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Journal Article

Citation

Clark CJ, Alonso A, Everson-Rose SA, Spencer RA, Brady SS, Resnick MD, Borowsky IW, Connett JE, Krueger RF, Nguyen-Feng VN, Feng SL, Suglia SF. Prev. Med. 2016; 87: 132-137.

Affiliation

Department of Epidemiology, Columbia University, New York, NY. Electronic address: sfs2150@cumc.columbia.edu.

Copyright

(Copyright © 2016, Elsevier Publishing)

DOI

10.1016/j.ypmed.2016.02.031

PMID

26921659

Abstract

BACKGROUND: Childhood maltreatment has been linked to adulthood cardiovascular disease (CVD). Little is known about the relationship between intimate partner violence (IPV) in late adolescence and young adulthood and CVD risk later in adulthood.

PURPOSE: To examine whether IPV perpetration and victimization experienced in late adolescence and young adulthood are associated with CVD risk among adults in the United States and whether this relationship differs by sex.

METHODS: Data include 9,976 participants (50% female) in the National Longitudinal Study of Adolescent to Adult Health. Physical and sexual IPV were measured at wave 3 (2001/02) with items from the revised Conflict Tactics Scales. Participants' 30-year risk of CVD was calculated at wave 4 (2008/09) using a Framingham prediction model. Linear regression models adjusted for confounders and IPV by sex interaction terms were tested to examine the relationship.

RESULTS: The mean CVD risk score was 13.18% (95% CI: 12.71, 13.64). A one-standard deviation increase in the victimization score was associated with a 0.28% (95% CI: 0.03, 0.54) increase in CVD risk. Perpetration was similarly positively associated with CVD risk (beta: 0.33, 95% CI: 0.03, 0.62). When measured as a composite, all violence types were associated with increased CVD risk but only prior exposure to both victimization and perpetration reached statistical significance (0.62%, 95% CI: 0.01, 1.22). No differences by sex were detected.

CONCLUSIONS: Effect sizes are not large, but early detection of increased CVD risk in this relatively young population is notable and worthy of further study to inform the clinical response.


Language: en

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