TY - JOUR
T1 - Evidence of improved right ventricular structure after LVAD support in patients with end-stage cardiomyopathy
AU - Küçüker, Seref A.
AU - Stetson, Sonny J.
AU - Becker, Katy A.
AU - Akgül, Ahmet
AU - Loebe, Matthias
AU - Lafuente, Javier A.
AU - Noon, George P.
AU - Koerner, Michael M.
AU - Entman, Mark L.
AU - Torre, Guillermo
N1 - Funding Information:
This work was supported in part by Grant HL-42550 from the National Heart, Lung, and Blood Institute (Dr. Entman) and was funded by the Turkish Health Ministry (Drs. Küçüker and Akgül).
PY - 2004/1
Y1 - 2004/1
N2 - Background: Although many reports demonstrate the hemodynamic benefits of left ventricular assist devices (LVAD) in right-sided circulation, it is not known whether the right ventricular myocardium goes through reverse remodeling after left ventricular mechanical circulatory support. Accordingly, the purposes of our studies were 1) to investigate the right ventricular changes that occur in fibrosis, in cellular hypertrophy, and in intra-myocardial tumor necrosis factor α (TNF-α) levels in patients receiving LVAD support; and 2) to determine whether the type of LVAD used influences right ventricular myocardial changes. Methods and results: We measured myocyte size, total collagen content, and TNF-α levels using semi-quantitative immunohistochemical analysis of myocardial samples from the right and left ventricles of control and failing myocardia, either supported by 1 of 2 distinct forms of LVADs or without support. We found that when compared with control, although myocyte size was not increased in the right ventricle of failing myocardia (p = not significant), total collagen content and myocardial TNF-α levels were decreased in the right ventricle compared with controls (p < 0.01 and p < 0.001, respectively). Conclusion: These data demonstrate that chronic left ventricular unloading with either pulsatile or continuous-flow devices decreases right ventricular total collagen and myocardial TNF-α content. We suggest that the decreased fibrosis and normalization of cytokine milieu observed may in part contribute to the recovery of right-sided cardiac function associated with chronic mechanical circulatory support.
AB - Background: Although many reports demonstrate the hemodynamic benefits of left ventricular assist devices (LVAD) in right-sided circulation, it is not known whether the right ventricular myocardium goes through reverse remodeling after left ventricular mechanical circulatory support. Accordingly, the purposes of our studies were 1) to investigate the right ventricular changes that occur in fibrosis, in cellular hypertrophy, and in intra-myocardial tumor necrosis factor α (TNF-α) levels in patients receiving LVAD support; and 2) to determine whether the type of LVAD used influences right ventricular myocardial changes. Methods and results: We measured myocyte size, total collagen content, and TNF-α levels using semi-quantitative immunohistochemical analysis of myocardial samples from the right and left ventricles of control and failing myocardia, either supported by 1 of 2 distinct forms of LVADs or without support. We found that when compared with control, although myocyte size was not increased in the right ventricle of failing myocardia (p = not significant), total collagen content and myocardial TNF-α levels were decreased in the right ventricle compared with controls (p < 0.01 and p < 0.001, respectively). Conclusion: These data demonstrate that chronic left ventricular unloading with either pulsatile or continuous-flow devices decreases right ventricular total collagen and myocardial TNF-α content. We suggest that the decreased fibrosis and normalization of cytokine milieu observed may in part contribute to the recovery of right-sided cardiac function associated with chronic mechanical circulatory support.
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U2 - 10.1016/S1053-2498(03)00057-3
DO - 10.1016/S1053-2498(03)00057-3
M3 - Article
C2 - 14734124
AN - SCOPUS:9144249608
SN - 1053-2498
VL - 23
SP - 28
EP - 35
JO - Journal of Heart and Lung Transplantation
JF - Journal of Heart and Lung Transplantation
IS - 1
ER -