Evidence map›Paper›PMID 21256510›Full record

ArticleThe Journal of pediatrics2011

Fucosyltransferase 2 non-secretor and low secretor status predicts severe outcomes in premature infants.

Ardythe L Morrow, Jareen Meinzen-Derr, Pengwei Huang, Kurt R Schibler, Tanya Cahill, Mehdi Keddache, Suhas G Kallapur, David S Newburg, Meredith Tabangin, Barbara B Warner and 1 more

Abstract readComparative StudyMulticenter Study
In one paragraph

Article in The Journal of pediatrics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 2 pooled it
8.4field-weighted citation impact, top 2% 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

60 citing papers in PubMed, 2 syntheses or guidelines pooled it, 122 citations in OpenAlex.

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  18. FUT2 gene as a genetic susceptible marker of infectious diseases: A Review.International journal of molecular epidemiology and genetics · 2022
    Review
  19. Review
  20. Maternal H-antigen secretor status is an early biomarker for potential preterm delivery.Journal of perinatology : official journal of the California Perinatal Association · 2021
    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

11 authors at 4 institutions in 1 country.

Ardythe L MorrowDivision of Neonatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45213, USA. Ardythe.Morrow@cchmc.org
Jareen Meinzen-Derr
Pengwei Huang
Kurt R Schibler
Tanya Cahill
Mehdi Keddache
Suhas G Kallapur
David S Newburg
Meredith Tabangin
Barbara B Warner
Xi Jiang
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati Medical Center · USBoston College · USWashington University in St. Louis · US

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Kathryn Ann Wikenheiser-Brokamp · 2007 to 2026
$24.4M
VIRAL GASTROENTERITIS PATHOGENSP01HD013021 · NICHD · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MORROW, ARDYTHE L · 1985 to 2013
$15.0M
NICHD Cooperative Multicenter Neonatal Research NetworkU10HD027853 · NICHD · UNIVERSITY OF CINCINNATI · PI SCHIBLER, KURT R · 1991 to 2015
$6.2M
Novel genetic and salivary glycan biomarkers for risk of NEC in ELBW infants.R01HD059140 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI MORROW, ARDYTHE L · 2009 to 2013
$3.3M
Role of EGF in Development of Necrotizing EnterocolitisR03DK061596 · NIDDK · CHILDREN'S HOSPITAL MED CTR (CINCINNATI) · PI WARNER, BARBARA B · 2002 to 2003
$279k
NICHD NIH HHS P01 HD013021NICHD NIH HHS P01HD13021NICHD NIH HHS R01 HD 059140NICHD NIH HHS R01 HD059140NICHD NIH HHS U10 HD 027853NICHD NIH HHS U10 HD027853NIDDK NIH HHS P30 DK078392NIDDK NIH HHS R03 DK061596NIDDK NIH HHS R03 DK61596
6 · The paper itself

Abstract

objectiveTo investigate secretor gene fucosyltransferase 2 (FUT2) polymorphism and secretor phenotype in relation to outcomes of prematurity. STUDY

designStudy infants were ≤32 weeks gestational age. Secretor genotype was determined from salivary DNA. Secretor phenotype was measured with H antigen, the carbohydrate produced by secretor gene enzymes, in saliva samples collected on day 9 ± 5. The optimal predictive cutoff point in salivary H values was identified with Classification and Regression Tree analysis. Study outcomes were death, necrotizing enterocolitis (NEC, Bell's stage II/III), and confirmed sepsis.

resultsThere were 410 study infants, 26 deaths, 30 cases of NEC, and 96 cases of sepsis. Analyzed by genotype, 13% of 95 infants who were non-secretors, 5% of 203 infants who were heterozygotes, and 2% of 96 infants who were secretor dominant died (P = .01). Analyzed by phenotype, 15% of 135 infants with low secretor phenotype died, compared with 2% of 248 infants with high secretor phenotype (predictive value = 76%, P < .001). Low secretor phenotype was associated (P < .05) with NEC, and non-secretor genotype was associated (P = .05) with gram negative sepsis. Secretor status remained significant after controlling for multiple clinical factors.

conclusionsSecretor genotype and phenotype may provide strong predictive biomarkers of adverse outcomes in premature infants.

Indexed as

Infant, PrematurePolymorphism, GeneticCause of DeathDNAEnterocolitis, NecrotizingFollow-Up StudiesFucosyltransferasesGalactoside 2-alpha-L-fucosyltransferaseGenotypeHumansInfant MortalityInfant, NewbornOhioPrognosisRetrospective StudiesSalivaDNAFucosyltransferasesGalactoside 2-alpha-L-fucosyltransferase

Identifiers

PMID21256510
PMCPMC3412418
OpenAlexW1977019826

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.