Cited 12 times in
Effect of tumor necrosis factor inhibitors on risk of cardiovascular disease in patients with axial spondyloarthritis
DC Field | Value | Language |
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dc.contributor.author | 권오찬 | - |
dc.contributor.author | 박민찬 | - |
dc.date.accessioned | 2022-08-23T00:11:59Z | - |
dc.date.available | 2022-08-23T00:11:59Z | - |
dc.date.issued | 2022-06 | - |
dc.identifier.issn | 1478-6354 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/189306 | - |
dc.description.abstract | Background: Axial spondyloarthritis (axSpA) is associated with an increased risk of cardiovascular disease. We aimed to evaluate the effect of tumor necrosis factor inhibitors (TNFis) on the risk of cardiovascular disease in patients with axSpA. Methods: This retrospective study included 450 patients with axSpA without pre-existing cardiovascular disease. The outcome was incident cardiovascular disease (myocardial infarction or stroke) after the diagnosis of axSpA. The effect of TNFis on cardiovascular risk was analyzed in the total study population and in an inverse probability of treatment weighting (IPTW)-adjusted population. Cox proportional hazards models were used to estimate the hazard ratios (HRs) and 95% confidence intervals (95% CIs) for cardiovascular disease, according to exposure to TNFis. Results: Of the 450 patients, 233 (51.8%) and 217 (48.2%) patients were and were not exposed to TNFis, respectively. Twenty cardiovascular diseases occurred during 2868 person-years of follow-up (incidence rate: 6.97/1000 person-years). In the total study population, exposure to TNFis was associated with a reduced cardiovascular risk when adjusted for traditional cardiovascular risk factors (HR 0.30, 95% CI 0.10-0.85, p = 0.024). However, when time-averaged erythrocyte sedimentation rate and C-reactive protein were additionally adjusted, this association was attenuated and lost statistical significance (HR 0.37, 95% CI 0.12-1.12, p = 0.077). Furthermore, in the IPTW-adjusted population, exposure to TNFis showed no significant reduction in cardiovascular risk (HR 0.60, 95% CI 0.23-1.54, p = 0.287). Conclusions: Although controlling inflammation through TNFis could be beneficial in cardiovascular risk reduction, our data indicate no TNFi-specific reduction in cardiovascular risk in patients with axSpA. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | BioMed Central | - |
dc.relation.isPartOf | ARTHRITIS RESEARCH & THERAPY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Axial Spondyloarthritis* | - |
dc.subject.MESH | Cardiovascular Diseases* / epidemiology | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Spondylarthritis* / complications | - |
dc.subject.MESH | Spondylarthritis* / drug therapy | - |
dc.subject.MESH | Spondylitis, Ankylosing* | - |
dc.subject.MESH | Tumor Necrosis Factor Inhibitors / therapeutic use | - |
dc.subject.MESH | Tumor Necrosis Factor-alpha | - |
dc.title | Effect of tumor necrosis factor inhibitors on risk of cardiovascular disease in patients with axial spondyloarthritis | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | Oh Chan Kwon | - |
dc.contributor.googleauthor | Min-Chan Park | - |
dc.identifier.doi | 10.1186/s13075-022-02836-4 | - |
dc.contributor.localId | A05818 | - |
dc.contributor.localId | A01470 | - |
dc.relation.journalcode | J00241 | - |
dc.identifier.eissn | 1478-6362 | - |
dc.identifier.pmid | 35698171 | - |
dc.subject.keyword | Axial spondyloarthritis | - |
dc.subject.keyword | Cardiovascular risk | - |
dc.subject.keyword | Inflammation | - |
dc.subject.keyword | Tumor necrosis factor inhibitor | - |
dc.contributor.alternativeName | Kwon, Oh Chan | - |
dc.contributor.affiliatedAuthor | 권오찬 | - |
dc.contributor.affiliatedAuthor | 박민찬 | - |
dc.citation.volume | 24 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 141 | - |
dc.identifier.bibliographicCitation | ARTHRITIS RESEARCH & THERAPY, Vol.24(1) : 141, 2022-06 | - |
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