Key result
The cyclic variation index of integrated backscatter was significantly lower in hypertensive patients than in athletes and controls at both the septum (p<0.002) and posterior wall (p<0.001).
Why the study?
Does the cyclic variation of the myocardial integrated backscatter signal differ between hypertensive cardiopathy, athlete's heart, and healthy controls?
Observational (n=30)
Does the cyclic variation of the myocardial integrated backscatter signal differ between hypertensive cardiopathy, athlete's heart, and healthy controls?
p-value: p=< 0.002
Hypertensive cardiopathy is associated with a significant reduction in the cyclic variation of the myocardial integrated backscatter signal compared to athlete's heart and healthy controls, suggesting altered intramural myocardial function.
May support differentiation of hypertensive from physiologic hypertrophy; leaves open clinical utility pending prospective validation.
BACKGROUND: Ultrasound tissue characterization studies realized through integrated backscatter analysis with end-diastolic sampling in hypertensive cardiopathy have demonstrated that abnormalities in the left ventricular myocardial ultrasonic texture are present in extreme forms of left ventricular hypertrophy (LVH). Such abnormalities are not evident in the athlete's heart. The aim of the present study was to analyze the ultrasonic backscatter myocardial indexes both as peak end-diastolic signal intensity and as cardiac-cyclic variation in two models of LVH: hypertensive cardiopathy and athlete's heart. METHODS: Three groups of 10 subjects each, all men of mean age (31.6+/-3.5 years), and of comparable weight and height, were analyzed. Group A comprised 10 cyclists of good professional level, while hypertensive patients were grouped in Group H. Both groups presented a comparable left ventricular mass (LVM). Group C included 10 healthy subjects acting as controls. The men with hypertension were selected on the basis of the results of ambulatory monitoring of the blood pressure according to ISH-World Health Organization guidelines (International Society of Hypertension). A 2D-color Doppler echocardiography with a digital echograph Sonos 5500 (Agilent Technologies, Andover, Massachusetts, USA), was carried out on all the subjects in the study for conventional analysis of the LVM and function. The ultrasonic myocardial integrated backscatter signal (IBS) was analyzed with an 'acoustic densitometry' module implemented on a AT echograph. The signal was also sampled with a region of interest (ROI) placed at interventricular septum and at posterior left ventricular wall level. The systo-diastolic variation of the backscatter was also considered, as cyclic variation index (CVIibs). RESULTS: According to the inclusion criteria, the LVM was comparable in groups A and H, but it was significantly higher than group C (left ventricular mass (body surface) (LVMbs)=154.5+/-18.7 (A), 146.8+/-25.5 (H), 101.4+/-12.4 (C), p < 0.001). The end-diastolic IBS did not show significant statistical differences among the three groups. The CVI(IBS) both at septum (30.5+/-5.3 (A), 13.2+/-13.1 (H), 27.2+/-7.3(C), p < 0.002) and posterior wall level (43.7+/-9.1 (A), 16.5+/-12.1 (H), 40.7+/-9.1 (C), p < 0.001) though, was significantly lower in the hypertensive patients than in both the athletes and the control group, where the results were comparable. CONCLUSION: A significant alteration of the myocardial CVIibs (both for septum and posterior wall) was found in the hypertensive model. This was probably the expression of an alteration in the intramural myocardial function.
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Bello et al. (2001) conducted an observational in Hypertensive cardiopathy and athlete's heart (n=30). Ultrasonic backscatter myocardial indexes analysis vs. Athlete's heart and healthy controls was evaluated on Cyclic variation index of integrated backscatter (CVIibs) at septum and posterior wall (p=< 0.002). The cyclic variation index of integrated backscatter was significantly lower in hypertensive patients than in athletes and controls at both the septum (p<0.002) and posterior wall (p<0.001).
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