Evidence map›Paper›PMID 18400978›Full record

ArticleClinical and vaccine immunology : CVI2008

Association of mannose-binding lectin gene polymorphism but not of mannose-binding serine protease 2 with chronic severe aortic regurgitation of rheumatic etiology.

Rajendranath Ramasawmy, Guilherme S Spina, Kellen C Fae, Alexandre C Pereira, Renato Nisihara, Iara Jose Messias Reason, Max Grinberg, Flavio Tarasoutchi, Jorge Kalil, Luiza Guilherme

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Review
  6. Article
  7. Article
  8. Review
  9. Observational
  10. Acute rheumatic fever and rheumatic heart disease.Nature reviews. Disease primers · 2016 · on this map
    Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Understanding rheumatic fever.Rheumatology international · 2012
    Review
  18. Article
  19. Article
  20. 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

10 authors at 4 institutions in 1 country.

Rajendranath RamasawmyHeart Institute (InCor), University of Sao Paulo School of Medicine, Sao Paulo, Brazil. ramasawm@usp.br
Guilherme S Spina
Kellen C Fae
Alexandre C Pereira
Renato Nisihara
Iara Jose Messias Reason
Max Grinberg
Flavio Tarasoutchi
Jorge Kalil
Luiza Guilherme
Hospital de Clínicas Universidade Federal do Paraná · BRMillennium Institute · BRUniversidade de São Paulo · BRUniversidade Federal do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N-Acetylglucosamine (GlcNAc) is the major immunoepitope of group A streptococcal cell wall carbohydrates. Antistreptococcal antibodies cross-reactive with anti-GlcNAc and laminin are present in sera of patients with rheumatic fever. The cross-reactivity of these antibodies with human heart valvular endothelium and the underlying basement membrane has been suggested to be a possible cause of immune-mediated valve lesion. Mannose-binding lectin (MBL) encoded by the MBL2 gene, a soluble pathogen recognition receptor, has high affinity for GlcNAc. We postulated that mutations in exon 1 of the MBL2 gene associated with a deficient serum level of MBL may contribute to chronic severe aortic regurgitation (AR) of rheumatic etiology. We studied 90 patients with severe chronic AR of rheumatic etiology and 281 healthy controls (HC) for the variants of the MBL2 gene at codons 52, 54, and 57 by using a PCR-restriction fragment length polymorphism-based method. We observed a significant difference in the prevalence of defective MBL2 alleles between patients with chronic severe AR and HC. Sixteen percent of patients with chronic severe AR were homozygotes or compound heterozygotes for defective MBL alleles in contrast to 5% for HC (P = 0.0022; odds ratio, 3.5 [95% confidence interval, 1.6 to 7.7]). No association was detected with the variant of the MASP2 gene. Our study suggests that MBL deficiency may contribute to the development of chronic severe AR of rheumatic etiology.

Indexed as

Polymorphism, GeneticAdultAllelesAortic Valve InsufficiencyCytokinesFemaleGene FrequencyGenotypeHumansMaleMannose-Binding LectinMannose-Binding Protein-Associated Serine ProteasesPolymorphism, Restriction Fragment LengthRheumatic DiseasesCytokinesMannose-Binding LectinMannose-Binding Protein-Associated Serine ProteasesMASP2 protein, human

Identifiers

PMID18400978
PMCPMC2446618
OpenAlexW1994282399

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.