Deo Sudha S, Bhagat Ameya R, Shah Rajnikant N
Department of Immunology, Sir. H.N. Medical Research Society, Girgaum, Mumbai, Maharashtra, India.
Department of Immunology, Sir. H.N. Hospital and Research Centre, Girgaum, Mumbai, Maharashtra, India.
Indian Dermatol Online J. 2013 Oct;4(4):279-82. doi: 10.4103/2229-5178.120637.
Vitiligo is an acquired skin disease that involves the interplay of complex genetic, immunological, neural and self-destructive mechanisms in its pathogenesis. According to autocytotoxic hypothesis, oxidative stress has been suggested to be the initial pathogenic event in melanocyte degeneration.
The aim of our investigation was to evaluate the role of oxidative stress by studying the role of catalase (CAT) in the destruction of melanocytes in patients with vitiligo and compare the same in healthy normal controls.
We determined the serum catalase enzyme by ELISA method. The catalase activity was studied in two groups, Group I-localized vitiligo: (i) active stage, (ii) static or inactive stage and Group II-generalized vitiligo: (i) active stage, (ii) static or inactive stage patients, and the levels were compared with healthy controls.
Group I active stage patients showed significant difference in the catalase levels with a P < 0.044 when compared with healthy controls, whereas Group II static stage patients did not show any significant difference (P < 0.095) although the catalase activity was increased.
Our study could not explain the cause of melanocyte damage in patients in the active stage of the disease. The increase in the oxidative stress as detected by catalase activity was more significant in Group I active disease than Group II active disease patients although the levels were higher than the healthy normals. This is the first study conducted on active and static stage of vitilgo in India. It is possible that the number of compounds of hydrogen peroxide produced is not balanced by the production of catalase in the body.
白癜风是一种获得性皮肤病,其发病机制涉及复杂的遗传、免疫、神经和自我破坏机制的相互作用。根据自身细胞毒性假说,氧化应激被认为是黑素细胞变性的初始致病事件。
我们研究的目的是通过研究过氧化氢酶(CAT)在白癜风患者黑素细胞破坏中的作用来评估氧化应激的作用,并与健康正常对照组进行比较。
我们采用ELISA法测定血清过氧化氢酶。在两组中研究过氧化氢酶活性,第一组为局限性白癜风:(i)活动期,(ii)静止或非活动期;第二组为泛发性白癜风:(i)活动期,(ii)静止或非活动期患者,并将其水平与健康对照组进行比较。
第一组活动期患者与健康对照组相比,过氧化氢酶水平有显著差异,P<0.044,而第二组静止期患者虽然过氧化氢酶活性增加,但未显示出任何显著差异(P<0.095)。
我们的研究无法解释疾病活动期患者黑素细胞损伤的原因。尽管过氧化氢酶活性检测到的氧化应激水平高于健康正常人,但第一组活动期疾病患者比第二组活动期疾病患者的氧化应激增加更为显著。这是印度首次对白癜风活动期和静止期进行的研究。体内产生的过氧化氢化合物数量可能与过氧化氢酶的产生不平衡。