Gohar Maha K, Atta Amal H, Nasr Mohamed M, Hussein Doaa N
Department of Medical Microbiology & Immunology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Department of Dermatology & Venereology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Egypt J Immunol. 2017 Jun;24(2):9-22.
Atopic dermatitis (AD) is a worldwide chronic inflammation of skin.Many factors and chemokines play role in pathogenesis of AD. Identifying the reliable biomarkers to diagnose and assess severity of AD is important. In this study we aimed to find a reliable biomarker to determine the severity of AD and monitor treatment as well as, examining the possible association between IL-18 gene [rs 187238] promoter polymorphism and AD disease. The study included 30 Egyptian patients with AD and 30 healthy controls. Patients were clinically evaluated according to SCORAD scoring system. For each subject levels of Thymus and activation regulated chemokine (TARC), IL-18, total IgE and Lactate dehydrogenase enzyme (LDH) in serum were measured and Polymorphism in IL-18 gene was analyzed using restriction fragment length polymorphism (RFLP). Patients were reevaluated after treatment. Serum levels of TARC, IL-18, IgE and LDH were significantly higher in patients than controls, and were associated with high SCORAD score. G allele was risk factor with OR 2.31 (1.10- 4.85) and significant p-value < 0.05 for AD. GG genotype was significantly associated with elevated serum levels of TARC, IL-18 and IgE. After treatment serum level of TARC showed significant decrease and was associated with low SCORAD score. We concluded that TARC, IL-18, total IgE and LDH are potential markers of severity in AD. G allele in IL-18 gene [rs 187238] is risk factor for AD while C allele is considered protective. TARC is also a reliable marker formonitoring treatment.
特应性皮炎(AD)是一种全球性的皮肤慢性炎症。许多因素和趋化因子在AD的发病机制中起作用。确定可靠的生物标志物以诊断和评估AD的严重程度很重要。在本研究中,我们旨在寻找一种可靠的生物标志物来确定AD的严重程度并监测治疗,同时研究白细胞介素-18基因[rs 187238]启动子多态性与AD疾病之间的可能关联。该研究包括30名埃及AD患者和30名健康对照。根据SCORAD评分系统对患者进行临床评估。测量每个受试者血清中的胸腺和活化调节趋化因子(TARC)、白细胞介素-18、总IgE和乳酸脱氢酶(LDH)水平,并使用限制性片段长度多态性(RFLP)分析白细胞介素-18基因的多态性。治疗后对患者进行重新评估。患者血清中TARC、白细胞介素-18、IgE和LDH水平明显高于对照组,且与高SCORAD评分相关。G等位基因是AD的危险因素,OR为2.31(1.10 - 4.85),p值<0.05具有统计学意义。GG基因型与血清TARC、白细胞介素-18和IgE水平升高显著相关。治疗后血清TARC水平显著下降,并与低SCORAD评分相关。我们得出结论,TARC、白细胞介素-18、总IgE和LDH是AD严重程度的潜在标志物。白细胞介素-18基因[rs 187238]中的G等位基因是AD的危险因素,而C等位基因被认为具有保护作用。TARC也是监测治疗的可靠标志物。