Predicting Posttraumatic Stress Disorder Among Survivors of Recent Interpersonal Violence.


Journal

Journal of interpersonal violence
ISSN: 1552-6518
Titre abrégé: J Interpers Violence
Pays: United States
ID NLM: 8700910

Informations de publication

Date de publication:
07 2022
Historique:
pubmed: 2 12 2020
medline: 8 7 2022
entrez: 1 12 2020
Statut: ppublish

Résumé

A substantial minority of women who experience interpersonal violence will develop posttraumatic stress disorder (PTSD). One critical challenge for preventing PTSD is predicting whose acute posttraumatic stress symptoms will worsen to a clinically significant degree. This 6-month longitudinal study adopted multilevel modeling and exploratory machine learning (ML) methods to predict PTSD onset in 58 young women, ages 18 to 30, who experienced an incident of physical and/or sexual assault in the three months prior to baseline assessment. Women completed baseline assessments of theory-driven cognitive and neurobiological predictors and interview-based measures of PTSD diagnostic status and symptom severity at 1-, 3-, and 6-month follow-ups. Higher levels of self-blame, generalized anxiety disorder severity, childhood trauma exposure, and impairment across multiple domains were associated with a pattern of high and stable posttraumatic stress symptom severity over time. Predictive performance for PTSD onset was similarly strong for a gradient boosting machine learning model including all predictors and a logistic regression model including only baseline posttraumatic stress symptom severity. The present findings provide directions for future work on PTSD prediction among interpersonal violence survivors that could enhance early risk detection and potentially inform targeted prevention programs.

Identifiants

pubmed: 33256508
doi: 10.1177/0886260520978195
pmc: PMC8164639
mid: NIHMS1664275
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

NP11460-NP11489

Subventions

Organisme : NIMHD NIH HHS
ID : U54 MD007586
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH108155
Pays : United States
Organisme : NIMH NIH HHS
ID : K01 MH101403
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA040966
Pays : United States
Organisme : NIMHD NIH HHS
ID : U54 MD007593
Pays : United States
Organisme : NIMHD NIH HHS
ID : R01 MD010757
Pays : United States

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Auteurs

Matthew C Morris (MC)

University of Mississippi Medical Center, Jackson, Mississippi, USA.

Francisco Sanchez-Sáez (F)

Universidad Internacional de La Rioja, Logroño, Spain.

Brooklynn Bailey (B)

The Ohio State University, Columbus, Ohio, USA.

Natalie Hellman (N)

University of Tulsa, Tulsa, Oklahoma, USA.

Amber Williams (A)

University of Mississippi Medical Center, Jackson, Mississippi, USA.

Julie A Schumacher (JA)

University of Mississippi Medical Center, Jackson, Mississippi, USA.

Uma Rao (U)

University of California, Irvine, California, USA.
Children's Hospital of Orange County, Orange, California, USA.

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Classifications MeSH