Kim Myungshin, Yoo Jaeeun, Kim Jiyeon, Park Joonhong, Han Eunhee, Jang Woori, Chae Hyojin, Lee Ji Hyun, Park Young Min, Kim Yonggoo
Department of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Catholic Genetic Laboratory Center, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
PLoS One. 2017 Dec 27;12(12):e0190077. doi: 10.1371/journal.pone.0190077. eCollection 2017.
FLG encodes a large protein called profilaggrin, which plays a key role in maintaining an effective skin barrier against the environment. In this study, we identified FLG single nucleotide variations (FLG-SNVs) and evaluated the association of FLG-SNVs with clinical phenotypes including atopic dermatitis (AD)-associated minor clinical features, presence of specific allergic sensitization, and serum parameters.
Eighty-one Korean patients with AD were enrolled. AD-associated minor clinical features as well as allergic rhinitis and asthma were diagnosed by specialists. FLG-SNVs were identified by Sanger sequencing of entire exons through long-range PCR. Allergic sensitization to a specific allergen was evaluated by multiple allergen simultaneous test. Serologic parameters such as serum eosinophil cationic protein (ECP) and eosinophil derived neurotoxin (EDN) were measured.
A total of seventy-three SNVs and 4 LOF mutations were successfully genotyped. rs71626704 and rs76413899 were significantly associated with a history of asthma and cheilitis (P = 0.002 and P = 0.033, respectively), however, the associations were not found statistically significant after adjustment by multiple comparisons. In addition, we detected haplotype blocks which were correlated with non-specific hand or foot dermatitis and scalp scale. We identified FLG-SNVs which were associated with sensitization to environmental allergens; rs62623409 and rs71625199 (P = 0.038 and P = 0.008, respectively). Patients with FLG P478S TT and history of allergic rhinitis showed a higher EDN level, and among those patients, the ones with asthma showed a higher ECP level.
This study revealed the association of FLG-SNVs with AD-associated minor clinical features. We firstly identified rs71625199 which was associated with higher environmental allergic sensitization. We also suggest that FLG P478S is a kind of disease modifier which affects serologic parameters such as EDN and ECP.
FLG基因编码一种名为丝聚合蛋白原的大型蛋白质,该蛋白在维持有效的皮肤屏障抵御外界环境方面发挥关键作用。在本研究中,我们鉴定了FLG单核苷酸变异(FLG-SNVs),并评估了FLG-SNVs与临床表型的关联,这些临床表型包括特应性皮炎(AD)相关的次要临床特征、特定过敏致敏的存在情况以及血清参数。
招募了81名韩国AD患者。由专家诊断AD相关的次要临床特征以及过敏性鼻炎和哮喘。通过长距离PCR对整个外显子进行桑格测序来鉴定FLG-SNVs。通过多种变应原同步检测评估对特定变应原的过敏致敏情况。检测血清学参数,如血清嗜酸性粒细胞阳离子蛋白(ECP)和嗜酸性粒细胞衍生神经毒素(EDN)。
共成功对73个SNV和4个功能丧失突变进行了基因分型。rs71626704和rs76413899分别与哮喘病史和唇炎显著相关(P = 0.002和P = 0.033),然而,经多重比较校正后,这些关联未发现具有统计学意义。此外,我们检测到与非特异性手足皮炎和头皮鳞屑相关的单倍型块。我们鉴定出与环境变应原致敏相关的FLG-SNVs;rs62623409和rs71625199(分别为P = 0.038和P = 0.008)。携带FLG P478S TT且有过敏性鼻炎病史的患者EDN水平较高,在这些患者中,患有哮喘的患者ECP水平较高。
本研究揭示了FLG-SNVs与AD相关次要临床特征的关联。我们首次鉴定出与较高环境过敏致敏相关的rs71625199。我们还表明,FLG P478S是一种疾病修饰因子,可影响EDN和ECP等血清学参数。