A longitudinal study on intrinsic connectivity of hippocampus associated with positive symptom in first-episode schizophrenia

Behavioural Brain Research

Volumn 283, Issue , 2015, Pages 78-86

  Duan, Hui Feng ^a   Gan, Jing Li ^a   Yang, Jia Ming ^a   Cheng, Zheng Xiang ^a   Gao, Cun You ^a   Shi, Zhen Juan ^a   Zhu, Xi Quan ^a   Liang, Xue Jun ^a   Zhao, Lan Min ^a  

^a PLA 91st Central Hospital   (China)

Author keywords

First episode schizophrenia; Functional connectivity; Hippocampus; Magnetic resonance imaging; Positive symptom

Indexed keywords

ADULT; ARTICLE; CEREBELLUM; CINGULATE GYRUS; CONTROLLED STUDY; FEMALE; FOLLOW UP; FRONTAL GYRUS; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HIPPOCAMPUS; HUMAN; IMAGE ANALYSIS; LONGITUDINAL STUDY; MAJOR CLINICAL STUDY; MALE; POSITIVE SYNDROME; POSTERIOR CINGULATE; PRECUNEUS; RESTING STATE NETWORK; RIGHT MIDDLE FRONTAL GYRUS; SCORING SYSTEM; TEMPORAL GYRUS; BRAIN MAPPING; DISEASE COURSE; NERVE TRACT; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY; PSYCHOLOGICAL RATING SCALE; REST; SCHIZOPHRENIA;

ADULT; BRAIN MAPPING; DISEASE PROGRESSION; FEMALE; FOLLOW-UP STUDIES; HIPPOCAMPUS; HUMANS; LONGITUDINAL STUDIES; MAGNETIC RESONANCE IMAGING; MALE; NEURAL PATHWAYS; PSYCHIATRIC STATUS RATING SCALES; REST; SCHIZOPHRENIA;

EID: 84922308723     PISSN: 01664328     EISSN: 18727549     Source Type: Journal    
DOI: 10.1016/j.bbr.2015.01.022     Document Type: Article

References (53)

1. Chakos M.H., Schobel S.A., Gu H., Gerig G., Bradford D., Charles C., et al. Duration of illness and treatment effects on hippocampal volume in male patients with schizophrenia. Br J Psychiatry 2005, 186:26-31.
2. Velakoulis D., Wood S.J., Wong M.T., McGorry P.D., Yung A., Phillips L., et al. Hippocampal and amygdala volumes according to psychosis stage and diagnosis: a magnetic resonance imaging study of chronic schizophrenia, first-episode psychosis, and ultra-high-risk individuals. Arch Gen Psychiatry 2006, 63:139-149.
3. Honea R., Crow T.J., Passingham D., Mackay C.E. Regional deficits in brain volume in schizophrenia: a meta-analysis of voxel-based morphometry studies. Am J Psychiatry 2005, 162:2233-2245.
4. Steen R.G., Mull C., McClure R., Hamer R.M., Lieberman J.A. Brain volume in first-episode schizophrenia: systematic review and meta-analysis of magnetic resonance imaging studies. Br J Psychiatry 2006, 188:510-518.
5. Glahn D.C., Laird A.R., Ellison-Wright I., Thelen S.M., Robinson J.L., Lancaster J.L., et al. Meta-analysis of gray matter anomalies in schizophrenia: application of anatomic likelihood estimation and network analysis. Biol Psychiatry 2008, 64:774-781.
6. Kasai K., Shenton M.E., Salisbury D.F., Hirayasu Y., Onitsuka T., Spencer M.H., et al. Progressive decrease of left Heschl gyrus and planum temporale gray matter volume in first-episode schizophrenia: a longitudinal magnetic resonance imaging study. Arch Gen Psychiatry 2003, 60:766-775.
7. Schaufelberger M.S., Lappin J.M., Duran F.L., Rosa P.G., Uchida R.R., Santos L.C., et al. Lack of progression of brain abnormalities in first-episode psychosis: a longitudinal magnetic resonance imaging study. Psychol Med 2011, 41:1677-1689.
8. Lappin J.M., Morgan C., Chalavi S., Morgan K.D., Reinders A.A., Fearon P., et al. Bilateral hippocampal increase following first-episode psychosis is associated with good clinical, functional and cognitive outcomes. Psychol Med 2014, 44:1279-1291.
9. Tamminga C.A., Stan A.D., Wagner A.D. The hippocampal formation in schizophrenia. Am J Psychiatry 2010, 167:1178-1193.
10. Lodge D.J., Grace A.A. Hippocampal dysregulation of dopamine system function and the pathophysiology of schizophrenia. Trends Pharmacol Sci 2011, 32:507-513.
11. Barch D.M., Csernansky J.G., Conturo T., Snyder A.Z. Working and long-term memory deficits in schizophrenia: is there a common prefrontal mechanism. J Abnormal Psychol 2002, 111:478-494.
12. Weiss A.P., Schacter D.L., Goff D.C., Rauch S.L., Alpert N.M., Fischman A.J., et al. Impaired hippocampal recruitment during normal modulation of memory performance in schizophrenia. Biol Psychiatry 2003, 53:48-55.
13. Zhou Y., Shu N., Liu Y., Song M., Hao Y., Liu H., et al. Altered resting-state functional connectivity and anatomical connectivity of hippocampus in schizophrenia. Schizophr Res 2008, 100:120-132.
14. Wolf R.C., Vasic N., Sambataro F., Hose A., Frasch K., Schmid M., et al. Temporally anticorrelated brain networks during working memory performance reveal aberrant prefrontal and hippocampal connectivity in patients with schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry 2009, 33:1464-1473.
15. Henseler I., Falkai P., Gruber O. Disturbed functional connectivity within brain networks subserving domain-specific subcomponents of working memory in schizophrenia: relation to performance and clinical symptoms. J Psychiatr Res 2010, 44:364-372.
16. Knochel C., Stablein M., Storchak H., Reinke B., Jurcoane A., Prvulovic D., et al. Multimodal assessments of the hippocampal formation in schizophrenia and bipolar disorder: evidences from neurobehavioral measures and functional and structural MRI. Neuroimage Clin 2014, 6:134-144.
17. Association A.P. Diagnostic and statistical manual of mental disorders 1994, DSM-IV: American Psychiatric Association, Washington, DC. 4th ed.
18. Kay S.R., Fiszbein A., Lindenmayer J.P., Opler L.A. Positive and negative syndromes in schizophrenia as a function of chronicity. Acta Psychiatr Scand 1986, 74:507-518.
19. Wang L., Zang Y., He Y., Liang M., Zhang X., Tian L., et al. Changes in hippocampal connectivity in the early stages of Alzheimer's disease: evidence from resting state fMRI. Neuroimage 2006, 31:496-504.
20. Fornito A., Zalesky A., Bassett D.S., Meunier D., Ellison-Wright I., Yucel M., et al. Genetic influences on cost-efficient organization of human cortical functional networks. J Neurosci 2011, 31:3261-3270.
21. Song X.W., Dong Z.Y., Long X.Y., Li S.F., Zuo X.N., Zhu C.Z., et al. REST: a toolkit for resting-state functional magnetic resonance imaging data processing. PLoS ONE 2011, 6:e25031.
22. Maldjian J.A., Laurienti P.J., Kraft R.A., Burdette J.H. An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets. Neuroimage 2003, 19:1233-1239.
23. Tregellas J.R., Davalos D.B., Rojas D.C., Waldo M.C., Gibson L., Wylie K., et al. Increased hemodynamic response in the hippocampus, thalamus and prefrontal cortex during abnormal sensory gating in schizophrenia. Schizophr Res 2007, 92:262-272.
24. Liang M., Zhou Y., Jiang T., Liu Z., Tian L., Liu H., et al. Widespread functional disconnectivity in schizophrenia with resting-state functional magnetic resonance imaging. Neuroreport 2006, 17:209-213.
25. Genzel L., Dresler M., Cornu M., Jager E., Konrad B., Adamczyk M., et al. Medial prefrontal-hippocampal connectivity and motor memory consolidation in depression and schizophrenia. Biol Psychiatry 2015, 77:177-186.
26. Poch C., Campo P. Neocortical-hippocampal dynamics of working memory in healthy and diseased brain states based on functional connectivity. Front Hum Neurosci 2012, 6:36.
27. Kraguljac N.V., White D.M., Hadley J., Reid M.A., Lahti A.C. Hippocampal-parietal dysconnectivity and glutamate abnormalities in unmedicated patients with schizophrenia. Hippocampus 2014, 24:1524-1532.
28. White T., Kendi A.T., Lehericy S., Kendi M., Karatekin C., Guimaraes A., et al. Disruption of hippocampal connectivity in children and adolescents with schizophrenia-a voxel-based diffusion tensor imaging study. Schizophr Res 2007, 90:302-307.
29. Harrison P.J. The hippocampus in schizophrenia: a review of the neuropathological evidence and its pathophysiological implications. Psychopharmacology 2004, 174:151-162.
30. Sigurdsson T., Stark K.L., Karayiorgou M., Gogos J.A., Gordon J.A. Impaired hippocampal-prefrontal synchrony in a genetic mouse model of schizophrenia. Nature 2010, 464:763-767.
31. Sommer I.E., Clos M., Meijering A.L., Diederen K.M., Eickhoff S.B. Resting state functional connectivity in patients with chronic hallucinations. PLoS ONE 2012, 7:e43516.
32. Rotarska-Jagiela A., van de Ven V., Oertel-Knochel V., Uhlhaas P.J., Vogeley K., Linden D.E. Resting-state functional network correlates of psychotic symptoms in schizophrenia. Schizophr Res 2010, 117:21-30.
33. Fransson P. Spontaneous low-frequency BOLD signal fluctuations: an fMRI investigation of the resting-state default mode of brain function hypothesis. Hum Brain Mapp 2005, 26:15-29.
34. Moscovitch M., Nadel L., Winocur G., Gilboa A., Rosenbaum R.S. The cognitive neuroscience of remote episodic, semantic and spatial memory. Curr Opin Neurobiol 2006, 16:179-190.
35. Bartsch T., Dohring J., Rohr A., Jansen O., Deuschl G. CA1 neurons in the human hippocampus are critical for autobiographical memory, mental time travel, and autonoetic consciousness. Proc Natl Acad Sci USA 2011, 108:17562-17567.
36. Vincent J.L., Snyder A.Z., Fox M.D., Shannon B.J., Andrews J.R., Raichle M.E., et al. Coherent spontaneous activity identifies a hippocampal-parietal memory network. J Neurophysiol 2006, 96:3517-3531.
37. Yu Y., Shen H., Zeng L.L., Ma Q., Hu D. Convergent and divergent functional connectivity patterns in schizophrenia and depression. PLoS ONE 2013, 8:e68250.
38. Takahashi T., Wood S.J., Yung A.R., Soulsby B., McGorry P.D., Suzuki M., et al. Progressive gray matter reduction of the superior temporal gyrus during transition to psychosis. Arch Gen Psychiatry 2009, 66:366-376.
39. Zipursky R.B., Reilly T.J., Murray R.M. The myth of schizophrenia as a progressive brain disease. Schizophr Bull 2013, 39:1363-1372.
40. Ayesa-Arriola R., Perez-Iglesias R., Rodriguez-Sanchez J.M., Pardo-Garcia G., Tabares-Seisdedos R., Ayuso-Mateos J.L., et al. Predictors of neurocognitive impairment at 3 years after a first episode non-affective psychosis. Prog Neuropsychopharmacol Biol Psychiatry 2013, 43:23-28.
41. Bauer E.P., Paz R., Pare D. Gamma oscillations coordinate amygdalo-rhinal interactions during learning. J Neurosci 2007, 27:9369-9379.
42. Rolls E.T. Hippocampo-cortical and cortico-cortical backprojections. Hippocampus 2000, 10:380-388.
43. Cobia D.J., Smith M.J., Wang L., Csernansky J.G. Longitudinal progression of frontal and temporal lobe changes in schizophrenia. Schizophr Res 2012, 139:1-6.
44. Quintana J., Wong T., Ortiz-Portillo E., Kovalik E., Davidson T., Marder S.R., et al. Prefrontal-posterior parietal networks in schizophrenia: primary dysfunctions and secondary compensations. Biol Psychiatry 2003, 53:12-24.
45. Tan H.Y., Sust S., Buckholtz J.W., Mattay V.S., Meyer-Lindenberg A., Egan M.F., et al. Dysfunctional prefrontal regional specialization and compensation in schizophrenia. Am J Psychiatry 2006, 163:1969-1977.
46. Murray G.K., Corlett P.R., Fletcher P.C. The neural underpinnings of associative learning in health and psychosis: how can performance be preserved when brain responses are abnormal. Schizophr Bull 2010, 36:465-471.
47. Kempton M.J., Stahl D., Williams S.C., DeLisi L.E. Progressive lateral ventricular enlargement in schizophrenia: a meta-analysis of longitudinal MRI studies. Schizophr Res 2010, 120:54-62.
48. de la Iglesia-Vaya M., Escarti M.J., Molina-Mateo J., Marti-Bonmati L., Gadea M., Castellanos F.X., et al. Abnormal synchrony and effective connectivity in patients with schizophrenia and auditory hallucinations. Neuroimage Clin 2014, 6:171-179.
49. Stephan K.E., Friston K.J., Frith C.D. Dysconnection in schizophrenia: from abnormal synaptic plasticity to failures of self-monitoring. Schizophr Bull 2009, 35:509-527.
50. Amad A., Cachia A., Gorwood P., Pins D., Delmaire C., Rolland B., et al. The multimodal connectivity of the hippocampal complex in auditory and visual hallucinations. Mol Psychiatry 2014, 19:184-191.
51. Rish I., Cecchi G., Thyreau B., Thirion B., Plaze M., Paillere-Martinot M.L., et al. Schizophrenia as a network disease: disruption of emergent brain function in patients with auditory hallucinations. PLoS ONE 2013, 8:e50625.
52. Friston K.J., Frith C.D. Schizophrenia: a disconnection syndrome. Clin Neurosci 1995, 3:89-97.
53. Seeley W.W., Menon V., Schatzberg A.F., Keller J., Glover G.H., Kenna H., et al. Dissociable intrinsic connectivity networks for salience processing and executive control. J Neurosci 2007, 27:2349-2356.