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J Am Coll Cardiol, 2001; 38:1357-1365 © 2001 by the American College of Cardiology Foundation |


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* Cattedra di Geriatria, Dipartimento di Medicina Clinica, Scienze Cardiovascolari ed Immunologiche, Università degli Studi di Napoli "Federico II," Naples, Italy
Cattedra di Medicina Interna, Dipartimento di Medicina Clinica, Scienze Cardiovascolari ed Immunologiche, Università degli Studi di Napoli "Federico II," Naples, Italy
Cattedra di Geriatria, Dipartimento delle Malattie del Metabolismo e dellInvecchiamento, Seconda Università di Napoli, Naples, Italy
Centro Medico di Telese Terme, Fondazione Salvatore Maugeri, IRCCS, Benevento, Italy
|| U.O. Riabilitazione, A.S.L. 4 Basso Molise, Fondazione Salvatore Maugeri, Larino/Termoli, Italy
¶ Department of Medicine-0682, University of California, San Diego, California, USA
Manuscript received December 12, 2000; revised manuscript received April 19, 2001, accepted July 19, 2001.
* Reprint requests and correspondence: Dr. Pasquale Abete, Dipartimento di Medicina Clinica e Scienze Cardiovascolari, Cattedra di Geriatria, Università degli Studi di Napoli "Federico II," Via S. Pansini, 5, 80131 Napoli, Italy.
p.abete{at}unina.it
| Abstract |
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The study investigated the effects of physical activity on preinfarction angina, a clinical equivalent of ischemic preconditioning (PC), in adult and elderly patients with acute myocardial infarction (AMI).
BACKGROUND
Preinfarction angina seems to confer protection against in-hospital mortality in adult but not in elderly patients. However, it has been experimentally demonstrated that exercise training restores the protective effect of PC in the aging heart.
METHODS
We retrospectively verified whether physical activity preserved the protective effect of preinfarction angina against in-hospital mortality in 557 elderly patients with AMI. Physical activity was quantified according to the Physical Activity Scale for the Elderly (PASE).
RESULTS
In-hospital mortality was 22.2% in elderly patients with preinfarction angina and 27.2% in those without (p = 0.20). When the PASE score was stratified in quartiles (0 to 40, 41 to 56, 57 to 90, >90), a high score was strongly associated with reduced in-hospital mortality (30.8%, 32.2%, 17.2% and 15.3%, respectively, p < 0.001 for trend). Interestingly, a high level of physical activity reduced in-hospital mortality in elderly patients with preinfarction angina (35.7%, 35.4%, 12.3% and 4.23%, respectively, p < 0.001 for trend) but not in those without (23.0%, 27.2%, 26.0% and 35.0%, respectively, p = 0.35 for trend). Accordingly, the protective role of preinfarction angina on in-hospital mortality was present only in elderly patients showing a high level of physical activity (adjusted odds ratio, 0.09; 95% confidence interval, 0.01 to 0.57; p < 0.05).
CONCLUSIONS
Physical activity and not preinfarction angina protects against in-hospital mortality in elderly patients with myocardial infarction. Nevertheless, the protective effect of preinfarction angina is preserved in elderly patients with a high level of physical activity.
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dogenous protective mechanisms against myocardial ischemia are brief, repeated episodes of myocardial ischemia, the so-called ischemic preconditioning (PC) that is a harbinger for the more prolonged ischemic episode (10,11). Patients with preinfarction angina, a clinical equivalent of PC, have a better outcome than those without angina (1216). Experimental (17,18) and clinical (19,20) studies show that aging reduces the efficiency of PC.
Several studies have indicated that physical activity reduces CHD-related mortality in elderly patients (2123). In addition, it has been experimentally demonstrated that exercise training restores PC in the aging heart (24). Consequently, the goal of our study was to verify retrospectively whether physical activity preserves clinically the cardioprotective effect afforded by preinfarction angina on several in-hospital end points, including mortality and cardiogenic shock, in elderly patients with acute myocardial infarction (AMI).
| Methods |
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65 years with AMI were admitted to our coronary care unit (CCU) regardless of their functional status. Patients were included in this retrospective study if they had at least two of the following criteria: 1) typical chest pain; 2) electrocardiographic (ECG) changes with evolution of Q waves (transmural infarction); and 3) elevation of creatine kinase (CK) levels. Nontransmural infarction was diagnosed by typical changes in the S-T segment and T-wave accompanied by increased CK levels. The medical records of these patients were individually reviewed according to criteria that have been described previously (19). Thrombolytic therapy was given to all patients except those presenting with complicating illness, absence of chest pain on admission or nonspecific ECG abnormalities considering age
65 years not a contraindication. Patients with advanced or terminal illness, cerebrovascular disease and such neuropsychiatric disorders as dementia and delirium were not included in the study. In particular, 11 patients (1.9%) with terminal illness, 13 patients (2.3%) with cerebrovascular disease and 23 patients (4.1%) with dementia were excluded according to the DSM-IV (American Psychiatric Association). The final number of patients included in the study was 510. Assessment of physical activity. Physical activity was evaluated with the Physical Activity Scale for the Elderly (PASE) (25). The total PASE score was computed by multiplying the amount of time spent in each activity (h/day) or participation (yes/no) in an activity by the empirically derived item weights and summing over all activities (Table 1). The item weights are based on comparison with physical activity derived by regressing a component score developed from a three-day motion sensor count, three-day physical activity diary, and global activity assessment (25). The total PASE score obtained was stratified in quartiles (0 to 40, 41 to 56, 57 to 90 and >90) for statistical analysis.
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In-hospital outcomes. In-hospital end points in the CCU were death, cardiogenic shock (marked and persistent hypotension with systolic arterial pressure <80 mm Hg and a reduction of cardiac index to <1.8 l/mm2), extension, persistent chest pain, creatine kinase-myoglobin fraction (CK-MB) peak, ventricular fibrillation and tachycardia and high-grade atrioventricular block.
Statistical analysis. The statistical power of detecting a clinically significant difference in elderly patients with AMI was 95%, under a type 1 error of 0.05 and an odds ratio (OR) as large as 3.00 (corresponding to a mortality rate of 20% in patients without physical activity before AMI). The power declined progressively to 85%, 75% and 60% with an OR of 2.50, 2.00 and 1.75, respectively. In the comparison between patients with and without preinfarction angina, categorical data and continuous variables were analyzed by chi-square test and the Student t test, respectively. In the comparison among patients stratified in quartiles of physical activity (0 to 40, 41 to 56, 57 to 90 and >90), categorical data were analyzed by chi-square tests (modified for linear trend) and continuous variables by analysis of variance. Logistic regression analysis was used to assess the role of preinfarction angina on death, cardiogenic shock and the combined end points independently from physical activity, chronic angina, thrombolytic therapy, primary percutaneous transluminal coronary angioplasty (PTCA), antianginal treatment and several demographic variables (age, gender, previous AMI, congestive heart failure, hypertension, diabetes, family history, smoking and cholesterolemia). The role of preinfarction angina on death, cardiogenic shock and the combined end points was also assessed in elderly patients stratified in quartiles of physical activity (0 to 40, 41 to 56, 57 to 90 and >90). The p values are reported for two-sided testing and are considered significant if less than 0.05.
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| Discussion |
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CHD and aging. More than 80% of all AMI-related deaths occur in patients >65 years old (15). Advanced age is a multivariate predictor of hospital mortality after AMI (7,8). In fact, in-hospital mortality was three times higher in older than in younger patients (8). Why mortality is higher in older patients with AMI remains unclear. Age-related changes such as increased myocardial mass (26), reduced diastolic relaxation (27), and impairment of angiogenesis (28) might render the AMI more susceptible to severe complications in elderly patients. In addition, comorbidity, which is very common in elderly patients, may predispose to complications and increased mortality after AMI (69). However, Tofler et al. (6) have demonstrated that even adverse baseline characteristics do not justify the increased in-hospital mortality observed in the elderly. Elderly patients are frequently treated with less aggressive therapy, including thrombolytic therapy (3,4,29). Nevertheless, Maggioni et al. (8) have demonstrated that age remains a powerful independent predictive factor of in-hospital mortality in patients with AMI who received thrombolytic therapy.
PC and aging. Our working hypothesis is that the higher mortality due to AMI might be explained at least in part by the age-related reduction of an endogenous protective mechanism such as PC (10). This phenomenon is characterized by reduced electromechanical dysfunction after a prolonged ischemic period when preceded by brief and repeated episodes of myocardial ischemia triggered by several mediators including adenosine and norepinephrine (11). The clinical equivalents of PC are preinfarction angina, warm-up phenomenon, and ischemic episodes during PTCA (11). In particular, preinfarction angina has been shown to reduce left ventricular impairment (12), infarct size (14) and the risk of right ventricular infarction (16), and to improve short-term prognosis (13) and in-hospital outcome (15) after AMI. However, these findings were observed only in adult patients with AMI. Age-related reduction of PC was first demonstrated in an experimental model and was attributed to an age-related reduction of norepinephrine release in response to myocardial ischemia and/or to age-related impairment of the sarcoplasmic reticulum (17,18), and then in clinical studies (19,20,30,31). Protective effect of preinfarction angina both against in-hospital outcomes (19) and in five-year survival rate was lost in elderly patients (20), indicating that the higher mortality observed in elderly patients might be justified in part by the age-related reduction of PC. Here, this mechanism seems to be preserved in elderly AMI patients who have high physical activity scores.
Physical activity, aging and CHD. Several epidemiological studies indicate that physical activity offers partial protection against primary or secondary events of CHD and associated mortality among middle-aged and older men (32). This is true in older men in whom disability is particularly frequent (33). In the Goteborg study, the most active men, after 20 years of follow-up, had a relative risk of death from CHD of 0.72 (95% CI: 0.560.92) (21). In the British Heart Study, light, moderate and vigorous activity reduced mortality and heart attacks in older men by 0.61 (95% CI: 0.480.86), 0.50 (95% CI: 0.310.79), and 0.65 (95% CI: 0.450.94), respectively (22). In the Honolulu Heart Program, the risk of CHD was reduced in physically capable elderly men with the distance walked (23). It is uncertain how physical activity could reduce mortality due to CHD in elderly people. Various factors have been implicated in this beneficial effect: a lipid-lowering effect (34), increased insulin sensitivity (35), reduced arterial pressure (36), increased coronary vasodilatory capacity (37) and coronary perfusion (38), correction of endothelial dysfunction (39), and the antiarrhythmic effect due to the reduction of heart rate and sympathetic activity (40). Similarly, experimental (4143) and clinical (4447) studies have demonstrated that physical activity can correct most of the cardiovascular alterations induced by aging. Indeed, exercise training preserves PC in the aging rat heart by safeguarding norepinephrine release in response to myocardial ischemia (24).
Study limitations. In general, data from retrospective studies should be viewed with caution. Prospective studies are needed to verify the absence of the protective effect of preinfarction angina in the elderly. Moreover, despite the inclusion criteria of our CCU, only 32% of the elderly patients underwent reperfusion therapy. In the experimental setting, a sustained, complete reperfusion is necessary after prolonged occlusion in order to obtain the reduction of infarct size (11). Thus, studies that contain one-third or even fewer patients receiving reperfusion therapy should be regarded with caution. However, when additional analysis in the "reperfused group" (145 thrombolytic therapy and 33 primary PTCA) was performed, no significant differences between elderly patients with preinfarction angina in comparison to those without preinfarction angina were found. In fact, the percentages of in-hospital mortality, cardiogenic shock and the combined end points in elderly patients with and without preinfarction angina were 24.1% versus 22.5% (p = 0.855, NS), 30.1% versus 38.7% (p = 0.316) and 30.3% versus 27.4% (p = 0.586), respectively. Similarly, CK-MB peak was 194 ± 118 IU/l in elderly patients with and 174 ± 162 in elderly patients without preinfarction angina (p = 0.399). Nevertheless, physical activity continues to exert its protective role also in this subgroup of patients (data not shown).
The effect of physical activity on the cardioprotection afforded by preinfarction angina should be due to a difference in the incidence of chronic angina, and thus to a well-developed collateral circulation (14,15). However, the incidence of chronic angina is greater both in elderly patients with the highest physical activity either with or without preinfarction angina (42.2% vs. 35.0%; p = 0.75). Hence, the beneficial effect of preinfarction angina in elderly patients with the highest physical activity is independent from chronic angina.
Conclusions. We confirm that the protective effect of preinfarction angina against in-hospital outcomes is reduced in elderly patients according to a growing bulk of evidence (48,49). Furthermore, we demonstrate that this beneficial effect is preserved in elderly patients who are characterized by a high level of physical activity. Thus, preservation of PC could explain, at least in part, the mechanism whereby physical activity exerts cardioprotective effects against AMI in elderly patients.
| Acknowledgments |
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| Footnotes |
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| References |
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