TY - JOUR
T1 - Oral magnesium therapy, exercise heart rate, exercise tolerance, and myocardial function in coronary artery disease patients
AU - Pokan, R.
AU - Hofmann, P.
AU - Von Duvillard, S. P.
AU - Smekal, G.
AU - Wonisch, M.
AU - Lettner, K.
AU - Schmid, P.
AU - Shechter, M.
AU - Silver, B.
AU - Bachl, N.
PY - 2006/9
Y1 - 2006/9
N2 - Background: Previous studies have demonstrated that in patients with coronary artery disease (CAD) upward deflection of the heart rate (HR) performance curve can be observed and that this upward deflection and the degree of the deflection are correlated with a diminished stress dependent left ventricular function. Magnesium supplementation improves endothelial function, exercise tolerance, and exercise induced chest pain in patients with CAD. Purpose: We studied trie effects of oral magnesium therapy on exercise dependent HR as related to exercise tolerance and resting myocardial function in patients with CAD. Methods: In a double blind controlled trial, 53 male patients with stable CAD were randomised to either oral magnesium 15 mmol twice daily (n = 28, age 61 ± 9 years, height 171± 7 cm, body weight 79 ± 10 kg, previous myocardial infarction, n = 7) or placebo (n = 25, age 58 ± 10 years, height 172 ± 6 cm, body weight 79 ± 10 kg, previous myocardial infarction, n = 6) for 6 months. Maximal oxygen uptake (VO 2max), the degree and direction of the deflection of the HR performance curve described as factor k<0 (upward deflection), and the left ventricular ejection fraction (LVEF) were the outcomes measured. Results: Magnesium therapy for 6 months significantly increased intracellular magnesium levels (32.7 ± 2.5 v 35.6 ± 2.1 mEq/l, p<0.001) compared to placebo (33.1 ± 3.1.9 v 33.8 ± 2.0 mEq/l, NS), VO2max (28.3 ± 6.2 v 30.6 ± 7.1 ml/kg/min, p<0.001; 29.3 ± 5.4 v 29.6± 5.2 ml/kg/min, NS), factor k (-0.298 ± 0.242 v -0.208 ± 0.260, p<0.05; -0.269 ± 0.336 v -0.272 ± 0.335, NS), and LVEF (58 ± 11 v 67 ± 10%, p<0.001; 55 ± 11 v 54 ± 12%, NS). Conclusion: The present study supports the intake of oral magnesium and its favourable effects on exercise tolerance and left ventricular function during rest and exercise in stable CAD patients.
AB - Background: Previous studies have demonstrated that in patients with coronary artery disease (CAD) upward deflection of the heart rate (HR) performance curve can be observed and that this upward deflection and the degree of the deflection are correlated with a diminished stress dependent left ventricular function. Magnesium supplementation improves endothelial function, exercise tolerance, and exercise induced chest pain in patients with CAD. Purpose: We studied trie effects of oral magnesium therapy on exercise dependent HR as related to exercise tolerance and resting myocardial function in patients with CAD. Methods: In a double blind controlled trial, 53 male patients with stable CAD were randomised to either oral magnesium 15 mmol twice daily (n = 28, age 61 ± 9 years, height 171± 7 cm, body weight 79 ± 10 kg, previous myocardial infarction, n = 7) or placebo (n = 25, age 58 ± 10 years, height 172 ± 6 cm, body weight 79 ± 10 kg, previous myocardial infarction, n = 6) for 6 months. Maximal oxygen uptake (VO 2max), the degree and direction of the deflection of the HR performance curve described as factor k<0 (upward deflection), and the left ventricular ejection fraction (LVEF) were the outcomes measured. Results: Magnesium therapy for 6 months significantly increased intracellular magnesium levels (32.7 ± 2.5 v 35.6 ± 2.1 mEq/l, p<0.001) compared to placebo (33.1 ± 3.1.9 v 33.8 ± 2.0 mEq/l, NS), VO2max (28.3 ± 6.2 v 30.6 ± 7.1 ml/kg/min, p<0.001; 29.3 ± 5.4 v 29.6± 5.2 ml/kg/min, NS), factor k (-0.298 ± 0.242 v -0.208 ± 0.260, p<0.05; -0.269 ± 0.336 v -0.272 ± 0.335, NS), and LVEF (58 ± 11 v 67 ± 10%, p<0.001; 55 ± 11 v 54 ± 12%, NS). Conclusion: The present study supports the intake of oral magnesium and its favourable effects on exercise tolerance and left ventricular function during rest and exercise in stable CAD patients.
UR - http://www.scopus.com/inward/record.url?scp=33748449019&partnerID=8YFLogxK
U2 - 10.1136/bjsm.2006.027250
DO - 10.1136/bjsm.2006.027250
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C2 - 16825271
AN - SCOPUS:33748449019
SN - 0306-3674
VL - 40
SP - 773
EP - 778
JO - British Journal of Sports Medicine
JF - British Journal of Sports Medicine
IS - 9
ER -