The Second Clinical Medical College of Guangxi Medical University, Nanning, China.
Department of Nephrology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, China.
J Clin Lab Anal. 2022 Sep;36(9):e24642. doi: 10.1002/jcla.24642. Epub 2022 Aug 10.
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is an autoimmune disease often accompanied by rapidly progressive renal failure, and the genetic background is still unknown. Our study was performed to test whether autophagy-related 16 like 1 (ATG16L1) rs4663402 and rs4663396 single nucleotide polymorphisms (SNPs) were associated with AAV in the Chinese Guangxi population.
One hundred seventy seven unrelated AAV patients and 216 healthy controls were included in this case-control study. Multiplex polymerase chain reaction combined with high-throughput sequencing was used for typing, and SNPStats and SHEsis were used for association analysis, pairwise linkage disequilibrium, and haplotype analysis.
rs4663402 and rs4663396 were in Hardy-Weinberg equilibrium in AAV and control groups. The frequencies of rs4663402 AA, AT, and TT genotypes were 82.5%, 16.9%, and 0.6%, respectively, in patients with AAV, and 83.5%, 16.2%, and 0.5%, respectively, in controls. The frequencies of rs4663396 CC, CT, and TT genotypes were 63.8%, 33.9%, and 2.3%, respectively, in patients with AAV, and 69.2%, 26.6%, and 4.2%, respectively, in controls. Haplotype analysis revealed two SNPs in a single haplotype block (D' = 1.0). Our logistic regression adjusted for sex and age showed no association between rs4663402 and rs4663396 and the risk for AAV in genetic models (p > 0.05). However, ATG16L1 rs4663396 CC and CT + TT genotypes exhibited statistically significant differences in the incidence of arthralgia (p = 0.03).
Our results indicated that ATG16L1 rs4663402 and rs4663396 polymorphisms were not associated with AAV in the Chinese Guangxi population. ATG16L1 rs4663396 CT + TT genotype may be associated with arthralgia.
抗中性粒细胞胞质抗体(ANCA)相关性血管炎(AAV)是一种自身免疫性疾病,常伴有快速进行性肾衰竭,其遗传背景尚不清楚。我们的研究旨在检测自噬相关 16 样蛋白 1(ATG16L1)rs4663402 和 rs4663396 单核苷酸多态性(SNP)是否与中国广西人群的 AAV 相关。
本病例对照研究纳入了 177 例无关 AAV 患者和 216 例健康对照。采用多重聚合酶链反应结合高通量测序进行分型,采用 SNPStats 和 SHEsis 进行关联分析、成对连锁不平衡和单倍型分析。
rs4663402 和 rs4663396 在 AAV 组和对照组中均处于哈迪-温伯格平衡状态。AAV 患者 rs4663402AA、AT 和 TT 基因型的频率分别为 82.5%、16.9%和 0.6%,对照组分别为 83.5%、16.2%和 0.5%。rs4663396CC、CT 和 TT 基因型的频率分别为 63.8%、33.9%和 2.3%,对照组分别为 69.2%、26.6%和 4.2%。单倍型分析显示,两个 SNP 位于单个单倍型块(D'=1.0)。我们的 logistic 回归调整了性别和年龄,在遗传模型中,rs4663402 和 rs4663396 与 AAV 的风险之间没有关联(p>0.05)。然而,ATG16L1rs4663396CC 和 CT+TT 基因型在关节痛的发生率上有统计学差异(p=0.03)。
我们的结果表明,ATG16L1 rs4663402 和 rs4663396 多态性与中国广西人群的 AAV 无关。ATG16L1 rs4663396CT+TT 基因型可能与关节痛有关。