Mobilization of stem cells in acute MI might signify the reparatory response. Aim of the Study. Prospective evaluation of correlation between CD34+CXCR4+ cell mobilization and improvement of LVEF and remodeling in patients with acute MI in 1-year followup. Methods. 50 patients with MI, 28 with stable angina (SAP), and 20 individuals with no CAD (CTRL). CD34+CXCR4+ cells, SDF-1, G-CSF, troponin I (TnI) and NT-proBNP were measured on admission and 1 year after MI. Echocardiography and ergospirometry were carried out after 1 year. Results. Number of CD34+CXCR4+ cells in acute MI was significantly higher in comparison with SAP and CTRL, but lower in patients with decreased LVEF â¤40%. In patients who had significant LVEF increase â¥5% in 1 year FU the number of cells in acute MI was significantly higher versus patients with no LVEF improvement. Number of cells was positively correlated (r = 0,41, P = 0,031) with absolute LVEF change and inversely with absolute change of ESD and EDD in 1-year FU. Mobilization of CD34+CXCR4+ cells in acute MI was negatively correlated with maximum TnI and NT-proBNP levels. Conclusion. Mobilization of CD34+CXCR4+ cells in acute MI shows significant positive correlation with improvement of LVEF after 1 year.
Mobilization of CD34+CXCR4+ stem/progenitor cells and the parameters of left ventricular function and remodeling in 1-year follow-up of patients with acute myocardial infarction.
CD34+CXCR4+干/祖细胞的动员以及急性心肌梗死患者1年随访期间左心室功能和重塑的参数
阅读:8
作者:Wyderka RafaÅ, Wojakowski Wojciech, Jadczyk Tomasz, MaÅlankiewicz Katarzyna, Parma Zofia, PawÅowski Tomasz, MusiaÅek Piotr, Majka Marcin, Król Marek, Kuczmik WacÅaw, Dworowy Sebastian, Korzeniowska Barbara, Ratajczak Mariusz Z, Tendera MichaÅ
| 期刊: | Mediators of Inflammation | 影响因子: | 4.200 |
| 时间: | 2012 | 起止号: | 2012;2012:564027 |
| doi: | 10.1155/2012/564027 | 研究方向: | 细胞生物学 |
| 疾病类型: | 心肌炎 | ||
特别声明
1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。
2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。
3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。
4、投稿及合作请联系:info@biocloudy.com。
