Literature DB >> 6122474

Ex uno multi: subtyping the schizophrenic syndrome.

D V Jeste, J E Kleinman, S G Potkin, D J Luchins, D R Weinberger.   

Abstract

We studied 93 chronic schizophrenic inpatients, who met the Research Diagnostic Criteria for schizophrenia. Data on a number of historical, epidemiologic, phenomenologic, biochemical, neuropathological, and treatment-response variables were analyzed, using univariate and multivariate statistical analyses. Patients were classified into pairs of subgroups, according to each of the following seven dimensions: (1) ventricle/brain ratio (VBR) assessed on computed tomography scans (normal vs. abnormal); (2) premorbid adjustment (good vs. poor); (3) therapeutic response to neuroleptics (good vs. poor); (4) platelet monoamine oxidase (MAO) activity (low vs. high); (5) paranoid features (present vs. absent); (6) tardive dyskinesia (present vs. absence); and (7) hemispheric asymmetry on computed tomography scans (normal vs. abnormal). These seven dimensions were chosen because earlier studies had shown that the variables involved were operationally definable and were of potential relevance to the subgrouping of schizophrenic patients. Our results suggested that two biological variables, viz., VBR and platelet MAO activity, might be useful in identifying two rather distinct subgroups among chronic schizophrenic patients. A subgroup with large VBR was associated with poor premorbid adjustment, neurological impairment, and poor therapeutic response to neuroleptics, while the subgroup with low platelet MAO activity was characterized by the presence of paranoid features and tardive dyskinesia. Possible explanations, implications, and limitations of our findings are discussed.

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Year:  1982        PMID: 6122474

Source DB:  PubMed          Journal:  Biol Psychiatry        ISSN: 0006-3223            Impact factor:   13.382


  5 in total

1.  Topographic subtypes of tardive dyskinesia in schizophrenic patients aged less than 60 years: relationship to demographic, clinical, treatment, and neuropsychological variables.

Authors:  O Gureje
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-12       Impact factor: 10.154

2.  Neurochemical and genetic bases of psychopathology: future directions.

Authors:  S Matthysse; M Kling
Journal:  Behav Genet       Date:  1982-02       Impact factor: 2.805

3.  Behavioral sensitization to beta-phenylethylamine (PEA): enduring modifications of specific dopaminergic neuron systems in the rat.

Authors:  T Kuroki; T Tsutsumi; M Hirano; T Matsumoto; Y Tatebayashi; K Nishiyama; H Uchimura; A Shiraishi; T Nakahara; K Nakamura
Journal:  Psychopharmacology (Berl)       Date:  1990       Impact factor: 4.530

Review 4.  Imaging phenotypes and genotypes in schizophrenia.

Authors:  Jessica A Turner; Padhraic Smyth; Fabio Macciardi; James H Fallon; James L Kennedy; Steven G Potkin
Journal:  Neuroinformatics       Date:  2006

5.  The relationship of structural brain imaging parameters to antipsychotic treatment response: a review.

Authors:  L Friedman; C Lys; S C Schulz
Journal:  J Psychiatry Neurosci       Date:  1992-06       Impact factor: 6.186

  5 in total

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