Evidence map›Paper›PMID 34504395›Full record

SynthesisMediators of inflammation2021

The Biological Disease-Modifying Antirheumatic Drugs and the Risk of Cardiovascular Events: A Systematic Review and Meta-Analysis.

Suiyuan Hu, Chu Lin, Xiaoling Cai, Xingyun Zhu, Fang Lv, Lin Nie, Linong Ji

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Mediators of inflammation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Heart failure in autoimmune rheumatic diseases.Rheumatology international · 2026
    Review
  4. Article
  5. Article
  6. Review
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  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Immunosenescence: an unexplored role in glomerulonephritis.Clinical & translational immunology · 2022
    Review
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 2 institutions in 1 country.

Suiyuan HuDepartment of Endocrinology and Metabolism, Peking University People's Hospital, Beijing, China.
Chu LinDepartment of Endocrinology and Metabolism, Peking University People's Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-2365-9831
Xiaoling CaiDepartment of Endocrinology and Metabolism, Peking University People's Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-7881-0543
Xingyun ZhuDepartment of Endocrinology and Metabolism, Peking University People's Hospital, Beijing, China.
Fang LvDepartment of Endocrinology and Metabolism, Peking University People's Hospital, Beijing, China.
Lin NieDepartment of Endocrinology and Metabolism, Beijing Airport Hospital, Beijing, China.
Linong JiDepartment of Endocrinology and Metabolism, Peking University People's Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-3262-2168
Peking University · CNAirport Shunyi District Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess the association between the use of biological disease-modifying antirheumatic drugs (bDMARDs) and the risk of cardiovascular events in patients with systemic inflammatory conditions.

methodsEligible cohort studies or randomized controlled trials (RCTs) from inception to January 2021 were included. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) for cardiovascular outcomes were calculated in the fixed- and random-effects model accordingly. Associated factors with risks of cardiovascular events were also studied in sensitivity analyses and metaregression analyses.

resultsCompared with non-bDMARD users, the risks of myocardial infarction (MI) (OR = 0.74, 95% CI, 0.63 to 0.87), heart failure (OR = 0.84, 95% CI, 0.74 to 0.95), cardiovascular (CV) death (OR = 0.62, 95% CI, 0.40 to 0.95), all-cause mortality (OR = 0.64, 95% CI, 0.58 to 0.70), and 3P-MACE (composite endpoint of MI, stroke, and CV death) (OR = 0.69, 95% CI, 0.53 to 0.89) were significantly reduced in bDMARD users, which were mainly driven by the risk reduction in patients with rheumatoid arthritis (RA). TNF-

conclusionsThe use of bDMARDs might be associated with the reduced risks of CV events, especially in patients with RA. The CV events might be less frequent in bDMARD users with TNF-

Indexed as

Antirheumatic AgentsArthritis, RheumatoidCardiovascular DiseasesCardiovascular SystemHeart FailureHumansInflammationLupus Erythematosus, SystemicMyocardial InfarctionOdds RatioPsoriasisRandomized Controlled Trials as TopicResearch DesignRiskRisk FactorsStrokeAntirheumatic AgentsTumor Necrosis Factor-alpha

Identifiers

PMID34504395
PMCPMC8423578
OpenAlexW3196805922

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.