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J Am Coll Cardiol, 2010; 55:671-679, doi:10.1016/j.jacc.2009.08.074
© 2010 by the American College of Cardiology Foundation
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CLINICAL RESEARCH: VALVULAR HEART DISEASE

Increased Oxidative Stress and Cardiomyocyte Myofibrillar Degeneration in Patients With Chronic Isolated Mitral Regurgitation and Ejection Fraction >60%

Mustafa I. Ahmed, MD*, James D. Gladden, BS*, Silvio H. Litovsky, MD*, Steven G. Lloyd, MD, PhD*, Himanshu Gupta, MD*, Seidu Inusah, MS*, Thomas Denney, Jr, PhD{ddagger}, Pamela Powell, MS*, David C. McGiffin, MD* and Louis J. Dell'Italia, MD*,{dagger},*

* Center for Heart Failure Research, Departments of Medicine, Cardiovascular Surgery, Pathology, and Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama
{dagger} Birmingham Veteran Affairs Medical Center, Birmingham, Alabama
{ddagger} Auburn University, Samuel Ginn College of Engineering, Auburn, Alabama

Manuscript received December 10, 2008; revised manuscript received August 20, 2009, accepted August 31, 2009.

* Reprint requests and correspondence: Dr. Louis J. Dell'Italia, UAB Center for Heart Failure Research, Division of Cardiology, 434 BMR2, 901 19th Street South, Birmingham, Alabama 35294-2180 (Email: loudell{at}uab.edu).

Objectives: This study assessed myocardial damage in patients with chronic isolated mitral regurgitation (MR) and left ventricular ejection fraction (LVEF) >60%.

Background: Typically, MR patients have decreased LVEF after mitral valve (MV) repair despite normal pre-operative LVEF.

Methods: Twenty-seven patients with isolated MR had left ventricular (LV) biopsies taken at time of MV repair. Magnetic resonance imaging with tissue tagging was performed in 40 normal subjects and in MR patients before and 6 months after MV repair.

Results: LVEF (66 ± 5% to 54 ± 9%, p < 0.0001) and LV end-diastolic volume index (108 ± 28 ml/m2 to 78 ± 24 ml/m2, p < 0.0001) decreased, whereas left ventricular end-systolic (LVES) volume index was 60% above normal pre- and post-MV repair (p < 0.05). The LV circumferential and longitudinal strain rates decreased below normal following MV repair (6.38 ± 1.38 vs. 5.11 ± 1.28, p = 0.0009, and 7.51 ± 2.58 vs. 5.31 ± 1.61, percentage of R to R interval, p < 0.0001), as LVES stress/LVES volume index ratio was depressed at baseline and following MV repair versus normal subjects (0.25 ± 0.10 and 0.28 ± 0.05 vs. 0.33 ± 0.12, p < 0.01). LV biopsies demonstrated cardiomyocyte myofibrillar degeneration versus normal subjects (p = 0.035). Immunostaining and immunoblotting demonstrated increased xanthine oxidase in MR versus normal subjects (p < 0.05). Lipofuscin deposition was increased in cardiomyocytes of MR versus normal subjects (0.62 ± 0.20 vs. 0.33 ± 0.11, percentage of area: p < 0.01).

Conclusions: Decreased LV strain rates and LVES wall stress/LVES volume index following MV repair indicate contractile dysfunction, despite pre-surgical LVEF >60%. Increased oxidative stress could cause myofibrillar degeneration and lipofuscin accumulation resulting in LV contractile dysfunction in MR.

Key Words: mitral regurgitation • oxidative stress • magnetic resonance imaging • tissue tagging

Abbreviations and Acronyms
  EF = ejection fraction
  LV = left ventricular
  LVED = left ventricular end-diastolic
  LVES = left ventricular end-systolic
  MR = mitral regurgitation
  MRI = magnetic resonance imaging
  MV = mitral valve
  XDH = xanthine dehydrogenase
  XO = xanthine oxidase


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