瘦素基因rs2167270多态性与特应性皮炎相关。

Dermato-Endocrinology Pub Date : 2018-03-26 eCollection Date: 2018-01-01 DOI:10.1080/19381980.2018.1454191
Saleem A Banihani, Rawan A Elmadhoun, Omar F Khabour, Karem H Alzoubi
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引用次数: 13

摘要

特应性皮炎是一种慢性炎症性皮肤病,由于复杂的环境、免疫和遗传相互作用而产生。脂肪因子是由白色脂肪组织的脂肪细胞分泌的生物活性介质,已知在机体代谢和免疫反应调节中起作用。瘦素是一种促炎脂肪因子,主要作用是调节食物摄入和能量消耗。很少有研究表明脂肪因子与特应性皮炎的发病机制有关。在本研究中,我们研究了3个瘦素基因多态性:-2548G>A (rs7799039)、-188 C/A (rs791620)和A19G (rs2167270)与特应性皮炎发病率的关系。164名患者和167名年龄和性别匹配的对照组使用聚合酶链反应-限制性片段长度多态性程序进行基因分型。rs2167270与特应性皮炎发病率有显著相关性(P < 0.05)。GG等位基因在患者组更为普遍,基因型频率为38.7%,而对照组为26.1%。另外2个被检多态性rs7799039和rs791620的基因型分布和等位基因频率在特应性皮炎患者与对照组之间无显著差异(P > 0.05)。提示rs2167270可能在特应性皮炎发病机制中发挥作用。
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The rs2167270 polymorphism of leptin gene is associated with atopic dermatitis.

Atopic dermatitis is a chronic inflammatory skin disease that arises because of complex environmental, immunological, and genetic interactions. Adipokines are bioactive mediators secreted from adipocytes of white adipose tissue and are known to have a role in body metabolism and regulation of immune responses. Leptin is a proinflammatory adipokine that functions mainly to regulate food intake and energy expenditure. Few studies have implicated adipokines in the pathogenesis of atopic dermatitis. In this study, we investigated the association of three leptin gene polymorphisms: -2548G>A (rs7799039), -188 C/A (rs791620), and A19G (rs2167270), with the incidence of atopic dermatitis. One hundred and sixty-four patients and one hundred and sixty-seven age- and gender-matched controls were genotyped using the polymerase chain reaction-restriction fragment length polymorphism procedure. A significant association was found between rs2167270 and the incidence of atopic dermatitis (P < 0.05). The GG allele was more prevalent in the patients' group with genotype frequency of 38.7%, compared to 26.1% for the control group. No significant differences were found in the genotype distribution or allelic frequency of the other two examined polymorphisms, rs7799039 and rs791620, between atopic dermatitis patients and controls (P > 0.05). The results suggest that rs2167270 might play a role in the pathogenesis of atopic dermatitis.

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