Evidence map›Paper›PMID 28288972›Full record

ArticleJournal of the American Heart Association2017

Interleukin 6 Inhibition and Coronary Artery Disease in a High-Risk Population: A Prospective Community-Based Clinical Study.

Bruno Cesar Bacchiega, Ana Beatriz Bacchiega, Magali Justina Gomez Usnayo, Ricardo Bedirian, Gurkirpal Singh, Geraldo da Rocha Castelar Pinheiro

Open access · goldAbstract readClinical Study
In one paragraph

Article in Journal of the American Heart Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 5 pooled it
12.2field-weighted citation impact, top 1% 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

85 citing papers in PubMed, 5 syntheses or guidelines pooled it, 157 citations in OpenAlex.

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  12. Characterizing Stroke Clots Using Single-Cell Sequencing.Journal of the American Heart Association · 2025
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25 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 2 countries.

Bruno Cesar BacchiegaDepartment of Internal Medicine, Rio de Janeiro State University, Rio de Janeiro, Brazil brunobacchiega@gmail.com.
Ana Beatriz BacchiegaDiscipline of Rheumatology, Rio de Janeiro State University, Rio de Janeiro, Brazil.
Magali Justina Gomez UsnayoDiscipline of Rheumatology, Rio de Janeiro State University, Rio de Janeiro, Brazil.
Ricardo BedirianDepartment of Internal Medicine, Rio de Janeiro State University, Rio de Janeiro, Brazil.
Gurkirpal SinghDivision of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, CA.
Geraldo da Rocha Castelar PinheiroDiscipline of Rheumatology, Rio de Janeiro State University, Rio de Janeiro, Brazil.
Universidade do Estado do Rio de Janeiro · BRStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtherosclerosis is a chronic inflammatory disease, with interleukin 6 (IL-6) as a major player in inflammation cascade. IL-6 blockade may reduce cardiovascular risk, but current treatments to block IL-6 also induce dyslipidemia, a finding with an uncertain prognosis. METHODS AND

resultsWe aimed to determine the endothelial function responses to the IL-6-blocking agent tocilizumab, anti-tumor necrosis factor α, and synthetic disease-modifying antirheumatic drug therapies in patients with rheumatoid arthritis in a 16-week prospective study. Sixty consecutive patients with rheumatoid arthritis were enrolled. Tocilizumab and anti-tumor necrosis factor α therapy were started in 18 patients each while 24 patients were treated with synthetic disease-modifying antirheumatic drugs. Forty patients completed the 16-week follow-up period. The main outcome was flow-mediated dilation percentage variation before and after therapy. In the tocilizumab group, flow-mediated dilation percentage variation increased statistically significantly from a pre-treatment mean of (3.43% [95% CI, 1.28-5.58] to 5.96% [95% CI, 3.95-7.97];

conclusionsEndothelial function is improved by tocilizumab in a high-risk population, even as it increases total cholesterol and low-density lipoprotein levels.

Indexed as

Interleukin-6 InhibitorsPopulation SurveillanceAdultAntibodies, Monoclonal, HumanizedAntirheumatic AgentsArthritis, RheumatoidBiomarkersBrazilCoronary Artery DiseaseDose-Response Relationship, DrugDrug Therapy, CombinationEndothelium, VascularFemaleFollow-Up StudiesHumansIncidenceAntibodies, Monoclonal, HumanizedAntirheumatic AgentsBiomarkersIL6 protein, humanInterleukin-6Interleukin-6 Inhibitorstocilizumabdyslipidemiaendothelial functioninflammationtocilizumab

Identifiers

PMID28288972
PMCPMC5524026
OpenAlexW2596497884

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.