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Mycoplasma, bacterial vaginosis-associated bacteria BVAB3, race, and risk of preterm birth in a high-risk cohort.
Foxman, Betsy; Wen, Ai; Srinivasan, Usha; Goldberg, Deborah; Marrs, Carl F; Owen, John; Wing, Deborah A; Misra, Dawn.
  • Foxman B; Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI. Electronic address: bfoxman@umich.edu.
  • Wen A; Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI.
  • Srinivasan U; Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI.
  • Goldberg D; Department of Ecology and Evolutionary Biology, University of Michigan Medical School, Ann Arbor, MI.
  • Marrs CF; Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI.
  • Owen J; Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, The University of Alabama at Birmingham, Birmingham, AL.
  • Wing DA; Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of California at Irvine School of Medicine, Irvine, CA.
  • Misra D; Department of Family Medicine and Public Health Sciences, School of Medicine, Wayne State University, Detroit, MI.
Am J Obstet Gynecol ; 210(3): 226.e1-7, 2014 Mar.
Article en En | MEDLINE | ID: mdl-24096128
ABSTRACT

OBJECTIVE:

Genital tract infection accounts for approximately 25-40% of all preterm births. We sought to assess the relationship between preterm birth and selected vaginal bacterial taxa associated with preterm birth either directly or through their association with bacterial vaginosis (BV). STUDY

DESIGN:

Vaginal fluid for Gram stain was collected between 17 and 22 weeks' gestation as part of a randomized trial of ultrasound-indicated cerclage for preterm birth prevention in women at high risk for recurrent spontaneous preterm birth. Bacterial deoxyribonucleic acid was extracted from the Gram stain slides and analyzed using quantitative polymerase chain reaction.

RESULTS:

Among the 499 participants, Mycoplasma was positively correlated with increased risk of preterm (risk ratio [RR], 1.83; 95% confidence interval [CI], 1.52-2.22) as was Mobiluncus (RR, 1.36; 95% CI, 1.07-1.73) and Atopobium (RR, 1.44; 95% CI, 1.1-1.87). However, there were strong interactions between the race/ethnic group and the presence of these and other individual taxa on risk of preterm birth. By contrast, bacterial vaginosis-associated bacteria (BVAB)-3 was consistently associated with a reduction in the risk of preterm birth for all racial/ethnic groups (0.55; 95% CI, 0.39-0.78).

CONCLUSION:

BV is characterized by a reduction of Lactobacillus, and lactic acid-producing bacteria and the presence of Mobiluncus; we found these factors and the presence of Mycoplasma to be associated with an increased risk of preterm birth. By contrast, the presence of a recently identified organism sufficient to cause BV, BVAB3, decreased the risk of preterm birth. These findings give insight into why treating BV has mixed impact on risk of preterm birth.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Complicaciones Infecciosas del Embarazo / Vaginosis Bacteriana / Nacimiento Prematuro / Trabajo de Parto Prematuro / Mycoplasma Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Complicaciones Infecciosas del Embarazo / Vaginosis Bacteriana / Nacimiento Prematuro / Trabajo de Parto Prematuro / Mycoplasma Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Año: 2014 Tipo del documento: Article