Hostname: page-component-586b7cd67f-vdxz6 Total loading time: 0 Render date: 2024-11-25T21:30:03.558Z Has data issue: false hasContentIssue false

Emotional reactivity in chronic schizophrenia: structural and functional brain correlates and the influence of adverse childhood experiences

Published online by Cambridge University Press:  09 June 2010

F. Benedetti*
Affiliation:
Department of Clinical Neurosciences, Scientific Institute and University Vita-Salute San Raffaele, Milan, Italy C.E.R.M.A.C. (Centro di Eccellenza Risonanza Magnetica ad Alto Campo), University Vita-Salute San Raffaele, Milan, Italy
D. Radaelli
Affiliation:
Department of Clinical Neurosciences, Scientific Institute and University Vita-Salute San Raffaele, Milan, Italy C.E.R.M.A.C. (Centro di Eccellenza Risonanza Magnetica ad Alto Campo), University Vita-Salute San Raffaele, Milan, Italy
S. Poletti
Affiliation:
Department of Clinical Neurosciences, Scientific Institute and University Vita-Salute San Raffaele, Milan, Italy C.E.R.M.A.C. (Centro di Eccellenza Risonanza Magnetica ad Alto Campo), University Vita-Salute San Raffaele, Milan, Italy Department of Pharmacological Sciences, Università degli Studi di Palermo, Italy
A. Falini
Affiliation:
C.E.R.M.A.C. (Centro di Eccellenza Risonanza Magnetica ad Alto Campo), University Vita-Salute San Raffaele, Milan, Italy Department of Neuroradiology, Scientific Institute and University Vita-Salute San Raffaele, Milan, Italy
R. Cavallaro
Affiliation:
Department of Clinical Neurosciences, Scientific Institute and University Vita-Salute San Raffaele, Milan, Italy
S. Dallaspezia
Affiliation:
Department of Clinical Neurosciences, Scientific Institute and University Vita-Salute San Raffaele, Milan, Italy C.E.R.M.A.C. (Centro di Eccellenza Risonanza Magnetica ad Alto Campo), University Vita-Salute San Raffaele, Milan, Italy
R. Riccaboni
Affiliation:
Department of Clinical Neurosciences, Scientific Institute and University Vita-Salute San Raffaele, Milan, Italy C.E.R.M.A.C. (Centro di Eccellenza Risonanza Magnetica ad Alto Campo), University Vita-Salute San Raffaele, Milan, Italy
G. Scotti
Affiliation:
C.E.R.M.A.C. (Centro di Eccellenza Risonanza Magnetica ad Alto Campo), University Vita-Salute San Raffaele, Milan, Italy Department of Neuroradiology, Scientific Institute and University Vita-Salute San Raffaele, Milan, Italy
E. Smeraldi
Affiliation:
Department of Clinical Neurosciences, Scientific Institute and University Vita-Salute San Raffaele, Milan, Italy C.E.R.M.A.C. (Centro di Eccellenza Risonanza Magnetica ad Alto Campo), University Vita-Salute San Raffaele, Milan, Italy
*
*Address for correspondence: F. Benedetti, M.D., Istituto Scientifico Ospedale San Raffaele, Department of Clinical Neurosciences, San Raffaele Turro, Via Stamira d'Ancona 20, Milan, Italy. (Email: [email protected])

Abstract

Background

Despite behavioural signs of flattened affect, patients affected by schizophrenia show enhanced sensitivity to negative stimuli. The current literature concerning neural circuitry for emotions supports dysregulations of cortico-limbic networks, but gives contrasting results. Adverse childhood experiences (ACEs) could persistently influence emotional regulation and neural correlates of response to emotional stimuli in healthy humans. This study evaluated the effect of ACEs and chronic undifferentiated schizophrenia on neural responses to emotional stimuli (negative facial expression).

Method

Brain blood-oxygen-level-dependent functional magnetic resonance imaging neural responses to a face-matching paradigm, and regional grey matter (GM) volumes were studied at 3.0 T in the amygdala, hippocampus, anterior cingulated cortex (ACC) and prefrontal cortex (PFC). The severity of ACEs was assessed. Participants included 20 consecutively admitted in-patients affected by chronic undifferentiated schizophrenia, and 20 unrelated healthy volunteers from the general population.

Results

Patients reported higher ACEs than controls. Worse ACEs proportionally led to decreasing responses in the amygdala and hippocampus, and to increasing responses in the PFC and ACC in all participants. Patients showed higher activations in the amygdala and hippocampus, and lower activations in the PFC and ACC. Higher ACEs were associated with higher GM volumes in the PFC and ACC, and schizophrenia was associated with GM reduction in all studied regions.

Conclusions

Structural and functional brain correlates of emotional reactivity are influenced by both current chronic undifferentiated schizophrenia and the severity of past ACEs.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Andreasen, NC, Pressler, M, Nopoulos, P, Miller, D, Ho, BC (2010). Antipsychotic dose equivalents and dose-years: a standardized method for comparing exposure to different drugs. Biological Psychiatry 67, 255262.CrossRefGoogle ScholarPubMed
BNF (2008). British National Formulary, 55th edn. British Medical Association; Royal Pharmaceutical Society of Great Britain. Pharmaceutical Press: London.Google Scholar
Ashburner, J, Friston, KJ (2005). Unified segmentation. Neuroimage 26, 839851.CrossRefGoogle ScholarPubMed
Barrelet, L, Ferrero, F, Szigethy, L, Giddey, C, Pellizzer, G (1990). Expressed emotion and first-admission schizophrenia. Nine-month follow-up in a French cultural environment. British Journal of Psychiatry 156, 357362.CrossRefGoogle Scholar
Benes, FM (2010). Amygdalocortical circuitry in schizophrenia: from circuits to molecules. Neuropsychopharmacology 35, 239257.CrossRefGoogle ScholarPubMed
Blasi, G, Popolizio, T, Taurisano, P, Caforio, G, Romano, R, Di Giorgio, A, Sambataro, F, Rubino, V, Latorre, V, Lo Bianco, L, Fazio, L, Nardini, M, Weinberger, DR, Bertolino, A (2009). Changes in prefrontal and amygdala activity during olanzapine treatment in schizophrenia. Psychiatry Research 173, 3138.CrossRefGoogle ScholarPubMed
Callicott, JH, Bertolino, A, Mattay, VS, Langheim, FJ, Duyn, J, Coppola, R, Goldberg, TE, Weinberger, DR (2000). Physiological dysfunction of the dorsolateral prefrontal cortex in schizophrenia revisited. Cerebral Cortex 10, 10781092.CrossRefGoogle ScholarPubMed
Ceccarelli, A, Rocca, MA, Pagani, E, Falini, A, Comi, G, Filippi, M (2009). Cognitive learning is associated with gray matter changes in healthy human individuals: a tensor-based morphometry study. Neuroimage 48, 585589.CrossRefGoogle ScholarPubMed
Collip, D, Myin-Germeys, I, Van Os, J (2008). Does the concept of ‘sensitization’ provide a plausible mechanism for the putative link between the environment and schizophrenia? Schizophrenia Bulletin 34, 220225.CrossRefGoogle ScholarPubMed
Cutting, LP, Aakre, JM, Docherty, NM (2006). Schizophrenic patients' perceptions of stress, expressed emotion, and sensitivity to criticism. Schizophrenia Bulletin 32, 743750.CrossRefGoogle ScholarPubMed
Das, P, Kemp, AH, Flynn, G, Harris, AW, Liddell, BJ, Whitford, TJ, Peduto, A, Gordon, E, Williams, LM (2007). Functional disconnections in the direct and indirect amygdala pathways for fear processing in schizophrenia. Schizophrenia Research 90, 284294.CrossRefGoogle ScholarPubMed
Fakra, E, Salgado-Pineda, P, Delaveau, P, Hariri, AR, Blin, O (2008). Neural bases of different cognitive strategies for facial affect processing in schizophrenia. Schizophrenia Research 100, 191205.CrossRefGoogle ScholarPubMed
Felitti, VJ, Anda, RF, Nordenberg, D, Williamson, DF, Spitz, AM, Edwards, V, Koss, MP, Marks, JS (1998). Relationship of childhood abuse and household dysfunction to many of the leading causes of death in adults. The Adverse Childhood Experiences (ACE) Study. American Journal of Preventive Medicine 14, 245258.Google ScholarPubMed
Goghari, VM, Sponheim, SR, Macdonald, AW 3rd (2010). The functional neuroanatomy of symptom dimensions in schizophrenia: a qualitative and quantitative review of a persistent question. Neuroscience and Biobehavioral Reviews 34, 468486.CrossRefGoogle ScholarPubMed
Good, CD, Johnsrude, IS, Ashburner, J, Henson, RN, Friston, KJ, Frackowiak, RS (2001). A voxel-based morphometric study of ageing in 465 normal adult human brains. Neuroimage 14, 2136.CrossRefGoogle ScholarPubMed
Gur, RC, Schroeder, L, Turner, T, McGrath, C, Chan, RM, Turetsky, BI, Alsop, D, Maldjian, J, Gur, RE (2002). Brain activation during facial emotion processing. Neuroimage 16, 651662.CrossRefGoogle ScholarPubMed
Gur, RE, Loughead, J, Kohler, CG, Elliott, MA, Lesko, K, Ruparel, K, Wolf, DH, Bilker, WB, Gur, RC (2007). Limbic activation associated with misidentification of fearful faces and flat affect in schizophrenia. Archives of General Psychiatry 64, 13561366.CrossRefGoogle ScholarPubMed
Hariri, AR, Mattay, VS, Tessitore, A, Kolachana, B, Fera, F, Goldman, D, Egan, MF, Weinberger, DR (2002). Serotonin transporter genetic variation and the response of the human amygdala. Science 297, 400403.CrossRefGoogle ScholarPubMed
Henry, JD, Green, MJ, de Lucia, A, Restuccia, C, McDonald, S, O'Donnell, M (2007). Emotion dysregulation in schizophrenia: reduced amplification of emotional expression is associated with emotional blunting. Schizophrenia Research 95, 197204.CrossRefGoogle ScholarPubMed
Holt, DJ, Kunkel, L, Weiss, AP, Goff, DC, Wright, CI, Shin, LM, Rauch, SL, Hootnick, J, Heckers, S (2006). Increased medial temporal lobe activation during the passive viewing of emotional and neutral facial expressions in schizophrenia. Schizophrenia Research 82, 153162.CrossRefGoogle ScholarPubMed
Honea, R, Crow, TJ, Passingham, D, Mackay, CE (2005). Regional deficits in brain volume in schizophrenia: a meta-analysis of voxel-based morphometry studies. American Journal of Psychiatry 162, 22332245.CrossRefGoogle ScholarPubMed
Hoschel, K, Irle, E (2001). Emotional priming of facial affect identification in schizophrenia. Schizophrenia Bulletin 27, 317327.CrossRefGoogle ScholarPubMed
Iritani, S (2007). Neuropathology of schizophrenia: a mini review. Neuropathology 27, 604608.CrossRefGoogle ScholarPubMed
Kay, SR, Fiszbein, A, Opler, LA (1987). The Positive and Negative Syndrome Scale (PANSS) for schizophrenia. Schizophrenia Bulletin 13, 261276.CrossRefGoogle ScholarPubMed
Kosaka, H, Omori, M, Murata, T, Iidaka, T, Yamada, H, Okada, T, Takahashi, T, Sadato, N, Itoh, H, Yonekura, Y, Wada, Y (2002). Differential amygdala response during facial recognition in patients with schizophrenia: an fMRI study. Schizophrenia Research 57, 8795.CrossRefGoogle ScholarPubMed
Kring, AM, Kerr, SL, Smith, DA, Neale, JM (1993). Flat affect in schizophrenia does not reflect diminished subjective experience of emotion. Journal of Abnormal Psychology 102, 507517.CrossRefGoogle Scholar
Li, H, Chan, RC, McAlonan, GM, Gong, QY (2009). Facial emotion processing in schizophrenia: a meta-analysis of functional neuroimaging data. Schizophrenia Bulletin. Published online 20 May 2009. doi:10.1093/schbul/sbn190.Google ScholarPubMed
Liberzon, I, Taylor, SF, Fig, LM, Decker, LR, Koeppe, RA, Minoshima, S (2000). Limbic activation and psychophysiologic responses to aversive visual stimuli. Interaction with cognitive task. Neuropsychopharmacology 23, 508516.CrossRefGoogle ScholarPubMed
McClure, RK, Phillips, I, Jazayerli, R, Barnett, A, Coppola, R, Weinberger, DR (2006). Regional change in brain morphometry in schizophrenia associated with antipsychotic treatment. Psychiatry Research 148, 121132.CrossRefGoogle ScholarPubMed
Myin-Germeys, I, Delespaul, PA, deVries, MW (2000). Schizophrenia patients are more emotionally active than is assumed based on their behavior. Schizophrenia Bulletin 26, 847854.CrossRefGoogle Scholar
Ochsner, KN, Gross, JJ (2005). The cognitive control of emotion. Trends in Cognitive Science 9, 242249.Google Scholar
Pezawas, L, Meyer-Lindenberg, A, Drabant, EM, Verchinski, BA, Munoz, KE, Kolachana, BS, Egan, MF, Mattay, VS, Hariri, AR, Weinberger, DR (2005). 5-HTTLPR polymorphism impacts human cingulate–amygdala interactions: a genetic susceptibility mechanism for depression. Nature Neuroscience 8, 828834.CrossRefGoogle ScholarPubMed
Phillips, ML, Drevets, WC, Rauch, SL, Lane, R (2003 a). Neurobiology of emotion perception I: The neural basis of normal emotion perception. Biological Psychiatry 54, 504514.CrossRefGoogle ScholarPubMed
Phillips, ML, Drevets, WC, Rauch, SL, Lane, R (2003 b). Neurobiology of emotion perception II: Implications for major psychiatric disorders. Biological Psychiatry 54, 515528.CrossRefGoogle ScholarPubMed
Phillips, ML, Williams, L, Senior, C, Bullmore, ET, Brammer, MJ, Andrew, C, Williams, SC, David, AS (1999). A differential neural response to threatening and non-'threatening negative facial expressions in paranoid and non-paranoid schizophrenics. Psychiatry Research 92, 1131.Google Scholar
Pruessner, JC, Dedovic, K, Khalili-Mahani, N, Engert, V, Pruessner, M, Buss, C, Renwick, R, Dagher, A, Meaney, MJ, Lupien, S (2008). Deactivation of the limbic system during acute psychosocial stress: evidence from positron emission tomography and functional magnetic resonance imaging studies. Biological Psychiatry 63, 234240.CrossRefGoogle ScholarPubMed
Rasetti, R, Mattay, VS, Wiedholz, LM, Kolachana, BS, Hariri, AR, Callicott, JH, Meyer-Lindenberg, A, Weinberger, DR (2009). Evidence that altered amygdala activity in schizophrenia is related to clinical state and not genetic risk. American Journal of Psychiatry 166, 216225.CrossRefGoogle Scholar
Repetti, RL, Taylor, SE, Seeman, TE (2002). Risky families: family social environments and the mental and physical health of offspring. Psychological Bulletin 128, 330366.CrossRefGoogle ScholarPubMed
Sanjuan, J, Lull, JJ, Aguilar, EJ, Marti-Bonmati, L, Moratal, D, Gonzalez, JC, Robles, M, Keshavan, MS (2007). Emotional words induce enhanced brain activity in schizophrenic patients with auditory hallucinations. Psychiatry Research 154, 2129.CrossRefGoogle ScholarPubMed
Scazufca, M, Kuipers, E, Menezes, PR (2001). Perception of negative emotions in close relatives by patients with schizophrenia. British Journal of Clinical Psychology 40, 167175.CrossRefGoogle ScholarPubMed
Schneider, F, Weiss, U, Kessler, C, Salloum, JB, Posse, S, Grodd, W, Muller-Gartner, HW (1998). Differential amygdala activation in schizophrenia during sadness. Schizophrenia Research 34, 133142.CrossRefGoogle ScholarPubMed
Stein, JL, Wiedholz, LM, Bassett, DS, Weinberger, DR, Zink, CF, Mattay, VS, Meyer-Lindenberg, A (2007). A validated network of effective amygdala connectivity. Neuroimage 36, 736745.CrossRefGoogle ScholarPubMed
Surguladze, S, Russell, T, Kucharska-Pietura, K, Travis, MJ, Giampietro, V, David, AS, Phillips, ML (2006). A reversal of the normal pattern of parahippocampal response to neutral and fearful faces is associated with reality distortion in schizophrenia. Biological Psychiatry 60, 423431.CrossRefGoogle ScholarPubMed
Suslow, T, Roestel, C, Arolt, V (2003). Affective priming in schizophrenia with and without affective negative symptoms. European Archives of Psychiatry and Clinical Neurosciences 253, 292300.CrossRefGoogle ScholarPubMed
Taylor, SE, Eisenberger, NI, Saxbe, D, Lehman, BJ, Lieberman, MD (2006). Neural responses to emotional stimuli are associated with childhood family stress. Biological Psychiatry 60, 296301.CrossRefGoogle ScholarPubMed
Taylor, SE, Lerner, JS, Sage, RM, Lehman, BJ, Seeman, TE (2004). Early environment, emotions, responses to stress, and health. Journal of Personality 72, 13651393.CrossRefGoogle ScholarPubMed
Taylor, SF, Liberzon, I, Decker, LR, Koeppe, RA (2002). A functional anatomic study of emotion in schizophrenia. Schizophrenia Research 58, 159172.CrossRefGoogle ScholarPubMed
Taylor, SF, Phan, KL, Britton, JC, Liberzon, I (2005). Neural response to emotional salience in schizophrenia. Neuropsychopharmacology 30, 984995.CrossRefGoogle ScholarPubMed
Taylor, SF, Phan, KL, Decker, LR, Liberzon, I (2003). Subjective rating of emotionally salient stimuli modulates neural activity. Neuroimage 18, 650659.CrossRefGoogle ScholarPubMed
Tompson, MC, Goldstein, MJ, Lebell, MB, Mintz, LI, Marder, SR, Mintz, J (1995). Schizophrenic patients' perceptions of their relatives' attitudes. Psychiatry Research 57, 155167.CrossRefGoogle ScholarPubMed
van Winkel, R, Stefanis, NC, Myin-Germeys, I (2008). Psychosocial stress and psychosis. A review of the neurobiological mechanisms and the evidence for gene–stress interaction. Schizophrenia Bulletin 34, 10951105.CrossRefGoogle ScholarPubMed
Velakoulis, D, Wood, SJ, Wong, MT, McGorry, PD, Yung, A, Phillips, L, Smith, D, Brewer, W, Proffitt, T, Desmond, P, Pantelis, C (2006). 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. Archives of General Psychiatry 63, 139149.CrossRefGoogle ScholarPubMed
White, T, Cullen, K, Rohrer, LM, Karatekin, C, Luciana, M, Schmidt, M, Hongwanishkul, D, Kumra, S, Charles Schulz, S, Lim, KO (2008). Limbic structures and networks in children and adolescents with schizophrenia. Schizophrenia Bulletin 34, 1829.CrossRefGoogle ScholarPubMed
Williams, LM, Das, P, Harris, AW, Liddell, BB, Brammer, MJ, Olivieri, G, Skerrett, D, Phillips, ML, David, AS, Peduto, A, Gordon, E (2004). Dysregulation of arousal and amygdala–prefrontal systems in paranoid schizophrenia. American Journal of Psychiatry 161, 480489.CrossRefGoogle ScholarPubMed
Williams, LM, Das, P, Liddell, BJ, Olivieri, G, Peduto, AS, David, AS, Gordon, E, Harris, AW (2007). Fronto-limbic and autonomic disjunctions to negative emotion distinguish schizophrenia subtypes. Psychiatry Research 155, 2944.CrossRefGoogle ScholarPubMed
Wood, SJ, Pantelis, C, Velakoulis, D, Yucel, M, Fornito, A, McGorry, PD (2008). Progressive changes in the development toward schizophrenia: studies in subjects at increased symptomatic risk. Schizophrenia Bulletin 34, 322329.CrossRefGoogle ScholarPubMed
Wright, P, Albarracin, D, Brown, RD, Li, H, He, G, Liu, Y (2008). Dissociated responses in the amygdala and orbitofrontal cortex to bottom-up and top-down components of emotional evaluation. Neuroimage 39, 894902.CrossRefGoogle ScholarPubMed