维生素D补充剂改善慢性自发性荨麻疹患者的荨麻疹症状和生活质量:一项前瞻性病例对照研究

Dermato-Endocrinology Pub Date : 2014-10-31 eCollection Date: 2016-01-01 DOI:10.4161/derm.29727
Tadech Boonpiyathad, Panitan Pradubpongsa, Atik Sangasapaviriya
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引用次数: 31

摘要

维生素D在免疫系统中起着重要作用;血清维生素D浓度降低与免疫功能失调有关。低维生素D状态可能与慢性自发性荨麻疹(CSU)有关。我们对60名CSU患者和40名健康人进行了一项前瞻性病例对照研究,评估了维生素D水平低的患病率,以及补充维生素D后的临床反应和生活质量。在基线和6周后测定血清25-羟基维生素D (25(OH)D)浓度。对于25(OH)D浓度< 30 ng/ml的患者,治疗包括20,000 IU/天麦角钙化醇(维生素D2)和非镇静抗组胺药物,持续6周。根据7天以上荨麻疹活动评分(UAS7)和皮肤科生活质量指数(DLQI)评估荨麻疹症状严重程度和生活质量。在100名参与者中,73%是女性;平均年龄39±16岁。CSU组维生素D缺乏症(25(OH)D < 20 ng/ml)显著高于对照组。CSU组25(OH)D浓度中位数为15 (7 ~ 52)ng/ml,显著低于对照组30 (25 ~ 46)ng/ml。总体而言,83%(50/60)的CSU患者(25(OH)D < 30 ng/ml)接受麦角钙化醇(维生素D2)补充治疗;6周后,与未补充维生素D组相比,这些患者的UAS7和DLQI评分有显著改善。该研究揭示了血清25(OH)D浓度较低与CSU的显著关联。维生素D补充剂可能改善CSU患者的症状和生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vitamin D supplements improve urticaria symptoms and quality of life in chronic spontaneous urticaria patients: A prospective case-control study.

Vitamin D supplements improve urticaria symptoms and quality of life in chronic spontaneous urticaria patients: A prospective case-control study.

Vitamin D supplements improve urticaria symptoms and quality of life in chronic spontaneous urticaria patients: A prospective case-control study.

Vitamin D supplements improve urticaria symptoms and quality of life in chronic spontaneous urticaria patients: A prospective case-control study.

Vitamin D plays an important role in the immune system; decreased serum vitamin D concentrations have been linked to dysregulated immune function. Low vitamin D status is probably associated with chronic spontaneous urticaria (CSU). We evaluated the prevalence of low vitamin D status, and the clinical response and quality of life following vitamin D supplementation, in a prospective case-control study with 60 CSU patients and 40 healthy individuals. Serum 25-hydroxy vitamin D (25(OH)D) concentrations were measured at baseline and after 6 weeks. For patients with 25(OH)D concentrations < 30 ng/ml, treatment included 20,000 IU/day of ergocalciferol (vitamin D2) and non-sedative antihistamine drugs for 6 weeks. Urticaria symptom severity and quality of life were assessed based on the Urticaria Activity Score over 7 days (UAS7) and the Dermatology Life Quality Index (DLQI). Of the 100 participants, 73% were female; the mean age was 39 ± 16 years. Vitamin D deficiency (measured as 25(OH)D < 20 ng/ml) was significantly higher in the CSU group than the control group. The median 25(OH)D concentration for the CSU group, 15 (7 - 52) ng/ml was significantly lower than for control group, 30 (25 - 46) ng/ml. Overall, 83% (50/60) of CSU patients (25(OH)D < 30 ng/ml) were treated with ergocalciferol (vitamin D2) supplementation; after 6 weeks, these patients showed significant improvements in UAS7 and DLQI scores compared with the non-vitamin D supplement group. This study revealed a significant association of lower serum 25(OH)D concentrations with CSU. Vitamin D supplements might improve symptoms and quality of life in CSU patients.

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