Evidence map›Paper›PMID 26371589›Full record

ArticleThe 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 Obstetricians2016

A toll-like receptor 9 (rs352140) variant is associated with placental inflammation in newborn infants.

Vijender Karody, Shawn Reese, Navin Kumar, Jennifer Liedel, Jason Jarzembowski, Venkatesh Sampath

Open access · greenAbstract read
In one paragraph

Article in 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, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Innate immunity - the hallmark ofWorld journal of clinical cases · 2021
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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

6 authors at 5 institutions in 1 country.

Vijender Karodya Department of Pediatrics , Medical College of Wisconsin and Children's Hospital of Wisconsin , Milwaukee , WI , USA .
Shawn Reeseb Department of Pediatrics , Wheaton Franciscan Healthcare , Milwaukee , WI , USA .
Navin Kumarc Department of Neonatology , Hurley Medical Center , Flint , MI , USA .
Jennifer Liedeld Department of Pediatric Critical Care , The Children's Hospital of Montefiore , Bronx , NY , USA .
Jason Jarzembowskif Department of Pathology , Medical College of Wisconsin and Children's Hospital of Wisconsin , Milwaukee , WI , USA.
Venkatesh Sampatha Department of Pediatrics , Medical College of Wisconsin and Children's Hospital of Wisconsin , Milwaukee , WI , USA .
Medical College of Wisconsin · USAlbert Einstein College of Medicine · USChildren's Hospital of Wisconsin · USHurley Medical Center · USWheaton Franciscan Healthcare · US

Funding

Clinical and Translational Science AwardKL2TR000056 · NCATS · MEDICAL COLLEGE OF WISCONSIN · PI SHAKER, REZA NONE · 2012 to 2015
$609k
NCATS NIH HHS 8KL2TR000056NCATS NIH HHS KL2 TR000056
6 · The paper itself

Abstract

objectiveChorioamnionitis contributes to premature birth and associated postnatal morbidity. The genetic basis of altered immune responses underlying placental inflammation (PI) remains understudied. The aim of this study was to evaluate the relationship among TLR signaling pathway polymorphisms and different patterns of PI.

methodsProspective cohort study in infants involving cord blood collection and placental examination for PI. One hundred and fifty-nine infants enrolled in study out of which 28 were term (eight with PI) and 131 preterm (47 with PI). DNA from blood was genotyped for SNPs in TLR2, 4, 5, 9, NFKBI, NFKBIA, TIRAP, and IRAK1 genes using multiplexed single base extension assay.

resultsWhile there were no differences in BW, GA, gender, race, and SPL among infants with or without PI, there was a higher incidence of PPROM, maternal smoking, drug use, and clinical chorioamnionitis among infants with PI. Out of nine TLR variants, only CT and/or TT genotypes of the TLR9 variant (rs352140) were significantly associated (p = 0.004) with any PI and maternal pattern of inflammation (p = 0.012) both by univariate analysis and logistic regression.

conclusionsThe presence of a variant T allele in a common SNP (rs352140) in the TLR9 gene whose product recognizes bacterial DNA is associated with increased PI.

Indexed as

Polymorphism, Single NucleotideAllelesChorioamnionitisFemaleGenetic Predisposition to DiseaseHumansInfant, NewbornInfant, PrematureInflammationMalePlacenta DiseasesPregnancyPremature Rupture of Fetal MembranesToll-Like Receptor 9TLR9 protein, humanToll-Like Receptor 9Chorioamnionitisinnate immunityplacental inflammationrs352140toll-like receptor 9 polymorphisms

Identifiers

PMID26371589
PMCPMC5238957
OpenAlexW1920508269

What OpenQuestion holds

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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.