Serum neopterin level in psoriatic patients treated with acitretin or narrowband ultraviolet B or both

E. Hegazy, M. E. El Taieb, Abd A. M. Eliew, Ali Younis, Ahmed K. Ibrahim, Fatma E. A. Elfatah, H. Ibrahim
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Abstract

A biological indicator of cellular immunity is neopterin. In certain studies, psoriasis patients had higher serum, and urine neopterin levels, which were reduced following therapy. To evaluate the effect of acitretin versus narrowband ultraviolet B (NB-UVB) and combinations of them on psoriasis vulgaris and correlate it with neopterin level In this case-control research, a total of 120 respondents (30 healthy volunteers) served as the control group, in addition to 90 psoriasis patients randomly allocated into three equal groups: group (I): 30 patients received Acitretin for 3 months. Group (II): 30 patients were treated with NB-UVB. Group (III): 30 patients received Acitretin and NB-UVB (3 sessions/week) for 3 months. Serum neopterin levels were measured pre- and post-treatment. All patients were clinically and photographically evaluated using the Psoriasis Area and Severity Index (PASI) score. The study was registered at clinicaltrial.com. Approval numbers: NCT05401006 and date of registration: 1/6/2022. In this study, statistically significant higher serum neopterin levels have been found in psoriatic patients than healthy controls. We found a significant decrease in PASI scores in all groups. The relative reduction percentage in the PASI score was substantially different between groups (P<0.001). The highest decrease percentage in PASI score was reported in group III compared with group II (NB-UVB) and group I (Acitretin group), (P<0.001). The median s. neopterin levels after treatment varied substantially among the three groups (P<0.001). When compared with healthy controls, serum neopterin levels in psoriatic patients were substantially greater (P<0.05).
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接受阿昔曲汀或窄带紫外线 B 或两者治疗的银屑病患者的血清蝶呤水平
细胞免疫的一个生物指标是新蝶呤。在某些研究中,银屑病患者血清和尿液中的新蝶呤水平较高,但在治疗后有所降低。 评估阿曲汀与窄带紫外线 B(NB-UVB)及其组合对寻常型银屑病的影响,并将其与新蝶呤水平联系起来 在这项病例对照研究中,共有 120 名受访者(30 名健康志愿者)作为对照组,此外还有 90 名银屑病患者被随机分配到三个相同的组别:组(I):30名患者接受阿曲汀治疗3个月。第二组30名患者接受NB-UVB治疗。第三组30 名患者接受阿曲汀和 NB-UVB 治疗(每周 3 次),为期 3 个月。测量治疗前后的血清蝶呤水平。使用银屑病面积和严重程度指数(PASI)对所有患者进行临床和照片评估。该研究已在 clinicaltrial.com 注册。批准号:NCT05401006 和注册日期:1/6/2022. 在这项研究中,我们发现银屑病患者的血清新蝶呤水平明显高于健康对照组。我们发现所有组别的 PASI 评分都有明显下降。各组间 PASI 评分的相对下降百分比差异很大(P<0.001)。与第二组(NB-UVB 组)和第一组(阿曲汀组)相比,第三组的 PASI 评分下降比例最高(P<0.001)。三组患者治疗后的中位蝶呤水平差异很大(P<0.001)。 与健康对照组相比,银屑病患者的血清蝶呤水平要高出很多(P<0.05)。
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