and volume of the amygdala in subjects diagnosed with bipolar disorder or schizophrenia. Biol Psychiatry 2007; 62: 884–893.
- 144 Pantazopoulos H, Lange N, Baldessarini RJ, Berretta S. Parvalbumin neurons in the entorhinal cortex of subjects diagnosed with bipolar disorder or schizophrenia. Biol Psychiatry 2007; 61: 640–652.
- 145 Wang AY, Lohmann KM, Yang CK et al. Bipolar disorder type 1 and schizophrenia are accompanied by decreased density of parvalbumin- and somatostatin-positive interneurons in the parahippocampal region. Acta Neuropathol 2011; 122: 615–626.
- 146 Knable MB, Barci BM, Webster MJ, Meador-Woodruff J, Torrey EF. Molecular abnormalities of the hippocampus in severe psychiatric illness: postmortem findings from the Stanley Neuropathology Consortium. Mol Psychiatry 2004; 9: 609–620.
- 147 Konradi C, Zimmerman EI, Yang CK et al. Hippocampal interneurons in bipolar disorder. Arch Gen Psychiatry 2011; 68: 340–350.
- 148 Torrey EF, Barci BM, Webster MJ, Bartko JJ, Meador-Woodruff JH, Knable MB. Neurochemical markers for schizophrenia, bipolar disorder, and major depression in postmortem brains. Biol Psychiatry 2005; 57: 252–260.
- 149 McIntosh AM, Whalley HC, McKirdy J et al. Prefrontal function and activation in bipolar disorder and schizophrenia. Am J Psychiatry 2008; 165: 378–384.
- 150 Altshuler LL, Bookheimer SY, Townsend J et al. Blunted activation in orbitofrontal cortex during mania: a functional magnetic resonance imaging study. Biol Psychiatry 2005; 58: 763–769.
- 151 Blumberg HP, Stern E, Ricketts S et al. Rostral and orbital prefrontal cortex dysfunction in the manic state of bipolar disorder. Am J Psychiatry 1999; 156: 1986–1988.
- 152 Blumberg HP, Leung HC, Skudlarski P et al. A functional magnetic resonance imaging study of bipolar disorder: state- and trait-related dysfunction in ventral prefrontal cortices. Arch Gen Psychiatry 2003; 60: 601–609.
- 153 Elliott R, Ogilvie A, Rubinsztein JS, Calderon G, Dolan RJ, Sahakian BJ. Abnormal ventral frontal response during performance of an affective go/no go task in patients with mania. Biol Psychiatry 2004; 55: 1163–1170.
- 154 Rubinsztein JS, Fletcher PC, Rogers RD et al. Decision-making in mania: a PET study. Brain 2001; 124: 2550–2563.
- 155 Strakowski SM, Eliassen JC, Lamy M et al. Functional magnetic resonance imaging brain activation in bipolar mania: evidence for disruption of the ventrolateral prefrontal-amygdala emotional pathway. Biol Psychiatry 2011; 69: 381–388.
- 156 Chen CH, Lennox B, Jacob R et al. Explicit and implicit facial affect recognition in manic and depressed States of bipolar disorder: a functional magnetic resonance imaging study. Biol Psychiatry 2006; 59: 31–39.
- 157 Townsend J, Bookheimer SY, Foland-Ross LC, Sugar CA, Altshuler LL. fMRI abnormalities in dorsolateral prefrontal cortex during a working memory task in manic, euthymic and depressed bipolar subjects. Psychiatry Res 2010; 182: 22–29.
- 158 Frangou S, Kington J, Raymont V, Shergill SS. Examining ventral and dorsal prefrontal function in bipolar disorder: a functional magnetic resonance imaging study. Eur Psychiatry 2008; 23: 300–308.
- 159 Kronhaus DM, Lawrence NS, Williams AM et al. Stroop performance in bipolar disorder: further evidence for abnormalities in the ventral prefrontal cortex. Bipolar Disord 2006; 8: 28–39.
- 160 Kruger S, Seminowicz D, Goldapple K, Kennedy SH, Mayberg HS. State and trait influences on mood regulation in bipolar disorder: blood flow differences with an acute mood challenge. Biol Psychiatry 2003; 54: 1274–1283.
- 161 Kruger S, Alda M, Young LT, Goldapple K, Parikh S, Mayberg HS. Risk and resilience markers in bipolar disorder: brain responses to emotional challenge in bipolar patients and their healthy siblings. Am J Psychiatry 2006; 163: 257–264.
- 162 Malhi GS, Lagopoulos J, Sachdev PS, Ivanovski B, Shnier R. An emotional Stroop functional MRI study of euthymic bipolar disorder. Bipolar Disord 2005; 7(Suppl. 5): 58–69.
- 163 Strakowski SM, Adler CM, Holland SK, Mills N, DelBello MP. A preliminary fMRI study of sustained attention in euthymic, unmedicated bipolar disorder. Neuropsychopharmacol 2004; 29: 1734–1740.
- 164 Leibenluft E, Rich BA, Vinton DT et al. Neural circuitry engaged during unsuccessful motor inhibition in pediatric bipolar disorder. Am J Psychiatry 2007; 164: 52–60.
- 165 Blumberg HP, Martin A, Kaufman J et al. Frontostriatal abnormalities in adolescents with bipolar disorder: preliminary observations from functional MRI. Am J Psychiatry 2003; 160: 1345–1347.
- 166 Kim E, Jung YC, Ku J et al. Reduced activation in the mirror neuron system during a virtual social cognition task in euthymic bipolar disorder. Prog Neuropsychopharmacol Biol Psychiatry 2009; 33: 1409–1416.
- 167 Pavuluri MN, Passarotti AM, Harral EM, Sweeney JA. An fMRI study of the neural correlates of incidental versus directed emotion processing in pediatric bipolar disorder. J Am Acad Child Adolesc Psychiatry 2009; 48: 308–319.
- 168 Van der Schot A, Kahn R, Ramsey N, Nolen W, Vink M. Trait and state dependent functional impairments in bipolar disorder. Psychiatry Res 2010; 184: 135–142.
- 169 Frangou S, Haldane M, Roddy D, Kumari V. Evidence for deficit in tasks of ventral, but not dorsal, prefrontal executive function as an endophenotypic marker for bipolar disorder. Biol Psychiatry 2005; 58: 838–839.
- 170 Deckersbach T, Dougherty DD, Savage C et al. Impaired recruitment of the dorsolateral prefrontal cortex and hippocampus during encoding in bipolar disorder. Biol Psychiatry 2006; 59: 138–146.
- 171 Lagopoulos J, Malhi GS. A functional magnetic resonance imaging study of emotional Stroop in euthymic bipolar disorder. NeuroReport 2007; 18: 1583–1587.
- 172 Malhi GS, Lagopoulos J, Sachdev PS, Ivanovski B, Shnier R, Ketter T. Is a lack of disgust something to fear? A functional magnetic resonance imaging facial emotion recognition study in euthymic bipolar disorder patients. Bipolar Disord 2007; 9: 345–357.
- 173 Blumberg HP, Stern E, Martinez D et al. Increased anterior cingulate and caudate activity in bipolar mania. Biol Psychiatry 2000; 48: 1045–1052.
- 174 Brooks JO 3rd, Wang PW, Bonner JC et al. Decreased prefrontal, anterior cingulate, insula, and ventral striatal metabolism in medication-free depressed outpatients with bipolar disorder. J Psychiatr Res 2009; 43: 181–188.
- 175 Caligiuri MP, Brown GG, Meloy MJ et al. An fMRI study of affective state and medication on cortical and subcortical brain regions during motor performance in bipolar disorder. Psychiatry Res 2003; 123: 171–182.
- 176 Malhi GS, Lagopoulos J, Sachdev P, Mitchell PB, Ivanovski B, Parker GB. Cognitive generation of affect in hypomania: an fMRI study. Bipolar Disord 2004; 6: 271–285.
- 177 Chang K, Adleman NE, Dienes K, Simeonova DI, Menon V, Reiss A. Anomalous prefrontal-subcortical activation in familial pediatric bipolar disorder - A functional magnetic resonance imaging investigation. Arch Gen Psychiatry 2004; 61: 781–792.
- 178 Caligiuri MP, Brown GG, Meloy MJ, Eberson S, Niculescu AB, Lohr JB. Striatopallidal regulation of affect in bipolar disorder. J Affect Disord 2006; 91: 235–242.
- 179 Marchand WR, Lee JN, Thatcher GW et al. A functional MRI study of a paced motor activation task to evaluate frontal-subcortical circuit function in bipolar depression. Psychiatry Res 2007; 155: 221–230.
- 180 Wessa M, Houenou J, Paillere-Martinot ML et al. Fronto-striatal overactivation in euthymic bipolar patients during an emotional go/nogo task. Am J Psychiatry 2007; 164: 638–646.
- 181 Strakowski SM, Adler CM, Holland SK, Mills NP, DelBello MP, Eliassen JC. Abnormal FMRI brain activation in euthymic bipolar disorder patients during a counting Stroop interference task. Am J Psychiatry 2005; 162: 1697–1705.
- 182 Loeber RT, Gruber SA, Cohen BM, Renshaw PF, Sherwood AR, Yurgelun-Todd DA. Cerebellar blood volume in bipolar patients correlates with medication. Biol Psychiatry 2002; 51: 370–376.
- 183 Atmaca M, Ozdemir H, Yildirim H. Corpus callosum areas in first-episode patients with bipolar disorder. Psychol Med 2007; 37: 699–704.
- 184 Brambilla P, Nicoletti MA, Sassi RB et al. Magnetic resonance imaging study of corpus callosum abnormalities in patients with bipolar disorder. Biol Psychiatry 2003; 54: 1294–1297.
- 185 Brambilla P, Nicoletti M, Sassi RB et al. Corpus callosum signal intensity in patients with bipolar and unipolar disorder. J Neurol Neurosurg Psychiatry 2004; 75: 221–225.
- 186 Caetano SC, Silveira CM, Kaur S et al. Abnormal corpus callosum myelination in pediatric bipolar patients. J Affect Disord 2008; 108: 297–301.
- 187 Coffman JA, Bornstein RA, Olson SC, Schwarzkopf SB, Nasrallah HA. Cognitive impairment and cerebral structure by MRI in bipolar disorder. Biol Psychiatry 1990; 27: 1188–1196.
- 188 Haznedar MM, Roversi F, Pallanti S et al. Fronto-thalamo-striatal gray and white matter volumes and anisotropy of their connections in bipolar spectrum illnesses. Biol Psychiatry 2005; 57: 733–742.
- 189 Beaulieu C. The basis of anisotropic water diffusion in the nervous system - a technical review. NMR Biomed 2002; 15: 435–455.
- 190 Adler CM, Holland SK, Schmithorst V et al. Abnormal frontal white matter tracts in bipolar disorder: a diffusion tensor imaging study. Bipolar Disord 2004; 6: 197–203.
- 191 Adler CM, Adams J, DelBello MP et al. Evidence of white matter pathology in bipolar disorder adolescents experiencing their first episode of mania: a diffusion tensor imaging study. Am J Psychiatry 2006; 163: 322–324.
- 192 Beyer JL, Taylor WD, MacFall JR et al. Cortical white matter microstructural abnormalities in bipolar disorder. Neuropsychopharmacol 2005; 30: 2225–2229.
- 193 Bruno S, Cercignani M, Ron MA. White matter abnormalities in bipolar disorder: a voxel-based diffusion tensor imaging study. Bipolar Disord 2008; 10: 460–468.
- 194 Houenou J, Wessa M, Douaud G et al. Increased white matter connectivity in euthymic bipolar patients: diffusion tensor tractography between the subgenual cingulate and the amygdalo-hippocampal complex. Mol Psychiatry 2007; 12: 1001–1010.
- 195 Regenold WT, D’Agostino CA, Ramesh N, Hasnain M, Roys S, Gullapalli RP. Diffusion-weighted magnetic resonance imaging of white matter in bipolar disorder: a pilot study. Bipolar Disord 2006; 8: 188–195.
- 196 Versace A, Almeida JR, Hassel S et al. Elevated left and reduced right orbitomedial prefrontal fractional anisotropy in adults with bipolar disorder revealed by tract-based spatial statistics. Arch Gen Psychiatry 2008; 65: 1041–1052.
- 197 Wang F, Jackowski M, Kalmar JH et al. Abnormal anterior cingulum integrity in bipolar disorder determined through diffusion tensor imaging. Br J Psychiatry 2008; 193: 126–129.
- 198 Zanetti MV, Jackowski MP, Versace A et al. State-dependent microstructural white matter changes in bipolar I depression. Eur Arch Psychiatry Clin Neurosci 2009; 259: 316–328.
- 199 Wang F, Kalmar JH, Edmiston E et al. Abnormal corpus callosum integrity in bipolar disorder: a diffusion tensor imaging study. Biol Psychiatry 2008; 64: 730–733.
- 200 Yurgelun-Todd DA, Silveri MM, Gruber SA, Rohan ML, Pimentel PJ. White matter abnormalities observed in bipolar disorder: a diffusion tensor imaging study. Bipolar Disord 2007; 9: 504–512.
- 201 Frazier JA, Breeze JL, Papadimitriou G et al. White matter abnormalities in children with and at risk for bipolar disorder. Bipolar Disord 2007; 9: 799–809.
- 202 Kieseppa T, van Erp TG, Haukka J et al. Reduced left hemispheric white matter volume in twins with bipolar I disorder. Biol Psychiatry 2003; 54: 896–905.
- 203 McDonald C, Bullmore ET, Sham PC et al. Association of genetic risks for schizophrenia and bipolar disorder with specific and generic brain structural endophenotypes. Arch Gen Psychiatry 2004; 61: 974–984.
- 204 Sprooten E, Sussmann JE, Clugston A et al. White matter integrity in individuals at high genetic risk of bipolar disorder. Biol Psychiatry 2011; 70: 350–356.
- 205 Versace A, Ladouceur CD, Romero S et al. Altered development of white matter in youth at high familial risk for bipolar disorder: a diffusion tensor imaging study. J Am Acad Child Adolesc Psychiatry 2010; 49: 1249–1259.
- 206 Chaddock CA, Barker GJ, Marshall N et al. White matter microstructural impairments and genetic liability to familial bipolar I disorder. Br J Psychiatry 2009; 194: 527–534.
- 207 Versace A, Almeida JR, Quevedo K et al. Right orbitofrontal corticolimbic and left corticocortical white matter connectivity differentiate bipolar and unipolar depression. Biol Psychiatry 2010; 68: 560–567.
- 208 Anand A, Li Y, Wang Y, Lowe MJ, Dzemidzic M. Resting state corticolimbic connectivity abnormalities in unmedicated bipolar disorder and unipolar depression. Psychiatry Res 2009; 171: 189–198.
- 209 Chepenik LG, Raffo M, Hampson M et al. Functional connectivity between ventral prefrontal cortex and amygdala at low frequency in the resting state in bipolar disorder. Psychiatry Res 2010; 182: 207–210.
- 210 Dickstein DP, Gorrostieta C, Ombao H et al. Fronto-temporal spontaneous resting state functional connectivity in pediatric bipolar disorder. Biol Psychiatry 2010; 68: 839–846.
- 211 Foland LC, Altshuler LL, Bookheimer SY, Eisenberger N, Townsend J, Thompson PM. Evidence for deficient modulation of amygdala response by prefrontal cortex in bipolar mania. Psychiatry Res 2008; 162: 27–37.
- 212 Rich BA, Fromm SJ, Berghorst LH et al. Neural connectivity in children with bipolar disorder: impairment in the face emotion processing circuit. J Child Psychol Psychiatry 2008; 49: 88–96.
- 213 Versace A, Thompson WK, Zhou D et al. Abnormal left and right amygdala–orbitofrontal cortical functional connectivity to emotional faces: state versus trait vulnerability markers of depression in bipolar disorder. Biol Psychiatry 2010; 67: 422–431.
- 214 Wang F, Kalmar JH, He Y et al. Functional and structural connectivity between the perigenual anterior cingulate and amygdala in bipolar disorder. Biol Psychiatry 2009; 66: 516–521.
- 215 Almeida JR, Versace A, Mechelli A et al. Abnormal amygdala–prefrontal effective connectivity to happy faces differentiates bipolar from major depression. Biol Psychiatry 2009; 66: 451–459.
- 216 Blumberg HP, Wang F, Chepenik LG et al. Influence of vascular endothelial growth factor variation on human hippocampus morphology. Biol Psychiatry 2008; 64: 901–903.
- 217 McIntosh AM, Moorhead TW, Job D et al. The effects of a neuregulin 1 variant on white matter density and integrity. Mol Psychiatry 2008; 13: 1054–1059.
- 218 Wang F, McIntosh AM, He Y, Gelernter J, Blumberg HP. The association of genetic variation in CACNA1C with structure and function of a frontotemporal system. Bipolar Disord 2011; 13: 696–700.