4.7 Article

Childhood adversities and adult psychopathology in the National Comorbidity Survey Replication (NCS-R) III: associations with functional impairment related to DSM-IV disorders

期刊

PSYCHOLOGICAL MEDICINE
卷 40, 期 5, 页码 847-859

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291709991115

关键词

Childhood adversity; disability; functional impairment; severity

资金

  1. National Institute of Mental Health (NIMH) [U01-MH60220, R01 MH070884]
  2. National Institute on Drug Abuse (NIDA)
  3. Robert Wood Johnson Foundation (RWJF) [044780]
  4. John W. Alden Trust
  5. John D. and Catherine T. MacArthur Foundation
  6. Pfizer Foundation
  7. US Public Health Service [R13-MH066849, R01-MH069864, R01 DA016558]
  8. Fogarty International Center (FIRCA) [R03-TW006481]
  9. Pan American Health Organization
  10. Ortho-McNeil Pharmaceutical, Inc.
  11. GlaxoSmithKline
  12. Bristol-Myers Squibb
  13. Substance Abuse and Mental Health Services Administration (SAMHSA)
  14. Eli Lilly Company

向作者/读者索取更多资源

Background. Despite evidence that childhood adversities (CAs) are associated with increased risk of mental disorders, little is known about their associations with disorder-related impairment. We report the associations between CAs and functional impairment associated with 12-month DSM-IV disorders in a national sample. Method. We used data from the US National Comorbidity Survey Replication (NCS-R). Respondents completed diagnostic interviews that assessed 12-month DSM-IV disorder prevalence and impairment. Associations of 12 retrospectively reported CAs with impairment among cases (n = 2242) were assessed using multiple regression analysis. Impairment measures included a dichotomous measure of classification in the severe range of impairment on the Sheehan Disability Scale (SDS) and a measure of self-reported number of days out of role due to emotional problems in the past 12 months. Results. CAs were positively and significantly associated with impairment. Predictive effects of CAs on the SIDS were particularly pronounced for anxiety disorders and were significant in predicting increased clays out of role associated with mood, anxiety and disruptive behavior disorders. Predictive effects persisted throughout the life course and were not accounted for by disorder co-morbidity. CAs associated with maladaptive family functioning (MFF; parental mental illness, substance disorder, criminality, family violence, abuse, neglect) were more consistently associated with impairment than other CAs. The joint effects of co-morbid MFF CAs were significantly subadditive. Simulations suggest that CAs account for 19.6% of severely impairing disorders and 17.4% of days out of role. Conclusions. CAs predict greater disorder-related impairment, highlighting the ongoing clinical significance of CAs at every stage of the life course.

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