Kemeriz Funda, Gönül Müzeyyen, Cengiz Fatma Pelin, Emiroğlu Nazan, Cemil Bengü Çevirgen
Department of Dermatology, Aksaray University Faculty of Medicine, Aksaray, Turkey.
Department of Dermatology, Dıskapı Research and Training Hospital, Ankara, Turkey.
Indian J Dermatol. 2019 Nov-Dec;64(6):447-450. doi: 10.4103/ijd.IJD_53_18.
Neopterin is a biochemical marker of cellular immunity. It has been reported that serum and urine neopterin levels increase in psoriasis and decrease with treatment. Nevertheless, assessment of a direct link between narrowband ultraviolet B (UVB) therapy and neopterin level in association with Psoriasis Area and Severity Index (PASI) scores has not been performed yet. We aimed to evaluate the serum neopterin level in patients with psoriasis treated with narrowband UVB therapy in association with disease severity.
The study included 35 patients with chronic plaque-type psoriasis who had PASI scores of >10 or below 10 but resistant to topical therapies and 30 healthy individuals. The narrowband UVB therapy was administered to the patient group ( = 35). Serum neopterin analysis was performed with an enzyme-linked immunosorbent assay method before and after treatment.
There was statistically significant correlation between neopterin level and PASI score in the patient group ( = 0.011). The serum neopterin level was significantly increased in patients with higher PASI score. Moreover, the serum neopterin level was found to be statistically higher in severe psoriasis group (PASI score ≥10, = 14) than the mild-moderate group (PASI score <10, = 21) ( = 0.001). Furthermore, a significant decrease was observed according to serum neopterin level after the narrowband UVB therapy in the remaining 20 patients who were able to comply with the scheduled therapy and follow-up procedure ( = 0.026).
Serum neopterin levels were found to be an useful marker for evaluating disease severity and efficacy of narrowband UVB treatment. Thus, our findings may provide a new approach with the management of disease and follow-up strategies in patients with psoriasis.
新蝶呤是细胞免疫的生化标志物。据报道,银屑病患者血清和尿液中的新蝶呤水平会升高,且随治疗而降低。然而,尚未对窄谱中波紫外线(UVB)疗法与新蝶呤水平之间的直接联系以及银屑病面积和严重程度指数(PASI)评分进行评估。我们旨在评估接受窄谱UVB治疗的银屑病患者血清新蝶呤水平与疾病严重程度之间的关系。
该研究纳入了35例慢性斑块型银屑病患者,其PASI评分>10或低于10但对局部治疗耐药,以及30名健康个体。对患者组(n = 35)进行窄谱UVB治疗。治疗前后采用酶联免疫吸附测定法进行血清新蝶呤分析。
患者组中新蝶呤水平与PASI评分之间存在统计学显著相关性(r = 0.011)。PASI评分较高的患者血清新蝶呤水平显著升高。此外,重度银屑病组(PASI评分≥10,n = 14)的血清新蝶呤水平在统计学上高于轻度 - 中度组(PASI评分<10,n = 21)(p = 0.001)。此外,在其余20例能够遵守预定治疗和随访程序的患者中,窄谱UVB治疗后血清新蝶呤水平显著下降(p = 0.026)。
血清新蝶呤水平被发现是评估疾病严重程度和窄谱UVB治疗疗效的有用标志物。因此,我们的研究结果可能为银屑病患者的疾病管理和随访策略提供一种新方法。