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Stability and Change of Psychopathology Symptoms Throughout Childhood and Adolescence
Assessing stability and change of children’s psychopathology symptoms can help elucidate whether specific behaviors are transient developmental variations or indicate persistent psychopathology. This study included 6930 children across early childhood (T1), late childhood (T2) and early adolescence...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9560913/ https://www.ncbi.nlm.nih.gov/pubmed/34184159 http://dx.doi.org/10.1007/s10578-021-01212-8 |
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author | Blok, Elisabet de Mol, C. Louk van der Ende, Jan Hillegers, Manon H. J. Althoff, Robert R. Shaw, Philip White, Tonya |
author_facet | Blok, Elisabet de Mol, C. Louk van der Ende, Jan Hillegers, Manon H. J. Althoff, Robert R. Shaw, Philip White, Tonya |
author_sort | Blok, Elisabet |
collection | PubMed |
description | Assessing stability and change of children’s psychopathology symptoms can help elucidate whether specific behaviors are transient developmental variations or indicate persistent psychopathology. This study included 6930 children across early childhood (T1), late childhood (T2) and early adolescence (T3), from the general population. Latent profile analysis identified psychopathology subgroups and latent transition analysis quantified the probability that children remained within, or transitioned across psychopathology subgroups. We identified four psychopathology subgroups; no problems (T1: 85.9%, T2: 79.0%, T3: 78.0%), internalizing (T1: 5.1%, T2: 9.2%, T3: 9.0%), externalizing (T1: 7.3%, T2: 8.3%, T3: 10.2%) and the dysregulation profile (DP) (T1: 1.7%, T2: 3.5%, T3: 2.8%). From T1 to T2, 44.7% of the children remained in the DP. Between T2 and T3, 33.6% remained in the DP; however, 91.4% were classified in one of the psychopathology subgroups. Our findings suggest that for many children, internalizing or externalizing symptoms encompass a transient phase within development. Contrary, the DP resembles a severe at-risk state in which the predictive value for being in one of the psychopathology subgroups increases over time. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10578-021-01212-8. |
format | Online Article Text |
id | pubmed-9560913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-95609132022-10-15 Stability and Change of Psychopathology Symptoms Throughout Childhood and Adolescence Blok, Elisabet de Mol, C. Louk van der Ende, Jan Hillegers, Manon H. J. Althoff, Robert R. Shaw, Philip White, Tonya Child Psychiatry Hum Dev Original Article Assessing stability and change of children’s psychopathology symptoms can help elucidate whether specific behaviors are transient developmental variations or indicate persistent psychopathology. This study included 6930 children across early childhood (T1), late childhood (T2) and early adolescence (T3), from the general population. Latent profile analysis identified psychopathology subgroups and latent transition analysis quantified the probability that children remained within, or transitioned across psychopathology subgroups. We identified four psychopathology subgroups; no problems (T1: 85.9%, T2: 79.0%, T3: 78.0%), internalizing (T1: 5.1%, T2: 9.2%, T3: 9.0%), externalizing (T1: 7.3%, T2: 8.3%, T3: 10.2%) and the dysregulation profile (DP) (T1: 1.7%, T2: 3.5%, T3: 2.8%). From T1 to T2, 44.7% of the children remained in the DP. Between T2 and T3, 33.6% remained in the DP; however, 91.4% were classified in one of the psychopathology subgroups. Our findings suggest that for many children, internalizing or externalizing symptoms encompass a transient phase within development. Contrary, the DP resembles a severe at-risk state in which the predictive value for being in one of the psychopathology subgroups increases over time. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10578-021-01212-8. Springer US 2021-06-28 2022 /pmc/articles/PMC9560913/ /pubmed/34184159 http://dx.doi.org/10.1007/s10578-021-01212-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/ 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Blok, Elisabet de Mol, C. Louk van der Ende, Jan Hillegers, Manon H. J. Althoff, Robert R. Shaw, Philip White, Tonya Stability and Change of Psychopathology Symptoms Throughout Childhood and Adolescence |
title | Stability and Change of Psychopathology Symptoms Throughout Childhood and Adolescence |
title_full | Stability and Change of Psychopathology Symptoms Throughout Childhood and Adolescence |
title_fullStr | Stability and Change of Psychopathology Symptoms Throughout Childhood and Adolescence |
title_full_unstemmed | Stability and Change of Psychopathology Symptoms Throughout Childhood and Adolescence |
title_short | Stability and Change of Psychopathology Symptoms Throughout Childhood and Adolescence |
title_sort | stability and change of psychopathology symptoms throughout childhood and adolescence |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9560913/ https://www.ncbi.nlm.nih.gov/pubmed/34184159 http://dx.doi.org/10.1007/s10578-021-01212-8 |
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