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      The Longitudinal Course of Schizophrenia Across the Lifespan: Clinical, Cognitive, and Neurobiological Aspects

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          Abstract

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          Abstract

          Despite several decades of research, our knowledge of the long-term course of schizophrenia (SZ) is hampered by a lack of homogeneity of both research methods and phenotypic definitions of SZ’s course. We provide a comprehensive review of the course of SZ by applying stringent methodological and diagnostic study-selection criteria. We report on positive and negative symptoms, cognition, and findings obtained by neuroimaging. In addition, we perform a meta-analysis of longitudinal studies of cognition in humans. We selected 35 human studies focusing on a narrow SZ phenotype, employing a follow-up duration of six months or more and consistent methodology at the different measurement points. For the meta-analysis on global cognitive change, eight and four studies were used to compare SZ to healthy and psychiatric controls, respectively. We find that the course of SZ is characterized by a constancy or even improvement of positive and negative symptoms and by fairly stable cognitive impairment, reflecting structural frontal and temporal cortical pathology. Progressive changes of the frontal cortex appear to develop in parallel with changes in symptomatology and executive impairment. Despite stable differences in cognition between patients and controls over the time intervals studied, high heterogeneity in the magnitude of effect sizes is present, and age is identified as one of its potential sources. Meta-regression shows these magnitudes to depend on the age at study inclusion. For future research, a combination of longitudinal and cross-sectional research designs is warranted to better account for potential cohort effects.

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          Long-term antipsychotic treatment and brain volumes: a longitudinal study of first-episode schizophrenia.

          Progressive brain volume changes in schizophrenia are thought to be due principally to the disease. However, recent animal studies indicate that antipsychotics, the mainstay of treatment for schizophrenia patients, may also contribute to brain tissue volume decrement. Because antipsychotics are prescribed for long periods for schizophrenia patients and have increasingly widespread use in other psychiatric disorders, it is imperative to determine their long-term effects on the human brain. To evaluate relative contributions of 4 potential predictors (illness duration, antipsychotic treatment, illness severity, and substance abuse) of brain volume change. Predictors of brain volume changes were assessed prospectively based on multiple informants. Data from the Iowa Longitudinal Study. Two hundred eleven patients with schizophrenia who underwent repeated neuroimaging beginning soon after illness onset, yielding a total of 674 high-resolution magnetic resonance scans. On average, each patient had 3 scans (≥2 and as many as 5) over 7.2 years (up to 14 years). Brain volumes. During longitudinal follow-up, antipsychotic treatment reflected national prescribing practices in 1991 through 2009. Longer follow-up correlated with smaller brain tissue volumes and larger cerebrospinal fluid volumes. Greater intensity of antipsychotic treatment was associated with indicators of generalized and specific brain tissue reduction after controlling for effects of the other 3 predictors. More antipsychotic treatment was associated with smaller gray matter volumes. Progressive decrement in white matter volume was most evident among patients who received more antipsychotic treatment. Illness severity had relatively modest correlations with tissue volume reduction, and alcohol/illicit drug misuse had no significant associations when effects of the other variables were adjusted. Viewed together with data from animal studies, our study suggests that antipsychotics have a subtle but measurable influence on brain tissue loss over time, suggesting the importance of careful risk-benefit review of dosage and duration of treatment as well as their off-label use.
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            Are there progressive brain changes in schizophrenia? A meta-analysis of structural magnetic resonance imaging studies.

            It is well established that schizophrenia is associated with structural brain abnormalities, but whether these are static or progress over time remains controversial. A systematic review of longitudinal volumetric studies using region-of-interest structural magnetic resonance imaging in patients with schizophrenia and healthy control subjects. The percentage change in volume between scans for each brain region of interest was obtained, and data were combined using random effects meta-analysis. Twenty-seven studies were included in the meta-analysis, with 928 patients and 867 control subjects, and 32 different brain regions of interest. Subjects with schizophrenia showed significantly greater decreases over time in whole brain volume, whole brain gray matter, frontal gray and white matter, parietal white matter, and temporal white matter volume, as well as larger increases in lateral ventricular volume, than healthy control subjects. The time between baseline and follow-up magnetic resonance imaging scans ranged from 1 to 10 years. The differences between patients and control subjects in annualized percentage volume change were -.07% for whole brain volume, -.59% for whole brain gray matter, -.32% for frontal white matter, -.32% for parietal white matter, -.39% for temporal white matter, and +.36% for bilateral lateral ventricles. These findings suggest that schizophrenia is associated with progressive structural brain abnormalities, affecting both gray and white matter. We found no evidence to suggest progressive medial temporal lobe involvement but did find evidence that this may be partly explained by heterogeneity between studies in patient age and illness duration. The causes and clinical correlates of these progressive brain changes should now be the focus of investigation. Copyright © 2011 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.
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              A GENERAL MODEL FOR THE STUDY OF DEVELOPMENTAL PROBLEMS.

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                Author and article information

                Journal
                Harv Rev Psychiatry
                Harv Rev Psychiatry
                HVP
                Harvard Review of Psychiatry
                Lippincott Williams & Wilkins
                1067-3229
                1465-7309
                March 2016
                19 October 2016
                : 24
                : 2
                : 118-128
                Affiliations
                From the Institute of Psychiatric Phenomics and Genomics (Drs. Heilbronner and Schulze, and Department of Psychiatry and Psychotherapy (Dr. Falkai), Ludwig-Maximilians-University Munich; Section on Psychiatric Genetics, Department of Psychiatry and Psychotherapy, University Medical Center Göttingen (Drs. Heilbronner and Schulze); Department of Psychiatry and Psychotherapy, Technical University Munich (Drs. Samara and Leucht).
                Author notes
                Correspondence: Thomas G. Schulze, MD, Institute of Psychiatric Phenomics and Genomics, Ludwig-Maximilians-University Munich, Nußbaumstraße 7, 80336 Munich, Germany. Email: Thomas.Schulze@ 123456med.uni-muenchen.de
                Article
                HVP50034 00005
                10.1097/HRP.0000000000000092
                5079232
                26954596
                2fb45647-3f86-4c53-bc37-ddb4b0d5bb1e
                © 2016 President and Fellows of Harvard College
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                Clinical Psychology & Psychiatry
                diagnosis,imaging,longitudinal,neuropsychology,psychosis,schizophrenia

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