Ni Jie, Ye Xinjian, Chen Yitong, Fu Haizhou, Wu Ziqiong, Lu Haiping, Chen Qianming
Stomatology Hospital, School of Stomatology, Zhejiang University School of Medicine, Zhejiang Provincial Clinical Research Center for Oral Diseases, Key Laboratory of Oral Biomedical Research of Zhejiang Province, Cancer Center of Zhejiang University, Engineering Research Center of Oral Biomaterials and Devices of Zhejiang Province, Hangzhou, China.
School of Stomatology, Zhejiang Chinese Medical University, Hangzhou, China.
Int Dent J. 2025 Jun;75(3):2194-2203. doi: 10.1016/j.identj.2024.12.014. Epub 2024 Dec 31.
The oral mucosa mirrors a range of latent systemic disorders, with potential clinical associations noted between autoimmune thyroid disease (AITD) and oral lichen planus (OLP). This study aims to explore the genetic relationship and underlying mechanisms mediating these conditions.
A 2-step Mendelian randomization (MR) analysis was conducted to elucidate the genetic relationship and mediating factors between AITD and OLP. Linkage disequilibrium score regression was employed to assess heritability and genetic correlations among phenotypes, followed by genetic colocalization analysis to discern shared genetic variants. A transcriptome-wide association study (TWAS) was also performed to pinpoint gene expression profiles.
Genetically predicted AITD is associated with an increased risk of OLP (OR[95% CI]: 1.44[1.19,1.74], P=1.61 × 10), potentially mediated by hypothyroidism. There is strong evidence of colocalization between AITD and OLP, with a shared PTPN22 gene variant driving this association. TWAS further identified RNASET2 and FGFR1OP within the HLA region as high-confidence shared genes for both conditions.
Our study provides novel evidence of a possible genetic association between AITD and OLP. These findings highlight the critical role of endocrine alterations in maintaining oral immune homeostasis, though further research is warranted to validate our findings.
口腔黏膜反映了一系列潜在的全身性疾病,自身免疫性甲状腺疾病(AITD)与口腔扁平苔藓(OLP)之间存在潜在的临床关联。本研究旨在探讨介导这些疾病的遗传关系及潜在机制。
进行了两步孟德尔随机化(MR)分析,以阐明AITD与OLP之间的遗传关系及介导因素。采用连锁不平衡评分回归评估表型之间的遗传力和遗传相关性,随后进行遗传共定位分析以识别共享的遗传变异。还进行了全转录组关联研究(TWAS)以确定基因表达谱。
遗传预测的AITD与OLP风险增加相关(OR[95%CI]:1.44[1.19,1.74],P = 1.61×10),可能由甲状腺功能减退介导。有强有力的证据表明AITD与OLP之间存在共定位,一个共享的PTPN22基因变异驱动了这种关联。TWAS进一步确定HLA区域内的RNASET2和FGFR1OP为这两种疾病的高可信度共享基因。
我们的研究为AITD与OLP之间可能的遗传关联提供了新证据。这些发现突出了内分泌改变在维持口腔免疫稳态中的关键作用,不过仍需进一步研究来验证我们的发现。