Evidence map›Paper›PMID 22225939›Full record

ArticleInternational journal of immunogenetics2012

Mannose-binding lectin genotype and serum levels in patients with chronic and allergic pulmonary aspergillosis.

E Harrison, A Singh, J Morris, N L Smith, M G Fraczek, C B Moore, D W Denning

Abstract read
In one paragraph

Article in International journal of immunogenetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review of current and future therapeutics in ABPA.Therapeutic advances in chronic disease · 2021
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Serum mannose-binding lectin concentration, but not genotype, is associated with Clostridium difficile infection recurrence: a prospective cohort study.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2014
    Article
  10. Long-term antifungal treatment improves health status in patients with chronic pulmonary aspergillosis: a longitudinal analysis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2013
    Article
  11. 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 2 institutions in 1 country.

E HarrisonThe National Aspergillosis Centre, The University Hospital of South Manchester, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.
A Singh
J Morris
N L Smith
M G Fraczek
C B Moore
D W Denning
Manchester Academic Health Science Centre · GBUniversity of Manchester · GB

Funding

Rapid and Expandable Nucleic Acid Platform to Detect Bloodstream InfectionsU01AI066561 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI PERLIN, DAVID S · 2005 to 2009
$3.5M
Medical Research CouncilNIAID NIH HHS AI066561NIAID NIH HHS U01 AI066561
6 · The paper itself

Abstract

Several studies suggest mannose-binding lectin (MBL) deficiency is associated with various manifestations of aspergillosis. MBL serum levels and function are genetically determined, but levels rise during inflammation. We address the relative frequency of deficient genotypes, the relationship between serum level and genotype and both age and disease manifestations in patients with chronic pulmonary (CPA) and allergic bronchopulmonary aspergillosis (ABPA) and severe asthma with fungal sensitization (SAFS). DNA was extracted from blood samples, and MBL2 genotyping was performed using the INNO-LiPA MBL2 kit. Serum MBL concentrations were determined using ELISA. One hundred and eight patients were evaluated, 70 (65%) with CPA, 38 (35%) with allergic disease (ABPA, SAFS or undefined) and 13 (12%) had both CPA and ABPA. The mean MBL serum level was 1849 μg L(-1) and did not differ between groups. Forty subjects (37%) had exon 1 genotypes producing nonfunctional MBL (A/B, A/C, A/D and O/O), a frequency not different from published normal controls. A/A subjects with CPA had higher levels (2981 μg L(-1)) compared with allergic A/A subjects (2202 μg L(-1)) (pc0.012). No single haplotype, genotype or allele was significantly related to any aspergillosis phenotype. Worse breathlessness was associated with higher MBL levels among A/A subjects (P = 0.009) and conversely nonfunctional genotypes. Mean MBL values were higher in those with an Medical Research Council (MRC) breathlessness score of 5 compared with those with and MRC score of 1 (P = 0.023). A/A allergic subjects (n = 27) in this study were ≈ 11 years younger than allergic A/O subjects (n = 11, P = 0.02). Subjects with worse respiratory status or more severe CPA had higher MBL serum levels (P = 0.023; P = 0.034). Bronchiectasis was not associated with MBL levels in CPA or allergic aspergillosis. MBL genotype and serum level modulate progression of aspergillosis.

Indexed as

Polymorphism, Single NucleotideAdultAgedAged, 80 and overAllelesAspergillosis, Allergic BronchopulmonaryChronic DiseaseEnzyme-Linked Immunosorbent AssayGene FrequencyGenetic Association StudiesGenotypeGenotyping TechniquesHaplotypesHumansLinkage DisequilibriumMannose-Binding LectinMannose-Binding LectinMBL2 protein, human

Identifiers

PMID22225939
PMCPMC3326202
OpenAlexW2097835864

What OpenQuestion holds

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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.