Evidence map›Paper›PMID 19733287›Full record

ArticleAmerican journal of obstetrics and gynecology2009

Polymorphisms in thrombophilia and renin-angiotensin system pathways, preterm delivery, and evidence of placental hemorrhage.

Julia Warner Gargano, Claudia B Holzman, Patricia K Senagore, M Lynne Reuss, Dorothy R Pathak, Karen H Friderici, Katherine Jernigan, Rachel Fisher

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in American journal of obstetrics and gynecology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Placental lesions associated with acute atherosis.The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians · 2015
    Article
  7. Article
  8. Article
  9. Article
  10. Maternal lipids at mid-pregnancy and the risk of preterm delivery.Acta obstetricia et gynecologica Scandinavica · 2012
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Evidence of placental haemorrhage and preterm delivery.BJOG : an international journal of obstetrics and gynaecology · 2010
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Julia Warner GarganoDepartment of Epidemiology, College of Human Medicine, Michigan State University, East Lansing, MI 48823, USA.
Claudia B Holzman
Patricia K Senagore
M Lynne Reuss
Dorothy R Pathak
Karen H Friderici
Katherine Jernigan
Rachel Fisher
Michigan State University · USSouthwest Women's Oncology · US

Funding

Etiologic Heterogeneity in Preterm DeliveryR01HD034543 · NICHD · MICHIGAN STATE UNIVERSITY · PI HOLZMAN, CLAUDIA B. · 1997 to 2005
$5.3M
Preterm Delivery and Maternal Cardiovascular Disease RiskR01HL103825 · NHLBI · MICHIGAN STATE UNIVERSITY · PI CATOV, JANET M, HOLZMAN, CLAUDIA B. · 2010 to 2013
$3.6M
Immune System Gene Polymorphisms and Preterm DeliveryU01DP000143 · DP · MICHIGAN STATE UNIVERSITY · PI HOLZMAN, CLAUDIA B. · 2005 to 2009
$2.1M
NCCDPHP CDC HHS U01 DP000143NCCDPHP CDC HHS U01 DP000143-01NHLBI NIH HHS R01 HL103825NICHD NIH HHS R01 HD034543NICHD NIH HHS R01 HD34543
6 · The paper itself

Abstract

objectiveThe purpose of this study was to analyze functional polymorphisms in candidate genes (methylenetetrahydrofolate reductase [MTHFR]677C>T, MTHFR1298A>C, factor 5 1691G>A [FVL], and angiotensinogen (AGT)-6G>A) in relation to a hypothesized placental hemorrhage pathway to preterm delivery (PTD). STUDY

designWe assessed maternal genotypes, pregnancy outcomes, and placental pathologic evidence among 560 white and 399 black women who were recruited at mid trimester into a prospective cohort study (1998-2004). Odds of dominant genotypes were calculated for PTDs with (n = 56) or without (n = 177) evidence of placental hemorrhage (referent = term) with the use of race-stratified polytomous logistic regression models.

resultsAmong white women, FVL GA/AA and AGT(-6) GA/AA were both associated with hemorrhage-related PTDs (odds ratio [OR], 4.8; 95% confidence interval [CI], 1.6-14.2 and OR, 3.8; 95% CI, 1.3-10.5, respectively), but not other PTDs (ORs, 1.2 and 0.9, respectively). FVL GA/AA was associated with placental abruption (OR, 5.8; 95% CI, 1.1-30) among white women. All results were null for MTHFR genotypes.

conclusionFVL and AGT variant genotypes were associated specifically with hemorrhage-related PTDs.

Indexed as

AdultAngiotensinogenFactor VFemaleGene FrequencyGenotypeHemorrhageHumansLogistic ModelsMethylenetetrahydrofolate Reductase (NADPH2)Placenta DiseasesPoint MutationPolymorphism, GeneticPregnancyPregnancy OutcomePremature BirthAngiotensinogenFactor Vfactor V LeidenMethylenetetrahydrofolate Reductase (NADPH2)

Identifiers

PMID19733287
PMCPMC3018335
OpenAlexW2062511932

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.