Duration of psoriatic arthritis as a risk factor for myocardial infarction

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Duration of psoriatic arthritis as a risk factor for myocardial infarction. / Egeberg, Alexander; Skov, Lone; Hansen, Peter Riis; Gislason, Gunnar H.; Wu, Jashin J.; Thyssen, Jacob P.; Mallbris, Lotus.

In: Rheumatology Advances in Practice, Vol. 2, No. 1, 2018, p. 1-5.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Egeberg, A, Skov, L, Hansen, PR, Gislason, GH, Wu, JJ, Thyssen, JP & Mallbris, L 2018, 'Duration of psoriatic arthritis as a risk factor for myocardial infarction', Rheumatology Advances in Practice, vol. 2, no. 1, pp. 1-5. https://doi.org/10.1093/rap/rky011

APA

Egeberg, A., Skov, L., Hansen, P. R., Gislason, G. H., Wu, J. J., Thyssen, J. P., & Mallbris, L. (2018). Duration of psoriatic arthritis as a risk factor for myocardial infarction. Rheumatology Advances in Practice, 2(1), 1-5. https://doi.org/10.1093/rap/rky011

Vancouver

Egeberg A, Skov L, Hansen PR, Gislason GH, Wu JJ, Thyssen JP et al. Duration of psoriatic arthritis as a risk factor for myocardial infarction. Rheumatology Advances in Practice. 2018;2(1):1-5. https://doi.org/10.1093/rap/rky011

Author

Egeberg, Alexander ; Skov, Lone ; Hansen, Peter Riis ; Gislason, Gunnar H. ; Wu, Jashin J. ; Thyssen, Jacob P. ; Mallbris, Lotus. / Duration of psoriatic arthritis as a risk factor for myocardial infarction. In: Rheumatology Advances in Practice. 2018 ; Vol. 2, No. 1. pp. 1-5.

Bibtex

@article{f5437a72518a4f66b6244fbd6e6abd07,
title = "Duration of psoriatic arthritis as a risk factor for myocardial infarction",
abstract = "Objectives The aim was to examine the association between disease duration and risk of myocardial infarction (MI) in patients with PsA. Methods We used nationwide registry data from Denmark to estimate incidence rates per 1000 person-years and the risk of MI [adjusted hazard ratios (HRs) with 95% CIs] in rheumatologistdiagnosed patients with PsA using Cox regression models. The study period was between 1 January 2008 and 31 December 2012. Results The study population comprised a total of 8071 patients with PsA and 4 348 857 general population control subjects. A total of 156 and 54 215 MIs occurred during follow-up among patients with PsA and the reference population, respectively. There was a significant association between the duration of PsA and risk of MI (adjusted HR = 1.02; 95% CI: 1.01, 1.03 for each additional year after PsA diagnosis). Stratified based on short ( < 2 years) and long (≥2 years) disease duration, the adjusted HRs were 0.96 (95% CI: 0.60, 1.52; P=0.8487) and 1.29 (95% CI: 1.09, 1.53; P=0.0026), respectively. Other significant predictors included age, sex, socio-economic status, smoking, alcohol abuse, diabetes, hypertension and previous cardiovascular disease. Conclusions We observed an increased risk of MI associated with longer duration of PsA. Our findings call for increased focus on disease duration in the cardiovascular risk assessment among patients with PsA.",
keywords = "Cardiovascular risk, Epidemiology, Myocardial infarction, Psoriatic arthritis",
author = "Alexander Egeberg and Lone Skov and Hansen, {Peter Riis} and Gislason, {Gunnar H.} and Wu, {Jashin J.} and Thyssen, {Jacob P.} and Lotus Mallbris",
year = "2018",
doi = "10.1093/rap/rky011",
language = "English",
volume = "2",
pages = "1--5",
journal = "Rheumatology Advances in Practice",
issn = "2514-1775",
publisher = "Oxford University Press",
number = "1",

}

RIS

TY - JOUR

T1 - Duration of psoriatic arthritis as a risk factor for myocardial infarction

AU - Egeberg, Alexander

AU - Skov, Lone

AU - Hansen, Peter Riis

AU - Gislason, Gunnar H.

AU - Wu, Jashin J.

AU - Thyssen, Jacob P.

AU - Mallbris, Lotus

PY - 2018

Y1 - 2018

N2 - Objectives The aim was to examine the association between disease duration and risk of myocardial infarction (MI) in patients with PsA. Methods We used nationwide registry data from Denmark to estimate incidence rates per 1000 person-years and the risk of MI [adjusted hazard ratios (HRs) with 95% CIs] in rheumatologistdiagnosed patients with PsA using Cox regression models. The study period was between 1 January 2008 and 31 December 2012. Results The study population comprised a total of 8071 patients with PsA and 4 348 857 general population control subjects. A total of 156 and 54 215 MIs occurred during follow-up among patients with PsA and the reference population, respectively. There was a significant association between the duration of PsA and risk of MI (adjusted HR = 1.02; 95% CI: 1.01, 1.03 for each additional year after PsA diagnosis). Stratified based on short ( < 2 years) and long (≥2 years) disease duration, the adjusted HRs were 0.96 (95% CI: 0.60, 1.52; P=0.8487) and 1.29 (95% CI: 1.09, 1.53; P=0.0026), respectively. Other significant predictors included age, sex, socio-economic status, smoking, alcohol abuse, diabetes, hypertension and previous cardiovascular disease. Conclusions We observed an increased risk of MI associated with longer duration of PsA. Our findings call for increased focus on disease duration in the cardiovascular risk assessment among patients with PsA.

AB - Objectives The aim was to examine the association between disease duration and risk of myocardial infarction (MI) in patients with PsA. Methods We used nationwide registry data from Denmark to estimate incidence rates per 1000 person-years and the risk of MI [adjusted hazard ratios (HRs) with 95% CIs] in rheumatologistdiagnosed patients with PsA using Cox regression models. The study period was between 1 January 2008 and 31 December 2012. Results The study population comprised a total of 8071 patients with PsA and 4 348 857 general population control subjects. A total of 156 and 54 215 MIs occurred during follow-up among patients with PsA and the reference population, respectively. There was a significant association between the duration of PsA and risk of MI (adjusted HR = 1.02; 95% CI: 1.01, 1.03 for each additional year after PsA diagnosis). Stratified based on short ( < 2 years) and long (≥2 years) disease duration, the adjusted HRs were 0.96 (95% CI: 0.60, 1.52; P=0.8487) and 1.29 (95% CI: 1.09, 1.53; P=0.0026), respectively. Other significant predictors included age, sex, socio-economic status, smoking, alcohol abuse, diabetes, hypertension and previous cardiovascular disease. Conclusions We observed an increased risk of MI associated with longer duration of PsA. Our findings call for increased focus on disease duration in the cardiovascular risk assessment among patients with PsA.

KW - Cardiovascular risk

KW - Epidemiology

KW - Myocardial infarction

KW - Psoriatic arthritis

U2 - 10.1093/rap/rky011

DO - 10.1093/rap/rky011

M3 - Journal article

C2 - 31431960

AN - SCOPUS:85063184044

VL - 2

SP - 1

EP - 5

JO - Rheumatology Advances in Practice

JF - Rheumatology Advances in Practice

SN - 2514-1775

IS - 1

ER -

ID: 222100640