The potential impact of systemic anti-inflammatory therapies in psoriasis on major adverse cardiovascular events: a Korean nationwide cohort study

Abstract This nationwide population-based cohort study aimed to investigate the impact of systemic anti-inflammatory treatment on the major adverse cardiovascular events (MACE) risk in patients with psoriasis from January 2006 to December 2018, using a database provided by the Korean National Health...

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Autores principales: Joo Ran Hong, Hojin Jeong, Hyeongsu Kim, Hyun Suk Yang, Ji Youn Hong, Sung Min Kim, Young Ah Cho, Yang Won Lee, Yong Beom Choe, Kyu Joong Ahn
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spelling oai:doaj.org-article:067715a19bb34e6a852907c3561050452021-12-02T18:27:48ZThe potential impact of systemic anti-inflammatory therapies in psoriasis on major adverse cardiovascular events: a Korean nationwide cohort study10.1038/s41598-021-87766-y2045-2322https://doaj.org/article/067715a19bb34e6a852907c3561050452021-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-87766-yhttps://doaj.org/toc/2045-2322Abstract This nationwide population-based cohort study aimed to investigate the impact of systemic anti-inflammatory treatment on the major adverse cardiovascular events (MACE) risk in patients with psoriasis from January 2006 to December 2018, using a database provided by the Korean National Health Insurance Service. Patients were grouped based on the following treatment modalities: biologics, phototherapy, methotrexate, cyclosporine, and mixed conventional systemic agents. Patients who had not received any systemic treatment were assigned to the control cohort. The incidence of MACE per 1000 person-year was 3.5, 9.3, 12.1, 28.4, 39.5, and 14.5 in the biologic, phototherapy, methotrexate, cyclosporine, mixed conventional systemic agents, and control cohorts, respectively. During the 36-month follow-up, the cumulative incidence of MACE in the phototherapy and biologic cohorts remained lower than that of other treatment modalities. Cyclosporine (hazard ratio (HR) = 2.11, 95% confidence interval (CI) = 1.64–2.71) and mixed conventional systemic agents (HR = 2.57, 95% CI = 2.05–3.22) treatments were associated with increased MACE risk. Methotrexate treatment was not associated with MACE. Our finding demonstrates that treatment modalities may affect cardiovascular comorbidities in patients with psoriasis. Thus, an appropriate combination of anti-psoriatic therapies should be considered to manage patients with high cardiovascular risk. IRB approval status: Waiver decision was obtained by the institutional review board, Konkuk University Hospital, Seoul, Republic of Korea (KUH1120107).Joo Ran HongHojin JeongHyeongsu KimHyun Suk YangJi Youn HongSung Min KimYoung Ah ChoYang Won LeeYong Beom ChoeKyu Joong AhnNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Joo Ran Hong
Hojin Jeong
Hyeongsu Kim
Hyun Suk Yang
Ji Youn Hong
Sung Min Kim
Young Ah Cho
Yang Won Lee
Yong Beom Choe
Kyu Joong Ahn
The potential impact of systemic anti-inflammatory therapies in psoriasis on major adverse cardiovascular events: a Korean nationwide cohort study
description Abstract This nationwide population-based cohort study aimed to investigate the impact of systemic anti-inflammatory treatment on the major adverse cardiovascular events (MACE) risk in patients with psoriasis from January 2006 to December 2018, using a database provided by the Korean National Health Insurance Service. Patients were grouped based on the following treatment modalities: biologics, phototherapy, methotrexate, cyclosporine, and mixed conventional systemic agents. Patients who had not received any systemic treatment were assigned to the control cohort. The incidence of MACE per 1000 person-year was 3.5, 9.3, 12.1, 28.4, 39.5, and 14.5 in the biologic, phototherapy, methotrexate, cyclosporine, mixed conventional systemic agents, and control cohorts, respectively. During the 36-month follow-up, the cumulative incidence of MACE in the phototherapy and biologic cohorts remained lower than that of other treatment modalities. Cyclosporine (hazard ratio (HR) = 2.11, 95% confidence interval (CI) = 1.64–2.71) and mixed conventional systemic agents (HR = 2.57, 95% CI = 2.05–3.22) treatments were associated with increased MACE risk. Methotrexate treatment was not associated with MACE. Our finding demonstrates that treatment modalities may affect cardiovascular comorbidities in patients with psoriasis. Thus, an appropriate combination of anti-psoriatic therapies should be considered to manage patients with high cardiovascular risk. IRB approval status: Waiver decision was obtained by the institutional review board, Konkuk University Hospital, Seoul, Republic of Korea (KUH1120107).
format article
author Joo Ran Hong
Hojin Jeong
Hyeongsu Kim
Hyun Suk Yang
Ji Youn Hong
Sung Min Kim
Young Ah Cho
Yang Won Lee
Yong Beom Choe
Kyu Joong Ahn
author_facet Joo Ran Hong
Hojin Jeong
Hyeongsu Kim
Hyun Suk Yang
Ji Youn Hong
Sung Min Kim
Young Ah Cho
Yang Won Lee
Yong Beom Choe
Kyu Joong Ahn
author_sort Joo Ran Hong
title The potential impact of systemic anti-inflammatory therapies in psoriasis on major adverse cardiovascular events: a Korean nationwide cohort study
title_short The potential impact of systemic anti-inflammatory therapies in psoriasis on major adverse cardiovascular events: a Korean nationwide cohort study
title_full The potential impact of systemic anti-inflammatory therapies in psoriasis on major adverse cardiovascular events: a Korean nationwide cohort study
title_fullStr The potential impact of systemic anti-inflammatory therapies in psoriasis on major adverse cardiovascular events: a Korean nationwide cohort study
title_full_unstemmed The potential impact of systemic anti-inflammatory therapies in psoriasis on major adverse cardiovascular events: a Korean nationwide cohort study
title_sort potential impact of systemic anti-inflammatory therapies in psoriasis on major adverse cardiovascular events: a korean nationwide cohort study
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/067715a19bb34e6a852907c356105045
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