Risk of Developing Hypertension in Atopic Dermatitis Patients Receiving Long-term and Low-dose Cyclosporine: A Nationwide Population-based Cohort Study

被引:0
作者
Woo, Yu Ri [1 ]
Choi, Arum [2 ]
Song, Seo Won [3 ]
Kim, Suyeun [1 ]
Son, Sang Wook [4 ]
Cho, Sang Hyun [1 ,4 ]
Kim, Sukil [2 ,6 ]
Kim, Jung Eun [3 ,5 ]
机构
[1] Catholic Univ Korea, Incheon St Marys Hosp, Coll Med, Dept Dermatol, Incheon St, Seoul, South Korea
[2] Catholic Univ Korea, Coll Med, Dept Prevent Med & Publ Hlth, Seoul, South Korea
[3] Catholic Univ Korea, Eunpyeong St Marys Hosp, Coll Med, Dept Dermatol, Eunpyeong St, Seoul, South Korea
[4] Korea Univ, Coll Med, Dept Dermatol, Seoul, South Korea
[5] Catholic Univ Korea, Eunpyeong St Marys Hosp, Coll Med, Dept Dermatol, 1021 Tongil Ro, Seoul 03312, South Korea
[6] Catholic Univ Korea, Coll Med, Dept Prevent Med & Publ Hlth, 222 Banpo Daero, Seoul 06591, South Korea
关键词
Atopic dermatitis; Cyclosporine; Dose-response relationship; drug; Hypertension; Risk; CONSENSUS GUIDELINES; EFFICACY; SAFETY; MECHANISM;
D O I
10.5021/ad.23.099
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Cyclosporine (CS) is a first-line immunosuppressive agent used to manage moderate to severe atopic dermatitis (AD). To date, the risk of developing hypertension associated with the long-term use of low-dose CS in AD patients is understudied. Objective: To determine the cumulative dose-dependent effect of CS on the risk of developing hypertension in patients with AD. Methods: A nationwide population-based retrospective cohort with 1,844,009 AD patients was built from the Korean National Health Insurance System database from 2005 to 2009. A Cox proportional-hazard regression analysis was performed according to patients' CS treatment history adjusted for potential confounders. Results: Current use of CS was associated with an increased risk of developing hypertension (adjusted hazard ratio, 4.442; 95% confidence interval, 3.761-5.247). Among the current CS users, a higher cumulative dose of CS (>= 39,725 mg) or longer cumulative use of CS (>= 182 days), was significantly associated with an increased risk of developing hypertension. Conclusion: The incidence of CS-associated hypertension is very low when using low-dose treatment regimens for AD. However, the current use or a high cumulative dose of CS for treating patients with AD increases the risk of developing hypertension. Precaution is needed when prescribing CS for long-term treatment of AD.
引用
收藏
页码:112 / 119
页数:8
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