Chawla Harsimran S, Kosta Susmit, Namdeo Chaitanya, Kataria Rajesh, Bhatia Kailash, Sahu Roshni, Joshi Pallavi
Department of Dermatology, Venerology and Leprosy, Sri Aurobindo Medical College and Post Graduate Institute, Sri Aurobindo University, Indore, Madhya Pradesh, India.
Department of Molecular and Virology Research and Diagnostic Laboratory, Sri Aurobindo Medical College and Post Graduate Institute, Sri Aurobindo University, Indore, Madhya Pradesh, India.
Indian Dermatol Online J. 2023 Aug 29;14(5):611-615. doi: 10.4103/idoj.idoj_636_22. eCollection 2023 Sep-Oct.
A genotype study of filaggrin gene loss-of-function mutations in central India can provide valuable insights into the prevalence and association of these mutations with atopic dermatitis (AD) and ichthyosis vulgaris (IV) in the region. The R501X and 2282del4 are both genetic variants in the human gene called filaggrin gene (), which encodes a protein that plays an important role in the formation and maintenance of the skin barrier. In this study, we determined the R501X and 2282del4 variants association with both AD and IV in Central Indian populations.
This case-control study was conducted in the Departments of Dermatology and Molecular and Virology Research and Diagnostic Laboratory at Sri Aurobindo Medical College and Post Graduate Institute, Indore (Madhya Pradesh). The study was approved by the Clinical Research and Ethics Committee. A total of 180 patients aged between 3 months - 60 years who attended the skin outpatient department between March-2021 to June-2022 were recruited in this study. Among them, 60 patients were in AD-group, 60 patients in IV-group, and 60 patients were in the healthy control group. Polymerase chain reaction followed by restriction fragment length polymorphism (PCR-RFLP) was used in genotyping for mutations (R501X and 2282del4).
The most common mutations were R501X (31.6% and 23.3%) and 2282del4 (18.3% and 13.3%) in AD and IV patients with heterozygous (AT) genotype, respectively. The combined mutation ( R501X and 2282del4) association was 10% and 5% in the AD and IV groups with heterozygous (AT) genotype, respectively, and in all the patients of control group with wild genotype (AA). There were no significant ( = 0.09) associations found with 2282del14 genotype.
The R501X mutation in the gene encoding filaggrin is one of the robust genetic associations of AD and IV. The 2282del4 polymorphism was marginally less as compared to R501X.
对印度中部丝聚合蛋白基因功能丧失突变进行基因分型研究,可为了解该地区这些突变的患病率及其与特应性皮炎(AD)和寻常型鱼鳞病(IV)的关联提供有价值的见解。R501X和2282del4都是人类丝聚合蛋白基因()中的遗传变异,该基因编码一种在皮肤屏障形成和维持中起重要作用的蛋白质。在本研究中,我们确定了印度中部人群中R501X和2282del4变异与AD和IV的关联。
本病例对照研究在印多尔(中央邦)圣奥罗宾多医学院及研究生学院的皮肤科、分子与病毒学研究及诊断实验室进行。该研究获得了临床研究与伦理委员会的批准。本研究共招募了2021年3月至2022年6月期间到皮肤科门诊就诊的180例年龄在3个月至60岁之间的患者。其中,AD组60例患者,IV组60例患者,健康对照组60例患者。采用聚合酶链反应(PCR)及限制性片段长度多态性分析(PCR-RFLP)对突变(R501X和2282del4)进行基因分型。
AD和IV患者中最常见的杂合子(AT)基因型突变分别为R501X(31.6%和23.3%)和2282del4(18.3%和13.3%)。AD组和IV组杂合子(AT)基因型的联合突变(R501X和2282del4)发生率分别为10%和5%,而对照组所有野生基因型(AA)患者中为0。2282del14基因型未发现显著关联(=0.09)。
丝聚合蛋白编码基因中的R501X突变是AD和IV的重要遗传关联之一。与R501X相比,2282del4多态性的关联程度略低。