Amr K, Abdel-Hameed M, Sayed K, Nour-Edin F, Abdel Hay R
Molecular Genetics, National Research Centre, Cairo, Egypt.
Clin Exp Dermatol. 2014 Aug;39(6):741-5. doi: 10.1111/ced.12394. Epub 2014 Jul 1.
Acne vulgaris is a multifactorial disease of the skin. Several studies have shown that sebocyte proliferation and/or lipogenesis, as well as inflammatory reactions, may be regulated by peroxisome proliferator-activated receptor (PPAR)γ-mediated pathways.
To investigate whether the Pro12Ala polymorphism of the PPARγ gene might be associated with the risk of acne, and to assess the effect of this polymorphism on acne severity.
This case-control study enrolled 100 patients with acne and 100 apparently healthy subjects. The clinical grade of acne was assessed using the Global Acne Grading System. We used PCR to identify the presence of the Pro12Ala polymorphism in exon 2 of PPARγ.
Our results revealed a statistically significant difference (P = 0.001) in the genotype distribution between patients and controls, with higher incidence of the Pro/Ala genotype in controls (51%) than in patients (28%). A statistically significant association (P < 0.001) between disease severity and genotype distribution was found, indicating that the Pro/Ala genotype is less prevalent in patients with severe acne.
Our results suggest that that the Ala allele might be a protective factor against acne development or may attenuate acne severity.
寻常痤疮是一种皮肤多因素疾病。多项研究表明,皮脂腺细胞增殖和/或脂肪生成以及炎症反应可能受过氧化物酶体增殖物激活受体(PPAR)γ介导的途径调控。
研究PPARγ基因Pro12Ala多态性是否可能与痤疮风险相关,并评估该多态性对痤疮严重程度的影响。
这项病例对照研究纳入了100例痤疮患者和100名明显健康的受试者。使用全球痤疮分级系统评估痤疮的临床分级。我们采用聚合酶链反应(PCR)来鉴定PPARγ基因第2外显子中Pro12Ala多态性的存在情况。
我们的结果显示,患者与对照组之间的基因型分布存在统计学显著差异(P = 0.001),对照组中Pro/Ala基因型的发生率(51%)高于患者组(28%)。发现疾病严重程度与基因型分布之间存在统计学显著关联(P < 0.001),表明Pro/Ala基因型在重度痤疮患者中不太常见。
我们的结果表明,Ala等位基因可能是预防痤疮发生的保护因素,或者可能减轻痤疮的严重程度。