Park Kui Young, Li Kapsok, Seok Joon, Seo Seong Jun
Department of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea .
J Korean Med Sci. 2016 Jul;31(7):1136-42. doi: 10.3346/jkms.2016.31.7.1136. Epub 2016 May 9.
Research of the FLG mutation in various ethnic groups revealed non-overlapping mutation patterns. In addition, Japanese and Chinese atopic patients showed somewhat different mutations. These ethnic differences make the research on Korean patients mandatory; however, no systematic research on Korean atopic dermatitis (AD) patients has been performed. This study aims to investigate the genetic polymorphism of FLG in Korean atopic dermatitis patients. The study was made up of three groups including 9 Ichthyosis vulgaris (IV) patients, 50 AD patients and 55 normal controls: the ichthyosis group was incorporated due to the reported association between the FLG mutation and IV. In comparison to other sequencing methods, the overlapping long-range PCR was used. We revealed the genetic polymorphism of filaggrin in Koreans, and at the same time, we discovered nonsense mutations in p.Y1767X and p.K4022X in Korean AD patients. By using FLG sequencing techniques confirmed in this study, new mutations or genetic polymorphisms with ethnic characteristics would be detected and further larger studies of repeat number polymorphisms could be performed.
对不同种族群体中丝聚合蛋白原(FLG)突变的研究揭示了不重叠的突变模式。此外,日本和中国的特应性患者表现出略有不同的突变。这些种族差异使得对韩国患者的研究成为必要;然而,尚未对韩国特应性皮炎(AD)患者进行系统研究。本研究旨在调查韩国特应性皮炎患者中FLG的基因多态性。该研究由三组组成,包括9例寻常型鱼鳞病(IV)患者、50例AD患者和55例正常对照:纳入鱼鳞病组是因为有报道称FLG突变与IV有关。与其他测序方法相比,使用了重叠长程PCR。我们揭示了韩国人中丝聚合蛋白的基因多态性,同时,我们在韩国AD患者中发现了p.Y1767X和p.K4022X的无义突变。通过使用本研究中确认的FLG测序技术,可以检测到具有种族特征的新突变或基因多态性,并可以进行更大规模的重复数多态性研究。