Evidence map›Paper›PMID 25184828›Full record

ArticlePloS one2014

Osteoprotegerin CGA haplotype protection against cerebrovascular complications in anti-CCP negative patients with rheumatoid arthritis.

Fernanda Genre, Raquel López-Mejías, Mercedes García-Bermúdez, Santos Castañeda, Carlos González-Juanatey, Javier Llorca, Alfonso Corrales, Begoña Ubilla, José A Miranda-Filloy, Trinitario Pina and 11 more

Open access · goldAbstract readClinical StudyMulticenter Study
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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Selected RANKL/RANK/OPG system genetic variants in diabetic foot patients.Journal of diabetes and metabolic disorders · 2018
    Article
  5. Mechanisms of vascular comorbidity in autoimmune diseases.Current opinion in rheumatology · 2018
    Review
  6. 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

21 authors at 10 institutions in 1 country.

Fernanda GenreEpidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Rheumatology Division, IDIVAL, Santander, Spain.
Raquel López-MejíasEpidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Rheumatology Division, IDIVAL, Santander, Spain.
Mercedes García-BermúdezInstituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, Spain.
Santos CastañedaDepartment of Rheumatology, Hospital Universitario la Princesa, IIS-Princesa, Madrid, Spain.
Carlos González-JuanateyCardiology Division, Hospital Universitario Lucus Augusti, Lugo, Spain.
Javier LlorcaDepartment of Epidemiology and Computational Biology, School of Medicine, University of Cantabria, and CIBER Epidemiología y Salud Pública (CIBERESP), IDIVAL, Santander, Spain.
Alfonso CorralesEpidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Rheumatology Division, IDIVAL, Santander, Spain.
Begoña UbillaEpidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Rheumatology Division, IDIVAL, Santander, Spain.
José A Miranda-FilloyDivision of Rheumatology, Hospital Universitario Lucus Augusti, Lugo, Spain.
Trinitario PinaEpidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Rheumatology Division, IDIVAL, Santander, Spain.
Carmen Gómez-VaqueroDepartment of Rheumatology, Hospital Universitario Bellvitge, Barcelona, Spain.
Luis Rodríguez-RodríguezDepartment of Rheumatology, Hospital Clínico San Carlos, Madrid, Spain.
Benjamín Fernández-GutiérrezDepartment of Rheumatology, Hospital Clínico San Carlos, Madrid, Spain.
Alejandro BalsaDepartment of Rheumatology, Hospital Universitario La Paz, Madrid, Spain.
Dora Pascual-SalcedoDepartment of Rheumatology, Hospital Universitario La Paz, Madrid, Spain.
Francisco J López-LongoDepartment of Rheumatology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Patricia CarreiraDepartment of Rheumatology, Hospital Universitario 12 de Octubre, Madrid, Spain.
Ricardo BlancoEpidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Rheumatology Division, IDIVAL, Santander, Spain.
Isidoro González-ÁlvaroDepartment of Rheumatology, Hospital Universitario la Princesa, IIS-Princesa, Madrid, Spain.
Javier MartínInstituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, Spain.
Miguel A González-GayEpidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Rheumatology Division, IDIVAL, Santander, Spain.
Instituto de Investigación Marqués de Valdecilla · ESConsejo Superior de Investigaciones Científicas · ESHospital Clínico San Carlos · ESHospital Universitario de La Princesa · ESHospital Universitario La Paz · ESHospital Universitario Lucus Augusti · ESBellvitge University Hospital · ESHospital General Universitario Gregorio Marañón · ESHospital Universitario 12 De Octubre · ESUniversidad de Cantabria · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRheumatoid arthritis is an inflammatory disease with high incidence of cardiovascular disease due to accelerated atherosclerosis. Osteoprotegerin (OPG) has been associated with increased risk of atherosclerotic disease in the general population. Several polymorphisms in the OPG gene with functional effects on cardiovascular disease in non-rheumatic individuals have been described. Therefore, we aimed to analyze the effect of three of these functional OPG polymorphisms on the risk of cardiovascular disease in a large and well-characterized cohort of Spanish patients with rheumatoid arthritis.

methodsThree OPG gene variants (rs3134063, rs2073618 and rs3134069) were genotyped by TaqMan assays in 2027 Spanish patients with rheumatoid arthritis. Anti-cyclic citrullinated peptide (anti-CCP) antibody testing was positive in 997 of 1714 tested. Also, 18.3% of the whole series had experienced cardiovascular events, including 5.4% with cerebrovascular accidents. The relationship between OPG variants and cardiovascular events was assessed using Cox regression.

resultsNo association between OPG gene variants and cardiovascular disease was observed in the whole group of rheumatoid arthritis patients or in anti-CCP positive patients. Nevertheless, a protective effect of CGA haplotype on the risk of cardiovascular disease in general, and specifically in the risk of cerebrovascular complications after adjusting for sex, age at disease diagnosis and traditional cardiovascular risk factors was disclosed in anti-CCP negative patients (HR = 0.54; 95%CI: 0.31-0.95; p = 0.032 and HR = 0.17; 95%CI: 0.04-0.78; p = 0.022, respectively).

conclusionOur results indicate a protective effect of the OPG CGA haplotype on cardiovascular risk, mainly due to a protective effect against cerebrovascular events in anti-CCP negative rheumatoid arthritis patients.

Indexed as

Arthritis, RheumatoidCerebrovascular DisordersHaplotypesPolymorphism, Single NucleotideAdultAgedAutoantibodiesFemaleHumansMaleMiddle AgedOsteoprotegerinPeptides, CyclicSpainAutoantibodiescyclic citrullinated peptideOsteoprotegerinPeptides, CyclicTNFRSF11B protein, human

Identifiers

PMID25184828
PMCPMC4153690
OpenAlexW2100460348

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.