Left ventricular assist device in end-stage heart failure: persistence of structural myocyte damage after unloading. An immunohistochemical analysis of the contractile myofilaments

J Am Coll Cardiol. 2002 Mar 20;39(6):963-9. doi: 10.1016/s0735-1097(02)01713-8.

Abstract

Objectives: We sought to evaluate the contractile proteins in cardiomyocytes of patients with end-stage heart failure (HF) before and after mechanical support with a left ventricular assist device (LVAD).

Background: Improvement of myocyte dysfunction has been suggested after LVAD support.

Methods: Fourteen patients' myocardial biopsies taken at the time of LVAD implantation and after explantation, at the time of heart transplantation, were processed for routine hematoxylin-eosin staining and immunohistochemistry using monoclonal antibodies against actin, myosin, tropomyosin, troponin C and T and titin. A grading scale from 1 (abnormal staining of all myocytes, no cross-striation) to 5 (normal fiber anatomy and striation) was used. The cross-sectional area of cardiomyocytes was also measured.

Results: The cardiomyocytes' cross-sectional area decreased after support, from 519 +/- 94 microm(2) to 319 +/- 53 microm(2) (p < 0.001). Actin, tropomyosin, troponin C, troponin T and titin at the time of LVAD implantation showed widespread distortion of architecture; their grades were 1.4 +/- 0.6, 2.3 +/- 1.0, 2.1 +/- 0.9, 2.1 +/- 1.2 and 2.0 +/- 0.6, respectively. In contrast, myosin morphology was preserved (4.6 +/- 0.7). After LVAD support, actin, tropomyosin, troponin C, troponin T and titin showed improvement (grades 2.7 +/- 1.3 [p = 0.004], 3.2 +/- 1.2 [p = 0.021], 3.3 +/- 0.9 [p = 0.004], 3.0 +/- 1.1 [p = 0.048] and 3.1 +/- 0.9 [p = 0.001], respectively), but no normalization. The myosin pattern deteriorated slightly (3.6 +/- 1.6 [p = 0.058]).

Conclusions: After LVAD support, during a period of 213 +/- 135 days in patients with end-stage HF, despite a decrease in the size of the cardiomyocytes, severe structural myocyte damage persisted. This does not support complete recovery of myocyte histologic features.

Publication types

  • Comparative Study
  • Evaluation Study

MeSH terms

  • Actin Cytoskeleton / chemistry
  • Adult
  • Biopsy
  • Coloring Agents / therapeutic use
  • Contractile Proteins / analysis
  • Coronary Artery Bypass / instrumentation
  • Female
  • Heart Atria / cytology
  • Heart Atria / pathology
  • Heart Atria / surgery
  • Heart Failure / pathology
  • Heart Failure / surgery*
  • Heart Ventricles / pathology
  • Heart Ventricles / surgery*
  • Heart-Assist Devices*
  • Hematoxylin / therapeutic use
  • Humans
  • Male
  • Myocardium / pathology
  • Prosthesis Implantation / instrumentation

Substances

  • Coloring Agents
  • Contractile Proteins
  • Hematoxylin