Association of Benzodiazepine Receptor Agonist Use With Changes in Psoriasis Severity in Adult Population: A Population-Based Study

To date, it remains uncertain whether benzodiazepine receptor agonists (BZRAs) are aggravating factors even though these drugs can elevate the levels of biomarkers associated with the development of psoriasis. Therefore, this study aimed to investigate the association of BZRA use with changes in pso...

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Main Authors: Ke-Ting Pan, I-Hsun Li, Hui-Han Kao, Yi-Hsien Chen, Pei-Xun Zhong, Li-Ting Kao
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-07-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2021.596375/full
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author Ke-Ting Pan
Ke-Ting Pan
I-Hsun Li
I-Hsun Li
I-Hsun Li
Hui-Han Kao
Hui-Han Kao
Yi-Hsien Chen
Pei-Xun Zhong
Pei-Xun Zhong
Li-Ting Kao
Li-Ting Kao
Li-Ting Kao
Li-Ting Kao
author_facet Ke-Ting Pan
Ke-Ting Pan
I-Hsun Li
I-Hsun Li
I-Hsun Li
Hui-Han Kao
Hui-Han Kao
Yi-Hsien Chen
Pei-Xun Zhong
Pei-Xun Zhong
Li-Ting Kao
Li-Ting Kao
Li-Ting Kao
Li-Ting Kao
author_sort Ke-Ting Pan
collection DOAJ
description To date, it remains uncertain whether benzodiazepine receptor agonists (BZRAs) are aggravating factors even though these drugs can elevate the levels of biomarkers associated with the development of psoriasis. Therefore, this study aimed to investigate the association of BZRA use with changes in psoriasis severity. All data were sourced from the National Health Insurance system in Taiwan. We conducted a population-based retrospective cross-sectional study of 15,727 psoriasis patients who received BZRAs (BZRA users), and 18,856 psoriasis patients who did not receive BZRAs (nonusers). At least a 1-year washout period without any BZRA prescriptions was required. The main outcome was the change in psoriasis severity between before and after BZRA exposure. This study detected the exacerbation of psoriasis severity in mild psoriasis population by using a logistic model. Then, this study carried another logistic model among those patients who had severe psoriasis to calculate the odds ratios (ORs) for the improvement of the psoriasis severity. Among patients with mild psoriasis, BZRA users had a significantly higher probability of psoriasis severity exacerbation (IPTW-adjusted OR = 1.46). Mild psoriasis patients who received high and low doses of BZRAs had 1.70- and 1.39-fold higher probabilities of psoriasis severity exacerbation, respectively, than the non-users. Furthermore, in the severe psoriasis population, more low-dose BZRA users improved psoriasis severity than non-users. In conclusion, this study provided clinical evidence of the effects of BZRA use on patients with psoriasis severity. Among patients with mild psoriasis, high-dose BZRA users may be associated with the changes in psoriasis severity. However, low-dose BZRA exposure only slightly exacerbated disease severity among patients with mild psoriasis. Accordingly, clinicians should evaluate the risks and benefits of the BZRA usage.
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spelling doaj.art-48a3275d478042388b8cdac0c4117d872022-12-21T20:04:17ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122021-07-011210.3389/fphar.2021.596375596375Association of Benzodiazepine Receptor Agonist Use With Changes in Psoriasis Severity in Adult Population: A Population-Based StudyKe-Ting Pan0Ke-Ting Pan1I-Hsun Li2I-Hsun Li3I-Hsun Li4Hui-Han Kao5Hui-Han Kao6Yi-Hsien Chen7Pei-Xun Zhong8Pei-Xun Zhong9Li-Ting Kao10Li-Ting Kao11Li-Ting Kao12Li-Ting Kao13Institute of Environmental Design and Engineering, Bartlett School, UCL, London, United KingdomGraduate Institute of Aerospace and Undersea Medicine, National Defense Medical Centre, Taipei, TaiwanDepartment of Pharmacy Practice, Tri-Service General Hospital, Taipei, TaiwanSchool of Pharmacy, National Defense Medical Center, Taipei, TaiwanDepartment of Pharmacology, National Defense Medical Center, Taipei, TaiwanGraduate Institute of Life Sciences, National Defense Medical Center, Taipei, TaiwanScience and Technology Policy Research and Information Center, National Applied Research Laboratories, Taipei, TaiwanDepartment of Dermatology, Tri-Service General Hospital, National Defense Medical Center, Taipei, TaiwanDepartment of Pharmacy Practice, Tri-Service General Hospital, Taipei, TaiwanSchool of Pharmacy, National Defense Medical Center, Taipei, TaiwanDepartment of Pharmacy Practice, Tri-Service General Hospital, Taipei, TaiwanSchool of Pharmacy, National Defense Medical Center, Taipei, TaiwanGraduate Institute of Life Sciences, National Defense Medical Center, Taipei, TaiwanSchool of Public Health, National Defense Medical Center, Taipei, TaiwanTo date, it remains uncertain whether benzodiazepine receptor agonists (BZRAs) are aggravating factors even though these drugs can elevate the levels of biomarkers associated with the development of psoriasis. Therefore, this study aimed to investigate the association of BZRA use with changes in psoriasis severity. All data were sourced from the National Health Insurance system in Taiwan. We conducted a population-based retrospective cross-sectional study of 15,727 psoriasis patients who received BZRAs (BZRA users), and 18,856 psoriasis patients who did not receive BZRAs (nonusers). At least a 1-year washout period without any BZRA prescriptions was required. The main outcome was the change in psoriasis severity between before and after BZRA exposure. This study detected the exacerbation of psoriasis severity in mild psoriasis population by using a logistic model. Then, this study carried another logistic model among those patients who had severe psoriasis to calculate the odds ratios (ORs) for the improvement of the psoriasis severity. Among patients with mild psoriasis, BZRA users had a significantly higher probability of psoriasis severity exacerbation (IPTW-adjusted OR = 1.46). Mild psoriasis patients who received high and low doses of BZRAs had 1.70- and 1.39-fold higher probabilities of psoriasis severity exacerbation, respectively, than the non-users. Furthermore, in the severe psoriasis population, more low-dose BZRA users improved psoriasis severity than non-users. In conclusion, this study provided clinical evidence of the effects of BZRA use on patients with psoriasis severity. Among patients with mild psoriasis, high-dose BZRA users may be associated with the changes in psoriasis severity. However, low-dose BZRA exposure only slightly exacerbated disease severity among patients with mild psoriasis. Accordingly, clinicians should evaluate the risks and benefits of the BZRA usage.https://www.frontiersin.org/articles/10.3389/fphar.2021.596375/fullbenzodiazepine receptor agonistsbenzodiazepinepsoriasisseveritysafety
spellingShingle Ke-Ting Pan
Ke-Ting Pan
I-Hsun Li
I-Hsun Li
I-Hsun Li
Hui-Han Kao
Hui-Han Kao
Yi-Hsien Chen
Pei-Xun Zhong
Pei-Xun Zhong
Li-Ting Kao
Li-Ting Kao
Li-Ting Kao
Li-Ting Kao
Association of Benzodiazepine Receptor Agonist Use With Changes in Psoriasis Severity in Adult Population: A Population-Based Study
Frontiers in Pharmacology
benzodiazepine receptor agonists
benzodiazepine
psoriasis
severity
safety
title Association of Benzodiazepine Receptor Agonist Use With Changes in Psoriasis Severity in Adult Population: A Population-Based Study
title_full Association of Benzodiazepine Receptor Agonist Use With Changes in Psoriasis Severity in Adult Population: A Population-Based Study
title_fullStr Association of Benzodiazepine Receptor Agonist Use With Changes in Psoriasis Severity in Adult Population: A Population-Based Study
title_full_unstemmed Association of Benzodiazepine Receptor Agonist Use With Changes in Psoriasis Severity in Adult Population: A Population-Based Study
title_short Association of Benzodiazepine Receptor Agonist Use With Changes in Psoriasis Severity in Adult Population: A Population-Based Study
title_sort association of benzodiazepine receptor agonist use with changes in psoriasis severity in adult population a population based study
topic benzodiazepine receptor agonists
benzodiazepine
psoriasis
severity
safety
url https://www.frontiersin.org/articles/10.3389/fphar.2021.596375/full
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