Differentiating patterns of amygdala-frontal functional connectivity in schizophrenia and bipolar disorder

Schizophrenia Bulletin

Volumn 40, Issue 2, 2014, Pages 469-477

  Liu, Hu ^a   Tang, Yanqing ^f   Womer, Fay ^b   Fan, Guoguang ^a   Lu, Tao ^a   Driesen, Naomi ^c   Ren, Ling ^a   Wang, Ye ^d   He, Yong ^c   Blumberg, Hilary P ^e   Xu, Ke ^a   Wang, Fei ^a,e  

^a CHINA MEDICAL UNIVERSITY   (China)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c BEIJING NORMAL UNIVERSITY   (China)

^d Shenyang Mental Health Center   (China)

^e YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f First Affiliated Hospital of China Medical University   (China)

Author keywords

amygdala; bipolar disorder; functional connectivity; prefrontal cortex; resting state; schizophrenia

Indexed keywords

ANTICONVULSIVE AGENT; ANTIDEPRESSANT AGENT; ATYPICAL ANTIPSYCHOTIC AGENT; LITHIUM; NEUROLEPTIC AGENT;

ADULT; AMYGDALOID NUCLEUS; ANTICONVULSANT THERAPY; ARTICLE; BASOLATERAL AMYGDALA; BIPOLAR DISORDER; BRAIN MAPPING; BRAIN REGION; CENTRAL NUCLEUS (AMYGDALA); CENTROMEDIAL AMYGDALA; CINGULATE GYRUS; CLINICAL ARTICLE; CLINICAL FEATURE; CONNECTOME; CONTROLLED STUDY; DIAGNOSTIC TEST ACCURACY STUDY; DISEASE SEVERITY; FEMALE; FUNCTIONAL MAGNETIC RESONANCE IMAGING; FUNCTIONAL NEUROIMAGING; HUMAN; MALE; MEDIAL AMYGDALA; MENTAL PATIENT; NERVE CELL DIFFERENTIATION; NEUROANATOMY; NEUROLOGIC DISEASE; PATHOPHYSIOLOGY; PREDICTIVE VALUE; PREFRONTAL CORTEX; PRIORITY JOURNAL; RESTING STATE NETWORK; SCHIZOPHRENIA; SUPERFICIAL AMYGDALA; YOUNG ADULT; COMPARATIVE STUDY; DEVICES; NUCLEAR MAGNETIC RESONANCE IMAGING; PROCEDURES;

ADULT; AMYGDALA; BIPOLAR DISORDER; CONNECTOME; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; PREFRONTAL CORTEX; SCHIZOPHRENIA;

EID: 84888054450     PISSN: 05867614     EISSN: 17451701     Source Type: Journal    
DOI: 10.1093/schbul/sbt044     Document Type: Article

References (53)

1. Murray RM, Sham P, Van Os J, Zanelli J, Cannon M, McDonald C. A developmental model for similarities and dissimilarities between schizophrenia and bipolar disorder. Schizophr Res. 2004;71:405-416.
2. Craddock N, O'Donovan MC, Owen MJ. Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology. Schizophr Bull. 2006;32:9-16.
3. Lichtenstein P, Yip BH, Björk C, et al. Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study. Lancet. 2009;373:234-239.
4. Phillips ML, Drevets WC, Rauch SL, Lane R. Neurobiology of emotion perception I: the neural basis of normal emotion perception. Biol Psychiatry. 2003;54:504-514.
5. Phillips ML, Drevets WC, Rauch SL, Lane R. Neurobiology of emotion perception II: implications for major psychiatric disorders. Biol Psychiatry. 2003;54:515-528.
6. Weidenhofer J, Bowden NA, Scott RJ, Tooney PA. Altered gene expression in the amygdala in schizophrenia: up-regulation of genes located in the cytomatrix active zone. Mol Cell Neurosci. 2006;31:243-250.
7. Benes FM. Searching for unique endophenotypes for schizophrenia and bipolar disorder within neural circuits and their molecular regulatory mechanisms. Schizophr Bull. 2007;33:932-936.
8. Ellison-Wright I, Glahn DC, Laird AR, Thelen SM, Bullmore E. The anatomy of first-episode and chronic schizophrenia: an anatomical likelihood estimation meta-Analysis. Am J Psychiatry. 2008;165:1015-1023.
9. Joyal CC, Laakso MP, Tiihonen J, et al. The amygdala and schizophrenia: a volumetric magnetic resonance imaging study in first-episode, neuroleptic-naive patients. Biol Psychiatry. 2003;54:1302-1304.
10. Bowley MP, Drevets WC, Ongür D, Price JL. Low glial numbers in the amygdala in major depressive disorder. Biol Psychiatry. 2002;52:404-412.
11. Womer FY, Kalmar JH, Wang F, Blumberg HP. A ventral prefrontal-Amygdala neural system in bipolar disorder: a view from neuroimaging research. Acta Neuropsychiatr. 2009;21:228-238.
12. Usher J, Leucht S, Falkai P, Scherk H. Correlation between amygdala volume and age in bipolar disorder - a systematic review and meta-Analysis of structural MRI studies. Psychiatry Res. 2010;182:1-8.
13. Curtis VA, Dixon TA, Morris RG, et al. Differential frontal activation in schizophrenia and bipolar illness during verbal fluency. J Affect Disord. 2001;66:111-121.
14. McIntosh AM, Whalley HC, McKirdy J, et al. Prefrontal function and activation in bipolar disorder and schizophrenia. Am J Psychiatry. 2008;165:378-384.
15. Weinberger DR, Berman KF, Zec RF. Physiologic dysfunction of dorsolateral prefrontal cortex in schizophrenia. I. Regional cerebral blood flow evidence. Arch Gen Psychiatry. 1986;43:114-124.
16. Whalley HC, Simonotto E, Flett S, et al. fMRI correlates of state and trait effects in subjects at genetically enhanced risk of schizophrenia. Brain. 2004;127:478-490.
17. 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.
18. 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.
19. Lewis DA, Cruz D, Eggan S, Erickson S. Postnatal development of prefrontal inhibitory circuits and the pathophysiology of cognitive dysfunction in schizophrenia. Ann N Y Acad Sci. 2004;1021:64-76.
20. Kringelbach ML. The human orbitofrontal cortex: linking reward to hedonic experience. Nat Rev Neurosci. 2005;6:691-702.
21. Delatour B, Witter MP. Projections from the parahippocampal region to the prefrontal cortex in the rat: evidence of multiple pathways. Eur J Neurosci. 2002;15:1400-1407.
22. Quirk GJ, Beer JS. Prefrontal involvement in the regulation of emotion: convergence of rat and human studies. Curr Opin Neurobiol. 2006;16:723-727.
23. Petrides M, Pandya DN. Efferent association pathways from the rostral prefrontal cortex in the macaque monkey. J Neurosci. 2007;27:11573-11586.
24. Schmahmann JD, Pandya DN. Fiber Pathways of the Brain. New York, NY: Oxford University Press; 2006.
25. Mufson EJ, Pandya DN. Some observations on the course and composition of the cingulum bundle in the rhesus monkey. J Comp Neurol. 1984;225:31-43.
26. Roy AK, Shehzad Z, Margulies DS, et al. Functional connectivity of the human amygdala using resting state fMRI. Neuroimage. 2009;45:614-626.
27. Gopin CB, Burdick KE, Derosse P, Goldberg TE, Malhotra AK. Emotional modulation of response inhibition in stable patients with bipolar I disorder: a comparison with healthy and schizophrenia subjects. Bipolar Disord. 2011;13:164-172.
28. Whalley HC, McKirdy J, Romaniuk L, et al. Functional imaging of emotional memory in bipolar disorder and schizophrenia. Bipolar Disord. 2009;11:840-856.
29. Amunts K, Kedo O, Kindler M, et al. Cytoarchitectonic mapping of the human amygdala, hippocampal region and entorhinal cortex: intersubject variability and probability maps. Anat Embryol. 2005;210:343-352.
30. Frazier JA, Giedd JN, Hamburger SD, et al. Brain anatomic magnetic resonance imaging in childhood-onset schizophrenia. Arch Gen Psychiatry. 1996;53:617-624.
31. Shad MU, Muddasani S, Prasad K, Sweeney JA, Keshavan MS. Insight and prefrontal cortex in first-episode schizophrenia. Neuroimage. 2004;22:1315-1320.
32. Glantz LA, Lewis DA. Decreased dendritic spine density on prefrontal cortical pyramidal neurons in schizophrenia. Arch Gen Psychiatry. 2000;57:65-73.
33. Black JE, Kodish IM, Grossman AW, et al. Pathology of layer V pyramidal neurons in the prefrontal cortex of patients with schizophrenia. Am J Psychiatry. 2004;161:742-744.
34. Goldman-Rakic PS. The physiological approach: functional architecture of working memory and disordered cognition in schizophrenia. Biol Psychiatry. 1999;46:650-661.
35. Gray JR, Braver TS, Raichle ME. Integration of emotion and cognition in the lateral prefrontal cortex. Proc Natl Acad Sci USA. 2002;99:4115-4120.
36. Corradi-Dell'Acqua C, Tomelleri L, Bellani M, et al. Thalamic-insular dysconnectivity in schizophrenia: evidence from structural equation modeling. Hum Brain Mapp. 2012;33:740-752.
37. Ongür D, Drevets WC, Price JL. Glial reduction in the subgenual prefrontal cortex in mood disorders. Proc Natl Acad Sci USA. 1998;95:13290-13295.
38. Rajkowska G. Postmortem studies in mood disorders indicate altered numbers of neurons and glial cells. Biol Psychiatry. 2000;48:766-777.
39. 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.
40. 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.
41. Goossens L, Kukolja J, Onur OA, et al. Selective processing of social stimuli in the superficial amygdala. Hum Brain Mapp. 2009;30:3332-3338.
42. Edwards J, Pattison PE, Jackson HJ, Wales RJ. Facial affect and affective prosody recognition in first-episode schizophrenia. Schizophr Res. 2001;48:235-253.
43. Harmer CJ, Grayson L, Goodwin GM. Enhanced recognition of disgust in bipolar illness. Biol Psychiatry. 2002;51:298-304.
44. Torta DM, Cauda F. Different functions in the cingulate cortex, a meta-Analytic connectivity modeling study. Neuroimage. 2011;56:2157-2172.
45. Krebs MO, Bourdel MC, Cherif ZR, et al. Deficit of inhibition motor control in untreated patients with schizophrenia: further support from visually guided saccade paradigms. Psychiatry Res. 2010;179:279-284.
46. Manschreck TC, Maher BA, Candela SF. Earlier age of first diagnosis in schizophrenia is related to impaired motor control. Schizophr Bull. 2004;30:351-360.
47. Deveney CM, Connolly ME, Jenkins SE, et al. Striatal dysfunction during failed motor inhibition in children at risk for bipolar disorder. Prog Neuropsychopharmacol Biol Psychiatry. 2012;38:127-133.
48. Weathers JD, Stringaris A, Deveney CM, et al. A developmental study of the neural circuitry mediating motor inhibition in bipolar disorder. Am J Psychiatry. 2012;169:633-641.
49. Lewis DA, Hashimoto T, Volk DW. Cortical inhibitory neurons and schizophrenia. Nat Rev Neurosci. 2005;6:312-324.
50. Bora E, Yücel M, Pantelis C. Cognitive impairment in affective psychoses: a meta-Analysis. Schizophr Bull. 2010;36: 112-125.
51. Lui S, Li T, Deng W, et al. Short-term effects of antipsychotic treatment on cerebral function in drug-naive first-episode schizophrenia revealed by "resting state" functional magnetic resonance imaging. Arch Gen Psychiatry. 2010;67:783-792.
52. Pavuluri MN, Ellis JA, Wegbreit E, Passarotti AM, Stevens MC. Pharmacotherapy impacts functional connectivity among affective circuits during response inhibition in pediatric mania. Behav Brain Res. 2012;226:493-503.
53. Cox RW. AFNI: software for analysis and visualization of functional magnetic resonance neuroimages. Comput Biomed Res. 1996;29:162-173.