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      Premorbid academic and social functioning in patients with schizophrenia and its associations with negative symptoms and cognition

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          The MATRICS Consensus Cognitive Battery, part 1: test selection, reliability, and validity.

          The lack of an accepted standard for measuring cognitive change in schizophrenia has been a major obstacle to regulatory approval of cognition-enhancing treatments. A primary mandate of the National Institute of Mental Health's Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) initiative was to develop a consensus cognitive battery for clinical trials of cognition-enhancing treatments for schizophrenia through a broadly based scientific evaluation of measures. The MATRICS Neurocognition Committee evaluated more than 90 tests in seven cognitive domains to identify the 36 most promising measures. A separate expert panel evaluated the degree to which each test met specific selection criteria. Twenty tests were selected as a beta battery. The beta battery was administered to 176 individuals with schizophrenia and readministered to 167 of them 4 weeks later so that the 20 tests could be compared directly. The expert panel ratings are presented for the initially selected 36 tests. For the beta battery tests, data on test-retest reliability, practice effects, relationships to functional status, practicality, and tolerability are presented. Based on these data, 10 tests were selected to represent seven cognitive domains in the MATRICS Consensus Cognitive Battery. The structured consensus method was a feasible and fair mechanism for choosing candidate tests, and direct comparison of beta battery tests in a common sample allowed selection of a final consensus battery. The MATRICS Consensus Cognitive Battery is expected to be the standard tool for assessing cognitive change in clinical trials of cognition-enhancing drugs for schizophrenia. It may also aid evaluation of cognitive remediation strategies.
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            Searching for a consensus five-factor model of the Positive and Negative Syndrome Scale for schizophrenia.

            Although the developers of the Positive and Negative Syndrome Scale (PANSS) grouped items into three subscales, factor analyses indicate that a five-factor model better characterizes PANSS data. However, lack of consensus on which model to use limits the comparability of PANSS variables across studies. We counted "votes" from published factor analyses to derive consensus models. One of these combined superior fit in our Caucasian sample (n=458, CFI=.970), and in distinct Japanese sample (n=164, CFI=.964), relative to the original three-subscale model, with a sorting of items into factors that was highly consistent across the studies reviewed. Published by Elsevier B.V.
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              The MATRICS Consensus Cognitive Battery, part 2: co-norming and standardization.

              The consensus cognitive battery developed by the National Institute of Mental Health's (NIMH's) Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) initiative includes 10 independently developed tests that are recommended as the standard battery for clinical trials of cognition-enhancing interventions for schizophrenia. To facilitate interpretation of results from the MATRICS Consensus Cognitive Battery using a common scaling across tests, normative data were obtained from a single representative U.S. community sample with the battery administered as a unit. The MATRICS Consensus Cognitive Battery was administered to 300 individuals from the general community at five sites in differing geographic regions. For each site, recruitment was stratified by age, gender, and education. A scientific survey sampling method was used to help avoid sampling bias. The battery was administered in a standard order to each participant in a single session lasting approximately 60 minutes. Descriptive data were generated, and age, gender, and education effects on performance were examined. Prominent age and education effects were observed across tests. The results for gender differed by measure, suggesting the need for age and gender corrections in clinical trials. The MATRICS Consensus Cognitive Battery components were co-normed, with allowance for demographic corrections. Co-norming a battery such as the MATRICS Consensus Cognitive Battery, comprising tests from independent test developers each with their own set of norms, facilitates valid interpretation of test scores and communication of findings across studies. These normative data will aid in estimating the magnitude of change during clinical trials of cognition-enhancing agents and make it possible to derive more directly interpretable composite scores.
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                Author and article information

                Journal
                Acta Psychiatrica Scandinavica
                Acta Psychiatr Scand
                Wiley
                0001690X
                September 2018
                September 2018
                July 08 2018
                : 138
                : 3
                : 253-266
                Affiliations
                [1 ]Department of Psychiatry; University of Campania L. Vanvitelli; Naples Italy
                [2 ]Section of Psychiatry; Department of Biotechnological and Applied Clinical Sciences; University of L'Aquila; L'Aquila Italy
                [3 ]Section of Psychiatry; Department of Neuroscience; University of Turin; Turin Italy
                [4 ]Department of Neurological and Psychiatric Sciences; University of Bari; Bari Italy
                [5 ]Department of Clinical and Molecular Biomedicine; Psychiatry Unit; University of Catania; Catania Italy
                [6 ]Section of Psychiatry; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics and Maternal and Child Health; University of Genoa; Genoa Italy
                [7 ]Psychiatry Unit; Department of Medical Sciences; University of Foggia; Foggia Italy
                [8 ]Department of Neurology and Psychiatry; Sapienza University of Rome; Rome Italy
                [9 ]Department of Molecular Medicine and Clinical Department of Mental Health; University of Siena; Siena Italy
                [10 ]Section of Psychiatry; Department of Clinical and Experimental Medicine; University of Pisa; Pisa Italy
                [11 ]Department of Neurosciences; Psychiatric Clinic; University of Padua; Padua Italy
                [12 ]Chair of Psychiatry; Department of Neuroscience and Imaging; G. d'Annunzio University; Chieti Italy
                [13 ]Department of Neurosciences, Mental Health and Sensory Organs; S. Andrea Hospital; Sapienza University of Rome; Rome Italy
                [14 ]Department of Neuroscience, Psychiatry Unit; University of Parma; Parma Italy
                [15 ]Chair of Psychiatry; Department of Medicine and Surgery; University of Salerno; Salerno Italy
                [16 ]Chair of Psychiatry; Department of Systems Medicine; Tor Vergata University of Rome; Rome Italy
                [17 ]Department of Psychiatry; University of Milan; Milan Italy
                [18 ]Section of Psychiatry; Department of Public Health, Clinical and Molecular Medicine; University of Cagliari; Cagliari Italy
                [19 ]Unit of Psychiatry; Department of Life, Health and Environmental Sciences; University of L'Aquila; L'Aquila Italy
                [20 ]Psychiatric Unit; School of Medicine; University of Brescia; Brescia Italy
                [21 ]Department of Mental Health; Spedali Civili Hospital; Brescia Italy
                [22 ]Psychiatric Unit; Department of Translational Medicine; University of Eastern Piedmont; Novara Italy
                Article
                10.1111/acps.12938
                29984409
                f2d3406f-19fb-483b-a4f6-91bea8fb8612
                © 2018

                http://doi.wiley.com/10.1002/tdm_license_1.1

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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