AN FDG-PET STUDY ON THE REGIONAL METABOLISM OF THE BRAIN IN SCHIZOPHRENIA

Main Article Content

Dr. R Karthikeyan

Keywords

Brain, Schizophrenia, Patients, Metabolism

Abstract

Recent technological development has proved beyond doubt that schizophrenia is biological in nature. FDG-PET functional neuroimaging has now emerged as an important tool in the examination of the biological basis of the psychopathology of schizophrenia. FDG-PET scanning was performed on male patients with schizophrenia diagnosis, and all of them were in the state of active psychosis according to the PANSS scale in resting conditions. The uptake of glucose cerebrally in the different regions of interest was examined throughout the schizophrenia spectrum. There was no significant impact upon cerebral glucose metabolism by the chronicity or severity of the illness. The negative type of schizophrenia patients had a significant reduction in metabolism in all the brain regions as compared to the positive type. Conversely, positive syndrome of schizophrenia showed extensive elevation of glucose metabolism in the medial temporal areas, basal ganglia and left thalamus. The cerebellum also showed hypometabolism. Although several brain structures have been implicated as the possible causative regions, and theories on how they work have been put forward, the fact that schizophrenia is significantly heterogeneous makes it a big challenge to specifically describe the disease process.

Abstract 42 | pdf Downloads 13

References

1. Ron MA, Harvey I. The brain in schizophrenia [Review]. J NeurolNeurosurg Psychiatry, 1990;53:725–6.
2. Ingvar DH, Franzen G. Distribution of cerebral activity in chronic schizophrenia. Lancet 1974;2:1484–6.
3. Mathew RJ, Duncan GC, Weinman ML, et al. Regional cerebral blood flow in schizophrenia. Arch Gen Psychiatry 1982; 39: 1121–4.
4. Ariel NR, Golden CJ, Berg RA, et al. Regional cerebral blood flow in schizophrenics. Arch Gen Psychiatry 1983;40:258–63.
5. Gur RE, Resnick SM, Alavi A, et al. Regional brain function in schizophrenia: I. A positron emission tomography study. Arch Gen Psychiatry 1987a;44:119–25.
6. Gur RE, Resnick SM, Gur RC, et al. Regional brain function in schizophrenia: I. Repeated evaluation with positron emission tomography study. Arch Gen Psychiatr y 1987b;44:126–9.
7. Shergill SS, Brammer MJ, Williams SC, et al. Mapping auditory hallucinations in schizophrenia using functional magnetic resonance imaging. Arch Gen Psychiatry 2000;57:1033–8.
8. Zakzanis KK, PoulinP , Hansen KT , et al. Searching the schizophrenic brain for temporal lobe deficits: A systematic review and meta-analysis. Psychol Med 2000;30:491–504.
9. Soyka M, Koch W ,Möller HJ, et al. Hypermetabolic pattern in frontal cortex and other brain regions in unmedicated schizophrenia patients: Results from a FDG-PET study. Eur Arch Psychiatry ClinNeurosci2005;255:308–12.
10. Andreasen NC, Paradiso S, O’Leary DS. ‘Cognitive dysmetria’ as an integrative theory of schizophrenia: A dysfunction in cortical–subcortical–cerebellar circuitry? Schizophr Bull 1998;24:203–18.
11. Kay SR, Fizsben A, Opler LA. The Positive and Negative Syndrome Scale for schizophrenia (PANSS). Schizophr Bull 1987a;13:261–76.
12. Buchsbaum MS, Ingvar DH, Kessler R, et al. Cerebral glucography with positron tomography. Use in normal subjects and in patients with schizophrenia. Arch Gen Psychiatry 1982;39:251–9.
13. Hazlett EA, Buchsbaum MS, Byne W, et al. Three-dimensional analysis with MRI and PET of the size, shape, and function of the thalamus in the schizophrenia spectrum. Am J Psychiatry 1999;156:1190–9.
14. Ramnani N, Miall C. Expanding cerebellar horizons. Trends CognNeurosci2001;5:135–6.
15. Potkin SG, Alva G, Fleming K, et al. A PET study of the pathophysiology of negative symptoms in schizophrenia. Positron emission tomography. Am J Psychiatry 2002;159:227–37.
16. Keller A, Castellanos FX, Vaituzis AC, et al. Progressive loss of cerebellar volume in childhood-onset schizophrenia. Am J Psychiatry 2003;160:128–33.
17. Mathew RJ, Duncan GC, Weinman ML, et al. Regional cerebral blood flow in schizophrenia. Arch Gen Psychiatry 1982;39: 1121–4