Osmania University, Dept. of Genetics, Hyderabad, Andhra Pradesh, Hyd -12, India.
Eur J Dermatol. 2011 Mar-Apr;21(2):173-7. doi: 10.1684/ejd.2011.1279.
Vitiligo is a depigmenting skin disorder with profound heterogenity in its aetio-pathophysiology, and is associated with inter-individual variation in progression of disease. Angiotensin converting enzyme (ACE) is a regulator of renin angiotensin system (RAS) that plays an important role in the physiology of the vasculature, blood pressure, inflammation, adipocyte distribution of various diseases. The present study was carried out in 243 vitiligo patients (132 males and 111 females), aged between 3-62 years with a mean age at onset of 21.6 ± 13.6 yrs, and in 205 healthy controls of south Indian origin. The main objectives of the present study were to evaluate the ACE I/D (insertion/deletion) polymorphism in the patient and control groups. Further, I/D genotypes were compared among the patients with and without the family history of vitiligo as well as the progression of the disease, through polymerase chain reaction (PCR) methods.
The results revealed a highly significant association of DD genotype with disease susceptibility (p < 0.01) in patients with a family history of vitiligo (p < 0.05) in terms of early age at onset. Further, the pre-dominance of ID genotype among patients revealed its association with a slow progression of the disease (p < 0.05). The present study is the first report to highlight the protective role of II genotype and the significant association of ID genotype with slow progression of the disease.
白癜风是一种色素脱失性皮肤病,其发病机制存在明显异质性,与疾病进展的个体间差异有关。血管紧张素转换酶(ACE)是肾素-血管紧张素系统(RAS)的调节剂,在血管生理学、血压、炎症、脂肪细胞分布等多种疾病中发挥重要作用。本研究在 243 例白癜风患者(男性 132 例,女性 111 例)和 205 例印度南部原籍的健康对照中进行。本研究的主要目的是评估患者和对照组中的 ACE I/D(插入/缺失)多态性。进一步通过聚合酶链反应(PCR)方法比较有和无白癜风家族史以及疾病进展的患者中的 I/D 基因型。
结果表明,DD 基因型与有家族史的白癜风患者的疾病易感性高度相关(p<0.01)(p<0.05),发病年龄较早。此外,患者中 ID 基因型的优势表明其与疾病的缓慢进展有关(p<0.05)。本研究首次报道了 II 基因型的保护作用以及 ID 基因型与疾病缓慢进展的显著相关性。