Identifying early changes in myocardial microstructure in hypertensive heart disease

PLoS One. 2014 May 15;9(5):e97424. doi: 10.1371/journal.pone.0097424. eCollection 2014.

Abstract

The transition from healthy myocardium to hypertensive heart disease is characterized by a series of poorly understood changes in myocardial tissue microstructure. Incremental alterations in the orientation and integrity of myocardial fibers can be assessed using advanced ultrasonic image analysis. We used a modified algorithm to investigate left ventricular myocardial microstructure based on analysis of the reflection intensity at the myocardial-pericardial interface on B-mode echocardiographic images. We evaluated the extent to which the novel algorithm can differentiate between normal myocardium and hypertensive heart disease in humans as well as in a mouse model of afterload resistance. The algorithm significantly differentiated between individuals with uncomplicated essential hypertension (N = 30) and healthy controls (N = 28), even after adjusting for age and sex (P = 0.025). There was a trend in higher relative wall thickness in hypertensive individuals compared to controls (P = 0.08), but no difference between groups in left ventricular mass (P = 0.98) or total wall thickness (P = 0.37). In mice, algorithm measurements (P = 0.026) compared with left ventricular mass (P = 0.053) more clearly differentiated between animal groups that underwent fixed aortic banding, temporary aortic banding, or sham procedure, on echocardiography at 7 weeks after surgery. Based on sonographic signal intensity analysis, a novel imaging algorithm provides an accessible, non-invasive measure that appears to differentiate normal left ventricular microstructure from myocardium exposed to chronic afterload stress. The algorithm may represent a particularly sensitive measure of the myocardial changes that occur early in the course of disease progression.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Algorithms
  • Animals
  • Aorta / pathology
  • Blood Pressure
  • Case-Control Studies
  • Disease Models, Animal
  • Disease Progression
  • Echocardiography / methods
  • Essential Hypertension
  • Female
  • Heart Diseases / physiopathology*
  • Heart Ventricles
  • Humans
  • Hypertension / physiopathology*
  • Image Processing, Computer-Assisted / methods*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Myocardium / pathology*