The First Affiliated Hospital, Harbin Medical University, Harbin, Heilongjiang 150080, PR China.
Mol Med Rep. 2012 Nov;6(5):1171-7. doi: 10.3892/mmr.2012.1032. Epub 2012 Aug 10.
Previous studies have shown that insertion/deletion polymorphisms in the angiotensin-converting enzyme (ACE) gene and the endothelial nitric oxide synthase (eNOS) gene are associated with Henoch-Schönlein purpura nephritis (HSPN). However, further studies are required to prove the relationship between HSPN and ACE and eNOS single nucleotide polymorphisms (SNPs). We studied six ACE SNPs and two eNOS SNPs by genotyping HSPN patients. Statistical analyses indicate that four ACE SNPs and two eNOS SNPs are associated with HSPN susceptibility. A cumulative effect analysis suggested that an increased number of unfavourable genotypes may lead to an increased risk of HSPN. By comparing alleles, genotypes and haplotypes that are associated with lupus nephritis (LN) and HSPN, we found genetic heterogeneity between HSPN and LN.
先前的研究表明,血管紧张素转换酶(ACE)基因和内皮型一氧化氮合酶(eNOS)基因的插入/缺失多态性与过敏性紫癜肾炎(HSPN)有关。然而,需要进一步的研究来证明 HSPN 与 ACE 和 eNOS 单核苷酸多态性(SNPs)之间的关系。我们通过基因分型 HSPN 患者研究了六个 ACE SNPs 和两个 eNOS SNPs。统计分析表明,四个 ACE SNPs 和两个 eNOS SNPs 与 HSPN 的易感性有关。累积效应分析表明,不利基因型数量的增加可能导致 HSPN 风险的增加。通过比较与狼疮肾炎(LN)和 HSPN 相关的等位基因、基因型和单倍型,我们发现 HSPN 和 LN 之间存在遗传异质性。