Source:http://linkedlifedata.com/resource/pubmed/id/20965572
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2010-11-24
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pubmed:abstractText |
Recent findings suggest that the association between inflammation-related genes and preterm delivery may be stronger in the presence of bacterial vaginosis (BV). Tumor necrosis factor-alpha (TNF?) and interleukin 1-beta (IL-1?) are pro-inflammatory cytokines capable of inducing preterm labor in non-human primates. In this study the authors tested associations among two TNF? promoter polymorphisms (-G308A and -G238A), a single IL-1? polymorphism (+C3954T), vaginal microbial findings, and risk of preterm delivery. Data were from the Pregnancy Outcomes and Community Health (POUCH) Study (n=777 term and n=230 preterm deliveries). Vaginal smears collected at mid-pregnancy (15-27 weeks gestation) were scored according to Nugent's criteria. A Nugent score of ? 4 was modeled as the cut-point for intermediate and positive BV. Logistic regression was used to estimate odds ratios for associations among independent covariates (vaginal flora, genotype) and preterm delivery. Results showed that women with a Nugent score of? 4 and the TNF? -238 A/G or A/A were at increased risk of delivering preterm (race/ethnicity adjusted OR 2.6, 95% CI 1.2, 5.8). The p-value for the genotype and Nugent score interaction=0.02. This study points to one more example of a potential gene-environment interaction in a preterm delivery pathway. Future tests of this finding will determine the robustness of these results.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1872-7603
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
87
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
82-9
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pubmed:meshHeading |
pubmed-meshheading:20965572-Adult,
pubmed-meshheading:20965572-Cohort Studies,
pubmed-meshheading:20965572-Cytokines,
pubmed-meshheading:20965572-Female,
pubmed-meshheading:20965572-Genotype,
pubmed-meshheading:20965572-Humans,
pubmed-meshheading:20965572-Interleukin-1beta,
pubmed-meshheading:20965572-Polymorphism, Single Nucleotide,
pubmed-meshheading:20965572-Pregnancy,
pubmed-meshheading:20965572-Pregnancy Outcome,
pubmed-meshheading:20965572-Premature Birth,
pubmed-meshheading:20965572-Risk Factors,
pubmed-meshheading:20965572-Tumor Necrosis Factor-alpha,
pubmed-meshheading:20965572-Vagina,
pubmed-meshheading:20965572-Vaginosis, Bacterial,
pubmed-meshheading:20965572-Young Adult
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pubmed:year |
2010
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pubmed:articleTitle |
Interplay of cytokine polymorphisms and bacterial vaginosis in the etiology of preterm delivery.
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pubmed:affiliation |
Department of Epidemiology, B601 West Fee Hall, Michigan State University, East Lansing, MI 48824, USA. njones@epi.msu.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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