Regional cerebral blood flow alterations in unipolar depression

Forty-seven symptomatic inpatients and outpatients with major depression (13 nonendogenous, 23 endogenous, and 11 psychotic by Research Diagnostic Criteria) were compared with 138 normal control subjects. Absolute regional cerebral blood flow (rCBF, ml/minute/100 g) was measured with 133Xe single photon emission computed tomography. Flow ratios (region of interest/global flow) and residual scores (the difference between patient flow ratios and expected normal flow ratios, as derived from the control population) were also computed. Results revealed significant age x region x depression subtype interactions for absolute, ratio, and residual flow data. Consequently, a test of group means (or analysis of covariance) could not be used to examine between-group differences. Multiple regression analyses were employed to study the effects of age on rCBF. This analysis revealed that different, though sometimes overlapping, regions exhibited different age effects on rCBF in different depressive subtypes. Thus, diagnostic-subtype-dependent age effects on rCBF precluded comparisons of mean values within or across regions for subject groups, but distinguished between symptomatic depressed patients and control subjects and among patient groups. Possible causes of such effects include variations in duration of illness or medication history or sensitization phenomena.

[1]  J R Moeller,et al.  Regional cerebral blood flow in mood disorders. I. Comparison of major depressives and normal controls at rest. , 1990, Archives of general psychiatry.

[2]  M. Reivich,et al.  Brain function in psychiatric disorders. II. Regional cerebral blood flow in medicated unipolar depressives. , 1984, Archives of general psychiatry.

[3]  R. V. Van Heertum,et al.  Single photon emission computed tomography (SPECT) with [123I]IMP in the differential diagnosis of psychiatric disorders. , 1989, The Journal of neuropsychiatry and clinical neurosciences.

[4]  M S Buchsbaum,et al.  Frontal cortex and basal ganglia metabolic rates assessed by positron emission tomography with [18F]2-deoxyglucose in affective illness. , 1986, Journal of affective disorders.

[5]  F R Sharp,et al.  c‐fos expression and (14C) 2‐deoxyglucose uptake in the caudal cerebellum of the rat during motor/sensory cortex stimulation , 1989, The Journal of comparative neurology.

[6]  J C Mazziotta,et al.  Cerebral metabolic rates for glucose in mood disorders. Studies with positron emission tomography and fluorodeoxyglucose F 18. , 1985, Archives of general psychiatry.

[7]  T. Curran,et al.  Expression of c-fos protein in brain: metabolic mapping at the cellular level. , 1988, Science.

[8]  E. Metter,et al.  Patterns of cerebral glucose utilization in depression, multiple infarct dementia, and Alzheimer's disease. , 1985, Research publications - Association for Research in Nervous and Mental Disease.

[9]  H. Sackeim,et al.  Acute Reductions of Regional Cerebral Blood Flow following Electroconvulsive Therapy a , 1986, Annals of the New York Academy of Sciences.

[10]  P. Linkowski,et al.  Regional Cerebral Blood Flow and Lateralized Hemispheric Dysfunction in Depression , 1983, British Journal of Psychiatry.

[11]  F. Goodwin Manic-Depressive Illness , 1990 .

[12]  R. Post,et al.  C-fos mRNA expression following electrical-induced seizure and acute nociceptive stress in mouse brain , 1989, Epilepsy Research.

[13]  Robert M. Post,et al.  Recurrent Affective Disorders: Lessons from Limbic Kindling , 1988 .

[14]  P. Leber Adverse drug reactions. Safe passage (how good a guarantee?). , 1982, Psychopharmacology bulletin.

[15]  F. Reischies,et al.  Clinical correlates of cerebral blood flow in depression , 1989, Psychiatry Research.

[16]  O Nickel,et al.  Regional cerebral blood flow in depression: associations with psychopathology. , 1989, Journal of affective disorders.

[17]  R. Mathew,et al.  Cerebral blood flow in depression. , 1980, The American journal of psychiatry.

[18]  L. DeLisi,et al.  Anteroposterior gradients in cerebral glucose use in schizophrenia and affective disorders. , 1984, Archives of general psychiatry.

[19]  H. Hippius,et al.  Pathological cerebral blood flow during motor function in schizophrenic and endogenous depressed patients , 1986, Biological Psychiatry.

[20]  E M Stokely,et al.  Normal Distribution of Regional Cerebral Blood Flow Measured by Dynamic Single-Photon Emission Tomography , 1986, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[21]  J. Mazziotta,et al.  Reduction of prefrontal cortex glucose metabolism common to three types of depression. , 1989, Archives of general psychiatry.

[22]  J. Risberg,et al.  Acute and Late Effects of Electroconvulsive Therapy a , 1986 .

[23]  A. Hirano,et al.  AN ATLAS OF THE HUMAN BRAIN FOR COMPUTERIZED TOMOGRAPHY. , 1978 .

[24]  L. DeLisi,et al.  Glucose utilization in the temporal cortex of affectively ill patients: Positron emission tomography , 1987, Biological Psychiatry.

[25]  J. Mendlewicz,et al.  Regional Cerebral Blood Flow in Patients with Affective Disorders , 1990, British Journal of Psychiatry.

[26]  S. Pappatà,et al.  Left prefrontal glucose hypometabolism in the depressed state: a confirmation. , 1990, The American journal of psychiatry.

[27]  S. Ohno,et al.  11C-glucose metabolism in manic and depressed patients , 1987, Psychiatry Research.

[28]  R. Post,et al.  Evidence for common alterations in cerebral glucose metabolism in major affective disorders and schizophrenia. , 1989, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology.

[29]  M. Hamilton A RATING SCALE FOR DEPRESSION , 1960, Journal of neurology, neurosurgery, and psychiatry.

[30]  J. Totah,et al.  INTERACTIVE GRAPHICS METHODS FOR REGIONAL QUANTIFICATION OF TOMOGRAPHIC BRAIN BLOOD FLOW IMAGES. , 1982 .

[31]  J. Risberg,et al.  Regional cerebral blood flow in depression and mania. , 1989, Archives of general psychiatry.

[32]  D. Rubinow,et al.  Conditioning and Sensitisation in the Longitudinal Course of Affective Illness , 1986, British Journal of Psychiatry.