Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation Research
Search: search_blue_button Advanced Search
Circulation Research. 2006;98:e48
doi: 10.1161/01.RES.0000214407.58341.c8
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Erbs, S.
Right arrow Articles by Hambrecht, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Erbs, S.
Right arrow Articles by Hambrecht, R.
(Circulation Research. 2006;98:e48.)
© 2006 American Heart Association, Inc.


Letter to the Editor

Intracoronary Administration of Circulating Blood-Derived Progenitor Cells After Recanalization of Chronic Coronary Artery Occlusion Improves Endothelial Function

Sandra Erbs, Axel Linke, Gerhard Schuler, Rainer Hambrecht

University of Leipzig, Heart Center, Department of Internal Medicine/Cardiology, Leipzig, Germany


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 

To the Editor:

We read with interest the letter by Dr Traverse.1 He pointed out that the beneficial effects of the therapy with circulating progenitor cells (CPC) rely on the increase in left ventricular (LV) function in CPC-treated patients as compared with a control group where LV performance did not change during the study period of 3 months.

However, we would like to use this opportunity to address a couple of questions that have been raised by Dr Traverse:

First, our study was the first randomized placebo-controlled trial ever that was designed to address the effects of an intracoronary CPC application on endothelial dysfunction after recanalization of chronic total occlusion (CTO).2 The primary end point of our study was coronary flow reserve in the reopened artery, which was found to be increased by 43% in patients of the CPC group. This was linked to an improvement in metabolism, an increase in local and global left ventricular function. In contrast, even though CTO was successfully recanalized, which results in a restoration of the antegrad flow that is clearly higher than the collateral flow, endothelial dysfunction persisted in the control group; the number of hibernating segments as well as the myocardial performance did not change significantly in these patients. These data are consistent with the hypothesis that the degree of endothelial dysfunction after recanalization of CTO is a main determinant of myocardial metabolism and LV function.2

Second, there is evidence that the suggestive observational data reported in the studies, which were cited . . . [Full Text of this Article]




This article has been cited by other articles:


Home page
Circ. Res.Home page
S. Dimmeler and A. Leri
Aging and Disease as Modifiers of Efficacy of Cell Therapy
Circ. Res., June 6, 2008; 102(11): 1319 - 1330.
[Abstract] [Full Text] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
S. Dimmeler, J. Burchfield, and A. M. Zeiher
Cell-Based Therapy of Myocardial Infarction
Arterioscler Thromb Vasc Biol, February 1, 2008; 28(2): 208 - 216.
[Abstract] [Full Text] [PDF]