How can studies of resting-state functional connectivity help us understand psychosis as a disorder of brain development?

Current Opinion in Neurobiology

Volumn 30, Issue , 2015, Pages 85-91

  Satterthwaite, Theodore D ^a   Baker, Justin T ^b,c  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b MCLEAN HOSPITAL   (United States)

^c MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN DISEASE; BRAIN FUNCTION; CLINICAL DECISION MAKING; DISEASE ASSOCIATION; HUMAN; INFORMATION PROCESSING; LONGITUDINAL STUDY; NEUROIMAGING; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PROGNOSIS; PSYCHOSIS; RESTING STATE FUNCTIONAL CONNECTIVITY; RESTING STATE NETWORK; REVIEW; ANIMAL; BLOOD; BRAIN; GROWTH, DEVELOPMENT AND AGING; IMAGE PROCESSING; PATHOLOGY; PSYCHOTIC DISORDERS; REST; VASCULARIZATION;

OXYGEN;

ANIMALS; BRAIN; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; MAGNETIC RESONANCE IMAGING; OXYGEN; PSYCHOTIC DISORDERS; REST;

EID: 84910031284     PISSN: 09594388     EISSN: 18736882     Source Type: Journal    
DOI: 10.1016/j.conb.2014.10.005     Document Type: Review

References (50)

1. Rapoport J.L., Giedd J.N., Gogtay N. Neurodevelopmental model of schizophrenia: update 2012. Mol Psychiatry 2012.
2. Insel T.R. Rethinking schizophrenia. Nature 2010, 468:187-193.
3. Biswal B., Yetkin F.Z., Haughton V.M., Hyde J.S. Functional connectivity in the motor cortex of resting human brain using echo-planar MRI. Magn Reson Med 1995, 34:537-541.
4. Power J.D., Cohen A.L., Nelson S.M., et al. Functional network organization of the human brain. Neuron 2011, 72:665-678.
5. Yeo B.T.T., Krienen F.M., Sepulcre J., et al. The organization of the human cerebral cortex estimated by intrinsic functional connectivity. J Neurophysiol 2011, 106:1125-1165.
6. Smith S.M., Fox P.T., Miller K.L., et al. Correspondence of the brain's functional architecture during activation and rest. Proc Natl Acad Sci U S A 2009, 106:13040-13045.
7. Gur R.C., Calkins M.E., Satterthwaite T.D., et al. Neurocognitive growth charting in psychosis spectrum youths. JAMA Psychiatry 2014.
8. Fair D.A., Dosenbach N.U.F., Church J.A., et al. Development of distinct control networks through segregation and integration. Proc Natl Acad Sci U S A 2007, 104:13507-13512.
9. Fair D.A., Cohen A.L., Dosenbach N.U.F., et al. The maturing architecture of the brain's default network. Proc Natl Acad Sci 2008, 105:4028.
10. Kelly A.M.C., Di Martino A., Uddin L.Q., et al. Development of anterior cingulate functional connectivity from late childhood to early adulthood. Cereb Cortex 2009, 19:640-657.
11. Uddin L.Q., Supekar K.S., Ryali S., Menon V. Dynamic reconfiguration of structural and functional connectivity across core neurocognitive brain networks with development. J Neurosci 2011, 31:18578-18589.
12. Thomason M.E., Dassanayake M.T., Shen S., et al. Cross-hemispheric functional connectivity in the human fetal brain. Sci Transl Med 2013, 5. 173ra24.
13. Satterthwaite T.D., Wolf D.H., Ruparel K., et al. Heterogeneous impact of motion on fundamental patterns of developmental changes in functional connectivity during youth. Neuroimage 2013, 83:45-57.
14. Anderson J.S., Ferguson M.A., Lopez-Larson M., Yurgelun-Todd D: Connectivity gradients between the default mode and attention control networks. Brain Connect 2011, 1:147-157.
15. Barber A.D., Caffo B.S., Pekar J.J., Mostofsky SH: Developmental changes in within- and between-network connectivity between late childhood and adulthood. Neuropsychologia 2013, 51:156-167.
16. Dosenbach N.U.F., Nardos B., Cohen A.L., et al. Prediction of individual brain maturity using fMRI. Science 2010, 329:1358-1361.
17. Barch D.M., Ceaser A: Cognition in schizophrenia: core psychological and neural mechanisms. Trends Cogn Sci 2012, 16:27-34.
18. Minzenberg M.J., Laird A.R., Thelen S., Carter C.S., Glahn D.C. Meta-analysis of 41 functional neuroimaging studies of executive function in schizophrenia. Arch Gen Psychiatry 2009, 66:811-822.
19. Volk D.W., Lewis D.A. Prefrontal cortical circuits in schizophrenia. Curr Top Behav Neurosci 2010, 4:485-508.
20. Anticevic A., Tang Y., Cho Y.T., et al. Amygdala connectivity differs among chronic, early course, and individuals at risk for developing schizophrenia. Schizophr Bull 2013.
21. Baker J.T., Holmes A.J., Masters G.A., et al. Disruption of cortical association networks in schizophrenia and psychotic bipolar disorder. JAMA Psychiatry 2014, 71:109-118.
22. Fornito A., Yoon J., Zalesky A., Bullmore E.T., Carter C.S. General and specific functional connectivity disturbances in first-episode schizophrenia during cognitive control performance. Biol Psychiatry 2011, 70:64-72.
23. Khadka S., Meda S.A., Stevens M.C., et al. Is aberrant functional connectivity a psychosis endophenotype?. A resting state functional magnetic resonance imaging study. Biol Psychiatry 2013, 74:458-466.
24. Mamah D., Barch D.M., Repovs G: Resting state functional connectivity of five neural networks in bipolar disorder and schizophrenia. J Affect Disord 2013, 150:601-609.
25. Palaniyappan L., Simmonite M., White T.P., Liddle E.B., Liddle PF: Neural primacy of the salience processing system in schizophrenia. Neuron 2013, 79:814-828.
26. Woodward N.D., Karbasforoushan H., Heckers S. Thalamocortical dysconnectivity in schizophrenia. Am J Psychiatry 2012, 169:1092-1099.
27. Woodward N.D., Rogers B., Heckers S. Functional resting-state networks are differentially affected in schizophrenia. Schizophr Res 2011, 130:86-93.
28. Whitfield-Gabrieli S., Thermenos H.W., Milanovic S., et al. Hyperactivity and hyperconnectivity of the default network in schizophrenia and in first-degree relatives of persons with schizophrenia. Proc Natl Acad Sci U S A 2009, 106:1279-1284.
29. Fryer S.L., Woods S.W., Kiehl K.A., et al. Deficient Suppression of default mode regions during working memory in individuals with early psychosis and at clinical high-risk for psychosis. Front Psychiatry 2013, 4:92.
30. Wotruba D., Michels L., Buechler R., et al. Aberrant coupling within and across the default mode, task-positive, and salience network in subjects at risk for psychosis. Schizophr Bull 2013.
31. Anticevic A., Cole M.W., Repovs G., et al. Characterizing thalamo-cortical disturbances in schizophrenia and bipolar illness. Cereb Cortex 2013.
32. Alexander-Bloch A.F., Gogtay N., Meunier D., et al. Disrupted modularity and local connectivity of brain functional networks in childhood-onset schizophrenia. Front Syst Neurosci 2010, 4:147.
33. Lynall M.-E., Bassett D.S., Kerwin R., et al. Functional connectivity and brain networks in schizophrenia. J Neurosci 2010, 30:9477-9487.
34. Tomasi D., Volkow N.D. Mapping small-world properties through development in the human brain: disruption in schizophrenia. PLoS One 2014, 9:e69617.
35. van den Heuvel M.P., Sporns O., Collin G., et al. Abnormal rich club organization and functional brain dynamics in schizophrenia. JAMA Psychiatry 2013, 70:783-792.
36. Yang G.J., Murray J.D., Repovs G., et al. Altered global brain signal in schizophrenia. Proc Natl Acad Sci U S A 2014, 111:7438-7443.
37. Satterthwaite T.D., Wolf D.H., Loughead J., et al. Impact of in-scanner head motion on multiple measures of functional connectivity: relevance for studies of neurodevelopment in youth. Neuroimage 2012, 60:623-632.
38. Satterthwaite T.D., Elliott M.A., Gerraty R.T., et al. An improved framework for confound regression and filtering for control of motion artifact in the preprocessing of resting-state functional connectivity data. Neuroimage 2013, 64:240-256.
39. Fournier M., Ferrari C., Baumann P.S., et al. Impaired metabolic reactivity to oxidative stress in early psychosis patients. Schizophr Bull 2014.
40. Fornito A., Harrison B.J., Goodby E., et al. Functional dysconnectivity of corticostriatal circuitry as a risk phenotype for psychosis. JAMA Psychiatry 2013, 70:1143-1151.
41. Power J.D., Barnes K.A., Snyder A.Z., Schlaggar B.L., Petersen SE: Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion. Neuroimage 2011, 59:2142-2154.
42. Van Dijk K.R.A., Sabuncu M.R., Buckner RL: The influence of head motion on intrinsic functional connectivity MRI. Neuroimage 2011, 59:431-438.
43. Fair D.A., Nigg J.T., Iyer S., et al. Distinct neural signatures detected for ADHD subtypes after controlling for micro-movements in resting state functional connectivity MRI data. Front Syst Neurosci 2012, 6:80.
44. Kundu P., Brenowitz N.D., Voon V., et al. Integrated strategy for improving functional connectivity mapping using multiecho fMRI. Proc Natl Acad Sci U S A 2013.
45. Addington J., Cadenhead K.S., Cannon T.D., et al. North American Prodrome Longitudinal Study: a collaborative multisite approach to prodromal schizophrenia research. Schizophr Bull 2007, 33:665-672.
46. Satterthwaite T.D., Elliott M.A., Ruparel K., et al. Neuroimaging of the Philadelphia neurodevelopmental cohort. Neuroimage 2014, 86:544-553.
47. Meda S.A., Ruano G., Windemuth A., et al. Multivariate analysis reveals genetic associations of the resting default mode network in psychotic bipolar disorder and schizophrenia. Proc Natl Acad Sci U S A 2014, 111:E2066-E2075.
48. Thompson P.M., Stein J.L., Medland S.E., et al. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging Behav 2014.
49. Feinberg D.A., Moeller S., Smith S.M., et al. Multiplexed echo planar imaging for sub-second whole brain FMRI and fast diffusion imaging. PLoS One 2010, 5:e15710.
50. Chang C., Glover G.H. Time-frequency dynamics of resting-state brain connectivity measured with fMRI. Neuroimage 2010, 50:81-98.