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Towards clinically actionable digital phenotyping targets in schizophrenia

Digital phenotyping has potential to quantify the lived experience of mental illness and generate real-time, actionable results related to recovery, such as the case of social rhythms in individuals with bipolar disorder. However, passive data features for social rhythm clinical targets in individua...

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Autores principales: Henson, Philip, Barnett, Ian, Keshavan, Matcheri, Torous, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200667/
https://www.ncbi.nlm.nih.gov/pubmed/32372059
http://dx.doi.org/10.1038/s41537-020-0100-1
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author Henson, Philip
Barnett, Ian
Keshavan, Matcheri
Torous, John
author_facet Henson, Philip
Barnett, Ian
Keshavan, Matcheri
Torous, John
author_sort Henson, Philip
collection PubMed
description Digital phenotyping has potential to quantify the lived experience of mental illness and generate real-time, actionable results related to recovery, such as the case of social rhythms in individuals with bipolar disorder. However, passive data features for social rhythm clinical targets in individuals with schizophrenia have yet to be studied. In this paper, we explore the relationship between active and passive data by focusing on temporal stability and variance at an individual level as well as large-scale associations on a population level to gain clinically actionable information regarding social rhythms. From individual data clustering, we found a 19% cluster overlap between specific active and passive data features for participants with schizophrenia. In the same clinical population, two passive data features in particular associated with social rhythms, “Circadian Routine” and “Weekend Day Routine,” and were negatively associated with symptoms of anxiety, depression, psychosis, and poor sleep (Spearman ρ ranged from −0.23 to −0.30, p < 0.001). Conversely, in healthy controls, more stable social rhythms were positively correlated with symptomatology (Spearman ρ ranged from 0.20 to 0.44, p < 0.05). Our results suggest that digital phenotyping in schizophrenia may offer clinically relevant information for understanding how daily routines affect symptomatology. Specifically, negative correlations between smartphone reported anxiety, depression, psychosis, and poor sleep in individuals with schizophrenia, but not in healthy controls, offer an actionable clinical target and area for further investigation.
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spelling pubmed-72006672020-05-06 Towards clinically actionable digital phenotyping targets in schizophrenia Henson, Philip Barnett, Ian Keshavan, Matcheri Torous, John NPJ Schizophr Article Digital phenotyping has potential to quantify the lived experience of mental illness and generate real-time, actionable results related to recovery, such as the case of social rhythms in individuals with bipolar disorder. However, passive data features for social rhythm clinical targets in individuals with schizophrenia have yet to be studied. In this paper, we explore the relationship between active and passive data by focusing on temporal stability and variance at an individual level as well as large-scale associations on a population level to gain clinically actionable information regarding social rhythms. From individual data clustering, we found a 19% cluster overlap between specific active and passive data features for participants with schizophrenia. In the same clinical population, two passive data features in particular associated with social rhythms, “Circadian Routine” and “Weekend Day Routine,” and were negatively associated with symptoms of anxiety, depression, psychosis, and poor sleep (Spearman ρ ranged from −0.23 to −0.30, p < 0.001). Conversely, in healthy controls, more stable social rhythms were positively correlated with symptomatology (Spearman ρ ranged from 0.20 to 0.44, p < 0.05). Our results suggest that digital phenotyping in schizophrenia may offer clinically relevant information for understanding how daily routines affect symptomatology. Specifically, negative correlations between smartphone reported anxiety, depression, psychosis, and poor sleep in individuals with schizophrenia, but not in healthy controls, offer an actionable clinical target and area for further investigation. Nature Publishing Group UK 2020-05-05 /pmc/articles/PMC7200667/ /pubmed/32372059 http://dx.doi.org/10.1038/s41537-020-0100-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Henson, Philip
Barnett, Ian
Keshavan, Matcheri
Torous, John
Towards clinically actionable digital phenotyping targets in schizophrenia
title Towards clinically actionable digital phenotyping targets in schizophrenia
title_full Towards clinically actionable digital phenotyping targets in schizophrenia
title_fullStr Towards clinically actionable digital phenotyping targets in schizophrenia
title_full_unstemmed Towards clinically actionable digital phenotyping targets in schizophrenia
title_short Towards clinically actionable digital phenotyping targets in schizophrenia
title_sort towards clinically actionable digital phenotyping targets in schizophrenia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200667/
https://www.ncbi.nlm.nih.gov/pubmed/32372059
http://dx.doi.org/10.1038/s41537-020-0100-1
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