Głażewska Edyta K, Niczyporuk Marek, Przylipiak Andrzej, Szmitkowski Maciej, Zajkowska Monika, Będkowska Ewa, Terlikowski Robert, Ławicki Sławomir
Department of Esthetic Medicine, Medical University of Bialystok, Bialystok, Poland.
Department of Biochemical Diagnostics, Medical University of Bialystok, Bialystok, Poland.
Postepy Dermatol Alergol. 2017 Aug;34(4):328-333. doi: 10.5114/ada.2017.69312. Epub 2017 Aug 1.
Matrix metalloproteinase-12 (MMP-12) may play an important role in the pathogenesis and spread of psoriatic disease.
To investigate plasma levels of the selected enzyme in plaque psoriasis patients before and after the course of narrowband UVB (NBUVB) therapy with respect to disease advancement.
The cohort included 49 patients suffering from plaque psoriasis, divided into groups according to severity of the disease. The control group consisted of 40 healthy volunteers. Plasma levels of MMP-12 were determined using immunoenzyme assay (ELISA), while the Psoriasis Area and Severity Index (PASI) was used to define disease advancement.
The results have shown a significantly decreased plasma level of MMP-12 in the total psoriasis patient group compared to healthy individuals, declining with the increase in disease advancement. The NBUVB therapy caused a decrease in the concentration of the analyzed enzyme, but this change was not statistically significant in the total group of psoriatic patients, while a significant change was detected in patients with a mild advancement of the disease.
Decreased synthesis of MMP-12 may lead to the stimulation of the epidermal angiogenesis process, which results in the appearance and spread of psoriatic scales. Based on the obtained results, macrophage metalloelastase seems to be a negatively reacting plasma biomarker of the studied disease.
基质金属蛋白酶-12(MMP-12)可能在银屑病的发病机制和扩散过程中发挥重要作用。
研究斑块状银屑病患者在窄谱中波紫外线(NBUVB)治疗前后血浆中该特定酶的水平与疾病进展的关系。
该队列包括49例斑块状银屑病患者,根据疾病严重程度分组。对照组由40名健康志愿者组成。采用免疫酶测定法(ELISA)测定血浆中MMP-12的水平,同时使用银屑病面积和严重程度指数(PASI)来定义疾病进展。
结果显示,与健康个体相比,银屑病患者总体组血浆中MMP-12水平显著降低,且随疾病进展加剧而下降。NBUVB治疗导致所分析酶的浓度降低,但在银屑病患者总体组中这一变化无统计学意义,而在疾病轻度进展的患者中检测到显著变化。
MMP-12合成减少可能会刺激表皮血管生成过程,从而导致银屑病鳞屑的出现和扩散。基于所得结果,巨噬细胞金属弹性蛋白酶似乎是所研究疾病的一种呈负反应的血浆生物标志物。