Evidence map›Paper›PMID 24751721›Full record

ArticlePloS one2014

Mannose binding lectin and susceptibility to rheumatoid arthritis in Brazilian patients and their relatives.

Isabela Goeldner, Thelma L Skare, Shirley R Utiyama, Renato M Nisihara, Hoang van Tong, Iara J T Messias-Reason, Thirumalaisamy P Velavan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Identification of mannose-binding lectin as a mechanism in progressive immunoglobulin A nephropathy.International journal of clinical and experimental pathology · 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 4 institutions in 3 countries.

Isabela GoeldnerDepartment of Medical Pathology, Federal University of Paraná, Curitiba, Brazil; Institute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Thelma L SkareRheumatology Unit, Evangelical Hospital, Curitiba, Brazil.
Shirley R UtiyamaDepartment of Medical Pathology, Federal University of Paraná, Curitiba, Brazil.
Renato M NisiharaDepartment of Medical Pathology, Federal University of Paraná, Curitiba, Brazil.
Hoang van TongInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Iara J T Messias-ReasonDepartment of Medical Pathology, Federal University of Paraná, Curitiba, Brazil.
Thirumalaisamy P VelavanInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany; Fondation Congolaise pour la Recherche Medicale, Brazzaville , Republic of Congo.
Universidade Federal do Paraná · BRUniversity of Tübingen · DEFondation Congolaise Pour La Recherche Médicale · CGHospital Universitário Evangélico de Curitiba · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRheumatoid arthritis (RA) is a commonly occurring systemic inflammatory auto immune disease and is believed to be associated with genetic factors. The innate immune complement protein Mannose binding lectin (MBL) and their MBL2 genetic variants are associated with different infectious and autoimmune diseases.

methodsIn a Brazilian cohort, we aim to associate the functional role of circulating MBL serum levels and MBL2 variants in clinically classified patients (n = 196) with rheumatoid arthritis including their relatives (n = 200) and ethnicity matched healthy controls (n = 200). MBL serum levels were measured by ELISA and functional MBL2 variants were genotyped by direct sequencing.

resultsThe exon1+54 MBL2*B variant was significantly associated with an increased risk and the reconstructed haplotype MBL2*LYPB was associated with RA susceptibility. Circulating serum MBL levels were observed significantly lower in RA patients compared to their relatives and controls. No significant contribution of MBL levels were observed with respect to functional class, age at disease onset, disease duration and/or other clinical parameters such as nodules, secondary Sjögren syndrome, anti-CCP and rheumatoid factor. Differential distribution of serum MBL levels with functional MBL2 variants was observed in respective RA patients and their relatives.

conclusionsOur results suggest MBL levels as a possible marker for RA susceptibility in a Brazilian population.

Indexed as

FamilyAdolescentAdultAgedAged, 80 and overAllelesArthritis, RheumatoidBrazilCase-Control StudiesChildCohort StudiesDisease SusceptibilityFemaleGenetic Predisposition to DiseaseHaplotypesHumansMannose-Binding LectinMBL2 protein, human

Identifiers

PMID24751721
PMCPMC3994105
OpenAlexW2095291245

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.