Evidence map›Paper›PMID 33388968›Full record

ArticleRheumatology international2021

Increased short-term risk of cardiovascular events in inflammatory rheumatic diseases: results from a population-based cohort.

Vital Da Silva Domingues, Ana M Rodrigues, Sara S Dias, Luís Delgado, Ebrahim Barkoudah, Jaime Branco, Helena Canhão

Abstract read
PubMed Publisher
In one paragraph

Article in Rheumatology international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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 6 institutions in 2 countries.

Vital Da Silva DominguesCentro Hospitalar do Porto, Porto, Portugal. vdomingues@igc.gulbenkian.pt.ORCID http://orcid.org/0000-0001-7339-0220
Ana M RodriguesCentro de Estudos de Doenças Crónicas (CEDOC), EpiDoc Unit, Unidade de Epidemiologia em Doenças Crónicas, NOVA Medical School, Universidade Nova de Lisboa (NMS/UNL), Lisboa, Portugal.ORCID http://orcid.org/0000-0003-2046-8017
Sara S DiasCentro de Estudos de Doenças Crónicas (CEDOC), EpiDoc Unit, Unidade de Epidemiologia em Doenças Crónicas, NOVA Medical School, Universidade Nova de Lisboa (NMS/UNL), Lisboa, Portugal.ORCID http://orcid.org/0000-0001-6782-7481
Luís DelgadoServiço de Imunologia Básica e Clínica, Departamento de Patologia, Faculdade de Medicina da Universidade do Porto, Porto, Portugal.ORCID http://orcid.org/0000-0003-2375-9071
Ebrahim BarkoudahBrigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-8224-5121
Jaime BrancoCentro de Estudos de Doenças Crónicas (CEDOC), EpiDoc Unit, Unidade de Epidemiologia em Doenças Crónicas, NOVA Medical School, Universidade Nova de Lisboa (NMS/UNL), Lisboa, Portugal.ORCID http://orcid.org/0000-0001-7024-4375
Helena CanhãoCentro de Estudos de Doenças Crónicas (CEDOC), EpiDoc Unit, Unidade de Epidemiologia em Doenças Crónicas, NOVA Medical School, Universidade Nova de Lisboa (NMS/UNL), Lisboa, Portugal.ORCID http://orcid.org/0000-0003-1894-4870
Universidade Nova de Lisboa · PTBrigham and Women's Hospital · USCentro Hospitalar do Porto · PTHospital de Egas Moniz · PTInstituto Politécnico de Leiria · PTUniversidade do Porto · PT

Funding

Sociedade Portuguesa de Reumatologia/Pfizer PT2017_002
6 · The paper itself

Abstract

Cardiovascular diseases represent the first cause of death globally. Inflammatory rheumatic disease (IRMD) patients, due to their lifelong inflammatory status, are at increased risk of developing premature cardiovascular disease. We aimed to assess the risk for cardiovascular events (CVE) in a population-based study. We followed 10,153 adults from the EpiDoC Cohort, a large Portuguese population-based prospective study (2011-2016). IRMD patients were identified at baseline and followed during 5 years. CVE were defined as a composite of self-reported myocardial infarction or angina pectoris, arrhythmias, valvular disease, stroke or transient ischemic attack and peripheral artery disease. Statistical analysis was performed by utilizing multivariate logistic regression and goodness-of-fit and area under ROC curve. At baseline, IRMD patients had similar age as the non-IRMD participants (mean age 55 vs 53 years-old; 72.1% female); dyslipidaemia and sedentary lifestyle were more common (40.7% vs 31.4%, p = 0.033; 87.3% vs 67%, p = 0.016, respectively). During an average follow-up of 2.6 years, 26 CVE were reported among IRMD patients. IRMD patients had higher odd of CVE (OR 1.64, 95% CI 1.04-2.58; p = 0.03), despite comparable mortality rates (1.7% vs 0.7%, p = 0.806). A stepwise approach attained that gender, age, history of hypertension, body mass index, IRMD and follow-up time are the most important predictive variables of CVE (AUC 0.80). IRMD patients, at community level, have an increased short-term risk of major CVE when compared to non-IRMD, and that highlights the potential benefit of a systematic screening and more aggressive cardiovascular risk assessment and management of these patients.

Indexed as

Risk AssessmentCardiovascular DiseasesCase-Control StudiesFemaleHeart Disease Risk FactorsHumansMaleMiddle AgedProspective StudiesRheumatic DiseasesROC CurveCardiovascular diseasesInflammationProspective studyRheumatic diseasesRisk assessment

Identifiers

PMID33388968
OpenAlexW3119385911

What Socratic 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 Socratic graph.