Relationship between left ventricular mass and hemodynamic responses to physical and mental stress

Objective: Increased left ventricular mass (LVM) is predictive of future cardiac morbidity and mortality. Although casual and ambulatory blood pressure (BP) predict LVM, other hemodynamic determinants of LVM are incompletely understood. The present study examines laboratory-induced hemodynamic responses (to exercise, cold: and mental stress) and 24-hour ambulatory measures as predictors of LVM. Methods: Thirty-six healthy non-hypertensive subjects (mean age 33.9 +/- 9.4 years; 23 women, 13 men) were tested with mental stress, cold presser, and treadmill exercise in the laboratory and 24-hour ambulatory BP monitoring. LVM was measured using two-dimensional targeted M-mode echocardiography and indexed for body surface area (LVMI). Results: All laboratory tasks produced significant hemodynamic responses (p's < 0.01). Systolic blood pressure responses to mental stress (r = 042, p < 0.01) and cold presser (r = 0.34, p < 0.05) were significantly related to LVM. After adjusting for body size, the mental stress-induced SEP responses was the only significant predictor of LVMI (r = 0.32, p < 0.05). Exercise SEP responses were associated to LVMI in men (r = 0.63, p = 0.02), but not in women (r = 0.02, p = n.s.). Multivariate regression analyses revealed that SEP during mental stress was significantly predictive of LVMI (beta = 0.65, p = 0.05), independent of baseline SEP, 24-hour ambulatory SEP, and other control variables. Conclusion: The present results indicate that-SEP responses to mental stress are significantly related to LVM among healthy individuals, independently of baseline SEP, 24-hour ambulatory BP, age, body size, and sex. Blood pressure responses to exercise show a robust association with LVM in men but not in women. Hemodynamic responses elicited during laboratory tasks may therefore reveal important information about the pathophysiological processes involved in the development of cardiac end-organ damage. (C) 2000 Elsevier Science Inc. All rights reserved.