期刊文献+

卡泊三醇对白癜风患者血清和皮肤组织中IL-18及IFN-γ水平的影响 被引量:3

Effects of Calcipotriol on the Levels of IL-18 and IFN-γ in Serum and Skin of Patients with Leucoderma
原文传递
导出
摘要 目的:探讨卡泊三醇对白癜风患者血清和皮肤组织中IL-18及IFN-γ水平的影响。方法:收集我院收治的白癜风患者122例,随机分为实验组和对照组。对照组予外用补骨脂酊治疗,实验组给予外用卡泊三醇软膏。观察并比较两组患者治疗前后皮损面积、不良反应发生情况以及血清和皮肤组织液中IL-18及IFN-γ水平的变化情况。结果:与治疗前相比,两组患者治疗后白斑皮损面积均显著缩小(P<0.05),血清及皮肤组织液IL-8与INF-γ水平均明显降低(P<0.05)。与对照组相比,实验组治疗后白斑皮损面积更小(P<0.05),血清及皮肤组织液IL-18及IFN-γ含量较低(P<0.05)。结论:卡泊三醇能够有效改善白癜风患者的临床症状,且安全性较高,值得临床推广应用,这可能与其降低白癜风患者血清及皮肤组织液中IL-18及IFN-γ水平有关。 Objective:To investigate the effect of calcipotriol on the levels of IL-18 and IFN-γ in serum and skin tissue of patients with leucoderma.Methods:122 patients with leucoderma who were treated in our hospital were selected and randomly divided into the control group and the experimental group.The patients in the control group were treated with the external vaseline,while the patients in the experimental group were treated with calcipotriol.Then the skin lesion areas,incidence of adverse reactions and levels of IL-18 and IFN-γ in serum and skin tissue of both groups were observed and compared before and after the treatment.Results:Compared with before treatment,the leukoplakia lesions areas of both groups significantly reduced(P0.05),the levels of IL-8 and INF-γ in serum and skin tissue obviously decreased in both groups after the treatment(P0.05).Compared with the control group,the leukoplakia lesions area were smaller in the experimental group after the treatment(P0.05),and the levels of IL-8 and INF-γ in serum and skin tissue were lower in the experimental group(P0.05).Conclusions:Calcipotriol could effectively improve the clinical syptom of patients with leucoderma and had high safety,which might be related to the decrease of IL-18 and IFN-γ levels in serum and skin tissue.
出处 《现代生物医学进展》 CAS 2016年第6期1150-1152,1130,共4页 Progress in Modern Biomedicine
基金 辽宁省自然科学基金项目(2040736)
关键词 卡泊三醇 白癜风 白介素-18 Γ干扰素 皮损面积 Calcipotriol Leucoderma IL-18 IFN-γ Skin lesions area
  • 相关文献

参考文献20

  • 1Ken C F, Chang C C, Wen L, et al. Biochemical characterization of a functional recombinant aryl-alcohol dehydrogenase from Taiwan of ungus camphorata[J]. Botanical Studies, 2014, 55(2): 195-200.
  • 2Liu C P, Dai C A, Chao C Y, et al. Novel proton exchange membrane based on cross linked poly (vinyl alcohol) for direct methanol fuel cells[J]. Journal of Power Sources, 2014, 249(1): 285-298.
  • 3Hsieh C H, Li-Ting S U, Wang Y C, et al. Does alcohol intoxication protect patients from severe injury and reduce hospital mortality? The association of alcohol consumption with the severity of injury and survival in trauma patients[J]. Am Surg, 2013, 79(12): 1289-1294.
  • 4Kil H S, Cho H Y, Lee S J, et al. Alternative synthesis for the preparation of 16- [(18) F]fluoroestradiol [J]. Journal of Labelled Compounds, 2013, 56(12): 619-626.
  • 5Wiener C. Association of smokeless tobacco use and smoking in adolescents in the United States [J]. Journal of the American Dental Association, 2013, 144(8): 930-938.
  • 6Morita K, Saruwatari J, Miyagawa H, et al. Association between aldehyde dehydrogenase 2 polymorphisms and the incidence of diabetic retinopathy among Japanese subjects with type 2 diabetes mellitus[J]. Cardiovascular Diabetology, 2013, 12(7): 247-258.
  • 7Ansari W E, Sebena R, Stock C. Socio-demographic correlates of six indicators of alcohol consumption: survey findings of students across seven universities in England, Wales and Northern Ireland [J]. Archives of Public Health, 2013, 71(1): 29.
  • 8Quigg z, Hughes K, Bellis M A. Student drinking patterns and blood alcohol concentration on commercially organised pub crawls in the UK[J]. Addictive Behaviors,2013,38( 12): 2924-2929.
  • 9Kahler C W, Metrik J, Spillane N S, et al. Acute effects of low and high dose alcohol on smoking lapse behavior in a laboratory analogue task[J]. Psychopharmacology,2014,231(24): 4649-4657.
  • 10Borra s E, Albalat R, Duester G, et al. The Xenopus alcohol dehydrogenase gene family: characterization and comparative analysis ineorpomting amphibian and reptilian genomes [J]. Bmc G-enomics, 2014, 15(13): 216.

同被引文献49

引证文献3

二级引证文献21

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部