The racial disparities in STI: Concurrency, STI prevalence, and heterogeneity in partner selection
Identifieur interne : 003080 ( Ncbi/Curation ); précédent : 003079; suivant : 003081The racial disparities in STI: Concurrency, STI prevalence, and heterogeneity in partner selection
Auteurs : Deven T. Hamilton [États-Unis] ; Martina Morris [États-Unis]Source :
- Epidemics [ 1755-4365 ] ; 2015.
Abstract
There is a large and persistent racial disparity in STI in the U.S. which has placed non-Hispanic-Blacks at disproportionately high risk. We tested a hypothesis that both individual-level risk factors (partner number, anal sex, condom use) and local-network features (concurrency and assortative mixing by race) combine to account for the association between race and chlamydia status.
Data from the Longitudinal Survey of Adolescent Health Wave III were used. Chlamydia status was determined using biomarkers. Individual-level risk behaviors were self-reported. Network location variables for concurrency and assortative mixing were imputed using egocentrically sample data on sexual partnerships.
After controlling for demographic attributes including age, sex, marital status, education and health care access there remained a strong association between race and chlamydia status (OR = 5.23, 95% CI] 3.83–7.15],
Url:
DOI: 10.1016/j.epidem.2015.02.003
PubMed: 25979282
PubMed Central: 4435828
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">The racial disparities in STI: Concurrency, STI prevalence, and heterogeneity in partner selection</title>
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<series><title level="j">Epidemics</title>
<idno type="ISSN">1755-4365</idno>
<idno type="eISSN">1878-0067</idno>
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<front><div type="abstract" xml:lang="en"><sec id="S1"><title>Background</title>
<p id="P1">There is a large and persistent racial disparity in STI in the U.S. which has placed non-Hispanic-Blacks at disproportionately high risk. We tested a hypothesis that both individual-level risk factors (partner number, anal sex, condom use) and local-network features (concurrency and assortative mixing by race) combine to account for the association between race and chlamydia status.</p>
</sec>
<sec id="S2"><title>Methods</title>
<p id="P2">Data from the Longitudinal Survey of Adolescent Health Wave III were used. Chlamydia status was determined using biomarkers. Individual-level risk behaviors were self-reported. Network location variables for concurrency and assortative mixing were imputed using egocentrically sample data on sexual partnerships.</p>
</sec>
<sec id="S3"><title>Results</title>
<p id="P3">After controlling for demographic attributes including age, sex, marital status, education and health care access there remained a strong association between race and chlamydia status (OR = 5.23, 95% CI] 3.83–7.15], <italic>p</italic>
< .001 for Non-Hispanic Blacks with Non-Hispanic Whites as the reference category). The inclusion of individual-level risk factors did not alter the association between race and chlamydia(OR = 5.23 for Non-Hispanic Blacks). The inclusion of concurrency and assortative mixing by race substantially reduced the association between race and chlamydia status (OR = 1.87, 95% CI [0.89–3.91] <italic>p</italic>
> .05 for Non-Hispanic Blacks).</p>
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