Genetic variation associated with preterm birth: a HuGE review
Open accessAbstract
Preterm birth (PTB) is a major public health concern because of its high prevalence, associated mortality and morbidity, and expense from both short-term hospitalization and long-term disability. In 2002, 11.9% of U.S. births occurred before 37 weeks gestation. Epidemiologic studies have identified many demographic, behavioral, and medical characteristics associated with PTB risk. In addition, recent evidence indicates a role for genetic susceptibility. We reviewed 18 studies published before June 1, 2004, that examined associations between polymorphisms in the maternal or fetal genome and PTB risk. Studies of a polymorphism in tumor necrosis factor-alpha, a proinflammatory cytokine, showed the most consistent increase in the risk of PTB. Environmental factors such as infection, stress, and obesity, which activate inflammatory pathways, have been associated with PTB, suggesting that environmental and genetic risk factors might operate and interact through related pathways. This review highlights maternal and fetal genetic susceptibilities to PTB, the potential relationships with environmental risk factors, and the need for additional well-designed studies of this critical public health problem.
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Fetal and maternal genotypes modify the risk of preterm delivery.
“The fetal and maternal genotypes modify the risk of preterm delivery.135”
From Epidemiology and causes of preterm birth (2008) · cites this paper as [135]
Genetic association studies have identified single-nucleotide polymorphisms in several genes associated with preterm labour and PPROM.
“Genetic association studies have been used to identify single-nucleotide polymorphisms in several genes associated with preterm labour and PPROM.133, 134, 135”
From Epidemiology and causes of preterm birth (2008) · cites this paper as [135]
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- Authors
- Crider, K. S., Whitehead, N., & Buus, R. M.
- Affiliations
- Centers for Disease Control and Prevention (US)
- Venue
- Genetics in Medicine
- Publisher
- Elsevier BV
- Published
- 2005-11
- Volume
- 7
- Issue
- 9
- Pages
- 593-604
- ISSN
- 1098-3600 (ISSN-L)
- OpenAlex
- W2063627864
- Cited by
- 190
- References
- 121
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 1 · 2023: 5 · 2022: 3 · 2021: 7 · 2020: 5 · 2019: 4 · 2018: 7 · 2017: 13 · 2016: 8 · 2015: 6 · 2014: 13 · 2013: 13 · 2012: 13
- FWCI
- 2.27
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Genetics in Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Preterm Birth and Chorioamnionitis
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Infant Development and Preterm Care
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Keywords
- preterm birth, genetic susceptibility, TNF-α, TNF-alpha polymorphism, genetic polymorphism, maternal genetic risk, inflammation, infection, stress, obesity, environmental risk factors, gene-environment interaction
- MeSH terms
- Environmental Exposure, Female, Fetal Proteins, Humans, Interleukins, Pregnancy, Risk Factors, Tumor Necrosis Factor-alpha, Genetic Variation, Receptors, Adrenergic, beta-2, Genetic Predisposition to Disease, Matrix Metalloproteinases, Vascular Endothelial Growth Factor A, Methylenetetrahydrofolate Reductase (NADPH2), Premature Birth, Toll-Like Receptor 4
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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