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Characterization and structure of hypomania in a British nonclinical adolescent sample

BACKGROUND: This study aimed to test the validity of using the Hypomania Checklist-16 [HCL-16] to measure hypomania in a British adolescent community sample. Limited research is available concerning the characterization of hypomania among community adolescent samples, particularly in the UK, despite...

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Autores principales: Hosang, Georgina M., Cardno, Alastair G., Freeman, Daniel, Ronald, Angelica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier/North-Holland Biomedical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113133/
https://www.ncbi.nlm.nih.gov/pubmed/27728870
http://dx.doi.org/10.1016/j.jad.2016.08.033
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author Hosang, Georgina M.
Cardno, Alastair G.
Freeman, Daniel
Ronald, Angelica
author_facet Hosang, Georgina M.
Cardno, Alastair G.
Freeman, Daniel
Ronald, Angelica
author_sort Hosang, Georgina M.
collection PubMed
description BACKGROUND: This study aimed to test the validity of using the Hypomania Checklist-16 [HCL-16] to measure hypomania in a British adolescent community sample. Limited research is available concerning the characterization of hypomania among community adolescent samples, particularly in the UK, despite its potential importance for early intervention policy development. METHOD: To explore the structure and characterization of hypomania in a British adolescent nonclinical cohort, over 1400 17 year olds (Mean=17.05 years; SD=0.88) completed the HCL-16 along with measures of different psychological and psychopathological dimensions. RESULTS: Principal components analysis revealed a 2-component solution for the HCL-16, described as active-elated and irritable/risk-taking. Hypomanic symptoms were significantly correlated with many psychopathological dimensions. There were distinct correlation patterns for the two HCL-16 subscales, with the irritability/risk-taking subscale showing significantly stronger associations with psychotic-like experiences, internalizing and externalizing problems, and reduced life satisfaction relative to the active-elated dimension. Adolescents at ‘high-risk’ for bipolar disorder reported more psychopathology relative to the comparison group. LIMITATIONS: Absence of the clinical diagnosis of bipolar disorder in the sample means that the classification of the ‘high-risk’ group cannot be confirmed. CONCLUSIONS: The structure of the HCL-16 in this UK adolescent sample mirrored that observed in adult and clinical cohorts. The observed links between the HCL-16 and psychopathological dimensions that have been previously associated with both hypomania and bipolar disorder lend support to the HCL-16's validity as a hypomania instrument for adolescents. Better understanding of hypomania prior to adulthood has considerable potential for informing early intervention approaches.
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spelling pubmed-51131332017-01-01 Characterization and structure of hypomania in a British nonclinical adolescent sample Hosang, Georgina M. Cardno, Alastair G. Freeman, Daniel Ronald, Angelica J Affect Disord Article BACKGROUND: This study aimed to test the validity of using the Hypomania Checklist-16 [HCL-16] to measure hypomania in a British adolescent community sample. Limited research is available concerning the characterization of hypomania among community adolescent samples, particularly in the UK, despite its potential importance for early intervention policy development. METHOD: To explore the structure and characterization of hypomania in a British adolescent nonclinical cohort, over 1400 17 year olds (Mean=17.05 years; SD=0.88) completed the HCL-16 along with measures of different psychological and psychopathological dimensions. RESULTS: Principal components analysis revealed a 2-component solution for the HCL-16, described as active-elated and irritable/risk-taking. Hypomanic symptoms were significantly correlated with many psychopathological dimensions. There were distinct correlation patterns for the two HCL-16 subscales, with the irritability/risk-taking subscale showing significantly stronger associations with psychotic-like experiences, internalizing and externalizing problems, and reduced life satisfaction relative to the active-elated dimension. Adolescents at ‘high-risk’ for bipolar disorder reported more psychopathology relative to the comparison group. LIMITATIONS: Absence of the clinical diagnosis of bipolar disorder in the sample means that the classification of the ‘high-risk’ group cannot be confirmed. CONCLUSIONS: The structure of the HCL-16 in this UK adolescent sample mirrored that observed in adult and clinical cohorts. The observed links between the HCL-16 and psychopathological dimensions that have been previously associated with both hypomania and bipolar disorder lend support to the HCL-16's validity as a hypomania instrument for adolescents. Better understanding of hypomania prior to adulthood has considerable potential for informing early intervention approaches. Elsevier/North-Holland Biomedical Press 2017-01-01 /pmc/articles/PMC5113133/ /pubmed/27728870 http://dx.doi.org/10.1016/j.jad.2016.08.033 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hosang, Georgina M.
Cardno, Alastair G.
Freeman, Daniel
Ronald, Angelica
Characterization and structure of hypomania in a British nonclinical adolescent sample
title Characterization and structure of hypomania in a British nonclinical adolescent sample
title_full Characterization and structure of hypomania in a British nonclinical adolescent sample
title_fullStr Characterization and structure of hypomania in a British nonclinical adolescent sample
title_full_unstemmed Characterization and structure of hypomania in a British nonclinical adolescent sample
title_short Characterization and structure of hypomania in a British nonclinical adolescent sample
title_sort characterization and structure of hypomania in a british nonclinical adolescent sample
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113133/
https://www.ncbi.nlm.nih.gov/pubmed/27728870
http://dx.doi.org/10.1016/j.jad.2016.08.033
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