Neural Correlates of Sad Feelings in Schizophrenia with and without Blunted Affect

• Published in: Canadian journal of psychiatry 2005-12, Vol.50 (14), p.909-917
• Main Authors: Stip, Emmanuel, Fahim, Cherine, Liddle, Peter, Mancini-Marïe, Adham, Mensour, Boualem, Bentaleb, Lahcen Ait, Beauregard, Mario
• Format: Article
• Language: English
• Subjects: Adult; Adult and adolescent clinical studies; Affect; Biological and medical sciences; Brain; Brain - anatomy & histology; Brain - metabolism; Brain - physiopathology; Diagnostic and Statistical Manual of Mental Disorders; Emotions; Female; Humans; Magnetic Resonance Imaging; Male; Medical research; Medical sciences; Middle Aged; NMR; Nuclear magnetic resonance; Oxygen - metabolism; Patients; Psychiatry; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Psychoses; Schizophrenia; Schizophrenia - diagnosis; Schizophrenia - metabolism; Schizophrenia - physiopathology; Severity of Illness Index; Social Environment
• ISSN: 0706-7437; 1497-0015
• DOI: 10.1177/070674370505001405

Objective: There have been reports that patients with schizophrenia have decreased activity in the prefrontal cortex during emotion processing. However, findings have been confounded by sample nonspecificity and explicit cognitive task interference with emotion processing. We aimed to further investigate this by examining the ventrolateral prefrontal cortex (VLPFC) activation in response to the passive viewing of sad film excerpts. Methods: We presented film excerpts depicting sad and neutral social situations to 25 schizophrenia patients (14 with blunted affect [BA+] and 11 without blunted affect [BA-]) in an implicit perception task to evoke prefronto-limbic activity illustrated by blood oxygenation level–dependent functional magnetic resonance imaging. Results: A random-effects analysis (2-sample t test) using statistical parametric mapping indicated that BA+ patients differed from BA–patients at a 0.05 level (P corrected for multiple comparisons). Consistent with our a priori hypothesis, BA–patients (relative to BA+ patients) showed significant activation in the right VLPFC. An exploratory analysis revealed the following loci of activation: caudate nucleus, VLPFC, middle prefrontal cortex, medial prefrontal cortex, anterior cingulate cortex, and anterior temporal pole in the BA–group; and hippocampus, cerebellum, anterior temporal pole, and midbrain in the BA+ group. Conclusions: We observed not only hypofrontality in the BA+ group but also dysfunctional circuitry distributed throughout the brain. The temporal and midbrain activation seen in the BA+ group may indicate that these brain regions were working harder to compensate for inactivation in other regions. These distributed dysfunctional circuits may form the neural basis of blunted affect through impairment of emotion processing in the brain that prevents it from processing input efficiently and producing output effectively, thereby leading to symptoms such as blunted affect.