CHU Nice, Department of Clinical Research and Innovation, Université Côte d'Azur, Nice, France.
CHU Nice, Department of Dermatology, Université Côte d'Azur, Nice, France.
J Eur Acad Dermatol Venereol. 2021 Aug;35(8):1725-1729. doi: 10.1111/jdv.17331. Epub 2021 May 13.
Despite a solid rationale, the usefulness of antioxidants in treating vitiligo has not been clearly demonstrated. Combining superoxide dismutase (SOD) with a wheat gliadin biopolymer protects it during the passage through the gastrointestinal tract.
To evaluate the efficacy of gliadin-protected SOD (GP-SOD), associated with narrowband ultraviolet B(NB-UVB), for treating vitiligo.
We conducted a 24-week monocentric interventional prospective randomized placebo-controlled trial in the tertiary center for vitiligo care in the department of Dermatology of Nice University hospital, Nice, France. Subjects with non-segmental vitiligo affecting more than 5% of the total body surface were included. The subjects received gliadin-protected SOD (GP-SOD; 1 g/day for 12 weeks followed by 0.5 g/day for 12 weeks) or placebo in combination with twice-weekly sessions of NB-UVB. The primary endpoint was the total repigmentation rate at 24 weeks, compared with baseline, as assessed by investigator-assessed Vitiligo Extent Score (VES) on standardized pictures.
A total of 50 patients were included. After 24 weeks, a greater improvement in VES was observed in the GP-SOD group (19.85%; SE 4.63, P < 0.0001) compared with the placebo group (8.83%; SE 4.72, P = 0.0676). Tolerance was good in both groups. No related side-effect was reported.
The use of GP-SOD appears to be a useful add-on to phototherapy in the treatment of vitiligo patients.
尽管有充分的理论依据,但抗氧化剂在治疗白癜风中的有效性尚未得到明确证实。将超氧化物歧化酶(SOD)与小麦谷蛋白生物聚合物结合使用可以在通过胃肠道时对其进行保护。
评估谷蛋白保护的 SOD(GP-SOD)与窄带紫外线 B(NB-UVB)联合治疗白癜风的疗效。
我们在法国尼斯大学医院皮肤科的白癜风治疗三级中心进行了一项为期 24 周的单中心干预性前瞻性随机安慰剂对照试验。纳入患有影响全身 5%以上面积的非节段性白癜风的受试者。受试者接受谷蛋白保护的 SOD(GP-SOD;1g/天,持续 12 周,然后 0.5g/天,持续 12 周)或安慰剂,同时每周两次接受 NB-UVB 治疗。主要终点是 24 周时与基线相比,研究者评估的白癜风范围和严重程度指数(VES)评估的总复色率。
共有 50 名患者入组。24 周后,GP-SOD 组 VES 改善更为显著(19.85%;SE 4.63,P<0.0001),而安慰剂组为 8.83%(SE 4.72,P=0.0676)。两组的耐受性均良好,均未报告相关不良反应。
GP-SOD 的使用似乎是白癜风患者光疗的一种有用的附加治疗方法。