愈尔敏汤治疗风湿热型慢性自发性荨麻疹疗效观察及对血清免疫指标的影响
DOI:
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

R758.24

基金项目:

四川省中医药管理局科学技术研究专项(2023MS579)


Observation on the Efficacy of Yu'ermin Decoction for Chronic Spontaneous Urticaria of Wind-Damp-Heat Type and Its Effect on Serum Immune Markers
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    目的:观察愈尔敏汤治疗风湿热型慢性自发性荨麻疹的临床疗效及对血清免疫指标的影响。方法: 选择2023年11月—2024年7月在古蔺县中医医院皮肤科就诊的风湿热型慢性自发性荨麻疹患者72例,按照随 机数字表法分为治疗组和对照组各36例。对照组采用氯雷他定片治疗,治疗组采用氯雷他定片联合愈尔敏汤 治疗。治疗4周,随访2周。评价2组临床疗效,比较2组治疗前后7天荨麻疹活动度评分(UAS7)、瘙痒视觉 模拟评分法(VAS) 评分、皮肤病生活质量指数(DLQI) 评分、血清免疫学指标[血清白细胞介素(IL) -17A、 IL-23、IL-33、肿瘤坏死因子-α(TNF-α)、γ-干扰素(IFN-γ)] 水平变化。结果:治疗后,治疗组总有效率为 94.44%(34/36),对照组为83.33% (30/36),2组比较,差异有统计学意义(P<0.05)。重复测量方差分析显 示,UAS7评分方面,组别、时间及交互效应均有显著性差异(P<0.05);治疗组各时间点及相邻时间点均较 前下降(P<0.05),对照组随访第2周与第1周无差异(P>0.05),而治疗第2周、随访第2周治疗组评分更 低(P<0.05)。2组瘙痒VAS评分均呈现显著下降趋势,组间、时间及交互效应均有显著性(P<0.05)。治疗 组VAS评分由(8.44±1.13) 分下降至(1.94±1.01) 分,各时间点均较治疗前下降(P<0.05);对照组VAS评 分亦由(8.28±0.94) 分下降至(3.08±1.38) 分,各时间点均较治疗前下降(P<0.05),但降幅小于治疗组。在 治疗第1周、随访第1周及随访第2周时,治疗组VAS评分低于对照组(P<0.05)。DLQI评分中,2组DLQI评 分均呈下降趋势,存在显著时间效应(P<0.05) 和组间效应(P<0.05),但组别×时间交互作用不显著(P> 0.05)。治疗组平均DLQI 评分从(25.08±3.41) 分下降至(5.31±2.07) 分,对照组从(24.72±2.94) 分下降 至(7.83±2.83) 分,2组各时间点均较治疗前显著下降(P<0.05);在治疗第3、4周及随访第1、2周时,治疗 组DLQI评分显著低于对照组,差异有统计学意义(P<0.05)。治疗后,治疗组IFN-γ水平较治疗前升高(P< 0.05), IL-33、IL-17A、IL-23、TNF-α 水平均较治疗前下降(P<0.05); 对照组IFN-γ 水平较治疗前升 高(P<0.05),IL-23、IL-33、TNF-α水平较治疗前下降(P<0.05),IL-17A水平治疗前后变化无统计学意 义(P>0.05)。治疗后,治疗组IL-17A水平低于对照组(P<0.05);IL-33、IL-23、TNF-α水平组间比较,差 异无统计学意义(P>0.05)。结论:氯雷他定片联合愈尔敏汤治疗风湿热型慢性自发性荨麻疹,可减轻患者临 床症状,调节免疫失衡,提高患者生活质量。

    Abstract:

    Abstract: Objective: To observe the clinical efficacy of Yu'ermin Decoction in the treatment of patients with chronic spontaneous urticaria (CSU) of wind-damp-heat type and its effect on serum immune markers. Methods:A total of 72 CSU patients of wind-damp-heat type who visited the Dermatology Department of Gulin County Hospital of Traditional Chinese Medicine from November 2023 to July 2024 were randomly divided into the treatment group and the control group (36 cases each). The control group received Loratadine Tablets alone; the treatment group received Loratadine Tablets combined with Yu'ermin Decoction. Both groups were treated for four weeks and followed up for two weeks. Clinical efficacy, 7-day Urticaria Activity Score (UAS7), Visual Analogue Scale (VAS) for pruritus, Dermatology Life Quality Index (DLQI),and serum immune markers [serum levels of interleukin (IL)-17A,IL-23, IL-33, tumor necrosis factor- α(TNF- α), interferon- γ (IFN- γ)] were compared between the two groups after treatment. Results: After treatment, the total effective rate was 94.44% (34/36) in the treatment group and 83.33% (30/36) in the control group, with the difference being significant (P<0.05). Repeated-measures ANOVA showed significant differences in terms of UAS7 scores for group, time, and group × time interaction effects (P< 0.05);UAS7 scores at every time point and between each pair of adjacent time points in the treatment group decreased compared to before treatment( P<0.05). In the control group,there was no significant difference between week one and week two of follow-up (P>0.05). The treatment group demonstrated significantly lower scores than the control group only at the two-week treatment time point and the two-week follow-up point (P<0.05). Both groups exhibited a significant decreasing trend in VAS scores for pruritus,with statistically significant main effects of group,time,and group × time interaction (P<0.05). The treatment group's VAS scores decreased from 8.44 ± 1.13 to 1.94 ± 1.01, showing significant reductions at all time points compared to before treatment (P<0.05). The control group's VAS scores also decreased from 8.28 ± 0.94 to 3.08 ± 1.38,with significant reductions at all time points compared to before treatment (P<0.05),although the magnitude of decrease was smaller than that in the treatment group. The treatment group had significantly lower VAS scores than the control group at week one of treatment, and weeks one and two of follow-up( P<0.05). For DLQI scores,both groups showed a decreasing trend with significant main effects of time and group (P<0.05), but the group × time interaction was not significant (P>0.05). The mean DLQI score in the treatment group decreased from 25.08 ± 3.41 to 5.31 ± 2.07,while that in the control group decreased from 24.72 ± 2.94 to 7.83 ± 2.83. Scores at all time points were significantly lower than those before treatment in both groups (P<0.05). The treatment group had significantly lower DLQI scores than the control group at treatment weeks three and four,and follow-up weeks one and two (P<0.05). After treatment, IFN- γ levels in the treatment group were significantly increased compared to before treatment (P<0.05), while levels of IL-33, IL-17A, IL-23, and TNF- α were significantly decreased (P<0.05). In the control group,levels of IL-23,IL-33,and TNF-α decreased compared to before treatment (P<0.05),and IFN-γ levels increased compared to before treatment (P<0.05),but the change in IL-17A was not statistically significant (P>0.05). After treatment, the IL-17A levels in the treatment group were significantly lower than those in the control group (P<0.05), while the differences in IL-33, IL-23, and TNF-α between the two groups were not statistically significant (P>0.05). Conclusion: The combination of Loratadine Tablets and Yu'ermin Decoction in treating CSU of wind-damp-heat type can alleviate clinical symptoms, modulate immune imbalance,and improve patients' quality of life.

    参考文献
    相似文献
    引证文献
引用本文

金凤,赵发伦,汪宁,聂玉钗,黄关秀.愈尔敏汤治疗风湿热型慢性自发性荨麻疹疗效观察及对血清免疫指标的影响[J].新中医,2026,58(2):46-52

复制
分享
相关视频

文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2026-01-29
  • 出版日期:
文章二维码