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Bipolar Disorder with frequent mood episodes in the National Comorbidity Survey Replication (NCS-R)

Virtually nothing is known about the epidemiology of rapid cycling bipolar disorder (BPD) in community samples. Nationally representative data are reported here for the prevalence and correlates of a surrogate measure of DSM-IV rapid cycling BPD from the National Comorbidity survey Replication (NCS-...

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Autores principales: Nierenberg, Andrew A., Akiskal, Hagop S., Angst, Jules, Hirschfeld, Robert M., Merikangas, Kathleen R., Petukhova, Maria, Kessler, Ronald C.
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891194/
https://www.ncbi.nlm.nih.gov/pubmed/19564874
http://dx.doi.org/10.1038/mp.2009.61
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author Nierenberg, Andrew A.
Akiskal, Hagop S.
Angst, Jules
Hirschfeld, Robert M.
Merikangas, Kathleen R.
Petukhova, Maria
Kessler, Ronald C.
author_facet Nierenberg, Andrew A.
Akiskal, Hagop S.
Angst, Jules
Hirschfeld, Robert M.
Merikangas, Kathleen R.
Petukhova, Maria
Kessler, Ronald C.
author_sort Nierenberg, Andrew A.
collection PubMed
description Virtually nothing is known about the epidemiology of rapid cycling bipolar disorder (BPD) in community samples. Nationally representative data are reported here for the prevalence and correlates of a surrogate measure of DSM-IV rapid cycling BPD from the National Comorbidity survey Replication (NCS-R), a national survey of the US household population. DSM-IV disorders were assessed in the NCS-R with the WHO Composite International Diagnostic Interview (CIDI). Although the CIDI did not assess rapid cycling, it did assess the broader category of 12-month BPD with frequent mood episodes (FME), having at least four episodes of mania/hypomania or major depression in the 12 months before interview. Roughly one-third of NCS-R respondents with lifetime DSM-IV BPD and half with 12-month BPD met criteria for FME. FME was associated with younger age-of-onset (of BP-I, but not BP-II) and higher annual persistence (73% of the years since first onset of illness with an episode) than non-FME BPD. No substantial associations of FME vs. non-FME BPD were found with socio-demographics, childhood risk factors (parental mental disorders, other childhood adversities), or comorbid DSM-IV disorders. However, FME manic episodes had greater clinical severity than non-FME episodes (assessed with a fully-structured version of the Young Mania Rating Scale) and FME hypomanic episodes had greater role impairment than non-FME episodes (assessed with the Sheehan Disability Scales). Whether these indicators of severity merely reflect attenuated effects of rapid cycling or independent effects of sub-threshold rapid cycling warrants further study given the high proportion of lifetime cases that met criteria for FME.
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spelling pubmed-28911942011-05-01 Bipolar Disorder with frequent mood episodes in the National Comorbidity Survey Replication (NCS-R) Nierenberg, Andrew A. Akiskal, Hagop S. Angst, Jules Hirschfeld, Robert M. Merikangas, Kathleen R. Petukhova, Maria Kessler, Ronald C. Mol Psychiatry Article Virtually nothing is known about the epidemiology of rapid cycling bipolar disorder (BPD) in community samples. Nationally representative data are reported here for the prevalence and correlates of a surrogate measure of DSM-IV rapid cycling BPD from the National Comorbidity survey Replication (NCS-R), a national survey of the US household population. DSM-IV disorders were assessed in the NCS-R with the WHO Composite International Diagnostic Interview (CIDI). Although the CIDI did not assess rapid cycling, it did assess the broader category of 12-month BPD with frequent mood episodes (FME), having at least four episodes of mania/hypomania or major depression in the 12 months before interview. Roughly one-third of NCS-R respondents with lifetime DSM-IV BPD and half with 12-month BPD met criteria for FME. FME was associated with younger age-of-onset (of BP-I, but not BP-II) and higher annual persistence (73% of the years since first onset of illness with an episode) than non-FME BPD. No substantial associations of FME vs. non-FME BPD were found with socio-demographics, childhood risk factors (parental mental disorders, other childhood adversities), or comorbid DSM-IV disorders. However, FME manic episodes had greater clinical severity than non-FME episodes (assessed with a fully-structured version of the Young Mania Rating Scale) and FME hypomanic episodes had greater role impairment than non-FME episodes (assessed with the Sheehan Disability Scales). Whether these indicators of severity merely reflect attenuated effects of rapid cycling or independent effects of sub-threshold rapid cycling warrants further study given the high proportion of lifetime cases that met criteria for FME. 2009-06-30 2010-11 /pmc/articles/PMC2891194/ /pubmed/19564874 http://dx.doi.org/10.1038/mp.2009.61 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Nierenberg, Andrew A.
Akiskal, Hagop S.
Angst, Jules
Hirschfeld, Robert M.
Merikangas, Kathleen R.
Petukhova, Maria
Kessler, Ronald C.
Bipolar Disorder with frequent mood episodes in the National Comorbidity Survey Replication (NCS-R)
title Bipolar Disorder with frequent mood episodes in the National Comorbidity Survey Replication (NCS-R)
title_full Bipolar Disorder with frequent mood episodes in the National Comorbidity Survey Replication (NCS-R)
title_fullStr Bipolar Disorder with frequent mood episodes in the National Comorbidity Survey Replication (NCS-R)
title_full_unstemmed Bipolar Disorder with frequent mood episodes in the National Comorbidity Survey Replication (NCS-R)
title_short Bipolar Disorder with frequent mood episodes in the National Comorbidity Survey Replication (NCS-R)
title_sort bipolar disorder with frequent mood episodes in the national comorbidity survey replication (ncs-r)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891194/
https://www.ncbi.nlm.nih.gov/pubmed/19564874
http://dx.doi.org/10.1038/mp.2009.61
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