Evidence map›Paper›PMID 28558032›Full record

ArticlePloS one2017

The association of mannose-binding lectin 2 polymorphisms with outcome in very low birth weight infants.

Annika Hartz, Julia Pagel, Alexander Humberg, Michael Preuss, Lena Schreiter, Jan Rupp, Julia Figge, Christian M Karsten, Peter Nürnberg, Egbert Herting and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. [Recent research on gene polymorphisms and genetic susceptibility of neonatal sepsis].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2024
    Review
  4. Review
  5. Review
  6. Association Between Variants of the Mannose-Binding Lectin 2 Gene and Susceptibility to Sepsis in the Hainan Island.Medical science monitor : international medical journal of experimental and clinical research · 2022
    Article
  7. Role ofDiagnostics (Basel, Switzerland) · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. 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

13 authors at 1 institution in 1 country.

Annika HartzDepartment of Pediatrics, University Hospital Lübeck, Lübeck, Germany.ORCID http://orcid.org/0000-0002-8785-2032
Julia PagelDepartment of Pediatrics, University Hospital Lübeck, Lübeck, Germany.
Alexander HumbergDepartment of Pediatrics, University Hospital Lübeck, Lübeck, Germany.
Michael PreussDepartment of Pediatrics, University Hospital Lübeck, Lübeck, Germany.
Lena SchreiterDepartment of Pediatrics, University Hospital Lübeck, Lübeck, Germany.
Jan RuppDepartment of Infectious Diseases and Microbiology, University Hospital Lübeck, Lübeck, Germany.
Julia FiggeInstitute of Systemic Inflammation Research, University Hospital Lübeck, Lübeck, Germany.
Christian M KarstenInstitute of Systemic Inflammation Research, University Hospital Lübeck, Lübeck, Germany.
Peter NürnbergCologne Center for Genomics, Cologne, Germany.
Egbert HertingDepartment of Pediatrics, University Hospital Lübeck, Lübeck, Germany.
Wolfgang GöpelDepartment of Pediatrics, University Hospital Lübeck, Lübeck, Germany.
Christoph HärtelDepartment of Pediatrics, University Hospital Lübeck, Lübeck, Germany.
German Neonatal Network (GNN)
University of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesStudies on the influence of mannose-binding lectin (MBL) deficiency on infection susceptibility in preterm infants have yielded controversial results. We investigated the association of genotype-based MBL levels with outcome in very-low-birth weight infants (VLBWI).

methodsWe genotyped 3 genetic variants of MBL2 (rs1800450, rs1800451, rs5030737) in 6878 VLBWI. MBL plasma levels were categorized as normal (wild type, A/A), low (heterozygotes, A/O) or undetectable (homozygotes, O/O). Primary outcome was the effect of genotype-based MBL2 levels on blood-culture proven and clinical sepsis during primary stay in hospital. We also evaluated burden of infection within 24 months after discharge.

resultsWe found no association between MBL levels and sepsis risk in the whole cohort. Infants without measurable MBL levels born between 32 0/7 to 36 6/7 weeks of gestation, however, had a higher rate of Gram-negative sepsis than infants with normal or reduced MBL levels. In a follow-up investigation at 24 months (n = 1070 infants), infants without measurable MBL levels suffered more frequently from stomatitis and urinary tract infection.

conclusionsIn a large cohort of VLBWI MBL2 deficiency had no major impact on infection risk unless children were born between 32 0/7 and 36 6/7 weeks of gestation.

Indexed as

Infant, Very Low Birth WeightPolymorphism, GeneticCohort StudiesHumansInfant, NewbornInfectionsMannose-Binding LectinMannose-Binding LectinsMetabolism, Inborn ErrorsMannose-Binding LectinMannose-Binding Lectins

Identifiers

PMID28558032
PMCPMC5448758
OpenAlexW2619172872

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.