File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Cardiovascular risk in patients with spondyloarthritis and association with anti-TNF drugs

TitleCardiovascular risk in patients with spondyloarthritis and association with anti-TNF drugs
Authors
Keywordscardiovascular event
cerebrovascular event
myocardial infarction
spondyloarthritis
stroke
Issue Date2021
PublisherSAGE Publications: Open Access Journals. The Journal's web site is located at https://journals.sagepub.com/home/taba
Citation
Therapeutic Advances in Musculoskeletal Disease, 2021, v. 13 How to Cite?
AbstractBackground: Cardiovascular (CVS) diseases are the leading cause of death worldwide and patients with rheumatic diseases have an increased CVS. CVS risk factors and CVS events are common in spondyloarthritis (SpA). Delineating the CVS risk in patients with SpA and identifying modifiable risk factors would be useful. Methods: Patients with SpA and patients with non-specific back pain (NSBP) were identified in rheumatology and orthopedics clinics, respectively. Clinical information and CVS events were retrieved. Baseline characteristics and incidence rates of CVS events were compared between two groups of patients using an age- and sex-matched cohort. Propensity score adjustment and Cox regression analysis were performed to determine the CVS risk associated with SpA. Results: A total of 5046 patients (SpA 2616 and NSBP 2430) were included from eight centers. Over 56,484 person-years of follow up, 160 strokes, 84 myocardial infarction (MI) and 262 major adverse cardiovascular events (MACE) were identified. Hypercholesterolemia was more prevalent in SpA (SpA 34.2%, NSBP 28.7%, p < 0.01). Crude incidence rates of MACE and stroke were higher in SpA patients. SpA was associated with a higher risk of MACE [hazard ratio (HR) 1.70; 95% confidence interval (CI) 1.29–2.26; p < 0.01] and cerebrovascular events (HR 1.50; 95% CI 1.08–2.07; p = 0.02). SpA patients with anti-TNF use had a reduced risk of MACE (HR 0.37, 95%CI 0.17–0.80, p = 0.01) and cerebrovascular events (HR 0.21, 95%CI 0.06–0.78, p = 0.02) compared with SpA patients without anti-TNF use. Conclusion: SpA is an independent CVS risk factor. Anti-tumor necrosis factor (TNF) drugs were associated with a reduced CVS risk in these patients.
Persistent Identifierhttp://hdl.handle.net/10722/301397
ISSN
2021 Impact Factor: 3.625
2020 SCImago Journal Rankings: 1.387
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChan, SCW-
dc.contributor.authorTeo, CK-
dc.contributor.authorLi, PH-
dc.contributor.authorLau, KK-
dc.contributor.authorLau, CS-
dc.contributor.authorChung, HY-
dc.date.accessioned2021-07-27T08:10:27Z-
dc.date.available2021-07-27T08:10:27Z-
dc.date.issued2021-
dc.identifier.citationTherapeutic Advances in Musculoskeletal Disease, 2021, v. 13-
dc.identifier.issn1759-720X-
dc.identifier.urihttp://hdl.handle.net/10722/301397-
dc.description.abstractBackground: Cardiovascular (CVS) diseases are the leading cause of death worldwide and patients with rheumatic diseases have an increased CVS. CVS risk factors and CVS events are common in spondyloarthritis (SpA). Delineating the CVS risk in patients with SpA and identifying modifiable risk factors would be useful. Methods: Patients with SpA and patients with non-specific back pain (NSBP) were identified in rheumatology and orthopedics clinics, respectively. Clinical information and CVS events were retrieved. Baseline characteristics and incidence rates of CVS events were compared between two groups of patients using an age- and sex-matched cohort. Propensity score adjustment and Cox regression analysis were performed to determine the CVS risk associated with SpA. Results: A total of 5046 patients (SpA 2616 and NSBP 2430) were included from eight centers. Over 56,484 person-years of follow up, 160 strokes, 84 myocardial infarction (MI) and 262 major adverse cardiovascular events (MACE) were identified. Hypercholesterolemia was more prevalent in SpA (SpA 34.2%, NSBP 28.7%, p < 0.01). Crude incidence rates of MACE and stroke were higher in SpA patients. SpA was associated with a higher risk of MACE [hazard ratio (HR) 1.70; 95% confidence interval (CI) 1.29–2.26; p < 0.01] and cerebrovascular events (HR 1.50; 95% CI 1.08–2.07; p = 0.02). SpA patients with anti-TNF use had a reduced risk of MACE (HR 0.37, 95%CI 0.17–0.80, p = 0.01) and cerebrovascular events (HR 0.21, 95%CI 0.06–0.78, p = 0.02) compared with SpA patients without anti-TNF use. Conclusion: SpA is an independent CVS risk factor. Anti-tumor necrosis factor (TNF) drugs were associated with a reduced CVS risk in these patients.-
dc.languageeng-
dc.publisherSAGE Publications: Open Access Journals. The Journal's web site is located at https://journals.sagepub.com/home/taba-
dc.relation.ispartofTherapeutic Advances in Musculoskeletal Disease-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectcardiovascular event-
dc.subjectcerebrovascular event-
dc.subjectmyocardial infarction-
dc.subjectspondyloarthritis-
dc.subjectstroke-
dc.titleCardiovascular risk in patients with spondyloarthritis and association with anti-TNF drugs-
dc.typeArticle-
dc.identifier.emailTeo, CK: tkc299@HKUCC-COM.hku.hk-
dc.identifier.emailLi, PH: liphilip@hku.hk-
dc.identifier.emailLau, KK: gkklau@hku.hk-
dc.identifier.emailLau, CS: cslau@hku.hk-
dc.identifier.emailChung, HY: jameschy@hku.hk-
dc.identifier.authorityLi, PH=rp02669-
dc.identifier.authorityLau, KK=rp01499-
dc.identifier.authorityLau, CS=rp01348-
dc.identifier.authorityChung, HY=rp02330-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1177/1759720X211032444-
dc.identifier.scopuseid_2-s2.0-85111399219-
dc.identifier.hkuros323647-
dc.identifier.volume13-
dc.identifier.isiWOS:000688106800001-
dc.publisher.placeUnited Kingdom-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats