Stanley Xavier Alphienes, Selvarajan Sandhiya, Chandrasekar Laxmisha, Kamalanathan Sadishkumar
Department of Pharmacology, Sri Ramachandra Institute of Higher Education and Research, Porur, Chennai, India.
Department of Clinical Pharmacology, JIPMER, Puducherry, India.
J Diet Suppl. 2020;17(4):415-428. doi: 10.1080/19390211.2019.1619009. Epub 2019 May 24.
Allergic contact dermatitis following exposure to is a chronic disease associated with frequent relapses and significant disturbance in the quality of life. The affected patients have lower circulating levels and decreased expression of IL-10. Hence, measures to increase its level may enhance the therapeutic outcome. The clinical trial was undertaken to evaluate the effect of cholecalciferol supplementation on treatment response and IL-10 level in dermatitis patients with vitamin D deficiency. A total of 72 patients were recruited and randomized to receive either cholecalciferol tablet 60,000 IU per week or matching placebo for 8 weeks with standard background treatment. Eczema Area Severity Index (EASI) and Dermatology Life Quality Index (DLQI) were assessed at baseline, 4 weeks, and 8 weeks while IL-10 and serum 25-hydroxyvitamin D levels were measured at baseline and 8 weeks. Levels of 25-hydroxyvitamin D and IL-10 showed a significant rise in both placebo and vitamin D groups following the intervention. The relatively higher increase in IL-10 level observed in the vitamin D group was statistically insignificant compared to placebo group. Significant reduction in EASI, as well as DLQI scores, was noted after 1 and 2 months, but the reduction in these scales was not significantly different between the groups. Cholecalciferol supplementation for 2 months did not reduce the disease severity in clinically diagnosed dermatitis patients. However, treatment initiation significantly improved plasma IL-10 levels after 2 months in both placebo and cholecalciferol groups.
接触[具体物质]后发生的过敏性接触性皮炎是一种慢性疾病,常伴有复发且严重影响生活质量。受影响的患者循环水平较低,白细胞介素-10(IL-10)表达减少。因此,提高其水平的措施可能会增强治疗效果。本临床试验旨在评估补充胆钙化醇对维生素D缺乏的[具体皮炎类型]皮炎患者治疗反应和IL-10水平的影响。共招募了72名患者,随机分为两组,一组每周服用60,000国际单位的胆钙化醇片,另一组服用匹配的安慰剂,为期8周,并给予标准背景治疗。在基线、4周和8周时评估湿疹面积严重程度指数(EASI)和皮肤病生活质量指数(DLQI),同时在基线和8周时测量IL-10和血清25-羟维生素D水平。干预后,安慰剂组和维生素D组的25-羟维生素D和IL-10水平均显著升高。与安慰剂组相比,维生素D组观察到的IL-10水平相对较高的升高在统计学上无显著差异。在1个月和2个月后,EASI以及DLQI评分均显著降低,但两组之间这些量表的降低无显著差异。补充胆钙化醇2个月并未降低临床诊断的[具体皮炎类型]皮炎患者的疾病严重程度。然而,在安慰剂组和胆钙化醇组中,治疗开始2个月后均显著改善了血浆IL-10水平。