Functional connectome organization predicts conversion to psychosis in clinical high-risk youth from the SHARP program

Guusje Collin, Larry J Seidman, Matcheri S Keshavan, William S Stone, Zhenghan Qi, Tianhong Zhang, Yingying Tang, Huijun Li, Sheeba Arnold Anteraper, Margaret A Niznikiewicz, Robert W McCarley, Martha E Shenton, Jijun Wang, Susan Whitfield-Gabrieli, Guusje Collin, Larry J Seidman, Matcheri S Keshavan, William S Stone, Zhenghan Qi, Tianhong Zhang, Yingying Tang, Huijun Li, Sheeba Arnold Anteraper, Margaret A Niznikiewicz, Robert W McCarley, Martha E Shenton, Jijun Wang, Susan Whitfield-Gabrieli

Abstract

The emergence of prodromal symptoms of schizophrenia and their evolution into overt psychosis may stem from an aberrant functional reorganization of the brain during adolescence. To examine whether abnormalities in connectome organization precede psychosis onset, we performed a functional connectome analysis in a large cohort of medication-naive youth at risk for psychosis from the Shanghai At Risk for Psychosis (SHARP) study. The SHARP program is a longitudinal study of adolescents and young adults at Clinical High Risk (CHR) for psychosis, conducted at the Shanghai Mental Health Center in collaboration with neuroimaging laboratories at Harvard and MIT. Our study involved a total of 251 subjects, including 158 CHRs and 93 age-, sex-, and education-matched healthy controls. During 1-year follow-up, 23 CHRs developed psychosis. CHRs who would go on to develop psychosis were found to show abnormal modular connectome organization at baseline, while CHR non-converters did not. In all CHRs, abnormal modular connectome organization at baseline was associated with a threefold conversion rate. A region-specific analysis showed that brain regions implicated in early-course schizophrenia, including superior temporal gyrus and anterior cingulate cortex, were most abnormal in terms of modular assignment. Our results show that functional changes in brain network organization precede the onset of psychosis and may drive psychosis development in at-risk youth.

Conflict of interest statement

Conflict of interest

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Image preprocessing and connectome analysis steps Overview of image preprocessing (A), connectome reconstruction (B), and modular community detection analysis (C). Of note, the colors of the modules shown in the connectivity matrices in panel C correspond to the modules as shown in Figure 2A.
Figure 2
Figure 2
Modular organization of the functional connectome A) Modular partitions of group-networks, plotted on cortical surface from superior, lateral, medial, and inferior angle, and subcortical structures (top to bottom row respectively). Colors indicate separate modules, with the prefrontal central-executive (CE) module in dark blue, the central sensorimotor (SM) module in green, the posterior visual (VIS) module in red, the (para)limbic (LIM) module in orange, the medial default mode (DM) module in light blue, and the cingulo-opercular (CO) module in yellow. B) Degree of similarity to average healthy network (SR) for individual subjects. Jittered data are plotted for each group, with mean (sd) values represented by the box behind the raw data. * indicates significant group-difference.
Figure 3
Figure 3
Regional findings of abnormal module assignment Surface plots showing exploratory regional findings (SRnode) at uncorrected p < .05 for surface-based (A) and MNI-based (B) processing methods respectively. * FDR-corrected significant effect for right superior temporal gyrus, anterior division.
Figure 4
Figure 4
Psychosis-free survival for typical vs. atypical baseline connectome organization Kaplan-Meier plot showing psychosis-free survival functions for CHRs with above-average (red) and below-average (blue) levels of SR (reflecting typical and atypical connectome organization respectively) as a functional of time since baseline (days).

References

    1. Liu CH, Keshavan MS, Tronick E, Seidman LJ. Perinatal risks and childhood premorbid indicators of later psychosis: Next steps for early psychosocial interventions. Schizophr Bull 2015; 41: 801–816.
    1. Keshavan MS, Delisi LE, Seidman LJ. Early and broadly defined psychosis risk mental states. Schizophr Res 2011; 126: 1–10.
    1. Fusar-poli P, Bonoldi I, Yung AR, Borgwardt S, Kempton MJ, Valmaggia L et al. Predicting psychosis: Meta-analysis of transition outcomes in individuals at high clinical risk. JAMA Psychiatry 2012; 69: 220–229.
    1. Yung AR, McGorry PD. The Prodromal Phase of First-episode Psychosis: Past and Current Conceptualizations. Schizophr Bull 1996; 22: 353–370.
    1. Tandon R, Nasrallah HA, Keshavan MS. Schizophrenia, ‘just the facts’ 4. Clinical features and conceptualization. Schizophr Res 2009; 110: 1–23.
    1. Insel TR. Rethinking schizophrenia. Nature 2010; 468: 187–193.
    1. Simon AE, Borgwardt S, Riecher-Rössler A, Velthorst E, de Haan L, Fusar-Poli P. Moving beyond transition outcomes: Meta-analysis of remission rates in individuals at high clinical risk for psychosis. Psychiatry Res 2013; 209: 266–272.
    1. Schlosser DA, Jacobson S, Chen Q, Sugar CA, Niendam TA, Li G et al. Recovery from an at-risk state: Clinical and functional outcomes of putatively prodromal youth who do not develop psychosis. Schizophr Bull 2012; 38: 1225–1233.
    1. Wang C, Lee J, Ho NF, Lim JKW, Poh JS, Rekhi G et al. Large-Scale Network Topology Reveals Heterogeneity in Individuals With at Risk Mental State for Psychosis: Findings From the Longitudinal Youth-at-Risk Study. Cereb Cortex 2017; Epub ahead: 1–10.
    1. Anticevic A, Haut K, Murray JD, Repovs G, Yang GJ, Diehl C et al. Association of thalamic dysconnectivity and conversion to psychosis in youth and young adults at elevated clinical risk. JAMA Psychiatry 2015; 72: 882–891.
    1. Gu S, Satterthwaite TD, Medaglia JD, Yang M, Gur RE, Gur RC et al. Emergence of system roles in normative neurodevelopment. Proc Natl Acad Sci USA 2015; 112: 13681–13686.
    1. Meunier D, Lambiotte R, Bullmore ET. Modular and hierarchically modular organization of brain networks. Front Neurosci 2010; 4: 200.
    1. Sporns O, Betzel RF. Modular Brain Networks. Annu Rev Psychol 2016; 67: 613–640.
    1. Fair DA, Cohen AL, Power JD, Dosenbach NUF, Church JA, Miezin FM et al. Functional brain networks develop from a ‘local to distributed’ organization. PLoS Comput Biol 2009; 5: e1000381.
    1. Satterthwaite TD, Wolf DH, Ruparel K, Erus G, Elliott MA, Eickhoff SB et al. Heterogeneous impact of motion on fundamental patterns of developmental changes in functional connectivity during youth. Neuroimage 2013; 83: 45–57.
    1. Collin G, Keshavan MS. Connectome development and a novel extension to the neurodevelopmental model of schizophrenia. Dialogues Clin Neurosci 2018; 20: 101–110.
    1. Sporns O. Contributions and challenges for network models in cognitive neuroscience. Nat Neurosci 2014; 17: 652–60.
    1. Zhang T, Li H, Tang Y, Niznikiewicz MA, Shenton ME, Keshavan MS et al. Validating the Predictive Accuracy of the NAPLS-2 Psychosis Risk Calculator in a Clinical High-Risk Sample From the SHARP (Shanghai At Risk for Psychosis) Program. Am J Psychiatry 2018; 175: 906–908.
    1. Zheng L, Wang J, Zhang T, Li H, Li C, Jiang K. The Chinese version of the SIPS/SOPS: a pilot study of reliability and validity. Chinese Ment Heal J 2012; 26: 571–576.
    1. Miller TJ, McGlashan TH, Rosen JL, Cadenhead K, Ventura J, Mcfarlane W et al. Prodromal assessment with the Structured Interview for Prodromal Syndromes and the Scale of Prodromal Symptoms: Predictive validity, interrater reliability, and training to reliability. Schizophr Bull 2003; 29: 703–715.
    1. Wechsler D WASI Manual Psychological Corporation, Harcourt Brace, San Antonio, TX, 1999.
    1. McGlashan T, Walsh B, Woods S. The Psychosis-Risk Syndrome: Handbook for Diagnosis and Follow-up. New York: Oxford University Press, 2010.
    1. Fornito A, Zalesky A, Breakspear M. Graph analysis of the human connectome: Promise, progress, and pitfalls. Neuroimage 2013; 80: 426–444.
    1. Sohn WS, Yoo K, Lee YB, Seo SW, Na DL, Jeong Y. Influence of ROI selection on resting functional connectivity: An individualized approach for resting fMRI analysis. Front Neurosci 2015; 9: 1–10.
    1. Fischl B FreeSurfer. Neuroimage 2012; 62: 774–81.
    1. Whitfield-Gabrieli S, Nieto-Castanon A. Conn: A functional connectivity toolbox for correlated and anticorrelated brain networks. Brain 2012; 2: 125–141.
    1. Makris N, Meyer JW, Bates JF, Yeterian EH, Kennedy DN, Caviness VS. MRI-Based Topographic Parcellation of Human Cerebral White Matter and Nuclei. Neuroimage 1999; 9: 18–45.
    1. Blondel VD, Guillaume J-L, Lambiotte R, Lefebvre E. Fast unfolding of communities in large networks. J Stat Mech 2008; : P10008.
    1. Rubinov M, Sporns O. Weight-conserving characterization of complex functional brain networks. Neuroimage 2011; 56: 2068–2079.
    1. Good BH, de Montjoye YA, Clauset A. Performance of modularity maximization in practical contexts. Phys Rev E 2010; 81: 46106.
    1. Doron KW, Bassett DS, Gazzaniga MS. Dynamic network structure of interhemispheric coordination. PNAS 2012; 109: 18661–18668.
    1. Traud AL, Kelsic ED, Mucha PJ, Porter MA. Comparing Community Structure to Characteristics in Online Collegiate Social Networks. SIAM Rev 2008; 53: 526–543.
    1. Bordier C, Nicolini C, Forcellini G, Bifone A. Disrupted modular organization of primary sensory brain areas in schizophrenia. NeuroImage Clin 2018; 18: 682–693.
    1. Lerman-Sinkoff DB, Barch DM. Network community structure alterations in adult schizophrenia: Identification and localization of alterations. NeuroImage Clin 2016; 10: 96–106.
    1. Hoffman R, Dobschka S. Cortical Pruning and the Development of Schizophrenia: A Computer Model. Schizophr Bull 1989; 15: 477–490.
    1. Hoffman R, McGlashan T. Parallel Distributed Processing and the Emergence of Schizophrenic Symptoms. Schizophr Bull 1993; 19: 119–140.
    1. Hoffman RE, McGlashan TH. Synaptic elimination, neurodevelopment, and the mechanism of hallucinated ‘voices’ in schizophrenia. Am J Psychiatry 1997; 154: 1683–1689.
    1. David AS. Dysmodularity: a neurocognitive model for schizophrenia. Schizophr Bull 1994; 20: 249–255.
    1. Yu Q, Plis SM, Erhardt EB, Allen EA, Sui J, Kiehl KA et al. Modular Organization of Functional Network Connectivity in Healthy Controls and Patients with Schizophrenia during the Resting State. Front Syst Neurosci 2012; 5: 1–16.
    1. Van den Heuvel MP, Sporns O, Collin G, Scheewe T, Mandl RCW, Cahn W et al. Abnormal rich club organization and functional brain dynamics in schizophrenia. JAMA psychiatry 2013; 70: 783–92.
    1. Schmidt A, Crossley NA, Harrisberger F, Smieskova R, Lenz C, Riecher-Rössler A et al. Structural network disorganization in subjects at clinical high risk for psychosis. Schizophr Bull 2017; 43: 583–591.
    1. Alexander-Bloch AF, Gogtay N, Meunier D, Birn R, Clasen L, Lalonde F et al. Disrupted modularity and local connectivity of brain functional networks in childhood-onset schizophrenia. Front Syst Neurosci 2010; 4: 147.
    1. Supekar K, Musen M, Menon V. Development of large-scale functional brain networks in children. PLoS Biol 2009; 7: e1000157.
    1. Casey B, Jones R, Somerville L. Braking and Accelerating of the Adolescent Brain. J Res Adolesc 2011; 21: 21–33.
    1. Skudlarski P, Jagannathan K, Anderson K, Stevens MC, Calhoun VD, Skudlarska BA et al. Brain connectivity is not only lower but different in schizophrenia: a combined anatomical and functional approach. Biol Psychiatry 2010; 68: 61–9.
    1. Pettersson-Yeo W, Allen P, Benetti S, McGuire P, Mechelli A. Dysconnectivity in schizophrenia: where are we now? Neurosci Biobehav Rev 2011; 35: 1110–24.
    1. Zalesky A, Cocchi L, Fornito A, Murray MM, Bullmore E. Connectivity differences in brain networks. Neuroimage 2012; 60: 1055–1062.
    1. Honea R, Sc B, Crow TJ, Ph D, Passingham D, Ph D et al. Regional Deficits in Brain Volume in Schizophrenia : A Meta-Analysis of Voxel-Based Morphometry Studies. Am J Psychiatry 2005; 162: 2233–2245.
    1. Glahn DC, Laird AR, Ellison-Wright I, Thelen SM, Robinson JL, Lancaster JL et al. Meta-Analysis of Gray Matter Anomalies in Schizophrenia: Application of Anatomic Likelihood Estimation and Network Analysis. Biol Psychiatry 2008; 64: 774–781.
    1. Vita A, De Peri L, Deste G, Sacchetti E. Progressive loss of cortical gray matter in schizophrenia: A meta-analysis and meta-regression of longitudinal MRI studies. Transl Psychiatry 2012; 2: e190–13.
    1. Shenton ME, Dickey CC, Frumin M, Mccarley RW. A review of MRI findings in schizophrenia. Schizophr Res 2001; 49: 1–52.
    1. Jung WH, Borgwardt S, Fusar-Poli P, Kwon JS. Gray matter volumetric abnormalities associated with the onset of psychosis. Front Psychiatry 2012; 3: 1–21.
    1. Tracy DK, Shergill SS. Mechanisms underlying auditory hallucinations - understanding perception without stimulus. Brain Sci 2013; 3: 642–669.
    1. Satterthwaite TD, Wolf DH, Loughead J, Ruparel K, Elliott MA, Hakonarson H 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.
    1. Power JD, Barnes KA, Snyder AZ, Schlaggar BL, Petersen SE. Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion. Neuroimage 2012; 59: 2142–2154.
    1. Behzadi Y, Restom K, Liau J, Liu TT. A component based noise correction method (CompCor) for BOLD and perfusion based fMRI. Neuroimage 2007; 37: 90–101.
    1. Murphy K, Birn RM, Handwerker DA, Jones TB, Bandettini PA. The impact of global signal regression on resting state correlations: are anti-correlated networks introduced? Neuroimage 2009; 44: 893–905.
    1. Chai XJ, Castañán AN, Öngür D, Whitfield-Gabrieli S. Anticorrelations in resting state networks without global signal regression. Neuroimage 2012; 59: 1420–1428.
    1. Murphy K, Birn RM, Bandettini PA. Resting-state FMRI confounds and cleanup. Neuroimage 2013; 80: 349–359.
    1. Rangaprakash D, Wu GR, Marinazzo D, Hu X, Deshpande G. Hemodynamic response function (HRF) variability confounds resting-state fMRI functional connectivity. Magn Reson Med 2018; 80: 1697–1713.

Source: PubMed

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