Immunopathology Group, Rheumatology Department, Hospital Universitario Marqués de Valdecilla-IDIVAL, 39011 Santander, Spain.
Division of Paediatrics, Hospital Universitario San Cecilio, 18016 Granada, Spain.
Int J Mol Sci. 2023 Aug 22;24(17):13063. doi: 10.3390/ijms241713063.
(rs11150612, rs11574637), rs17019602, rs4077515, (rs2738048, rs10086568), and rs2412971 are mucosal immune defence polymorphisms, that have an impact on IgA production, described as risk for IgA nephropathy (IgAN). Since IgAN and Immunoglobulin-A vasculitis (IgAV) share molecular mechanisms, with the aberrant deposit of IgA1 being the main pathophysiologic feature of both entities, we assessed the potential influence of the seven abovementioned polymorphisms on IgAV pathogenesis. These seven variants were genotyped in 381 Caucasian IgAV patients and 997 matched healthy controls. No statistically significant differences were observed in the genotype and allele frequencies of these seven polymorphisms when the whole cohort of IgAV patients and those with nephritis were compared to controls. Similar genotype and allele frequencies of all polymorphisms were disclosed when IgAV patients were stratified according to the age at disease onset or the presence/absence of gastrointestinal or renal manifestations. Likewise, no and haplotype differences were observed when the whole cohort of IgAV patients, along with those with nephritis and controls, as well as IgAV patients, stratified according to the abovementioned clinical characteristics, were compared. Our results suggest that mucosal immune defence polymorphisms do not represent novel genetic risk factors for IgAV pathogenesis.
(rs11150612、rs11574637)、rs17019602、rs4077515、(rs2738048、rs10086568)和 rs2412971 是黏膜免疫防御多态性,对 IgA 产生有影响,被描述为 IgA 肾病 (IgAN) 的风险因素。由于 IgAN 和免疫球蛋白 A 血管炎 (IgAV) 具有共同的分子机制,IgA1 的异常沉积是这两种疾病的主要病理生理特征,因此我们评估了上述七种多态性对 IgAV 发病机制的潜在影响。这七种变体在 381 例高加索 IgAV 患者和 997 名匹配的健康对照中进行了基因分型。当将整个 IgAV 患者队列和肾炎患者与对照组进行比较时,这些七种多态性的基因型和等位基因频率没有统计学上的显著差异。当根据疾病发病年龄或胃肠道或肾脏表现的存在/缺失对 IgAV 患者进行分层时,所有多态性的基因型和等位基因频率也相似。同样,当将整个 IgAV 患者队列、肾炎患者和对照组以及根据上述临床特征分层的 IgAV 患者进行比较时,没有观察到 和 单倍型差异。我们的研究结果表明,黏膜免疫防御多态性不代表 IgAV 发病机制的新遗传风险因素。