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      A pilot study to determine whether combinations of objectively measured activity parameters can be used to differentiate between mixed states, mania, and bipolar depression

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          Abstract

          Background

          Until recently, actigraphy studies in bipolar disorders focused on sleep rather than daytime activity in mania or depression, and have failed to analyse mixed episodes separately. Furthermore, even those studies that assessed activity parameters reported only mean levels rather than complexity or predictability of activity. We identified cases presenting in one of three acute phases of bipolar disorder and examined whether the application of non-linear dynamic models to the description of objectively measured activity can be used to predict case classification.

          Methods

          The sample comprised 34 adults who were hospitalized with an acute episode of mania ( n = 16), bipolar depression ( n = 12), or a mixed state ( n = 6), who agreed to wear an actiwatch for a continuous period of 24 h. Mean level, variability, regularity, entropy, and predictability of activity were recorded for a defined 64-min active morning and active evening period. Discriminant function analysis was used to determine the combination of variables that best classified cases based on phase of illness.

          Results

          The model identified two discriminant functions: the first was statistically significant and correlated with intra-individual fluctuation in activity and regularity of activity (sample entropy) in the active morning period; the second correlated with several measures of activity from the evening period (e.g. Fourier analysis, autocorrelation, sample entropy). A classification table generated from both functions correctly classified 79% of all cases based on phase of illness ( χ 2 = 36.21; df 4; p = 0.001). However, 42% of bipolar depression cases were misclassified as being in manic phase.

          Conclusions

          The findings should be treated with caution as this was a small-scale pilot study and we did not control for prescribed treatments, medication adherence, etc. However, the insights gained should encourage more widespread adoption of statistical approaches to the classification of cases alongside the application of more sophisticated modelling of activity patterns. The difficulty of accurately classifying cases of bipolar depression requires further research, as it is unclear whether the lower prediction rate reflects weaknesses in a model based only on actigraphy data, or if it reflects clinical reality i.e. the possibility that there may be more than one subtype of bipolar depression.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s40345-017-0076-6) contains supplementary material, which is available to authorized users.

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          Most cited references29

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          Using Support Vector Machine to identify imaging biomarkers of neurological and psychiatric disease: a critical review.

          Standard univariate analysis of neuroimaging data has revealed a host of neuroanatomical and functional differences between healthy individuals and patients suffering a wide range of neurological and psychiatric disorders. Significant only at group level however these findings have had limited clinical translation, and recent attention has turned toward alternative forms of analysis, including Support-Vector-Machine (SVM). A type of machine learning, SVM allows categorisation of an individual's previously unseen data into a predefined group using a classification algorithm, developed on a training data set. In recent years, SVM has been successfully applied in the context of disease diagnosis, transition prediction and treatment prognosis, using both structural and functional neuroimaging data. Here we provide a brief overview of the method and review those studies that applied it to the investigation of Alzheimer's disease, schizophrenia, major depression, bipolar disorder, presymptomatic Huntington's disease, Parkinson's disease and autistic spectrum disorder. We conclude by discussing the main theoretical and practical challenges associated with the implementation of this method into the clinic and possible future directions. Copyright © 2012 Elsevier Ltd. All rights reserved.
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            Approaching a consensus cognitive battery for clinical trials in schizophrenia: the NIMH-MATRICS conference to select cognitive domains and test criteria.

            To stimulate the development of new drugs for the cognitive deficits of schizophrenia, the National Institute of Mental Health (NIMH) established the Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) initiative. This article presents an overview of decisions from the first MATRICS consensus conference. The goals of the meeting were to 1) identify the cognitive domains that should be represented in a consensus cognitive battery and 2) prioritize key criteria for selection of tests for the battery. Seven cognitive domains were selected based on a review of the literature and input from experts: working memory, attention/vigilance, verbal learning and memory, visual learning and memory, reasoning and problem solving, speed of processing, and social cognition. Based on discussions at this meeting, five criteria were considered essential for test selection: good test-retest reliability, high utility as a repeated measure, relationship to functional outcome, potential response to pharmacologic agents, and practicality/tolerability. The results from this meeting constitute the initial steps for reaching a consensus cognitive battery for clinical trials in schizophrenia.
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              Sleep-related functioning in euthymic patients with bipolar disorder, patients with insomnia, and subjects without sleep problems.

              The authors investigated sleep-related functioning in euthymic patients with bipolar disorder. Euthymic patients with bipolar disorder (N=20), patients with insomnia (N=20), and subjects with good sleep (N=20) were compared on data from interviews and questionnaires and on findings from eight consecutive days and nights of sleep diary keeping (subjective sleep estimate) and actigraphy (objective sleep estimate). Seventy percent of the euthymic patients with bipolar disorder exhibited a clinically significant sleep disturbance. Compared with the other groups, the bipolar disorder group exhibited impaired sleep efficiency, higher levels of anxiety and fear about poor sleep, lower daytime activity levels, and a tendency to misperceive sleep. The bipolar disorder group held a level of dysfunctional beliefs about sleep that was comparable to that in the insomnia group and significantly higher than that in the good sleeper group. Insomnia is a significant problem among euthymic patients with bipolar disorder. Components of cognitive behavior therapy for insomnia, especially stimulus control and cognitive therapy, may be a helpful adjunct to treatment for patients with bipolar disorder.
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                Author and article information

                Contributors
                jan.scott@newcastle.ac.uk
                arne.valeer@ntnu.no
                ole.fasmer@uib.no
                gunnar.morker@ntnu.no
                karoline.krane-gartiser@ntnu.no
                Journal
                Int J Bipolar Disord
                Int J Bipolar Disord
                International Journal of Bipolar Disorders
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                2194-7511
                1 March 2017
                1 March 2017
                2017
                : 5
                : 5
                Affiliations
                [1 ]ISNI 0000 0001 0462 7212, GRID grid.1006.7, Academic Psychiatry, Institute of Neuroscience, , Newcastle University, ; Newcastle upon Tyne, UK
                [2 ]ISNI 0000 0001 1516 2393, GRID grid.5947.f, Department of Neuroscience, NTNU, , Norwegian University of Science and Technology, ; Trondheim, Norway
                [3 ]ISNI 0000 0004 0627 3560, GRID grid.52522.32, Department of Psychiatry, , St. Olav’s University Hospital, ; Trondheim, Norway
                [4 ]ISNI 0000 0004 1936 7443, GRID grid.7914.b, Department of Clinical Medicine, Section for Psychiatry, Faculty of Medicine and Dentistry, , University of Bergen, ; Bergen, Norway
                [5 ]ISNI 0000 0000 9753 1393, GRID grid.412008.f, Division of Psychiatry, , Haukeland University Hospital, ; Bergen, Norway
                Author information
                http://orcid.org/0000-0002-7203-8601
                Article
                76
                10.1186/s40345-017-0076-6
                5331021
                28155205
                1ec9d4d2-798e-4dae-be79-c7b4567cf061
                © The Author(s) 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 25 November 2016
                : 17 January 2017
                Categories
                Research
                Custom metadata
                © The Author(s) 2017

                actigraphy,non-linear dynamics,mixed states,discriminant analysis,classification,illness phase

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