Evidence map›Paper›PMID 24398289›Full record

SynthesisEpidemiology and infection2014

Mannose-binding lectin polymorphisms and the risk of sepsis: evidence from a meta-analysis.

A-Q Zhang, C-L Yue, W Pan, J-W Gao, L Zeng, W Gu, J-X Jiang

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Epidemiology and infection, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Mannose-Binding Lectin Levels in Critically Ill Children With Severe Infections.Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2017
    Trial
  4. Genetic associations in sepsis and ARDS.Frontiers in pharmacology · 2026
    Review
  5. Review
  6. Role ofDiagnostics (Basel, Switzerland) · 2022
    Article
  7. Review
  8. Article
  9. Article
  10. Variants in the Mannose-binding Lectin Gene MBL2 do not Associate With Sepsis Susceptibility or Survival in a Large European Cohort.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2015
    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

7 authors at 1 institution in 1 country.

A-Q ZhangState Key Laboratory of Trauma, Burns and Combined Injury,Institute of Surgery Research, Daping Hospital, Third Military Medical University,Chongqing,China.
C-L YueState Key Laboratory of Trauma, Burns and Combined Injury,Institute of Surgery Research, Daping Hospital, Third Military Medical University,Chongqing,China.
W PanState Key Laboratory of Trauma, Burns and Combined Injury,Institute of Surgery Research, Daping Hospital, Third Military Medical University,Chongqing,China.
J-W GaoState Key Laboratory of Trauma, Burns and Combined Injury,Institute of Surgery Research, Daping Hospital, Third Military Medical University,Chongqing,China.
L ZengState Key Laboratory of Trauma, Burns and Combined Injury,Institute of Surgery Research, Daping Hospital, Third Military Medical University,Chongqing,China.
W GuState Key Laboratory of Trauma, Burns and Combined Injury,Institute of Surgery Research, Daping Hospital, Third Military Medical University,Chongqing,China.
J-X JiangState Key Laboratory of Trauma, Burns and Combined Injury,Institute of Surgery Research, Daping Hospital, Third Military Medical University,Chongqing,China.
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several studies have evaluated the association between mannose-binding lectin (MBL) polymorphisms and sepsis. However, the results are inconclusive and conflicting. To better understand the roles of MBL polymorphisms in sepsis, we conducted a comprehensive meta-analysis. All relevant studies were searched from PubMed, EMBASE and Web of Knowledge databases, with the last report up to 7 May 2013. Twenty-nine studies addressing four MBL polymorphisms (-550G/C, -221G/C, structure variant A/O, Gly54Asp) were analysed for susceptibility to sepsis and one study for sepsis-related mortality. Overall, significant associations between structure variant A/O and susceptibility to sepsis were observed for AO + OO vs. AA [odds ratio (OR) 1·27, 95% confidence interval (CI) 1·05-1·52, P = 0·01] and O vs. A (OR 1·19, 95% CI 1·02-1·40, P = 0·03). In subgroup analysis based on age group, increased risk was found in the paediatric group in the dominant model (OR 1·72, 95% CI 1·16-2·56, P = 0·007). Moreover, there was a slight association between the +54A/B polymorphism and susceptibility to sepsis in Caucasians (recessive model: OR 10·64, 95% CI 1·24-91·65, P = 0·03). However, no association was observed for -550G/C and -221G/C polymorphisms both overall and in subgroup analysis. For sepsis-related mortality, only one study suggested AO/OO was associated with in-hospital mortality in pneumococcal sepsis patients after controlling for confounding variables. Our meta-analysis indicated that MBL structure variants might be associated with susceptibility to sepsis but further studies with a large sample size should be conducted to confirm these findings.

Indexed as

AdultAge FactorsChildGenetic Predisposition to DiseaseHumansMannose-Binding LectinOdds RatioPolymorphism, GeneticSepsisMannose-Binding Lectin

Identifiers

PMID24398289
PMCPMC9151319
OpenAlexW2088964002

What OpenQuestion holds

Textmetadata
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.