首页> 外文会议>International Congress on Coronary Artery Disease. >CNP transcriptomic profiling in HF patients as a function of clinical severity
【24h】

CNP transcriptomic profiling in HF patients as a function of clinical severity

机译:CNP在HF患者中转录组分析作为临床严重程度的函数

获取原文

摘要

The aim of this study was to evaluate the transcriptomic profiling of C-type natriuretic peptide (CNP) and of its specific receptor, NPR-B, in human leukocytes of heart failure (HF) patients (NYHAI-II, n=7; NYHA III-IV, n=13) as a function of clinical severity by Real-time PCR. A control group (C, n=8) was also evaluated. Significantly higher levels of CNP mRNA expression were found in HF as a function of clinical severity (p=0.005 C vs NYHA III-IV, p=0.017 NYHA I-II vs NYHA III-IV) and NPR-B transcript levels resulted down-regulated in HF patients with higher NYHA class (p=0.001 C vs NYHA III-IV, p<0.0001 NYHA I-II vs. NYHA III-IV). These results suggest a co-regulation of NPR-B and CNP expression supporting the relevance of this receptor in human disease characterized by a marked inflammatory/immune component.
机译:本研究的目的是评估C型利钠肽(CNP)和其特异性受体,NPR-B,心力衰竭(HF)患者(NYHAI-II,N = 7; NYHA的特异性受体 III-IV,n = 13)作为实时PCR临床严重程度的函数。 还评估对照组(C,N = 8)。 在HF中发现显着较高水平的CNP mRNA表达作为临床严重程度的函数(P = 0.005℃Vs Nyha III-IV,P = 0.017 Nyha I-II Vs Nyha III-IV)和NPR-B转录水平导致下来 - 患HF患者患有较高的NYHA级别的患者(p = 0.001℃,P <0.0001 nyha I-II与Nyha III-IV)。 这些结果表明,NPR-B和CNP表达的共调节,其支持该受体在人类疾病中的相关性,其特征在于标记的炎症/免疫组分。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号