A csontvelo eredetu CD34+ ossejtek hatása a bal kamra funkciójára akut miokardiális infarktust követoen

Translated title of the contribution: Effects of autologous bone marrow derived CD34+ stem cells on the left ventricular function following myocardial infarction

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Both experimental and human clinical studies executed in the last 5 years suggested that bone marrow derived cells may participate in the healing process after myocardial infarction. A number of small clinical trials indicated mild or moderate beneficial effect of intracoronary administration of bone marrow derived stem cells after myocardial infarction. Most of the studies used mononuclear cell fraction; due to the cellular heterogeneity of this cell population the type of the effective subpopulation was not known. We investigated the safety and functional effects of the autologous bone marrow CD34± stein cells after intracoronary administration in patients with recent myocardial infarction. 8 patients with impaired left ventricular function were transplanted with CD34± bone marrow stein cells 12 ± 1 day after the acute coronary event. 2D-echocardiography, FDG-PET and MIBI-SPECT were performed before transplantation and 6 month later. During the 6-month follow-up the global left ventricular function (basal EF 37,3 ± 2,9%, after cell therapy 44,8 ± 4,1%) and regional viability/metabolism increased significantly (17,6 ± 13,5%). The increase of myocardial perfusion in the infarct region was tendentious but not significant. Our results demonstrate for the first time that the CD34+ subpopulation of bone marrow derived stem cells improves left ventricular function and viability after myocardial infarction.

Translated title of the contributionEffects of autologous bone marrow derived CD34+ stem cells on the left ventricular function following myocardial infarction
Original languageHungarian
Pages (from-to)243-249
Number of pages7
JournalOrvosi hetilap
Volume148
Issue number6
DOIs
Publication statusPublished - Feb 11 2007

ASJC Scopus subject areas

  • Medicine(all)

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