Research Group On Genetic Epidemiology and Atherosclerosis in Systemic Diseases and in Metabolic Bone Diseases of the Musculoskeletal System, IDIVAL, Division of Rheumatology, Hospital Universitario Marqués de Valdecilla, Avenida Cardenal Herrera Oria s/n, 39011, Santander, Spain.
López Albo´ Post-Residency Programme, Hospital Universitario Marqués de Valdecilla, Santander, Spain.
Sci Rep. 2021 Aug 9;11(1):16163. doi: 10.1038/s41598-021-95762-5.
Cytokines signalling pathway genes are crucial factors of the genetic network underlying the pathogenesis of Immunoglobulin-A vasculitis (IgAV), an inflammatory vascular condition. An influence of the interleukin (IL)33- IL1 receptor like (IL1RL)1 signalling pathway on the increased risk of several immune-mediated diseases has been described. Accordingly, we assessed whether the IL33-IL1RL1 pathway represents a novel genetic risk factor for IgAV. Three tag polymorphisms within IL33 (rs3939286, rs7025417 and rs7044343) and three within IL1RL1 (rs2310173, rs13015714 and rs2058660), that also were previously associated with several inflammatory diseases, were genotyped in 380 Caucasian IgAV patients and 845 matched healthy controls. No genotypes or alleles differences were observed between IgAV patients and controls when IL33 and IL1RL1 variants were analysed independently. Likewise, no statistically significant differences were found in IL33 or IL1RL1 genotype and allele frequencies when IgAV patients were stratified according to the age at disease onset or to the presence/absence of gastrointestinal (GI) or renal manifestations. Similar results were disclosed when IL33 and IL1RL1 haplotypes were compared between IgAV patients and controls and between IgAV patients stratified according to the clinical characteristics mentioned above. Our results suggest that the IL33-IL1RL1 signalling pathway does not contribute to the genetic network underlying IgAV.
细胞因子信号通路基因是免疫球蛋白 A 血管炎 (IgAV) 发病机制中遗传网络的关键因素,IgAV 是一种炎症性血管疾病。已经描述了白细胞介素 (IL)33-IL1 受体样 (IL1RL)1 信号通路对多种免疫介导疾病的风险增加的影响。因此,我们评估了 IL33-IL1RL1 通路是否代表 IgAV 的新遗传风险因素。IL33 内的三个标签多态性(rs3939286、rs7025417 和 rs7044343)和 IL1RL1 内的三个多态性(rs2310173、rs13015714 和 rs2058660),先前也与几种炎症性疾病相关,在 380 名白种人 IgAV 患者和 845 名匹配的健康对照中进行了基因分型。当单独分析 IL33 和 IL1RL1 变体时,未观察到 IgAV 患者和对照组之间的基因型或等位基因差异。同样,当根据疾病发病年龄或胃肠道 (GI) 或肾脏表现的存在/不存在对 IgAV 患者进行分层时,在 IL33 或 IL1RL1 基因型和等位基因频率方面未发现统计学上的显著差异。当在 IgAV 患者和对照组之间以及在根据上述临床特征分层的 IgAV 患者之间比较 IL33 和 IL1RL1 单倍型时,也揭示了类似的结果。我们的结果表明,IL33-IL1RL1 信号通路不会导致 IgAV 遗传网络。