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中国临床药理学与治疗学 ›› 2019, Vol. 24 ›› Issue (4): 458-463.doi: 10.12092/j.issn.1009-2501.2019.04.015

• 药物治疗学 • 上一篇    下一篇

复方甘草酸苷对PPD患者抗菌肽LL-37的表达及临床预后的影响

宋 欣,王 雪,周黄红,赵天一   

  1. 丽水市中心医院皮肤性病科,丽水 323000,浙江
  • 收稿日期:2018-08-09 修回日期:2019-03-17 出版日期:2019-04-26 发布日期:2019-05-01
  • 作者简介:宋欣,女,副主任医师,研究方向:病毒性皮肤病,色素性皮肤病、银屑病。 E-mail:zhubang055@163.com
  • 基金资助:

    浙江省卫生和计划生育委员会医药卫生科技计划项目(2018PR905)

Effect of compound glycyrrhizin on the expression and clinical prognosis of antibacterial peptide LL-37 in patients with pigmentary purpuric skin disease

SONG Xin, WANG Xue, ZHOU Huanghong, ZHAO Tianyi   

  1. Department of Dermatology Diseases,Lishui Central Hospital, Lishui 323000, Zhejiang, China
  • Received:2018-08-09 Revised:2019-03-17 Online:2019-04-26 Published:2019-05-01

摘要:

目的:观察复方甘草酸苷对着色紫癜性皮肤病(pigmented purpuric dermatosis,PPD)患者抗菌肽LL-37的表达及其对患者临床预后的影响。方法:选取本院2015年4月到2018年4月间收治的54例PPD患者为研究对象,随机抽签将其分为观察组和对照组,每组27例,另外选取30例正常受试者作为正常组。对照组口服甲泼尼龙片、皮损处涂抹氟芬那酸丁酯软膏进行治疗;观察组在此基础上给予口服复方甘草酸苷片治疗;正常组不做任何治疗处理,1个月后进行观察评价。比较观察组和对照组患者的疗效、不良反应发生率及复发率,比较三组血清中LL-37水平与皮损处LL-37水平以及三组血清TNF-α、IL-6、IL-17炎性因子水平。结果:治疗前,观察组和对照组患者血清LL-37水平、皮损处LL-37水平以及血清TNF-α、IL-6、IL-17水平比较无明显差异(P>0.05),治疗后,两组患者血清LL-37水平、皮损处LL-37水平与血清TNF-α、IL-6、IL-17水平均显著降低(P<0.05),且观察组血清LL-37水平、皮损处LL-37水平与血清TNF-α、IL-6、IL-17水平均明显低于对照组(P<0.05)。观察组治疗有效率为70.37%,显著高于对照组51.85%(P<0.05);观察组不良反应发生率为18.52%,略低于对照组33.33%,但差异无统计学意义(P>0.05);观察组复发率为11.11%,略低于对照组18.52%,但差异无统计学意义(P>0.05)。结论:复方甘草酸苷能够降低PPD患者体内抗菌肽LL-37的表达水平,减轻炎性反应,同时不良反应发生率和复发率更低,疗效及安全性更佳,值得临床推广。

关键词: 复方甘草酸苷, 着色紫癜性皮肤病, LL-37, 临床疗效

Abstract:

AIM:To study the therapeutic effect and the antimicrobial peptide LL-37 level of compound glycyrrhizin in patients with pigmented purpuric dermatosis(PPD). METHODS:A total of 54 patients with PPD admitted to our hospital from April 2015 to April 2018 were enrolled in the study.They were randomly divided into observation group and control group,27 cases in each group,and 30 normal subjects were selected as a normal group.In the control group,oral methylprednisolone tablets and butyl flufenamate ointment were applied to the skin lesions;the observation group was given oral compound glycyrrhizin tablets;the normal group was not treated, and after 1 month,the evaluation was observed.The efficacy,adverse reaction rate and recurrence rate of the observation group and the control group were compared.The LL-37 level in serum of the three groups and the LL-37 level in skin lesions and the TNF-α,IL-6 and IL-17 levels in serum of the three groups were compared.RESULTS:Before treatment,there was no significant difference about the LL-37 level in serum and the LL-37 level in skin lesions and the TNF-α,IL-6 and IL-17 levels in serum between the observation group and the control group(P>0.05).After treatment,the LL-37 level in serum and the LL-37 level in skin lesions and the TNF-α,IL-6 and IL-17 levels in serum were decreased in both groups(P<0.05).The levels of TNF-α,IL-6 and IL-17 in observation group were significantly lower than those of the control group(P<0.05).Before and after treatment,serum LL-37 levels,skin LL-37 levels,and TNF-α,IL-6,and IL-17 levels were significantly higher in the observation group and the control group than those in the normal group (P<0.05).The effective rate of treatment in the observation group was 70.37%,which was significantly higher than that in the control group(51.85%) (P<0.05).The incidence of adverse reactions in the observation group was 18.52%,which was slightly lower than that in the control group(33.33%),but the difference was not statistically significant (P>0.05).The recurrence rate in the observation group was 11.11%,which was slightly lower than that in the control group 18.52%,but the difference was not Statistically significant (P>0.05).CONCLUSION:Compound glycyrrhizin can reduce the expression level of antibacterial peptide LL-37 in patients with pigmentary purpuric skin disease,reduce the inflammatory response,and the incidence of adverse reactions and recurrence rate is lower,the efficacy and safety are better,it is worthy of clinical promotion.

Key words: compound glycyrrhizin, pigmented purpuric skin disease, LL-37, clinical efficacy

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