Association between cardio‐cerebrovascular disease and systemic antipsoriatic therapy in psoriasis patients using population‐based data: A nested case–control study

Author:

Kim Bo Ri12ORCID,Lee Kun Hee3ORCID,Kim Jinseob4ORCID,Kim Jee Woo12ORCID,Paik Kyungho12ORCID,Myung Woojae56ORCID,Lee Hyewon78ORCID,Choi Chong Won12ORCID,Youn Sang Woong12ORCID

Affiliation:

1. Department of Dermatology Seoul National University Bundang Hospital Seongnam Republic of Korea

2. Department of Dermatology Seoul National University College of Medicine Seoul Republic of Korea

3. Department of Applied Statistics Yonsei University Seoul Republic of Korea

4. Zarathu Co., Ltd. Seoul Republic of Korea

5. Department of Neuropsychiatry Seoul National University Bundang Hospital Seongnam Republic of Korea

6. Department of Psychiatry Seoul National University College of Medicine Seoul Republic of Korea

7. Department of Health Administration and Management, College of Medical Sciences Soonchunhyang University Asan Republic of Korea

8. Department of Software Convergence Soonchunhyang University Graduate School Asan Republic of Korea

Abstract

AbstractThe effect of antipsoriatic therapy on cardio‐cerebrovascular disease (CCVD) is not well described. Thus, we performed a population‐based nested case–control study to investigate the effect of systemic antipsoriatic therapy on CCVD in psoriasis patients. Using nationwide cohort data from the Korean National Health Insurance Claims database, newly diagnosed psoriasis patients were identified. Among the enrolled participants, postenrollment development of CCVD events (ischemic heart disease, myocardial infarction, cerebral infarction, and cerebral hemorrhage) was investigated. To evaluate the effect of systemic antipsoriatic therapy on CCVD risk, we calculated the proportion of the treatment period with systemic antipsoriatic therapy during the study period (PTP [%]: the sum of all systemic antipsoriatic therapy durations divided by total observation period). Among 251 813 participants, 6262 experienced CCVD events during the study period (CCVD group). Controls included 245 551 patients without CCVD history during the study period (non‐CCVD group). The non‐CCVD group had greater PTP than the CCVD group (CCVD 2.12 ± 7.92, non‐CCVD 2.64 ± 9.64; P < 0.001). In multiple logistic regression analysis, PTP was inversely associated with the CCVD risk after adjusting for age, sex, diabetes, hypertension, and dyslipidemia. A 10% increase in PTP reduced CCVD risk by 0.96 (95% confidence interval 0.93 to 0.99). Reduced CCVD risk was robust for both conventional antipsoriatic therapy and biologics. Our study found that systemic antipsoriatic therapy use was inversely associated with CCVD risk in psoriasis patients. These findings suggested that systemic antipsoriatic therapy could reduce CCVD development in patients with psoriasis.

Publisher

Wiley

Subject

Dermatology,General Medicine

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