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左西替利嗪和孟鲁司特对慢性自身免疫性荨麻疹患者临床症状、血清水平及COX-1和COX-2酶皮肤表达的影响——一项初步研究

The effect of levocetirizine and montelukast on clinical symptoms, serum level and skin expression of COX-1 and COX-2 enzymes in patients suffering from chronic autoimmune urticaria - a pilot study.

作者信息

Korczyñska-Krawczyk Paulina, Kupryś-Lipiñska Izabela, Kupczyk Maciej, Wągrowska-Danilewicz Małgorzata, Szemraj Janusz, Bienias Wojciech, Narbutt Joanna, Śmigielski Janusz, Kuna Piotr

机构信息

Department of Internal Medicine, Asthma and Allergy, Norbert Barlicki Memorial University Hospital No. 1, Medical University of Lodz, Lodz, Poland.

Department of Nephropathology, Medical University of Lodz, Lodz, Poland.

出版信息

Postepy Dermatol Alergol. 2020 Feb;37(1):73-80. doi: 10.5114/ada.2018.79731. Epub 2018 Nov 23.

DOI:10.5114/ada.2018.79731
PMID:32467688
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7247068/
Abstract

INTRODUCTION

Chronic autoimmune urticaria (CAU) lasts over 6 weeks and is characterized by circulating IgE autoantibodies or IgG against IgE or IgE receptor.

AIM

To assess the clinical, laboratory and histological effects of 4-week levocetirizine and montelukast therapy in patients suffering from CAU.

MATERIAL AND METHODS

Of 296 tested patients with chronic urticaria 40 had a positive ASST test. Only 17 (16 female/1 male; medium age: 44 years) fulfilled all study inclusion/exclusion criteria. The study was designed as an open, randomized trial with two arms: levocetirizine or montelukast treatment for 4 weeks following a 2-week wash-out period. All participants completed urticaria activity score (UAS) and visual analogue scale (VAS) questionnaires before and after both therapies. Blood samples and skin bioptats were obtained before and after treatment to evaluate COX-1 and COX-2 serum concentrations and skin expression.

RESULTS

Clinical response to therapy measured with the UAS and VAS was better in the levocetirizine group. Both drugs caused a significant decrease in COX-1 and COX-2 serum level. COX-1 and COX-2 expression in epidermal and dermal inflammatory infiltration did not change significantly in either study group, but a significant decrease of COX-1 expression was observed when the groups were combined for analysis, and the decrease in COX-2 expression in the epidermis was of borderline significance.

CONCLUSIONS

The effectiveness of levocetirizine and montelukast in treating CAU may be partly related to the reduction of COX-1 and COX-2 serum level and tissue expression, but further studies on a larger group of patients are needed to support this observation.

摘要

引言

慢性自身免疫性荨麻疹(CAU)持续超过6周,其特征是存在针对IgE或IgE受体的循环IgE自身抗体或IgG。

目的

评估4周左西替利嗪和孟鲁司特治疗对CAU患者的临床、实验室及组织学影响。

材料与方法

在296例接受检测的慢性荨麻疹患者中,40例ASST试验呈阳性。仅有17例(16例女性/1例男性;平均年龄:44岁)符合所有研究纳入/排除标准。该研究设计为一项开放性随机试验,分为两组:经过2周洗脱期后,一组接受左西替利嗪治疗,另一组接受孟鲁司特治疗,为期4周。所有参与者在两种治疗前后均完成荨麻疹活动评分(UAS)和视觉模拟量表(VAS)问卷。在治疗前后采集血样和皮肤活检样本,以评估COX-1和COX-2的血清浓度及皮肤表达情况。

结果

用UAS和VAS衡量,左西替利嗪组的治疗临床反应更佳。两种药物均使COX-1和COX-2血清水平显著降低。在任一研究组中,表皮和真皮炎症浸润中的COX-1和COX-2表达均无显著变化,但在合并两组进行分析时,观察到COX-1表达显著降低,表皮中COX-2表达的降低具有临界显著性。

结论

左西替利嗪和孟鲁司特治疗CAU的有效性可能部分与COX-1和COX-2血清水平及组织表达的降低有关,但需要对更大规模的患者群体进行进一步研究以支持这一观察结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/41c136d130b2/PDIA-37-79731-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/bfb90af6fcc0/PDIA-37-79731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/d2e6bc45bf72/PDIA-37-79731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/22cd6a666665/PDIA-37-79731-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/e724fae85f79/PDIA-37-79731-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/41c136d130b2/PDIA-37-79731-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/bfb90af6fcc0/PDIA-37-79731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/d2e6bc45bf72/PDIA-37-79731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/22cd6a666665/PDIA-37-79731-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/e724fae85f79/PDIA-37-79731-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7247068/41c136d130b2/PDIA-37-79731-g005.jpg

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