Huang Jiangfeng, Jiang Ling, Hu Yibo, Fu Chuhan, Zhang Keyi, Wen Yaqing, Zhou Shu, Huang Jinhua, Chen Jing, Zeng Qinghai
Department of Dermatology, Third Xiangya Hospital, Central South University, Changsha, China.
J Cosmet Dermatol. 2025 Jun;24(6):e70211. doi: 10.1111/jocd.70211.
The existence of a definite direct causal relationship between vitiligo and diverse autoimmune disorders remains unknown due to the influence of confounding factors and potential reverse causality.
Mendelian randomization (MR) is a technique employed to explore causal connections between two phenotypes. In our research, bidirectional two-sample MR analyses were utilized to evaluate the causal connections between vitiligo and multiple autoimmune diseases (systemic lupus erythematosus, Graves' disease, inflammatory bowel disease, alopecia areata [AA], type 1 diabetes mellitus [T1MD], and rheumatoid arthritis [RA]). Furthermore, we utilized summary-based Mendelian randomization (SMR) analysis to search for common susceptibility loci between two diseases that reciprocally elevate each other's risk. Finally, colocalization analyses were used to validate the robustness of the selected genes.
There was an indication of potential causation between RA and vitiligo (IVW OR = 1.19; 95% CI = 1.05-1.13; p = 0.008). Furthermore, evident causal connections exist between vitiligo and AA (IVW OR = 1.14; 95% CI = 1.04-1.26; p = 0.008), T1MD (IVW OR = 1.14; 95% CI = 1.06-1.23; p < 0.001), and RA (IVW OR = 1.08; 95% CI = 1.03-1.13; p < 0.001). In SMR analyses and colocalization analyses, we identified three shared genes associated with both vitiligo and RA, including: FCRL3, FADS1, and FADS2.
Our findings demonstrated that vitiligo and RA mutually act as risk factors for each other. Additionally, vitiligo had significant causal relationships with AA and type 1 diabetes.
由于混杂因素的影响和潜在的反向因果关系,白癜风与多种自身免疫性疾病之间是否存在明确的直接因果关系尚不清楚。
孟德尔随机化(MR)是一种用于探索两种表型之间因果关系的技术。在我们的研究中,采用双向双样本MR分析来评估白癜风与多种自身免疫性疾病(系统性红斑狼疮、格雷夫斯病、炎症性肠病、斑秃[AA]、1型糖尿病[T1MD]和类风湿性关节炎[RA])之间的因果关系。此外,我们利用基于汇总数据的孟德尔随机化(SMR)分析来寻找两种相互增加对方风险的疾病之间的共同易感基因座。最后,进行共定位分析以验证所选基因的稳健性。
有迹象表明RA与白癜风之间存在潜在因果关系(IVW比值比=1.19;95%置信区间=1.05-1.13;p=0.008)。此外,白癜风与AA(IVW比值比=1.14;95%置信区间=1.04-1.26;p=0.008)、T1MD(IVW比值比=1.14;95%置信区间=1.06-1.23;p<0.001)和RA(IVW比值比=1.08;95%置信区间=1.03-1.13;p<0.001)之间存在明显的因果关系。在SMR分析和共定位分析中,我们鉴定出三个与白癜风和RA均相关的共享基因,包括:FCRL3、FADS1和FADS2。
我们的研究结果表明,白癜风和RA互为危险因素。此外,白癜风与AA和1型糖尿病之间存在显著的因果关系。