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Obstetrics & Gynecology 1999;93:117-123
© 1999 by The American College of Obstetricians and Gynecologists
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ORIGINAL RESEARCH

Association Between Bacterial Vaginosis and Fetal Fibronectin at 24–29 Weeks’ Gestation

LISA M. PASTORE, PhD, RACHEL A. ROYCE, PhD, TRACY P. JACKSON, JOHN M. THORP, Jr, MD, DAVID A. SAVITZ, PhD and USHA S. KREADEN, MSC

From the Department of Epidemiology, School of Public Health, University of North Carolina at Chapel Hill, and the Department of Obstetrics and Gynecology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, and Adeza Biomedical Corporation, Sunnyvale, California.

Address reprint requests to: Lisa M. Pastore, PhD Epidemiology Department, CB 7400 University of North Carolina Chapel Hill, NC 27599-7400 E-mail: lpastore{at}sph.unc.edu

Objective: To investigate the relationship between fetal fibronectin and bacterial vaginosis, which are associated with an increased risk for preterm delivery.

Methods: Researchers for the Pregnancy, Infection and Nutrition Study, a cohort study of pregnant women at three central North Carolina sites, collected genital tract specimens from all enrolled women between 24 and 29 weeks’ gestation. Among women with last menstrual periods between March 10, 1995, and August 15, 1996, 868 pregnancies were eligible for this analysis. Fetal fibronectin was assessed by a dipstick immunoassay kit. Bacterial vaginosis was evaluated by Nugent-scored, Gram-stained vaginal smears (scores of 7–10 considered positive).

Results: Overall, 6.3% of women had positive fetal fibronectin test results, and 18.8% had bacterial vaginosis. The unadjusted relative risk (RR) of fetal fibronectin-positivity comparing women with bacterial vaginosis to those without bacterial vaginosis was 1.6 (95% confidence interval [CI] 1.1, 2.5). Using multiple logistic regression to adjust for race, maternal age, parity, and location of care, women who had bacterial vaginosis and smoked at the time of recruitment were at substantially increased risk of fetal fibronectin-positivity (RR 7.8, 95% CI 2.2, 27.8) compared with smokers without bacterial vaginosis. Among nonsmokers, bacterial vaginosis was not associated with fetal fibronectin-positivity (RR 1.0, 95% CI 0.4, 2.4). These results were essentially unchanged after adding the requirement of vaginal pH exceeding 4.5 to the bacterial vaginosis definition.

Conclusion: Fetal fibronectin was associated positively with bacterial vaginosis, but only among women who smoked. These results might provide clues as to the biologic relationship between smoking, infection, and preterm delivery.




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