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Soc Sci Med. 2010 Dec;71(12):2108-16. doi: 10.1016/j.socscimed.2010.09.011. Epub 2010 Sep 29.

Metropolitan isolation segregation and Black-White disparities in very preterm birth: a test of mediating pathways and variance explained.

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  • 1Emory University, Epidemiology, Atlanta, GA 30322, USA. mkram02@emory.edu

Abstract

Residential isolation segregation (a measure of residential inter-racial exposure) has been associated with rates of preterm birth (<37 weeks gestation) experienced by Black women. Epidemiologic differences between very preterm (<32 weeks gestation) and moderately preterm births (32-36 weeks) raise questions about whether this association is similar across gestational ages, and through what pathways it might be mediated. Hierarchical Bayesian models were fit to answer three questions: is the isolation-prematurity association similar for very and moderately preterm birth; is this association mediated by maternal chronic disease, socioeconomic status, or metropolitan area crime and poverty rates; and how much of the geographic variation in Black-White very preterm birth disparities is explained by isolation segregation? Singleton births to Black and White women in 231 U.S. metropolitan statistical areas in 2000-2002 were analyzed and isolation segregation was calculated for each. We found that among Black women, isolation is associated with very preterm birth and moderately preterm birth. The association may be partially mediated by individual level socioeconomic characteristics and metropolitan level violent crime rates. There is no association between segregation and prematurity among White women. Isolation segregation explains 28% of the geographic variation in Black-White very preterm birth disparities. Our findings highlight the importance of isolation segregation for the high-burden outcome of very preterm birth, but unexplained excess risk for prematurity among Black women is substantial.

Copyright © 2010 Elsevier Ltd. All rights reserved.

PMID:
20947234
[PubMed - indexed for MEDLINE]
PMCID:
PMC2992580
Free PMC Article

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