Chang Y-C, Wu W-M, Chen C-H, Lee S-H, Hong H-S, Hsu L-A
Department of Dermatology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, No. 199, Tung-Hwa North Road, Taipei, Taiwan.
Br J Dermatol. 2007 Apr;156(4):642-5. doi: 10.1111/j.1365-2133.2006.07716.x. Epub 2007 Jan 30.
BACKGROUND: Genetic factors play an important role in susceptibility for psoriasis. The angiotensin I-converting enzyme (ACE) is expressed by keratinocytes. Administration of ACE inhibitors may induce or exacerbate psoriasis in clinical practice. Thus, ACE gene variants may contribute to the genetic background of psoriasis. OBJECTIVES: To assess the role of the ACE insertion/deletion (I/D) polymorphism in psoriasis among ethnically Chinese Taiwanese subjects. METHODS: In total, 312 patients with psoriasis and 615 control subjects were analysed for the ACE I/D polymorphism by polymerase chain reaction. RESULTS: A marginally significant difference (P=0 x 035) was found in the distribution of ACE I/D genotype frequencies between patients with psoriasis and controls. The frequency of the II genotype in patients with psoriasis was significantly higher than that in the control group (55 x 1% vs. 46 x 7%, respectively, P=0 x 015). Although the I allele frequency in patients with psoriasis (72 x 4%) was higher than that in the control group (68 x 2%), the difference was not significantly different (P=0 x 062). After adjusting for age and gender, carriers of the II genotype were 1 x 45 (95% confidence interval 1 x 09-1 x 92) times more likely than noncarriers to have psoriasis (P=0 x 010). CONCLUSIONS: Our results suggest that the presence of the I allele may confer susceptibility to development of psoriasis among ethnically Chinese Taiwanese individuals.
背景:遗传因素在银屑病易感性中起重要作用。血管紧张素I转换酶(ACE)由角质形成细胞表达。在临床实践中,使用ACE抑制剂可能诱发或加重银屑病。因此,ACE基因变异可能与银屑病的遗传背景有关。 目的:评估ACE插入/缺失(I/D)多态性在台湾汉族人群银屑病中的作用。 方法:采用聚合酶链反应对312例银屑病患者和615例对照者进行ACE I/D多态性分析。 结果:银屑病患者与对照者之间ACE I/D基因型频率分布存在边缘显著差异(P = 0.035)。银屑病患者中II基因型频率显著高于对照组(分别为55.1%和46.7%,P = 0.015)。虽然银屑病患者中I等位基因频率(72.4%)高于对照组(68.2%),但差异无统计学意义(P = 0.062)。在调整年龄和性别后,II基因型携带者患银屑病比非携带者高1.45倍(95%置信区间1.09 - 1.92)(P = 0.010)。 结论:我们的结果表明,I等位基因的存在可能使台湾汉族个体易患银屑病。
J Renin Angiotensin Aldosterone Syst. 2013-7-11
Clin Cosmet Investig Dermatol. 2024-11-11
Dermatol Ther (Heidelb). 2023-9
Br J Pharmacol. 2020-8
J Clin Aesthet Dermatol. 2010-1