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Short-Term Estrogen Administration Ameliorates Dobutamine-Induced Myocardial Ischemia in Postmenopausal Women With Coronary Artery Disease
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JACC Vol. 30, No. 6 November 15, 1997:1466 –71
Short-Term Estrogen Administration Ameliorates Dobutamine-Induced Myocardial Ischemia in Postmenopausal Women With Coronary Artery Disease METE ALPASLAN, MD, HIROAKI SHIMOKAWA, MD, MARI KUROIWA-MATSUMOTO, MD, YASUHIKO HARASAWA, MD, AKIRA TAKESHITA, MD, FACC Fukuoka, Japan
Objectives. This study was designed to examine whether shortterm estrogen administration ameliorates dobutamine-induced myocardial ischemia in postmenopausal women with coronary artery disease (CAD). Background. Estrogen replacement therapy in postmenopausal women is associated with a marked reduction in the risk of CAD. Estrogen has been reported to have both short- and long-term effects on the cardiovascular system. However, it remains to be examined whether short-term estrogen administration ameliorates myocardial ischemia caused by increased myocardial oxygen demand in postmenopausal women with CAD. Methods. Eight postmenopausal women with proved CAD underwent dobutamine stress echocardiography (DSE). DSE was performed three times in a placebo-controlled, double-blind manner: 1) 30 min after intravenous administration of saline solution (placebo) and after 2) a low dose (1.25 mg) and 3) a high dose (10 mg) of conjugated estrogen. The effects of estrogen were compared at the maximal comparable stage of DSE, which was the
maximal DSE level that the same patient achieved in all three examinations. Results. Estrogen dose-dependently ameliorated the dobutamineinduced worsening of symptoms (prolonging time to onset of symptoms by 52% [low dose] and 72% [high dose]), electrocardiographic findings (decreasing the magnitude of summed ST segment changes by 36% [low dose] and 76% [high dose]) and left ventricular wall motion (reducing the wall motion score index by 50% [low dose] and 77% [high dose], all p < 0.01 by analysis of variance). There was no significant difference in blood pressure, heart rate or rate-pressure product among the three examinations at the maximal comparable stage of DSE. Conclusions. Estrogen has short-term anti-ischemic effects on the myocardial ischemia induced by increased myocardial oxygen demand in postmenopausal women with CAD. (J Am Coll Cardiol 1997;30:1466 –71) ©1997 by the American College of Cardiology
Epidemiologic studies have shown that estrogen replacement therapy achieves an ;50% reduction in the risk of coronary heart disease among postmenopausal women (1). Estrogen replacement therapy has more beneficial effects in reducing the incidence of cardiovascular events in postmenopausal women with coronary artery disease (CAD) than in those without CAD. Sullivan et al. (2) reported that estrogen replacement therapy in postmenopausal women with CAD reduced the mortality rate at 10 years from 35% to 14%. Beneficial effects of estrogen are not totally attributable to their favorable effects on plasma lipid levels (3). Another possible mechanism for the beneficial effects of estrogen is its vascular effects, including endothelium-dependent relaxation
(4 – 6), endothelium-independent and calcium antagonistic vasodilating effect (7–9) and antioxidant effect (10). It has recently been reported (11) that sublingual administration of 17-beta-estradiol has short-term beneficial effects on myocardial ischemia during treadmill exercise testing in postmenopausal women with CAD. However, exercise tolerance during treadmill testing may be determined both by cardiac factors (e.g., mechanical function of the heart) and by noncardiac factors (e.g., pulmonary function and peripheral arterial disease). Thus, this beneficial effect of estrogen may in part be due to the noncardiac effects of the hormone. To our knowledge, the short-term effects of estrogen administration on left ventricular (LV) wall motion during myocardial ischemia have not been directly investigated. This study was thus designed to examine whether shortterm estrogen administration ameliorates the myocardial ischemia during dobutamine stress echocardiography (DSE) in postmenopausal women with CAD.
From the Research Institute of Angiocardiology and Cardiovascular Clinic, Kyushu University School of Medicine, Fukuoka, Japan. This work was supported in part by grants-in-aid from the Ministry of Education, Science, Sports and Culture, Tokyo, Japan. Manuscript received February 12, 1997; revised manuscript received July 31, 1997, accepted August 14, 1997. Address for correspondence: Dr. Hiroaki Shimokawa, The Research Institute of Angiocardiology and Cardiovascular Clinic, Kyushu University School of Medicine, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-82, Japan. E-mail: [email protected]. ©1997 by the American College of Cardiology Published by Elsevier Science Inc.
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JACC Vol. 30, No. 6 November 15, 1997:1466 –71
ALPASLAN ET AL. ANTI-ISCHEMIC EFFECT OF ESTROGEN
Abbreviations and Acronyms ANOVA 5 analysis of variance CAD 5 coronary artery disease ECG 5 electrocardiogram, electrocardiographic DSE 5 dobutamine stress echocardiography (echocardiographic) LV 5 left ventricular
Methods Subjects. Eight postmenopausal women with CAD proved by coronary arteriography were included in this study. The mean age was 69 years (range 53 to 79). No patient was receiving estrogen replacement therapy. All patients gave a written informed consent before the examination. No other patients were examined in the present study, and thus no exclusion took place before the examination. Study protocol was approved by the Human Research Committee at the Research Institute of Angiocardiology, Kyushu University School of Medicine. The clinical characteristics of the patients are shown in Table 1. DSE. DSE was performed three times in 2 weeks, in a placebo-controlled, double-blind manner: 1) 30 min after intravenous bolus administration of saline solution (5 ml) and after 2) a low dose (1.25 mg) and 3) a high dose (10 mg) of estrogen diluted in 5 ml of saline solution. The three examinations were performed at the same time of day in the same patient. Among the medications only beta-adrenergic receptor blocking agents were discontinued 1 day before the examination. No patient was receiving verapamil or diltiazem, which could suppress the heart rate response to dobutamine. The presence of unstable angina, profound anemia, electrolyte imbalance or uncontrolled hypertension (systolic blood pressure .190 or diastolic blood pressure .100 mm Hg, or both) was regarded as a contraindication for DSE. The patients were in the left lateral decubitus position throughout the study. They were asked to report the onset of chest pain or discomfort, or both, during the examination. Dobutamine was administered intravenously by an infusion pump. The starting dose of dobutamine was 5 mg/kg per min
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and the dose of dobutamine was increased in stepwise manner to 10, 20, 30, 40 and 50 mg/kg per min every 4 min until one of the following general end points was reached: target heart rate (85% of age-predicted maximal heart rate), peak dose, ischemic electrocardiographic (ECG) changes (.1 mm ST segment depression or elevation in more than two leads), severe hypertension (systolic blood pressure .220 mm Hg or diastolic blood pressure .110 mm Hg, or both), hypotension (.20 mm Hg decrease in systolic blood pressure compared with the rest blood pressure), chest pain or patient refusal to continue. When the patient experienced only mild chest discomfort or dyspnea without any of the preceding end points, the dobutamine infusion was continued until an end point was reached. However, a patient’s report of such chest discomfort or dyspnea was regarded as the onset of symptoms. Two-dimensional echocardiograms were obtained at rest, 3 min after dobutamine infusion at each stage and 10 min after the end of the dobutamine infusion. Atropine was not used in any patient. Echocardiographic images included parasternal long-axis, parasternal short-axis, apical two-chamber and apical four-chamber views; they were stored on S-VHS videotapes (Black Magnetite, Maxell, Tokyo, Japan) for off-line analysis. Twelve-lead ECGs were recorded at each stage (Auto Cardiner FCP-4301, Fukuda Denshi, Tokyo, Japan) and the patient also was continuously monitored by three-lead ECGs during the examination. Blood pressure was measured at each stage with a cuff manometer in the right or left arm opposite to the dobutamine infusion side. Time to onset of symptoms (chest pain, chest discomfort or dyspnea) was also recorded. ST segment depression was measured 0.08 s after the J point, and ST elevation was measured 0.02 s after the J point. The sum of ST shift was calculated by summing the ST elevations or depressions in 12-lead ECGs (12). We have previously confirmed that our DSE examination is reproducible to detect the presence of CAD. Our DSE examination has a sensitivity of 79% and a specificity of 92% (unpublished observations). Analysis of DSE. Echocardiograms were independently interpreted in blinded manner by two experienced cardiologists familiar with the analysis of LV wall motion. LV wall motion was analyzed in a 16-segment model as suggested by
Table 1. Clinical Characteristics of the Eight Postmenopausal Women Patient No.
Age (yr)
Coronary Artery Disease
Old Myocardial Infarction
Risk Factors
1 2 3 4 5 6 7 8
53 75 75 58 79 72 70 75
1-VD (LAD) 3-VD Left main trunk 1-VD (LAD) 1-VD (LAD) 2-VD (LAD, RCA) 1-VD (RCA) 3-VD
No Yes (apical) No Yes (anterolateral) No No Yes (inferior) No
Hypertension, NIDDM Hypertension, NIDDM, hyperlipidemia Hypertension, NIDDM, hyperlipidemia Hypertension Hypertension Hyperlipidemia Hypertension, NIDDM, hyperlipidemia Hypertension, hyperlipidemia
LAD 5 left anterior descending coronary artery; NIDDM 5 non–insulin-dependent diabetes mellitus; RCA 5 right coronary artery; VD 5 vessel disease.
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Figure 1. Time course of serum estrogen levels. Data are expressed as mean value 6 SEM (n 5 8). Serum levels of estrone and estradiol, but not those of estriol, increased significantly after intravenous administration of both low (solid circles [1.25 mg]) and high dose (open circles [10 mg]) conjugated estrogen. Serum levels of estrogen remained increased throughout DSE. Crossmarks 5 saline. *p , 0.01 versus control.
the American Society of Echocardiography (13). Wall motion index was scored in the following manner (14): normal 5 1; hypokinesia, severe hypokinesia or failure of hyperkinesia to develop 5 2; akinesia 5 3; dyskinesia 5 4; and aneurysmal 5 5. Hyperdynamic wall motion was regarded as the normal response to dobutamine infusion (14). Wall motion score index was calculated for every stage of DSE. Scoring was not performed if a particular segment was not clear enough for interpretation. The scores were summed and divided by the number of available segments to obtain the wall motion score index. The tolerance to dobutamine varied even in the same patient among the three examinations. Thus, the changes in the wall motion score index or the ST segment level from rest conditions to the maximal comparable stage of DSE, that is the maximal DSE level that the same patient could achieve in all three examinations, was determined to examine the effect of estrogen. The changes in wall motion score index were determined by the two cardiologists, and the mean value was used for the analysis. We confirmed that there was an excellent intraobserver (r 5 0.95, p , 0.001) and interobserver (r 5 0.96, p , 0.001) consistency (by a single-variable linear regression analysis). Measurements of serum levels of estrogen and lipid peroxides. Venous blood was sampled three times during each DSE examination: before and 30 min after the injection of test medication (just before starting DSE) and 10 min after the end of dobutamine infusion. The serum levels of the three estrogen fractions (estrone, estradiol and estriol) were analyzed by
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radioimmunoassay (15). Serum levels of lipid peroxides were also analyzed by the thiuobarbituric acid method (16). Drugs. Conjugated estrogen (Premarin, 20 mg/5 ml physiologic saline solution for intravenous use) was purchased from Asahi Chemicals (Tokyo, Japan) and dobutamine chloride from Shionogi Co. Ltd. (Osaka, Japan). Statistical analysis. Results are expressed as the mean value 6 SEM. Throughout the text, n means the number of patients. Data obtained from three examinations (saline solution and a low and a high dose of estrogen) were analyzed by analysis of variance (ANOVA) for repeated measures; if a significant F value was found, the Scheffe´ test for multiple comparisons was used to identify any differences among the three groups. A p value , 0.05 was considered statistically significant.
Results Serum levels of estrogen and lipid peroxides. After injection of a low dose of estrogen, serum levels of estrone and estradiol significantly increased to premenopausal levels whereas those of estriol did not change (Fig. 1). After administration of a high dose of estrogen, serum levels of estrone and estradiol further increased to supraphysiologic levels whereas those of estriol again did not change (Fig. 1). The serum levels of estrone and estradiol remained increased without a significant decrease during the examination period (Fig. 1). Serum levels of lipid peroxides under control conditions were within normal ranges (2 to 6 nmol/ml) in all three examinations: 3.3 6 0.2, 3.5 6 0.2 and 3.5 6 0.2 nmol/ml in the examinations with saline and low and high dose estrogen, respectively. These lipid peroxide levels did not change significantly after administration of either estrogen or dobutamine (data not shown). End point of DSE. Among the 24 DSE examinations, the dobutamine infusion was stopped because of chest pain in 14, achievement of the peak dose of dobutamine in 6, and ischemic ST segment changes in 4. Thus, the maximal comparable stage
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Table 2. Hemodynamic Variables
Saline solution HR Systolic BP Diastolic BP RPP (3103) Estrogen Low dose HR Systolic BP Diastolic BP RPP (3103) High dose HR Systolic BP Diastolic BP RPP (3103)
Control
Before DSE
At a Maximal Comparable Stage
62 6 3 136 6 6 72 6 4 8,525 6 634
58 6 3 137 6 6 73 6 4 8,090 6 511
95 6 6* 149 6 6 71 6 4 14,223 6 1,118*
60 6 3 134 6 5 68 6 3 8,187 6 586
58 6 3 135 6 3 66 6 3 7,961 6 442
99 6 6* 139 6 7 67 6 4 13,962 6 1,358*
58 6 3 143 6 3 77 6 6 8,252 6 486
56 6 2 138 6 4 72 6 6 7,711 6 302
92 6 4* 142 6 6 67 6 6 13,280 6 1,017*
*p , 0.01 versus control. Data are expressed as mean value 6 SEM (n 5 8). BP 5 blood pressure (mm Hg); DSE 5 dobutamine stress echocardiography; HR 5 heart rate (beats/min); RPP 5 rate-pressure product calculated as heart rate 3 systolic blood pressure.
of DSE (as expressed by the dobutamine dose, mg/kg per min) was 10 (n 5 1), 20 (n 5 4), 40 (n 5 2) and 50 (n 5 1). The patients reported that the dobutamine-induced chest pain was similar to that experienced in their daily life. Changes in hemodynamic variables. No significant difference was noted in heart rate, blood pressure or rate-pressure product among the three examinations (Table 2). Administration of estrogen, both low and high dose, did not significantly change heart rate, blood pressure or rate-pressure product before and 30 min after estrogen administration. However, at the maximal comparable stage of DSE, heart rate and ratepressure product, but not blood pressure, significantly increased over values in control conditions (Table 2). Effect of estrogen on symptoms. Estrogen significantly and dose-dependently prolonged the time to the onset of symptoms (p , 0.01 by ANOVA) (Fig. 2). The mean value of the percent prolongation of the time to the onset of symptoms was 52% at a low dose and 72% at a high dose of the hormone (Fig. 2). Effects of estrogen on ECG changes. Estrogen significantly and dose-dependently reduced the magnitude of the summed ST segment changes (p , 0.01 by ANOVA) (Fig. 3). The mean value of the percent reduction of the ST segment changes was 36% at a low dose and 76% at a high dose of the hormone (Fig. 3). Effect of estrogen on wall motion abnormalities. Estrogen significantly and dose-dependently ameliorated the worsening of the wall motion score index at the maximal comparable stage of DSE (p , 0.01 by ANOVA) (Fig. 4). The mean value of the percent reduction of the wall motion score index was 50% at a low dose and 77% at a high dose of the hormone (Fig. 4). Influence of baseline wall motion abnormalities. The preceding beneficial effects of estrogen on dobutamine-induced
Figure 2. Time (min) to onset of symptoms. Data are presented as mean value 6 SEM (n 5 8). The time to onset of symptoms of 24 min indicates that the patient completed the DSE examination without chest pain. Estrogen (E) dose-dependently prolonged the onset of symptoms during DSE (p , 0.01 by ANOVA).
symptoms, ECG changes and wall motion abnormalities were noted in our postmenopausal patients with CAD, regardless of the presence or absence of baseline wall motion abnormalities (data not shown).
Discussion The novel finding of the present study is that short-term administration of conjugated estrogen significantly ameliorated the dobutamine-induced myocardial ischemia in postmenopausal women with CAD. DSE. Dobutamine is a synthetic catecholamine and has effects on beta1-, beta2- and alpha1-adrenergic receptors (17,18). Dobutamine increases myocardial oxygen demand by increasing heart rate and myocardial contractility (17,18) mainly due to beta1-adrenergic receptor stimulation. The Figure 3. Summed ST segment changes (mm) from control to the maximal comparable stages of DSE. Data are presented as mean value 6 SEM (n 5 8). Estrogen (E) dose-dependently decreased the magnitude of summed ST segment changes from control levels to maximal comparable stages of DSE (p , 0.01 by ANOVA).
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Figure 4. Changes in wall motion index score evaluated by echocardiography. Data are presented as mean value 6 SEM (n 5 8). Estrogen (E) dose-dependently ameliorated the wall motion index score (p , 0.01 by ANOVA).
beta2- and alpha1-adrenergic agonist activities of dobutamine are relatively milder than its beta1-adrenergic activity. Because beta2- and alpha1-adrenergic effects of dobutamine are balanced in peripheral vasculature, dobutamine infusion, especially at low doses, has minimal effects on blood pressure (17). In the presence of CAD, the increased myocardial oxygen demand by dobutamine is associated with an inadequate increase in coronary blood flow, resulting in myocardial ischemia and abnormal LV wall motion that can be detected by cross-sectional echocardiography (14). DSE has several advantages over exercise echocardiography (19). First, myocardial ischemia can be easily induced by dobutamine infusion in almost all patients, whereas exercise echocardiography cannot always be performed in all patients. Second, because DSE allows echocardiographic imaging at every stage of dobutamine infusion, we were able to analyze LV wall motion at the maximal comparable stage of DSE in our study, whereas exercise echocardiography can be performed only after exercise. In the present study, heart rate responses were slightly lower than those in previous reports (17,18). We consider that this difference occurred in part because only two of our patients could achieve a dobutamine infusion rate of 50 mg/kg per min in four DSE examinations, and in part because the relatively older age of our patients (mean 69 years) may have blunted the heart rate response to the dobutamine stimulation. However, because rate-pressure products were comparable among the three examinations in our study, we were able to examine the effects of estrogen at the maximal comparable level of myocardial oxygen demand. Anti-ischemic effect of estrogen. In the present study, we observed the short-term anti-ischemic effects of estrogen, which may be attributed to the following vascular effects of this hormone: 1. Estrogen may ameliorate the extent of myocardial ischemia by enhancing the endothelium-dependent vasodilation of the coronary artery. Previous studies have demonstrated that
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an increase in sympathetic tone, such as that caused by mental stress (20), exercise (21) or cold pressor test (22), causes dilation of normal coronary arteries and paradoxic constriction of atherosclerotic coronary arteries with dysfunctional endothelium. Thus, enhanced endothelium-dependent relaxation may play a protective role to delay or prevent the occurrence of myocardial ischemia in patients with CAD. Physiologic levels of 17-beta-estradiol were shown (23) to immediately and selectively potentiate endothelium-dependent dilation in both large coronary arteries and coronary microvessels in postmenopausal women. We (24) also recently demonstrated that estrogen immediately improves both nitric oxide–mediated and non-nitric oxide (possibly endothelium-derived hyperpolarizing factor)–mediated endothelium-dependent forearm vasodilation in postmenopausal women. In the present study, it is possible that potentiation of endothelium-dependent vasodilation by estrogen increased the myocardial blood flow and ameliorated the dobutamine-induced worsening of symptoms, ECG findings and LV wall motion. 2. The endothelium-independent and calcium antagonistic vasodilating effects of estrogen may also explain in part its anti-ischemic effect. As functional estrogen receptor has been demonstrated on vascular smooth muscle cells in the human saphenous vein and mammary artery (25), it is highly possible that this also is the case in the human coronary artery. 3. An antioxidant effect of estrogen might be involved in the anti-ischemic effect of the hormone. However, this possibility may be less likely, at least in the present study, because the levels of lipid peroxides, a marker of systemic production of oxygen-derived free radicals (26), did not decrease with a low or a high dose of estrogen. In the present study, we used conjugated estrogen because it is the only estrogen agent that can be used for intravenous administration in our country. As serum levels of both estrone and estradiol were increased after administration of conjugated estrogen in our study, both estrogen fractions may contribute to the anti-ischemic effect of estrogen. Whereas comparative vascular effects of estrone and estradiol remain to be examined, estradiol is three times as potent as estrone in its anti-oxidant effect (27). A comparison of the serum levels of estrone and estradiol (Fig. 1) with the anti-ischemic effects of estrogen (Fig. 2 to 4) indicates that the logarithmic values of the estrogen levels appear to correlate with the hormone’s anti-ischemic effects. It also should be noted that even a low dose of estrogen (1.25 mg intravenously) that achieved physiologic serum levels of the hormone exerted anti-ischemic effects in postmenopausal women with CAD. Limitations of the study. Several limitations of our study could be cited. 1) We included only eight patients. However, the anti-ischemic effects of estrogen were evident even with this small number. 2) We investigated only the immediate effects of estrogen. A recent study (28) found that long-term estrogen replacement therapy that achieved physiologic levels of estrogen did not improve exercise tolerance by treadmill test in healthy postmenopausal women. It remains to be examined
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whether long-term estrogen replacement therapy increases exercise tolerance in postmenopausal women with CAD. 3) We did not store the images in a digitized format or review in a quad screen format but recorded them on S-VHS tapes. Side by side cine loop format is generally accepted to be a superior way for analyzing DSE. However, a recent study (29) suggested that, although digitized analysis would be more appropriate, traditional videotape analysis may also be used in DSE. 4) We included three patients with baseline wall motion abnormalities. However, the beneficial effects of estrogen were noted in our postmenopausal patients with CAD, regardless of the presence or absence of baseline wall motion abnormalities. In summary, we were able to demonstrate that short-term estrogen administration ameliorates dobutamine-induced myocardial ischemia. Our finding may have important clinical implications for understanding both the pathogenesis and the management of CAD in postmenopausal women. We thank Chie Fukagawa and Drs. Shin-ichi Ando, Hiroaki Yamamoto and Jun-ichi Oyama for their kind cooperation in this study.
References 1. Grodstein F, Stampfer M. The epidemiology of coronary heart disease and estrogen replacement in postmenopausal women. Prog Cardiovasc Dis 1995;38:199 –210. 2. Sullivan JM, Vander Zwaag R, Lemp GF, et al. Postmenopausal estrogen use and coronary atherosclerosis. Ann Intern Med 1988;108:358 – 63. 3. Barret-Connor E, Bush TL. Estrogen and coronary heart disease in women. JAMA 1991;265:1861–7. 4. Gilligan DM, Quyyumi AA, Cannon RO. Effects of physiological levels of estrogen on coronary vasomotor function in postmenopausal women. Circulation 1994;89:2545–51. 5. Williams JK, Adams MR, Klopfenstein HS. Estrogen modulates responses of atherosclerotic coronary arteries. Circulation 1990;81:1680 –7. 6. Williams JK, Adams MR, Herrington DM, Clarkson TB. Short term administration of estrogen and vascular responses of atherosclerotic coronary arteries. J Am Coll Cardiol 1992;20:452–7. 7. Jiang C, Sarrel PM, Lindsay DC, Poole-Wilson PA, Collins P. Endotheliumindependent relaxation of rabbit coronary artery by 17b-oestradiol in vitro. Br J Pharmacol 1991;104:1033–7. 8. Collins P, Rosano GMC, Lindsay D, Sarrel PM, Poole-Wilson PA. Cardiovascular protection by estrogen—a calcium antagonistic effect? Lancet 1993;341:1264 –5. 9. Han SZ, Karaki H, Ouchi Y, Akishita M, Orimo H. 17b-estradiol inhibits Ca21 influx and Ca21 release induced by thromboxane A2 in porcine coronary artery. Circulation 1995;91:2619 –26. 10. Sacks MN, Rader DJ, Cannon RO. Oestrogen and inhibition of oxidation of low density lipoproteins in postmenopausal women. Lancet 1994;343:269 – 70.
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11. Rosano GMC, Sarrel PM, Poole-Wilson PA, Collins P. Beneficial effects of oestrogen on exercise-induced myocardial ischemia in women with CAD. Lancet 1993;342:133– 6. 12. Cohen M, Rentrop P. Limitation of myocardial ischemia by collateral circulation during sudden controlled coronary artery occlusion in human subjects: a prospective study. Circulation 1986;74:469 –76. 13. Bourdillon PDV, Broderick TM, Sawada SG, et al. Regional wall motion index for infarct and noninfarct regions after reperfusion in acute myocardial infarction: comparison with global wall motion index. J Am Soc Echocardiogr 1989;2:398 – 407. 14. Bartunek J, Marwick TH, Rodrigues ACT, et al. Dobutamine-induced wall motion abnormalities: correlations with myocardial fractional flow reserve and quantitative coronary angiography. J Am Coll Cardiol 1996;27:1429 –36. 15. Meness RR, Rosenfield CR. Local and systemic estradiol 17b: effects on uterine and systemic vasodilation. Am J Physiol 1989;256:E536 – 42. 16. Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Annal Biochem 1979;95:351– 8. 17. Ruffalo RR. The pharmacology of dobutamine. Am J Med Sci 1987;294: 244 – 8. 18. Vanoverschelde JLJ, Wijns W, Essamri B, et al. Hemodynamic and mechanical determinants of myocardial O2 consumption in normal human heart: effects of dobutamine. Am J Physiol 1993;265:H1884 –92. 19. Pelikka PA, Roger VL, Oh JK, Miller FA, Seward JB, Tajik AJ. Stress echocardiography—Part II: dobutamine stress echocardiography: techniques, implementation, clinical applications, and correlations. Mayo Clin Proc 1995;70:16 –27. 20. Yeung AC, Vekshtein VI, Krantz DS, et al. The effect of atherosclerosis on the vasomotor response of coronary arteries to mental stress. N Engl J Med 1989;325:1551– 6. 21. Gordon JB, Ganz P, Nabel EG, et al. Atherosclerosis influences the vasomotor response of epicardial coronary arteries to exercise. J Clin Invest 1989;83:1946 –52. 22. Zeiher AM, Drexler H, Wollschla¨ger H, Just H. Modulation of coronary vasomotor tone in humans: progressive endothelial dysfunction with different early stages of coronary arteries. Circulation 1991;83:391– 401. 23. Reis SE, Gloth ST, Blumenthal RS, et al. Ethinyl estradiol acutely attenuates abnormal coronary vasomotor responses to acetylcholine in postmenopausal women. Circulation 1994;89:52– 60. 24. Tagawa H, Shimokawa H, Tagawa T, et al. Short-term estrogen augments both nitric oxide–mediated and non nitric oxide–mediated endotheliumdependent forearm vasodilation in postmenopausal women. J Cardiovasc Pharmacol 1997;30:481. 25. Karas RH, Patterson BL, Mendelson ME. Human vascular smooth muscle cells contain functional estrogen receptor. Circulation 1994;89:1943–50. 26. Paller MS, Hoidal JR, Ferris TF. Oxygen free radicals in ischemic acute renal failure in the rat. J Clin Invest 1984;74:1156 – 64. 27. Taniguchi S, Yanase T, Kobayashi K, et al. Catecol estrogen are more potent antioxidants than estrogens for the Cu21-catalyzed oxidation of low or high density lipoprotein: antioxidative effects of steroids on lipoproteins. Endocrine J 1994;41:605–11. 28. Snabes MC, Herd JA, Schuyler N, Dunn K, Spence DW, Young RL. In normal postmenopausal women physiologic estrogen replacement therapy fails to improve exercise tolerance: a randomized, double-blind, placebocontrolled, crossover trial. Am J Obstet Gynecol 1996;175:110 – 4. 29. Castini D, Gentile F, Ornaghi M, et al. Dobutamine echocardiography: usefulness of digital image processing. Eur Heart J 1995;16:1420 – 4.
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Short-Term Estrogen Administration Ameliorates Dobutamine-Induced Myocardial Ischemia in Postmenopausal Women With Coronary Artery Disease METE ALPASLAN, MD, HIROAKI SHIMOKAWA, MD, MARI KUROIWA-MATSUMOTO, MD, YASUHIKO HARASAWA, MD, AKIRA TAKESHITA, MD, FACC Fukuoka, Japan
Objectives. This study was designed to examine whether shortterm estrogen administration ameliorates dobutamine-induced myocardial ischemia in postmenopausal women with coronary artery disease (CAD). Background. Estrogen replacement therapy in postmenopausal women is associated with a marked reduction in the risk of CAD. Estrogen has been reported to have both short- and long-term effects on the cardiovascular system. However, it remains to be examined whether short-term estrogen administration ameliorates myocardial ischemia caused by increased myocardial oxygen demand in postmenopausal women with CAD. Methods. Eight postmenopausal women with proved CAD underwent dobutamine stress echocardiography (DSE). DSE was performed three times in a placebo-controlled, double-blind manner: 1) 30 min after intravenous administration of saline solution (placebo) and after 2) a low dose (1.25 mg) and 3) a high dose (10 mg) of conjugated estrogen. The effects of estrogen were compared at the maximal comparable stage of DSE, which was the
maximal DSE level that the same patient achieved in all three examinations. Results. Estrogen dose-dependently ameliorated the dobutamineinduced worsening of symptoms (prolonging time to onset of symptoms by 52% [low dose] and 72% [high dose]), electrocardiographic findings (decreasing the magnitude of summed ST segment changes by 36% [low dose] and 76% [high dose]) and left ventricular wall motion (reducing the wall motion score index by 50% [low dose] and 77% [high dose], all p < 0.01 by analysis of variance). There was no significant difference in blood pressure, heart rate or rate-pressure product among the three examinations at the maximal comparable stage of DSE. Conclusions. Estrogen has short-term anti-ischemic effects on the myocardial ischemia induced by increased myocardial oxygen demand in postmenopausal women with CAD. (J Am Coll Cardiol 1997;30:1466 –71) ©1997 by the American College of Cardiology
Epidemiologic studies have shown that estrogen replacement therapy achieves an ;50% reduction in the risk of coronary heart disease among postmenopausal women (1). Estrogen replacement therapy has more beneficial effects in reducing the incidence of cardiovascular events in postmenopausal women with coronary artery disease (CAD) than in those without CAD. Sullivan et al. (2) reported that estrogen replacement therapy in postmenopausal women with CAD reduced the mortality rate at 10 years from 35% to 14%. Beneficial effects of estrogen are not totally attributable to their favorable effects on plasma lipid levels (3). Another possible mechanism for the beneficial effects of estrogen is its vascular effects, including endothelium-dependent relaxation
(4 – 6), endothelium-independent and calcium antagonistic vasodilating effect (7–9) and antioxidant effect (10). It has recently been reported (11) that sublingual administration of 17-beta-estradiol has short-term beneficial effects on myocardial ischemia during treadmill exercise testing in postmenopausal women with CAD. However, exercise tolerance during treadmill testing may be determined both by cardiac factors (e.g., mechanical function of the heart) and by noncardiac factors (e.g., pulmonary function and peripheral arterial disease). Thus, this beneficial effect of estrogen may in part be due to the noncardiac effects of the hormone. To our knowledge, the short-term effects of estrogen administration on left ventricular (LV) wall motion during myocardial ischemia have not been directly investigated. This study was thus designed to examine whether shortterm estrogen administration ameliorates the myocardial ischemia during dobutamine stress echocardiography (DSE) in postmenopausal women with CAD.
From the Research Institute of Angiocardiology and Cardiovascular Clinic, Kyushu University School of Medicine, Fukuoka, Japan. This work was supported in part by grants-in-aid from the Ministry of Education, Science, Sports and Culture, Tokyo, Japan. Manuscript received February 12, 1997; revised manuscript received July 31, 1997, accepted August 14, 1997. Address for correspondence: Dr. Hiroaki Shimokawa, The Research Institute of Angiocardiology and Cardiovascular Clinic, Kyushu University School of Medicine, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-82, Japan. E-mail: [email protected]. ©1997 by the American College of Cardiology Published by Elsevier Science Inc.
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JACC Vol. 30, No. 6 November 15, 1997:1466 –71
ALPASLAN ET AL. ANTI-ISCHEMIC EFFECT OF ESTROGEN
Abbreviations and Acronyms ANOVA 5 analysis of variance CAD 5 coronary artery disease ECG 5 electrocardiogram, electrocardiographic DSE 5 dobutamine stress echocardiography (echocardiographic) LV 5 left ventricular
Methods Subjects. Eight postmenopausal women with CAD proved by coronary arteriography were included in this study. The mean age was 69 years (range 53 to 79). No patient was receiving estrogen replacement therapy. All patients gave a written informed consent before the examination. No other patients were examined in the present study, and thus no exclusion took place before the examination. Study protocol was approved by the Human Research Committee at the Research Institute of Angiocardiology, Kyushu University School of Medicine. The clinical characteristics of the patients are shown in Table 1. DSE. DSE was performed three times in 2 weeks, in a placebo-controlled, double-blind manner: 1) 30 min after intravenous bolus administration of saline solution (5 ml) and after 2) a low dose (1.25 mg) and 3) a high dose (10 mg) of estrogen diluted in 5 ml of saline solution. The three examinations were performed at the same time of day in the same patient. Among the medications only beta-adrenergic receptor blocking agents were discontinued 1 day before the examination. No patient was receiving verapamil or diltiazem, which could suppress the heart rate response to dobutamine. The presence of unstable angina, profound anemia, electrolyte imbalance or uncontrolled hypertension (systolic blood pressure .190 or diastolic blood pressure .100 mm Hg, or both) was regarded as a contraindication for DSE. The patients were in the left lateral decubitus position throughout the study. They were asked to report the onset of chest pain or discomfort, or both, during the examination. Dobutamine was administered intravenously by an infusion pump. The starting dose of dobutamine was 5 mg/kg per min
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and the dose of dobutamine was increased in stepwise manner to 10, 20, 30, 40 and 50 mg/kg per min every 4 min until one of the following general end points was reached: target heart rate (85% of age-predicted maximal heart rate), peak dose, ischemic electrocardiographic (ECG) changes (.1 mm ST segment depression or elevation in more than two leads), severe hypertension (systolic blood pressure .220 mm Hg or diastolic blood pressure .110 mm Hg, or both), hypotension (.20 mm Hg decrease in systolic blood pressure compared with the rest blood pressure), chest pain or patient refusal to continue. When the patient experienced only mild chest discomfort or dyspnea without any of the preceding end points, the dobutamine infusion was continued until an end point was reached. However, a patient’s report of such chest discomfort or dyspnea was regarded as the onset of symptoms. Two-dimensional echocardiograms were obtained at rest, 3 min after dobutamine infusion at each stage and 10 min after the end of the dobutamine infusion. Atropine was not used in any patient. Echocardiographic images included parasternal long-axis, parasternal short-axis, apical two-chamber and apical four-chamber views; they were stored on S-VHS videotapes (Black Magnetite, Maxell, Tokyo, Japan) for off-line analysis. Twelve-lead ECGs were recorded at each stage (Auto Cardiner FCP-4301, Fukuda Denshi, Tokyo, Japan) and the patient also was continuously monitored by three-lead ECGs during the examination. Blood pressure was measured at each stage with a cuff manometer in the right or left arm opposite to the dobutamine infusion side. Time to onset of symptoms (chest pain, chest discomfort or dyspnea) was also recorded. ST segment depression was measured 0.08 s after the J point, and ST elevation was measured 0.02 s after the J point. The sum of ST shift was calculated by summing the ST elevations or depressions in 12-lead ECGs (12). We have previously confirmed that our DSE examination is reproducible to detect the presence of CAD. Our DSE examination has a sensitivity of 79% and a specificity of 92% (unpublished observations). Analysis of DSE. Echocardiograms were independently interpreted in blinded manner by two experienced cardiologists familiar with the analysis of LV wall motion. LV wall motion was analyzed in a 16-segment model as suggested by
Table 1. Clinical Characteristics of the Eight Postmenopausal Women Patient No.
Age (yr)
Coronary Artery Disease
Old Myocardial Infarction
Risk Factors
1 2 3 4 5 6 7 8
53 75 75 58 79 72 70 75
1-VD (LAD) 3-VD Left main trunk 1-VD (LAD) 1-VD (LAD) 2-VD (LAD, RCA) 1-VD (RCA) 3-VD
No Yes (apical) No Yes (anterolateral) No No Yes (inferior) No
Hypertension, NIDDM Hypertension, NIDDM, hyperlipidemia Hypertension, NIDDM, hyperlipidemia Hypertension Hypertension Hyperlipidemia Hypertension, NIDDM, hyperlipidemia Hypertension, hyperlipidemia
LAD 5 left anterior descending coronary artery; NIDDM 5 non–insulin-dependent diabetes mellitus; RCA 5 right coronary artery; VD 5 vessel disease.
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Figure 1. Time course of serum estrogen levels. Data are expressed as mean value 6 SEM (n 5 8). Serum levels of estrone and estradiol, but not those of estriol, increased significantly after intravenous administration of both low (solid circles [1.25 mg]) and high dose (open circles [10 mg]) conjugated estrogen. Serum levels of estrogen remained increased throughout DSE. Crossmarks 5 saline. *p , 0.01 versus control.
the American Society of Echocardiography (13). Wall motion index was scored in the following manner (14): normal 5 1; hypokinesia, severe hypokinesia or failure of hyperkinesia to develop 5 2; akinesia 5 3; dyskinesia 5 4; and aneurysmal 5 5. Hyperdynamic wall motion was regarded as the normal response to dobutamine infusion (14). Wall motion score index was calculated for every stage of DSE. Scoring was not performed if a particular segment was not clear enough for interpretation. The scores were summed and divided by the number of available segments to obtain the wall motion score index. The tolerance to dobutamine varied even in the same patient among the three examinations. Thus, the changes in the wall motion score index or the ST segment level from rest conditions to the maximal comparable stage of DSE, that is the maximal DSE level that the same patient could achieve in all three examinations, was determined to examine the effect of estrogen. The changes in wall motion score index were determined by the two cardiologists, and the mean value was used for the analysis. We confirmed that there was an excellent intraobserver (r 5 0.95, p , 0.001) and interobserver (r 5 0.96, p , 0.001) consistency (by a single-variable linear regression analysis). Measurements of serum levels of estrogen and lipid peroxides. Venous blood was sampled three times during each DSE examination: before and 30 min after the injection of test medication (just before starting DSE) and 10 min after the end of dobutamine infusion. The serum levels of the three estrogen fractions (estrone, estradiol and estriol) were analyzed by
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radioimmunoassay (15). Serum levels of lipid peroxides were also analyzed by the thiuobarbituric acid method (16). Drugs. Conjugated estrogen (Premarin, 20 mg/5 ml physiologic saline solution for intravenous use) was purchased from Asahi Chemicals (Tokyo, Japan) and dobutamine chloride from Shionogi Co. Ltd. (Osaka, Japan). Statistical analysis. Results are expressed as the mean value 6 SEM. Throughout the text, n means the number of patients. Data obtained from three examinations (saline solution and a low and a high dose of estrogen) were analyzed by analysis of variance (ANOVA) for repeated measures; if a significant F value was found, the Scheffe´ test for multiple comparisons was used to identify any differences among the three groups. A p value , 0.05 was considered statistically significant.
Results Serum levels of estrogen and lipid peroxides. After injection of a low dose of estrogen, serum levels of estrone and estradiol significantly increased to premenopausal levels whereas those of estriol did not change (Fig. 1). After administration of a high dose of estrogen, serum levels of estrone and estradiol further increased to supraphysiologic levels whereas those of estriol again did not change (Fig. 1). The serum levels of estrone and estradiol remained increased without a significant decrease during the examination period (Fig. 1). Serum levels of lipid peroxides under control conditions were within normal ranges (2 to 6 nmol/ml) in all three examinations: 3.3 6 0.2, 3.5 6 0.2 and 3.5 6 0.2 nmol/ml in the examinations with saline and low and high dose estrogen, respectively. These lipid peroxide levels did not change significantly after administration of either estrogen or dobutamine (data not shown). End point of DSE. Among the 24 DSE examinations, the dobutamine infusion was stopped because of chest pain in 14, achievement of the peak dose of dobutamine in 6, and ischemic ST segment changes in 4. Thus, the maximal comparable stage
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Table 2. Hemodynamic Variables
Saline solution HR Systolic BP Diastolic BP RPP (3103) Estrogen Low dose HR Systolic BP Diastolic BP RPP (3103) High dose HR Systolic BP Diastolic BP RPP (3103)
Control
Before DSE
At a Maximal Comparable Stage
62 6 3 136 6 6 72 6 4 8,525 6 634
58 6 3 137 6 6 73 6 4 8,090 6 511
95 6 6* 149 6 6 71 6 4 14,223 6 1,118*
60 6 3 134 6 5 68 6 3 8,187 6 586
58 6 3 135 6 3 66 6 3 7,961 6 442
99 6 6* 139 6 7 67 6 4 13,962 6 1,358*
58 6 3 143 6 3 77 6 6 8,252 6 486
56 6 2 138 6 4 72 6 6 7,711 6 302
92 6 4* 142 6 6 67 6 6 13,280 6 1,017*
*p , 0.01 versus control. Data are expressed as mean value 6 SEM (n 5 8). BP 5 blood pressure (mm Hg); DSE 5 dobutamine stress echocardiography; HR 5 heart rate (beats/min); RPP 5 rate-pressure product calculated as heart rate 3 systolic blood pressure.
of DSE (as expressed by the dobutamine dose, mg/kg per min) was 10 (n 5 1), 20 (n 5 4), 40 (n 5 2) and 50 (n 5 1). The patients reported that the dobutamine-induced chest pain was similar to that experienced in their daily life. Changes in hemodynamic variables. No significant difference was noted in heart rate, blood pressure or rate-pressure product among the three examinations (Table 2). Administration of estrogen, both low and high dose, did not significantly change heart rate, blood pressure or rate-pressure product before and 30 min after estrogen administration. However, at the maximal comparable stage of DSE, heart rate and ratepressure product, but not blood pressure, significantly increased over values in control conditions (Table 2). Effect of estrogen on symptoms. Estrogen significantly and dose-dependently prolonged the time to the onset of symptoms (p , 0.01 by ANOVA) (Fig. 2). The mean value of the percent prolongation of the time to the onset of symptoms was 52% at a low dose and 72% at a high dose of the hormone (Fig. 2). Effects of estrogen on ECG changes. Estrogen significantly and dose-dependently reduced the magnitude of the summed ST segment changes (p , 0.01 by ANOVA) (Fig. 3). The mean value of the percent reduction of the ST segment changes was 36% at a low dose and 76% at a high dose of the hormone (Fig. 3). Effect of estrogen on wall motion abnormalities. Estrogen significantly and dose-dependently ameliorated the worsening of the wall motion score index at the maximal comparable stage of DSE (p , 0.01 by ANOVA) (Fig. 4). The mean value of the percent reduction of the wall motion score index was 50% at a low dose and 77% at a high dose of the hormone (Fig. 4). Influence of baseline wall motion abnormalities. The preceding beneficial effects of estrogen on dobutamine-induced
Figure 2. Time (min) to onset of symptoms. Data are presented as mean value 6 SEM (n 5 8). The time to onset of symptoms of 24 min indicates that the patient completed the DSE examination without chest pain. Estrogen (E) dose-dependently prolonged the onset of symptoms during DSE (p , 0.01 by ANOVA).
symptoms, ECG changes and wall motion abnormalities were noted in our postmenopausal patients with CAD, regardless of the presence or absence of baseline wall motion abnormalities (data not shown).
Discussion The novel finding of the present study is that short-term administration of conjugated estrogen significantly ameliorated the dobutamine-induced myocardial ischemia in postmenopausal women with CAD. DSE. Dobutamine is a synthetic catecholamine and has effects on beta1-, beta2- and alpha1-adrenergic receptors (17,18). Dobutamine increases myocardial oxygen demand by increasing heart rate and myocardial contractility (17,18) mainly due to beta1-adrenergic receptor stimulation. The Figure 3. Summed ST segment changes (mm) from control to the maximal comparable stages of DSE. Data are presented as mean value 6 SEM (n 5 8). Estrogen (E) dose-dependently decreased the magnitude of summed ST segment changes from control levels to maximal comparable stages of DSE (p , 0.01 by ANOVA).
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Figure 4. Changes in wall motion index score evaluated by echocardiography. Data are presented as mean value 6 SEM (n 5 8). Estrogen (E) dose-dependently ameliorated the wall motion index score (p , 0.01 by ANOVA).
beta2- and alpha1-adrenergic agonist activities of dobutamine are relatively milder than its beta1-adrenergic activity. Because beta2- and alpha1-adrenergic effects of dobutamine are balanced in peripheral vasculature, dobutamine infusion, especially at low doses, has minimal effects on blood pressure (17). In the presence of CAD, the increased myocardial oxygen demand by dobutamine is associated with an inadequate increase in coronary blood flow, resulting in myocardial ischemia and abnormal LV wall motion that can be detected by cross-sectional echocardiography (14). DSE has several advantages over exercise echocardiography (19). First, myocardial ischemia can be easily induced by dobutamine infusion in almost all patients, whereas exercise echocardiography cannot always be performed in all patients. Second, because DSE allows echocardiographic imaging at every stage of dobutamine infusion, we were able to analyze LV wall motion at the maximal comparable stage of DSE in our study, whereas exercise echocardiography can be performed only after exercise. In the present study, heart rate responses were slightly lower than those in previous reports (17,18). We consider that this difference occurred in part because only two of our patients could achieve a dobutamine infusion rate of 50 mg/kg per min in four DSE examinations, and in part because the relatively older age of our patients (mean 69 years) may have blunted the heart rate response to the dobutamine stimulation. However, because rate-pressure products were comparable among the three examinations in our study, we were able to examine the effects of estrogen at the maximal comparable level of myocardial oxygen demand. Anti-ischemic effect of estrogen. In the present study, we observed the short-term anti-ischemic effects of estrogen, which may be attributed to the following vascular effects of this hormone: 1. Estrogen may ameliorate the extent of myocardial ischemia by enhancing the endothelium-dependent vasodilation of the coronary artery. Previous studies have demonstrated that
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an increase in sympathetic tone, such as that caused by mental stress (20), exercise (21) or cold pressor test (22), causes dilation of normal coronary arteries and paradoxic constriction of atherosclerotic coronary arteries with dysfunctional endothelium. Thus, enhanced endothelium-dependent relaxation may play a protective role to delay or prevent the occurrence of myocardial ischemia in patients with CAD. Physiologic levels of 17-beta-estradiol were shown (23) to immediately and selectively potentiate endothelium-dependent dilation in both large coronary arteries and coronary microvessels in postmenopausal women. We (24) also recently demonstrated that estrogen immediately improves both nitric oxide–mediated and non-nitric oxide (possibly endothelium-derived hyperpolarizing factor)–mediated endothelium-dependent forearm vasodilation in postmenopausal women. In the present study, it is possible that potentiation of endothelium-dependent vasodilation by estrogen increased the myocardial blood flow and ameliorated the dobutamine-induced worsening of symptoms, ECG findings and LV wall motion. 2. The endothelium-independent and calcium antagonistic vasodilating effects of estrogen may also explain in part its anti-ischemic effect. As functional estrogen receptor has been demonstrated on vascular smooth muscle cells in the human saphenous vein and mammary artery (25), it is highly possible that this also is the case in the human coronary artery. 3. An antioxidant effect of estrogen might be involved in the anti-ischemic effect of the hormone. However, this possibility may be less likely, at least in the present study, because the levels of lipid peroxides, a marker of systemic production of oxygen-derived free radicals (26), did not decrease with a low or a high dose of estrogen. In the present study, we used conjugated estrogen because it is the only estrogen agent that can be used for intravenous administration in our country. As serum levels of both estrone and estradiol were increased after administration of conjugated estrogen in our study, both estrogen fractions may contribute to the anti-ischemic effect of estrogen. Whereas comparative vascular effects of estrone and estradiol remain to be examined, estradiol is three times as potent as estrone in its anti-oxidant effect (27). A comparison of the serum levels of estrone and estradiol (Fig. 1) with the anti-ischemic effects of estrogen (Fig. 2 to 4) indicates that the logarithmic values of the estrogen levels appear to correlate with the hormone’s anti-ischemic effects. It also should be noted that even a low dose of estrogen (1.25 mg intravenously) that achieved physiologic serum levels of the hormone exerted anti-ischemic effects in postmenopausal women with CAD. Limitations of the study. Several limitations of our study could be cited. 1) We included only eight patients. However, the anti-ischemic effects of estrogen were evident even with this small number. 2) We investigated only the immediate effects of estrogen. A recent study (28) found that long-term estrogen replacement therapy that achieved physiologic levels of estrogen did not improve exercise tolerance by treadmill test in healthy postmenopausal women. It remains to be examined
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whether long-term estrogen replacement therapy increases exercise tolerance in postmenopausal women with CAD. 3) We did not store the images in a digitized format or review in a quad screen format but recorded them on S-VHS tapes. Side by side cine loop format is generally accepted to be a superior way for analyzing DSE. However, a recent study (29) suggested that, although digitized analysis would be more appropriate, traditional videotape analysis may also be used in DSE. 4) We included three patients with baseline wall motion abnormalities. However, the beneficial effects of estrogen were noted in our postmenopausal patients with CAD, regardless of the presence or absence of baseline wall motion abnormalities. In summary, we were able to demonstrate that short-term estrogen administration ameliorates dobutamine-induced myocardial ischemia. Our finding may have important clinical implications for understanding both the pathogenesis and the management of CAD in postmenopausal women. We thank Chie Fukagawa and Drs. Shin-ichi Ando, Hiroaki Yamamoto and Jun-ichi Oyama for their kind cooperation in this study.
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