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神经生长因子及其受体的连锁和关联研究作为儿童 IgA 肾病的新易感基因。

Linkage and association study of neurotrophins and their receptors as novel susceptibility genes for childhood IgA nephropathy.

机构信息

Department of Pediatrics, School of Medicine, Kyung Hee University, Seoul 130-702, Republic of Korea.

出版信息

Pediatr Res. 2011 Apr;69(4):299-305. doi: 10.1203/PDR.0b013e31820b9365.

Abstract

Neurotrophins (NTs) and their receptors (NTRs) are known to be important for pathogenesis of various inflammatory diseases that occur in not only neuronal but also nonneuronal tissues, including kidney. Here, we investigated association between childhood IgA nephropathy (IgAN) and single nucleotide polymorphisms (SNPs) of genes encoding NTs [nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF)] and NTRs [nerve growth factor receptor (NGFR) and neurotrophic tyrosine kinase receptor 1-3 (NTRK1-3)]. The genotyping data of 197 patients and 289 control subjects revealed significant association between NGF SNP rs11102930 and presence of IgAN. Patient subgroup analysis revealed that that the presence of nephrotic range proteinuria (>40 mg/m/h) was associated with rs6334 of NTRK1 and rs11030104, rs7103411, rs7103873, and rs6484320 of BDNF. Significant genotype differences were observed in podocyte foot process effacement for rs1187321 and rs1187323 of NTRK2. Furthermore, some SNPs showed significantly different genotype distribution between patients with or without pathologically advanced disease markers, specifically in rs6334 of NTRK1. Our results suggest that SNPs of NTs and NTRs are associated with susceptibility, pathological advancement, podocyte foot process effacement, and development of proteinuria in childhood IgAN.

摘要

神经递质(NTs)及其受体(NTRs)在不仅在神经元组织而且在非神经元组织中发生的各种炎症性疾病的发病机制中起着重要作用,包括肾脏。在这里,我们研究了编码 NTs [神经生长因子(NGF)和脑源性神经营养因子(BDNF)]和 NTRs [神经生长因子受体(NGFR)和神经营养酪氨酸激酶受体 1-3(NTRK1-3)]的基因的单核苷酸多态性(SNPs)与儿童 IgA 肾病(IgAN)之间的关联。197 名患者和 289 名对照的基因分型数据显示,NGF SNP rs11102930 与 IgAN 的存在之间存在显著关联。患者亚组分析显示,肾病范围蛋白尿(>40mg/m/h)与 NTRK1 的 rs6334 和 BDNF 的 rs11030104、rs7103873、rs7103411 和 rs6484320 有关。在 NTRK2 的 rs1187321 和 rs1187323 中观察到足细胞足突消失的显著基因型差异。此外,一些 SNP 在具有或不具有病理进展疾病标志物的患者之间表现出明显不同的基因型分布,特别是在 NTRK1 的 rs6334 中。我们的结果表明,NT 和 NTR 的 SNPs 与儿童 IgAN 的易感性、病理进展、足细胞足突消失和蛋白尿的发展有关。

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