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IJGSM 2017;3(1):3-14

Gender differences in coronary heart disease in elderly populations

Caterina Trevisan1, Giuseppe Sergi1, Nicola Veronese1, Stefania Maggi2, Enzo Manzato1,2

1. Department of Medicine (DIMED), Geriatrics Division, University of Padua, Italy;

2. National Research Council, Institute of Neuroscience, Aging Branch, Padua, Italy.

Received 16 January 2017; accepted 7 March 2017.

Summary. Coronary heart diseases (CHDs) represent one of the leading causes of death in developed countries, and particularly in elderly populations. There are several gender-specific differences in the risk factors, presentation, management, and prognosis of CHDs in middle-aged and elderly adults. Elderly women, for example, tend to present with these diseases at an older age compared to men and are characterized by a greater number of risk factors and comorbidities at diagnosis. As far as symptomatic acute coronary syndromes are concerned, older women are less likely to report critical arterial obstruction, but seem to be more frequently affected by adverse outcomes and higher mortality. These features, which need to be considered during the management of coronary artery diseases in clinical practice, often lead to a lower rate of diagnostic investigations and less invasive therapeutic strategies for females compared to males. Some have hypothesized that the clinical approach toward CHDs in older women may be affected by a biased view due to the scarcity of literature involving women and elderly patients. The misperception that women have a lower cardiovascular risk compared to men and the fact that fewer older people were enrolled in the first large clinical trials have, in fact, led to under-recognized and under-treated CHDs in these patient groups. As most recent studies have considered middle-aged and elderly adults together, it is hard to know if the variability observed in the CHDs’ features is attributable to gender or to advanced age. Gender- and age-related differences in the characteristics and outcomes of CHDs represent therefore a field requiring further investigation to improve the management of such diseases in the elderly population.

Key words: coronary heart diseases, gender differences, elderly.

Differenze di genere nelle coronaropatie in età geriatrica

Riassunto. Le coronaropatie costituiscono una delle principali cause di morte nei Paesi industrializzati, soprattutto per la popolazione in età geriatrica. Negli anziani, come negli adulti, le malattie coronariche si caratterizzano per una molteplicità di differenze di genere che coinvolgono fattori di rischio, modalità di manifestazione e strategie terapeutiche di tali patologie. Rispetto agli uomini, per esempio, l’esordio delle coronaropatie è più tardivo nelle donne anziane, le quali presentano generalmente un più ampio corredo di comorbilità e di fattori di rischio cardiovascolare al momento della loro insorgenza. Le coronaropatie sintomatiche in età geriatrica, inoltre, si associano meno strettamente alla presenza di stenosi arteriose critiche nel sesso femminile, che però risulta essere gravato da prognosi peggiori e maggiore mortalità rispetto al genere maschile. Il riscontro di tali peculiarità ha inevitabilmente influenzato la gestione delle patologie coronariche nella pratica clinica, portando a un minor tasso di indagini diagnostiche e di trattamenti invasivi rivolti a pazienti di sesso femminile. Tale approccio clinico, tuttavia, non si avvale di fondate basi scientifiche, dal momento che non vi sono ancora solide e concordi indicazioni rispetto alla gestione delle patologie coronariche sia in pazienti anziani che di sesso femminile. Alla base della sottostima e del ridotto riconoscimento delle coronaropatie in tali tipologie di pazienti vi sono diversi fattori; tra questi, la convinzione che le donne abbiano un minore rischio cardiovascolare rispetto agli uomini, e la scarsa partecipazione di soggetti anziani nei primi ampi studi sperimentali rappresentano due aspetti di notevole rilevanza. Inoltre, dato che la maggior parte degli studi clinici effettuati negli ultimi anni considera insieme pazienti anziani e adulti, risulta particolarmente arduo valutare se la variabilità nelle caratteristiche e nella prognosi delle coronaropatie sia imputabile al genere o all’età avanzata. L’ambito delle differenze di genere nelle coronaropatie in età geriatrica richiede dunque ulteriori approfondimenti al fine di elaborare nuove indicazioni diagnostico-terapeutiche che tengano in considerazione la variabilità genere- ed età-correlata di tali patologie.

Parole chiave: coronaropatie, differenze di genere, età geriatrica.


The increase in life expectancy in developed countries has led to a change in the main causes of death in the general population, formerly linked to acute infectious diseases and now associated with chronic pathologies1. Cardiovascular diseases (CVDs), in particular, today constitute the leading cause of death in elderly populations and have a mortality rate that exceeds that of cancer for persons aged 65 and over2,3. As far as cardiovascular pathologies are concerned, coronary heart diseases (CHDs) have one of the highest standardized death rates, accounting for 593.7 deaths per 100,000 inhabitants across European countries2.

In middle-aged and elderly adults, CHDs are characterized by a number of gender differences affecting their epidemiology, presentation and outcomes. Nonetheless, the current literature still shows a gap in the knowledge about gender- and age-specific characteristics of CHDs due to an under-representation of women and of older people in the principal clinical trials that have been carried out4. As demonstrated by Lee et al., only 9% of patients older than 75 and 25% of women were included in studies carried out between 1991 and 2000, percentages that are well below the representation of those patients within the entire myocardial infarction (MI) population4. Considering that the onset of CHDs is later in women5,6, it could be hypothesized that part of the current gender gap depends on the age gap as the under-enrolment of elderly subjects may have limited the knowledge regarding CHDs particularly in older women4. These gender- and age-related gaps in the literature could be ascribed to several reasons. As regards advanced age, recruitment difficulties and lower compliance with medical treatments among elderly people can partially explain their low representation in clinical trials4. Moreover, the reluctance to expose older subjects to invasive therapies given the presence of multiple comorbidities or simply the preconception that age per se represents a factor that increases risk of adverse events also play a part in this bias4,7,8.

With regard to the gender gap, the belief that the female gender represents an independent factor that lowers the risk of CVDs has led many to underestimate the risk of heart diseases in women9,10. One of the most accredited hypotheses underlying this misperception is the belief that endogenous oestrogens have cardioprotective effects on the metabolic, coagulative and inflammatory pathways during fertile age11,12. Hormonal changes after menopause do not, however, entirely explain the decrease in the male/female ratio of CHD mortality occurring in advanced ages13 and the growing rate of women patients that has recently been observed14. This tendency was underlined by a large study based on a Finnish population showing that, while in 1980 middle-aged men represented the most dominant CHD group, in 2000 the dominant group was made up of women aged over 7514.

Gender differences in CHD risk and symptoms in the geriatric population are therefore an important, complex topic that requires further investigation since generalizing results from trials including mostly men and younger persons to female and elderly patients cannot be considered a reliable approach. Moreover, considering that elderly people account for a large proportion of hospitalizations, being able to reliably evaluate CHD in older men and women could aid in identifying coronary pathologies at an early stage or patients at high risk of developing them and improve clinical practice15. Given these considerations, this study sets out to examine the current literature regarding gender-specific differences with regard to risk factors, presentation, management and prognosis of coronary heart diseases in elderly populations.

Risk factors for coronary heart diseases in the elderly

The risk patterns for CHDs in older persons are characterized by a multitude of comorbid, behavioural and lifestyle factors accumulated with aging. Women, in particular, who generally develop CHDs approximately 7-10 years later than men, are more likely to present with a large number of cardiovascular risk factors at diagnosis5,6. In addition to the different prevalence rates of cardiovascular risk factors in men and women, their relevance in influencing the onset of CHDs shows further gender-related variability that could change between middle-aged and elderly adults.

The impact of excess weight on CHDs, for example, has been widely investigated in large longitudinal studies, and its negative metabolic and inflammatory consequences have been confirmed in both middle-aged and older individuals. However changes in body composition such as the increase and redistribution of fat in the visceral compartment occurring at older ages16-18 seem to influence this association. According to the study by Rimm et al., while obesity predicts CHD risk independently of fat distribution in men younger than 65, at older ages abdominal adiposity was a stronger predictor of CHD risk than body mass index (BMI)19. Similar results have been observed for the female gender in whom the central redistribution and accumulation of adipose tissue in post-menopausal age and the metabolic syndrome were more strongly associated with higher risk of coronary artery diseases than BMI20,21.

Other components of the metabolic syndrome and particularly lipid metabolism, are influenced by the fall in oestrogen beginning in the perimenopausal period. After menopause, in fact, LDL cholesterol increases in women and tends to exceed the levels found in men9,22-24, although women demonstrate larger and less atherogenic LDL25. Conversely, HDL concentrations fall slightly in women during the post-menopausal period, but they maintain higher levels22,26 and stronger inverse associations with CHDs and related mortality compared with men27,28.

The impact of diabetes and hypertension on coronary artery diseases has also been found to be stronger in women than in men. Although previous meta-analyses comparing the impact of diabetes on CHDs produced contrasting results29-31, Huxley et al. reported a 50% higher risk for fatal CHDs in diabetic women compared to middle-aged or elderly men32. Diabetic women tend, in fact, to have a higher-risk cardiovascular profile than men with worse lipid concentrations and blood pressure values32. As regards blood pressure, ageing is characterized by a progressive rise in systolic values in both genders, but after early adulthood this increase is steeper in women. This pattern is probably due to variations in endogenous oestrogen levels33 leading to higher average blood pressure values in women from the seventh decade of life34. Though increasing blood pressure has been associated to higher CHD incidence and mortality in both genders, its impact in older women seems to be greater than in men35,36. Conversely, mean diastolic blood pressure tends to gradually fall beginning at 60 in both men and women34, with the latter generally showing lower values. A consequent higher prevalence of isolated systolic hypertension has, therefore, been reported in elderly women compared with same-aged men and represents an additional factor increasing cardiovascular risk37.

Lifestyle factors and risk behaviours are other important determinants of cardiovascular risk in older populations. Though smoking is generally more common in men, its impact on the onset of ischemic heart diseases primarily seems to concern women. Compared with non-smokers, in fact, Prescott et al. demonstrated that female smokers had about a 50% higher relative risk of myocardial infarction than men across all age groups38. The risk difference between genders seemed to be attenuated in the population aged over 65 years, suggesting that in addition to its pro-inflammatory effect, the interaction between smoking and sex hormones could play a significant role38. With regard to dietary style and physical activity, no significant associations were found between dietary fat intake and coronary artery diseases in older persons39, while a meta-analysis by Sattelmair et al. reported that physical activity has a beneficial effect on CHD risk in both men and women, with stronger results for the latter40.

Presentation of coronary heart diseases in older men and women

Gender differences have been observed in the diagnosis and presentation of coronary artery diseases in both middle-aged and elderly adults. This variability could be attributable to gender-specific physiological and pathological characteristics of those diseases that may be exacerbated by aging.

From a pathophysiological viewpoint, women have smaller coronary vessels and stiffer aortas, present more often with microvascular dysfunction and poorer vascular reactivity compared to men, determining a lower vasodilator response41. The atherosclerotic process in coronary arteries may also differ in the two genders since women with CHD have demonstrated less widespread obstruction and a lower probability of presenting three-vessel coronary diseases or left-main stenosis6,42 and collateral vessels43. Plaque composition is characterized by lower necrotic core content and calcium in women who have a lower probability of plaque rupture42. Coronary calcification seems, however, more associated with mortality in women who also have thin-cap fibroatheromas with a higher vulnerability42. The characteristics of vessels and atherosclerotic plaques could influence clinical and electrocardiographic signs of CHDs that tend to be poorly correlated with the angiographic report of obstructive coronary disease, especially in women. In a sample of patients with unstable angina and non-Q wave myocardial infarction, Hochman et al. demonstrated that women had a higher probability of non-critical obstructions44, and this finding has been confirmed for all age groups including for individuals over 8045. Similarly, Sharaf et al. found that only 43% of middle aged and elderly women with suspected ischemic chest pain had a stenosis >50% and more than one third had no detectable obstructions46. Sex-specific features have also been observed in the non-invasive diagnostic testing of coronary diseases, which is less reliable in women than in men. Factors such as a higher resting heart rate, longer QT intervals and lower exercise capacity could, in fact, affect the overall predictive value of ECG and treadmill testing in women47,48. Reliable diagnostic tools for CHDs are particularly relevant in geriatric populations in which acute coronary syndrome (ACS) can show heterogeneous clinical patterns. Hence, the importance of the growing use in clinical practice of more sophisticated diagnostic imaging that has improved the identification of coronary disease in both genders9,47.

The clinical presentation of CHDs can present some sex-specific differences in elderly population, although older age seems to be a stronger predictor compared to gender of ACS presentation49,50. Since women at CHD onset tend to be older than men, they may therefore show different symptomatology for ACS. As regards symptomatic cases of CHDs, despite the fact that the prevalence of angina is higher in women than in men in middle age, after 65 years of age this disparity tends to be attenuated51. In particular, the prevalence of typical chest pain, the primary symptom complaint, has been found to be similar in men and women between the ages of 65 and 74, while it seems to be significantly lower in women than in men over 7552. As previously mentioned, chest pain in women is less associated with the presence of obstructive coronary artery disease. More than half of symptomatic women without relevant coronary artery diseases nevertheless continue to report symptoms of CHDs53, and the presence of chest pain even in women with normal coronary arteries has been associated with a higher risk of death and adverse cardiovascular events compared to asymptomatic women54. Moreover, among symptomatic CHDs, women generally report a higher number of symptoms than men, and they are more likely to have atypical vegetative signs such as nausea, vomiting and indigestion6,52. Though the prevalence of MI without chest pain and discomfort declines in advanced age, many studies report a higher rate of non-chest pain MI in women than in men, even after adjusting for age49,55,56. Patients with non-specific chest pain require particular attention because the pattern has also been associated with a significantly higher risk for nonfatal CHDs, hospitalized angina and new cardiovascular events55, in particular in women over 6557,58.

Management of acute coronary syndrome in the elderly

Compared to other older adults admitted to hospital for ACS, women are generally older and present with a higher number of comorbidities, such as diabetes, hypertension and prior congestive heart failure, which increase their mortality risk and may be important for the therapeutic approaches that can be considered5,6,56,59. Management of ACS often proves to be more difficult in elderly patients as a result of the delay in accessing the emergency unit since the time between the onset of symptoms is a fundamental prognostic variable for revascularization strategies60,61. This refers particularly to female patients who often present with a longer delay from symptom onset to hospital access (median values range from 1.8 to 7.2 hours for women and from 1.4 to 3.5 hours for men)61–63. In addition to common atypical presentation of CHDs, prehospital delay in older women could be due to the fact that women tend to underestimate their cardiovascular risk61,64 and are often unaware of the relevance of key symptoms65,66. An interesting study by Mosca et al. confirmed this pattern and found that only 53% of the women interviewed would call the emergency service if they thought they were having symptoms of a heart attack66.

Gender differences have also been found in the type of CHDs at presentation, with men more commonly presenting with ST-elevation myocardial infarction (STEMI)5,6 and, among non ST-elevation ACS, a higher rate of non ST-elevation myocardial infarction (NSTEMI) compared to women5. The higher prevalence of unstable angina in women instead reflects the angiographic features previously mentioned, namely a lower prevalence of complete coronary occlusion5,44,67. A confounding condition that may further prevent recognition of CHD in older persons is Takotsubo cardiomyopathy. This syndrome consists in a transient left ventricular dysfunction triggered by emotional or physical stress, shows a higher prevalence in the elderly and in the female gender and its clinical pattern is similar to that of ACS68,69. Since clinical and electrocardiographic characteristics are the most common tools used to evaluate CHDs, age- and gender-related differences in CHD presentation should be taken into consideration when the management of these patients is being evaluated70,71.

Management of ST-elevation myocardial infarction

Acute revascularization by percutaneous coronary intervention (PCI) or thrombolysis represents the gold standard for the treatment of acute MI and high-risk ACS72, and better outcomes have been demonstrated for shorter times to reperfusion62. Primary coronary angioplasty is, in particular, now considered the first choice for reperfusion in STEMI73. However, despite the fact that 51% of those procedures are performed on patients over 65, only one third of annual PCIs in the United States involve female patients74. This data has been confirmed by several authors, who have reported that women with MI were half as likely as men to receive invasive revascularization procedures75–80, in particular for mild disease6,81. As was observed by Clarke et al., the “gender bias” regarding admission to coronary care with a confident MI diagnosis has been confirmed across all age groups and is exacerbated in patients older than 75, even after considering the final diagnosis of CHD and Killip classification81. Moreover, as regards coronary care, women reported longer door-to-reperfusion time, showing a mean delay of 8.3 minutes compared with men, and therefore a worse time-related prognosis82-84. PCI may be less likely performed in older women because of the higher risk of bleeding after revascularization, observed, in particular, when glycoprotein IIb/IIIa inhibitors are used85,86. However, as demonstrated by Cho et al., this additional antiplatelet treatment seems in any case to protect both genders from major adverse outcomes and to only slightly increase the risk of minor bleeding in women86.

As regards thrombolysis, studies on fibrinolytic therapy after MI in older patients have produced contrasting results, especially for patients older than 75 who often showed a survival disadvantage after thrombolytic therapy, probably due to the age-related increased risk of stroke, bleeding, and sudden death due to mechanical rupture87–89. A higher bleeding rate has been observed in particular in women5,85,90, especially in those cases when thrombolysis was associated to heparin therapies91 which could be attributable to excessive doses of fibrinolytic and antithrombotic drugs that need to be adjusted based on renal function85.

Management of non ST-elevation myocardial infarction and unstable angina

Special attention should be dedicated to the management of NSTEMI, which largely depends on clinical, electrocardiographic and biochemical factors, in middle-aged and elderly adults92. While in some studies women have demonstrated better long-term outcomes than men when NSTEMI was treated with early invasive revascularization93,94, others reported a higher risk of major adverse cardiac events after PCI for NSTEMI in the female gender95,96. Moreover, Alfredsson et al. found better long-term prognoses for women with NSTEMI, in particular for the oldest group79,97, although they were less likely to be investigated71,97 and intensively treated71,76,79,98,99. The current guidelines, therefore, recommend classifying women according to their low or high risk, on the basis of biomarker values100. As confirmed by a recent meta-analysis, despite the fact that early invasive treatment leads to similar benefits for men and high-risk women as far as mortality, myocardial infarction and rehospitalization for ACS are concerned, the current guidelines for low-risk women continue to be a conservative therapy strategy101.

Medical treatment of acute coronary syndromes

Pharmacological therapy for ACS also seems to be affected by an age- and sex-related variability. Despite the fact that the benefit of aspirin, beta-blocker, statins, and ACE-inhibitors has been proved for both sexes102, fewer women are prescribed these drugs after ACS6,78,81,103–109. A gender-related variability has also been identified for the therapeutic efficacy of some medical treatments. Women, for example, have shown a higher residual platelet activity after dual antiplatelet therapy compared with men, confirming that there is a variable response to therapy110,111. In addition to the gender gap in the prescription of therapies for secondary prevention of CHDs, older age could represent another variable that must be considered when prescribing treatments. Pharmacokinetic and pharmacodynamic changes112, collateral effects and drug interactions due to polypharmacy113, and concomitant comorbidities (e.g. hypotension, recent bleeding history, arrhythmias, and chronic pulmonary diseases), in fact, all may influence medical prescriptions and need be taken into consideration when preventive therapies are being evaluated for elderly patients.

Gender-differences in mortality from coronary heart diseases in older patients

Mortality linked to CHDs has gradually fallen in Italy over the past forty years in both genders probably because of the reduction in major risk factors and the improvement in therapeutic strategies114. This pattern refers, in particular, to elderly populations, with a higher rate of prevented or postponed death observed for men between 65 and 84 and for women older than 75114. The relevance of knowledge about the main determinants of mortality for CHDs in older men and women is thus confirmed in this context given its importance in formulating preventive strategies and in improving clinical practice.

Although female gender has long been considered a factor that per se increases the overall mortality for CHDs, a prognostic value now seems to be associated to a number of factors with gender-specific features, such as the type and severity of disease, the subjects’ characteristics at presentation, and the intensity of CHD management5,6,44,115.

As far as subjects with STEMI are concerned, many studies have demonstrated a higher in-hospital mortality and short-term rate of ischemic events in women compared to men5,56,75,82,90,116–121. A recent study by Raphael et al. reported an increased death rate after STEMI attributable to non-cardiac causes in women and to cardiac causes in men122. The rate of post-procedure complications also seems to show some sex-specific differences. While benefits in terms of survival and reduced intracranial bleeding after primary PCI were similar in men and women with acute myocardial infarction (AMI), women more often than men experienced coronary vascular injuries and bleeding complications, irrespective of coronary size and other confounders123. Similar results have been reported for fibrinolysis that was associated with a higher incidence but a lower mortality linked to bleeding in women compared to men124, although the association may have depended on age and comorbidities and does not seem to be confirmed in terms of long-term survival125,126. However, the sex-age interaction influencing outcomes after MI seems to be stronger in younger age groups, while gender differences in the elderly population seem to be attenuated56,127,128. As regards NSTEMI and unstable angina, similar or better outcomes were found in women compared to their male counterparts5,44,92,128-130. However, as for MI, these results were partially minimized when age, comorbidities and disease management were considered5,6,90,117,127, further confirming that gender per se does not represent an independent prognostic factor for CHDs. According to the Thrombolysis in Myocardial Infarction (TIMI) IIIB trial, for example, outcomes including death, nonfatal MI and failure of therapy at 6-weeks in subjects with unstable angina and non-Q wave MI were associated with the severity of the coronary disease and not with gender44. A study by Dey et al. confirmed that disease severity is a negative prognostic factor and found a higher overall death rate in women than in men (4.5% vs 2.6%) only for advanced coronary artery diseases6. On the other hand, the risk of new infarction, stroke, and rehospitalization seemed to be increased in women, irrespective of age, cardiac catheterization and the number of diseased vessels6.

Psychological burden and functional impairment after CHDs in older subjects

Higher risks of depression and anxiety have been demonstrated in patients after CHDs, and an approximate 20% prevalence of major depressive disorder has been observed during the first year after MI131–134. The hypothesis that psychological burden after CHDs could have a negative impact on medical prognosis and mortality has been confirmed by several studies132,134,135, and Feng et al. reported that patients who experienced post-MI anxiety had a 9-fold increased risk of recurrent MI133. These findings, therefore, consolidate the importance of identifying and treating depression and anxiety in patients with CHDs. In addition to a history of prior depressive episodes, belonging to the female gender seems to increase the risk of developing depression after AMI132-134,136,137. Women, moreover, showed a higher burden and worse quality of life that was associated with the number and severity of angina symptoms, irrespective of the evidence of myocardial ischemia138. Similarly, a study by Bjerkeset et al. reported other sex-related differences in psychological distress during a 5-year follow-up139. Despite a higher initial risk for anxiety and depression, women and in particular older women demonstrated a risk reduction after two years; conversely, the risk for depression in men rose two years after AMI, suggesting that men have less coping resources compared to women aiding them in adapting to the long-term consequences of CHDs139-141. Contradicting previous studies, Zaninotto et al. reported similar results in a sample of older men and women and demonstrated that the latter had better quality of life and an improvement in depressive symptoms over time142–144. Among the number of factors influencing quality of life after CHDs, physical impairment and limitation in self-sufficiency involve all age groups and have a greater weight for the female gender145. Despite the fact that women demonstrated similar benefits from cardiovascular rehabilitation, fewer are admitted to rehabilitative programs than men, probably because they are older and have more comorbidities at presentation146. Unless it is prevented, the loss of functional status after CHDs hastens the age-related decline in older patients and increases the risk of developing other comorbidities, cognitive impairment147,148 and, finally, disability. Elderly patients suffering from CHDs are therefore at higher risk of becoming frail149, developing a progressive loss of physiological resilience to stressors 150 that can worsen CHD outcomes151,152 considering that frailty syndrome, which may be a consequence of CHDs, is also associated with a higher risk of developing other CVDs150,153–155.


Coronary heart diseases are characterized by several gender differences and age-related features. Sex-specific variability in prevalence, risk factors and presentation of CHDs can lead to difficulties and delays in identifying those pathologies, in particular for women. These patterns, together with the complex clinical condition of older patients who are often characterized by a number of comorbidities, need to be taken into consideration when the management of CHDs is being decided for elderly subjects. For the time being, women continue to be under-investigated and under-treated for CHDs thus resulting in a higher risk of negative outcomes that can progressively impair functional status and give rise to conditions such as frailty and disability. Better management of CHDs in older men and women, therefore, could prevent clinical and functional deterioration and delay worsening of quality of life, all aspects linked to a higher burden for our aging society and healthcare system.


1. Sahyoun NR, Lentzner H, Hoyert D, Robinson KN. Trends in causes of death among the elderly. Aging Trends 2001; (1): 1-10.

2. Eurostat. Causes of death statistics - people over 65. 2016 [cited 2016 Dec 30]. Available from:

3. National Institutes of Health-National Heart, Lung, and Blood Institute. Incidence and Prevalence: 2006 Chart Book on Cardiovascular and Lung Diseases. Bethesda, United States; 2006.

4. Lee PY. Representation of elderly persons and women in published randomized trials of acute coronary syndromes. JAMA 2001; 286(6): 708-13.

5. Hochman JS, Tamis JE, Thompson TD, et al. Sex, clinical presentation, and outcome in patients with acute coronary syndromes. Global Use of Strategies to Open Occluded Coronary Arteries in Acute Coronary Syndromes IIb Investigators. N Engl J Med 1999; 341(4):226-32.

6. Dey S, Flather MD, Devlin G, et al. Sex-related differences in the presentation, treatment and outcomes among patients with acute coronary syndromes: the Global Registry of Acute Coronary Events. Heart 2009; 95(1): 20-6.

7. Krumholz HM. Thrombolytic therapy for eligible elderly patients with acute myocardial infarction. JAMA 1997; 277(21): 1683-8.

8. Gurwitz JH. Recent age-related trends in the use of thrombolytic therapy in patients who have had acute myocardial infarction. Ann Intern Med 1996;124(3):283-91.

9. Maas AHEM, Appelman YEA. Gender differences in coronary heart disease. Neth Heart J 2010; 18(12): 598-602.

10. Daly CA, Clemens F, Sendon JLL, et al. The clinical characteristics and investigations planned in patients with stable angina presenting to cardiologists in Europe: from the Euro Heart Survey of Stable Angina. Eur Heart J 2005; 26(10): 996-1010.

11. Collins P, Rosano GM, Sarrel PM, et al. 17 beta-Estradiol attenuates acetylcholine-induced coronary arterial constriction in women but not men with coronary heart disease. Circulation 1995; 92(1):24-30.

12. Sutton-Tyrrell K, Lassila HC, Meilahn E, Bunker C, Matthews KA, Kuller LH. Carotid atherosclerosis in premenopausal and postmenopausal women and its association with risk factors measured after menopause. Stroke 1998; 29(6):1116-21.

13. Furman RH. Are gonadal hormones (estrogens and androgens) of significance in the development of ischemic heart disease. Ann N Y Acad Sci 1968; 149(2): 822–33.

14. Kattainen A, Salomaa V, Härkänen T, et al. Coronary heart disease: from a disease of middle-aged men in the late 1970s to a disease of elderly women in the 2000s. Eur Heart J 2006; 27(3): 296-301.

15. Go AS, Mozaffarian D, Roger VL, et al. Heart disease and stroke statistics--2013 update: a report from the American Heart Association. Circulation 2013; 127(1): e6–245.

16. Perissinotto E, Pisent C, Sergi G, Grigoletto F, Enzi G. Anthropometric measurements in the elderly: age and gender differences. Br J Nutr 2007; 87(2):177-86.

17. Kuk JL, Saunders TJ, Davidson LE, Ross R. Age-related changes in total and regional fat distribution. Ageing Res Rev 2009; 8(4): 339-48.

18. Goodpaster BH, Krishnaswami S, Harris TB, et al. Obesity, regional body fat distribution, and the metabolic syndrome in older men and women. Arch Intern Med 2005; 165(7): 777-83.

19. Rimm EB, Stampfer MJ, Giovannucci E, et al. Body size and fat distribution as predictors of coronary heart disease among middle-aged and older US men. Am J Epidemiol 1995; 141(12): 1117-27.

20. Prineas RJ, Folsom AR, Kaye SA. Central adiposity and increased risk of coronary artery disease mortality in older women. Ann Epidemiol 1993; 3(1): 35-41.

21. Kip KE, Marroquin OC, Kelley DE, et al. Clinical importance of obesity versus the metabolic syndrome in cardiovascular risk in women: a report from the Women’s Ischemia Syndrome Evaluation (WISE) study. Circulation 2004; 109(6): 706-13.

22. Kannel WB, Castelli WP, Gordon T, McNamara PM. Serum cholesterol, lipoproteins, and the risk of coronary heart disease. The Framingham study. Ann Intern Med 1971; 74(1): 1-12.

23. Stevenson JC, Crook D, Godsland IF. Influence of age and menopause on serum lipids and lipoproteins in healthy women. Atherosclerosis 1993; 98(1):83-90.

24. Kannel WB. Metabolic risk factors for coronary heart disease in women: perspective from the Framingham Study. Am Heart J 1987; 114(2): 413-9.

25. Nikkilä M, Pitkäjärvi T, Koivula T, et al. Women have a larger and less atherogenic low density lipoprotein particle size than men. Atherosclerosis 1996; 119(2): 181-90.

26. Kuller LH, Gutai JP, Meilahn E, Matthews KA, Plantinga P. Relationship of endogenous sex steroid hormones to lipids and apoproteins in postmenopausal women. Arterioscler Thromb Vasc Biol 1990; 10(6).

27. Gordon DJ, Probstfield JL, Garrison RJ, et al. High-density lipoprotein cholesterol and cardiovascular disease. Four prospective American studies. Circulation 1989; 79(1): 8-15.

28. Jacobs DR, Mebane IL, Bangdiwala SI, Criqui MH, Tyroler HA. High density lipoprotein cholesterol as a predictor of cardiovascular disease mortality in men and women: the follow-up study of the Lipid Research Clinics Prevalence Study. Am J Epidemiol 1990; 131(1): 32-47.

29. Kanaya AM, Grady D, Barrett-Connor E, et al. Explaining the sex difference in coronary heart disease mortality among patients with type 2 diabetes mellitus. Arch Intern Med 2002; 162(15):1737-45.

30. Orchard TJ. The impact of gender and general risk factors on the occurrence of atherosclerotic vascular disease in non-insulin-dependent diabetes mellitus. Ann Med 1996; 28(4): 323-33.

31. Lee WL, Cheung AM, Cape D, Zinman B. Impact of diabetes on coronary artery disease in women and men: a meta-analysis of prospective studies. Diabetes Care 2000; 23(7): 962-8.

32. Huxley R, Barzi F, Woodward M. Excess risk of fatal coronary heart disease associated with diabetes in men and women: meta-analysis of 37 prospective cohort studies. BMJ 2006; 332(7533): 73-8.

33. Barton M, Meyer MR. Postmenopausal hypertension: mechanisms and therapy. Hypertension 2009; 54(1):11-8.

34. Burt VL, Whelton P, Roccella EJ, et al. Prevalence of hypertension in the US adult population. Results from the Third National Health and Nutrition Examination Survey, 1988-1991. Hypertension 1995; 25(3): 305-13.

35. Jousilahti P, Vartiainen E, Tuomilehto J, Puska P. Sex, age, cardiovascular risk factors, and coronary heart disease: a prospective follow-up study of 14 786 middle-aged men and women in Finland. Circulation 1999; 99(9): 1165–72.

36. Vasan RS, Larson MG, Leip EP, et al. Impact of high-normal blood pressure on the risk of cardiovascular disease. N Engl J Med 2001; 345(18):1291-7.

37. Martins D, Nelson K, Pan D, Tareen N, Norris K. The effect of gender on age-related blood pressure changes and the prevalence of isolated systolic hypertension among older adults: data from NHANES III. J Gend Specif Med 2001; 4(3):10–3, 20.

38. Prescott E, Hippe M, Schnohr P, Hein HO, Vestbo J. Smoking and risk of myocardial infarction in women and men: longitudinal population study. BMJ 1998; 316(7137):1043-7.

39. Jakobsen MU, Overvad K, Dyerberg J, Schroll M, Heitmann BL. Dietary fat and risk of coronary heart disease: possible effect modification by gender and age. Am J Epidemiol 2004; 160(2):141-9.

40. Sattelmair J, Pertman J, Ding EL, Kohl HW, Haskell W, Lee I-M. Dose response between physical activity and risk of coronary heart disease: a meta-analysis. Circulation 2011; 124(7):789-95.

41. Pepine CJ, Kerensky RA, Lambert CR, et al. Some thoughts on the vasculopathy of women with ischemic heart disease. J Am Coll Cardiol 2006; 47(3):S30-5.

42. Lansky AJ, Ng VG, Maehara A, et al. Gender and the extent of coronary atherosclerosis, plaque composition, and clinical outcomes in acute coronary syndromes. JACC Cardiovasc Imaging 2012; 5(3): S62-72.

43. Johansson S, Bergstrand R, Ulvenstam G, et al. Sex differences in preinfarction characteristics and longterm survival among patients with myocardial infarction. Am J Epidemiol 1984; 119(4):610-23.

44. Hochman JS, McCabe CH, Stone PH, et al. Outcome and profile of women and men presenting with acute coronary syndromes: a report from TIMI IIIB. TIMI Investigators. Thrombolysis in myocardial infarction. J Am Coll Cardiol 1997; 30(1): 141-8.

45. Shaw LJ, Lewis JF, Hlatky MA, et al. Women’s ischemic syndrome evaluation: current status and future research directions: Report of the National Heart, Lung and Blood Institute Workshop: October 2-4, 2002: Section 5: Gender-related risk factors for ischemic heart disease. Circulation 2004; 109(6): 56e – 58.

46. Sharaf BL, Pepine CJ, Kerensky RA, et al. Detailed angiographic analysis of women with suspected ischemic chest pain (pilot phase data from the NHLBI-sponsored Women’s Ischemia Syndrome Evaluation [WISE] Study Angiographic Core Laboratory). Am J Cardiol 2001; 87(8):937-41; A3.

47. Mieres JH, Gulati M, Bairey Merz N, et al. Role of noninvasive testing in the clinical evaluation of women with suspected ischemic heart disease. Circulation 2014; 130(4): 350-79.

48. Kwok Y, Kim C, Grady D, Segal M, Redberg R. Meta-analysis of exercise testing to detect coronary artery disease in women. Am J Cardiol 1999; 83(5): 660-6.

49. Canto JG, Goldberg RJ, Hand MM, et al. Symptom presentation of women with acute coronary syndromes. Arch Intern Med 2007; 167(22):2405-13.

50. Gulati M, Shaw LJ, Bairey Merz CN. Myocardial ischemia in women: lessons from the NHLBI WISE study. Clin Cardiol 2012; 35(3):141-8.

51. Hemingway H, Langenberg C, Damant J, Frost C, Pyorala K, Barrett-Connor E. Prevalence of angina in women versus men: a systematic review and meta-analysis of international variations across 31 countries. Circulation 2008; 117(12): 1526–36.

52. Milner KA, Vaccarino V, Arnold AL, Funk M, Goldberg RJ. Gender and age differences in chief complaints of acute myocardial infarction (Worcester heart attack study). T Am J Cardiol 2004; 93(5): 606-8.

53. Shaw LJ, Merz CNB, Pepine CJ, et al. The economic burden of angina in women with suspected ischemic heart disease: Results from the National Institutes of Health-National Heart, Lung, and Blood Institute-Sponsored Women’s Ischemia Syndrome Evaluation. Circulation 2006; 114(9):894-904.

54. Gulati M, Cooper-DeHoff RM, McClure C, et al. Adverse cardiovascular outcomes in women with nonobstructive coronary artery disease: a report from the Women’s Ischemia Syndrome Evaluation Study and the St James Women Take Heart Project. Arch Intern Med 2009; 169(9): 843-50.

55. Brieger D, Eagle KA, Goodman SG, et al. Acute coronary syndromes without chest pain, an underdiagnosed and undertreated high-risk group. Chest 2004; 126(2):461-9.

56. Vaccarino V, Parsons L, Every NR, Barron HV, Krumholz HM. Sex-based differences in early mortality after myocardial infarction. N Engl J Med 1999; 341(4): 217-25.

57. Robinson JG, Wallace R, Limacher M, et al. Cardiovascular risk in women with non-specific chest pain (from the Women’s Health Initiative Hormone Trials). Am J Cardiol 2008; 102(6): 693-9.

58. Robinson JG, Wallace R, Limacher M, et al. Elderly women diagnosed with nonspecific chest pain may be at increased cardiovascular risk. J Women’s Health 2006; 15(10): 1151–60.

59. Milcent C, Dormont B, Durand-Zaleski I, Steg PG. Gender differences in hospital mortality and use of percutaneous coronary intervention in acute myocardial infarction: microsimulation analysis of the 1999 nationwide French hospitals database. Circulation 2007; 115(7):833-9.

60. Nguyen HL, Gore JM, Saczynski JS, et al. Age and sex differences and 20-year trends (1986 to 2005) in prehospital delay in patients hospitalized with acute myocardial infarction. Circ Cardiovasc Qual Outcomes 2010; 3(6): 590-8.

61. Graham G. Acute coronary syndromes in women: recent treatment trends and outcomes. Clin Med Insights Cardiol 2016; 10:1-10.

62. De Luca G, Suryapranata H, Ottervanger JP, Antman EM. Time delay to treatment and mortality in primary angioplasty for acute myocardial infarction: every minute of delay counts. Circulation 2004; 109(10): 1223-5.

63. Diercks DB, Owen KP, Kontos MC, et al. Gender differences in time to presentation for myocardial infarction before and after a national women’s cardiovascular awareness campaign: A temporal analysis from the Can Rapid Risk Stratification of Unstable Angina Patients Suppress ADverse Outcomes with Early Implementation (CRUSADE) and the National Cardiovascular Data Registry Acute Coronary Treatment and Intervention Outcomes Network-Get with the Guidelines. Am Heart J 2010; 160(1): 80-7.

64. Oertelt-Prigione S, Seeland U, Kendel F, et al. Cardiovascular risk factor distribution and subjective risk estimation in urban women--the BEFRI study: a randomized cross-sectional study. BMC Med 2015; 13:52.

65. Rosenfeld AG, Lindauer A, Darney BG. Understanding treatment-seeking delay in women with acute myocardial infarction: descriptions of decision-making patterns. Am J Crit Care 2005;14(4):285-93.

66. Mosca L, Mochari-Greenberger H, Dolor RJ, Newby LK, Robb KJ. Twelve-year follow-up of american women’s awareness of cardiovascular disease risk and barriers to heart health. Circ Cardiovasc Qual Outcomes 2010; 3(2): 120-7.

67. Tunstall-Pedoe H, Morrison C, Woodward M, Fitzpatrick B, Watt G. Sex differences in myocardial infarction and coronary deaths in the Scottish MONICA population of Glasgow 1985 to 1991. Presentation, diagnosis, treatment, and 28-day case fatality of 3991 events in men and 1551 events in women. Circulation 1996; 93(11):1981-92.

68. Templin C, Ghadri JR, Diekmann J, et al. Clinical features and outcomes of Takotsubo (stress) cardiomyopathy. N Engl J Med 2015; 373(10):929-38.

69. Deshmukh A, Kumar G, Pant S, Rihal C, Murugiah K, Mehta JL. Prevalence of Takotsubo cardiomyopathy in the United States. Am Heart J 2012; 164(1): 66-71.e1.

70. Radovanovic D, Erne P, Urban P, et al. Gender differences in management and outcomes in patients with acute coronary syndromes: results on 20 290 patients from the AMIS Plus Registry. Heart 2007; 93(11): 1369-75.

71. Hvelplund A, Galatius S, Madsen M, et al. Women with acute coronary syndrome are less invasively examined and subsequently less treated than men. Eur Heart J 2010; 31(6): 684-90.

72. Wijns W, Kolh P, Danchin N, et al. Guidelines on myocardial revascularization: The Task Force on Myocardial Revascularization of the European Society of Cardiology (ESC) and the European Association for Cardio-Thoracic Surgery (EACTS). Eur Heart J 2010; 31(20): 2501-55.

73. Andersen HR, Nielsen TT, Rasmussen K, et al. A Comparison of coronary angioplasty with fibrinolytic therapy in acute myocardial infarction. N Engl J Med 2003; 349(8):733-42.

74. Mozaffarian D, Benjamin EJ, Go AS, et al. Heart disease and stroke statistics-2016 Update: A Report from the American Heart Association. Circulation 2016; 133(4): e38-360.

75. Kudenchuk PJ, Maynard C, Martin JS, Wirkus M, Weaver WD. Comparison of presentation, treatment, and outcome of acute myocardial infarction in men versus women (the Myocardial Infarction Triage and Intervention Registry). Am J Cardiol 1996; 78(1): 9-14.

76. Worrall-Carter L, MacIsaac A, Scruth E, Rahman MA. Gender difference in the use of coronary interventions for patients with acute coronary syndrome: Experience from a major metropolitan hospital in Melbourne, Australia. Aust Crit Care 2017; 30(1):3-10.

77. Halvorsen S, Eritsland J, Abdelnoor M, et al. Gender differences in management and outcome of acute myocardial infarctions treated in 2006-2007. Cardiology 2009; 114(2): 83-8.

78. Bangalore S, Fonarow GC, Peterson ED, et al. Age and gender differences in quality of care and outcomes for patients with ST-segment elevation myocardial infarction. Am J Med 2012; 125(10):1000-9.

79. Zhang Z, Fang J, Gillespie C, Wang G, Hong Y, Yoon PW. Age-Specific Gender Differences in In-Hospital Mortality by Type of Acute Myocardial Infarction. Am J Cardiol 2012; 109(8):1097-103.

80. Ayanian JZ, Epstein AM. Differences in the use of procedures between women and men hospitalized for coronary heart disease. N Engl J Med 1991; 325(4): 221–5.

81. Clarke KW, Gray D, Keating NA, Hampton JR. Do women with acute myocardial infarction receive the same treatment as men? BMJ 1994; 309(6954): 563-6.

82. Haimi I, Lee HJ, Mehta S, et al. CRT-200.92 Gender disparities in ST-elevation myocardial infarction care and outcomes in emerging countries: a Global Lumen Organization for Women (GLOW) Initiative and Call to Action. JACC Cardiovasc Interv 2016; 9(4): S31.

83. Vakili BA, Kaplan RC, Brown DL. Sex-based differences in early mortality of patients undergoing primary angioplasty for first acute myocardial infarction. Circulation 2001; 104(25): 3034-8.

84. Sadowski M, Gasior M, Gierlotka M, Janion M, Polonski L. Gender-related differences in mortality after ST-segment elevation myocardial infarction: a large multicentre national registry. EuroIntervention 2011; 6(9): 1068-72.

85. Alexander KP, Chen AY, Newby LK, et al. Sex differences in major bleeding with glycoprotein iib/iiia inhibitors: results from the CRUSADE (Can Rapid risk stratification of Unstable angina patients Suppress ADverse outcomes with Early implementation of the ACC/AHA guidelines) Initiative. Circulation 2006; 114(13): 1380-7.

86. Cho L, Topol EJ, Balog C, et al. Clinical benefit of glycoprotein IIb/IIIa blockade with abciximab is independent of gender: Pooled analysis from EPIC, EPILOG and EPISTENT trials. J Am Coll Cardiol 2000; 36(2):381-6.

87. Maggioni AA, Maseri A, Fresco C, et al. Age-related increase in mortality among patients with first myocardial infarctions treated with thrombolysis. N Engl J Med 1993; 329(20): 1442–8.

88. Thiemann DR, Coresh J, Schulman SP, Gerstenblith G, Oetgen WJ, Powe NR. Lack of benefit for intravenous thrombolysis in patients with myocardial infarction who are older than 75 years. Circulation 2000; 101(19): 2239-46.

89. Wallentin L, Goldstein P, Armstrong PW, et al. Efficacy and safety of tenecteplase in combination with the low-molecular-weight heparin enoxaparin or unfractionated heparin in the prehospital setting. Circulation 2003; 108(2): 135-42.

90. Stone GW, Grines CL, Browne KF, et al. Comparison of in-hospital outcome in men versus women treated by either thrombolytic therapy or primary coronary angioplasty for acute myocardial infarction. Am J Cardiol. Excerpta Medica 1995; 75(15): 987-92.

91. Antman EM, Morrow DA, McCabe CH, et al. Enoxaparin versus unfractionated heparin with fibrinolysis for ST-elevation myocardial infarction. N Engl J Med 2006; 354(14): 1477-88.

92. Berger JS, Elliott L, Gallup D, et al. Sex differences in mortality following acute coronary syndromes. JAMA 2009; 302(8): 874–82.

93. Mueller C, Neumann F-J, Roskamm H, et al. Women do have an improved long-term outcome after non-ST-elevation acute coronary syndromes treated very early and predominantly with percutaneous coronary intervention: a prospective study in 1,450 consecutive patients. J Am Coll Cardiol 2002; 40(2): 245-50.

94. Glaser R, Herrmann HC, Murphy SA, et al. Benefit of an early invasive management strategy in women with acute coronary syndromes. JAMA 2002; 288(24): 3124-9.

95. Lansky AJ. Outcomes of percutaneous and surgical revascularization in women. Prog Cardiovasc Dis 2004; 46(4): 305-19.

96. Glaser R, Selzer F, Jacobs AK, et al. Effect of gender on prognosis following percutaneous coronary intervention for stable angina pectoris and acute coronary syndromes. Am J Cardiol 2006; 98(11): 1446-50.

97. Roe YL, Zeitz CJ, Mittinty MN, McDermott RA, Chew DP. Impact of age, gender and indigenous status on access to diagnostic coronary angiography for patients presenting with non-ST segment elevation acute coronary syndromes in Australia. Intern Med J 2013; 43(3): 317-22.

98. Gurjeva OS, Roe MT, Murphy SA, Moliterno DJ, Cannon CP, GUARANTEE investigators. Unfortunate impact of age on the management and outcomes of unstable angina and non-ST elevation myocardial infarction (The GUARANTEE Registry). Crit Pathw Cardiol 2005; 4(2): 81-7.

99. Alfredsson J, Stenestrand U, Wallentin L, Swahn E. Gender differences in management and outcome in non-ST-elevation acute coronary syndrome. Heart 2007; 93(11): 1357-62.

100. Anderson JL, Adams CD, Antman EM, et al. ACC/AHA 2007 Guidelines for the management of patients with unstable angina/non–st-elevation myocardial infarction. J Am Coll Cardiol 2007; 50(7): e1-157.

101. O’Donoghue M, Boden WE, Braunwald E, et al. Early invasive vs conservative treatment strategies in women and men with unstable angina and non-ST-segment elevation myocardial infarction: a meta-analysis. JAMA 2008; 300(1):71-80.

102. Mosca L, Banka CL, Benjamin EJ, et al. Evidence-based guidelines for cardiovascular disease prevention in women: 2007 Update. Circulation 2007; 115(11): 1481-501.

103. Mosca L, Grundy SM, Judelson D, et al. Guide to preventive cardiology for women. Circulation 1999; 99(18): 2480-4.

104. Gan SC, Beaver SK, Houck PM, MacLehose RF, Lawson HW, Chan L. Treatment of acute myocardial infarction and 30-day mortality among women and men. N Engl J Med 2000; 343(1):8-15.

105. Blomkalns AL, Chen AY, Hochman JS, et al. Gender disparities in the diagnosis and treatment of non–ST-segment elevation acute coronary syndromes. J Am Coll Cardiol 2005; 45(6): 832-7.

106. Vaccarino V, Rathore SS, Wenger NK, et al. Sex and racial differences in the management of acute myocardial infarction, 1994 through 2002. N Engl J Med 2005; 353(7): 671-82.

107. DeWilde S, Carey IM, Richards N, Whincup PH, Cook DG. Trends in secondary prevention of ischaemic heart disease in the UK 1994 2005: use of individual and combination treatment. Heart 2008; 94(1): 83-8.

108. Ballo P, Balzi D, Barchielli A, Turco L, Franconi F, Zuppiroli A. Gender differences in statin prescription rates, adequacy of dosing, and association of statin therapy with outcome after heart failure hospitalization: a retrospective analysis in a community setting. Eur J Clin Pharmacol 2016; 72(3): 311-9.

109. Bugiardini R, Yan AT, Yan RT, et al. Factors influencing underutilization of evidence-based therapies in women. Eur Heart J 2011; 32(11): 1337-44.

110. Levin RI. The puzzle of aspirin and sex. N Engl J Med 2005; 352(13): 1366-8.

111. Price MJ, Nayak KR, Barker CM, Kandzari DE, Teirstein PS. Predictors of heightened platelet reactivity despite dual-antiplatelet therapy in patients undergoing percutaneous coronary intervention. Am J Cardiol 2009; 103(10): 1339-43.

112. Hammerlein A, Derendorf H, Lowenthal DT. Pharmacokinetic and pharmacodynamic changes in the elderly. Clin Pharmacokinet 1998; 35(1): 49-64.

113. Sergi G, De Rui M, Sarti S, Manzato E. Polypharmacy in the elderly: can comprehensive geriatric assessment reduce inappropriate medication use? Drugs Aging 2011; 28(7): 509-18.

114. Palmieri L, Bennett K, Giampaoli S, Capewell S. Explaining the decrease in coronary heart disease mortality in Italy between 1980 and 2000. Am J Public Health 2010; 100(4): 684-92.

115. Shaw LJ, Bairey Merz CN, et al. Insights From the NHLBI-Sponsored Women’s Ischemia Syndrome Evaluation (WISE) Study: Part I: Gender differences in traditional and novel risk factors, symptom evaluation, and gender-optimized diagnostic strategies. J Am Coll Cardiol 2006; 47(3): S4-20.

116. He J, Klag MJ, Whelton PK, Zhoa Y, Weng X. Short- and long-term prognosis after acute myocardial infarction in Chinese men and women. Am J Epidemiol 1994; 139(7): 693-703.

117. Fiebach NH, Viscoli CM, Horwitz RI, et al. Differences between women and men in survival after myocardial infarction. JAMA 1990; 263(8): 1092-6.

118. Weaver WD, White HD, Wilcox RG, et al. Comparisons of characteristics and outcomes among women and men with acute myocardial infarction treated with thrombolytic therapy. JAMA 1996; 275(10): 777-82.

119. Chang W-C, Kaul P, Westerhout CM, et al. Impact of Sex on long-term mortality from acute myocardial infarction vs unstable angina. Arch Intern Med 2003; 163(20): 2476-84.

120. Lee KL, Woodlief LH, Topol EJ, et al. Predictors of 30-day mortality in the era of reperfusion for acute myocardial infarction. Results from an international trial of 41,021 patients. GUSTO-I Investigators. Circulation 1995; 91(6): 1659–68.

121. Wijnbergen I, Tijssen J, van ’t Veer M, Michels R, Pijls NHJ. Gender differences in long-term outcome after primary percutaneous intervention for ST-segment elevation myocardial infarction. Catheter Cardiovasc Interv 2013; 82(3): 379-84.

122. Raphael CE, Spoon D, Lennon R, et al. GENDER differences in cause of death following percutaneous coronary intervention. J Am Coll Cardiol 2016; 67(13): 329.

123. Argulian E, Patel AD, Abramson JL, et al. Gender differences in short-term cardiovascular outcomes after percutaneous coronary interventions. Am J Cardiol 2006; 98(1): 48-53.

124. Mehta RH, Stebbins AS, Lopes RD, et al. Comparison of incidence of bleeding and mortality of men versus women with ST-elevation myocardial infarction treated with fibrinolysis. Am J Cardiol 2012; 109(3): 320-6.

125. Nicolau JC, Ferraz MA, Nogueira PR, Garzon SAC, Serrano C V, Ramires JAF. The role of gender in the long-term prognosis of patients with myocardial infarction submitted to fibrinolytic treatment. Ann Epidemiol. 2004;14(1): 17-23.

126. Goldberg RJ, Gorak EJ, Yarzebski J, et al. A communitywide perspective of sex differences and temporal trends in the incidence and survival rates after acute myocardial infarction and out-of-hospital deaths caused by coronary heart disease. Circulation 1993; 87(6): 1947-53.

127. MacIntyre K, Stewart S, Capewell S, et al. Gender and survival: a population-based study of 201,114 men and women following a first acute myocardial infarction. J Am Coll Cardiol 2001; 38(3): 729-35.

128. Claassen M, Sybrandy KC, Appelman YE, Asselbergs FW. Gender gap in acute coronary heart disease: Myth or reality? World J Cardiol 2012; 4(2): 36-47.

129. Assiri AS. Gender differences in clinical presentation and management of patients with acute coronary syndrome in Southwest of Saudi Arabia. J Saudi Heart Assoc 2011; 23(3): 135-41.

130. Naito R, Miyauchi K, Konishi H, et al. Gender difference in long-term clinical outcomes following percutaneous coronary intervention during 1984–2008. Atherosclerosis 2016; 247: 105-10.

131. Thombs BD, Bass EB, Ford DE, et al. Prevalence of depression in survivors of acute myocardial infarction. J Gen Intern Med 2006; 21(1) :30-8.

132. Lesperance F, Frasure-Smith N, Talajic M. Major depression before and after myocardial infarction: its nature and consequences. Psychosom Med 1996; 58(2): 99-110.

133. Feng H-P, Chien W-C, Cheng W-T, Chung C-H, Cheng S-M, Tzeng W-C. Risk of anxiety and depressive disorders in patients with myocardial infarction. Medicine (Baltimore) 2016; 95(34): e4464.

134. Frasure-Smith N, Lespérance F, Juneau M, Talajic M, Bourassa MG. Gender, depression, and one-year prognosis after myocardial infarction. Psychosom Med 1999; 61(1): 26-37.

135. Frasure-Smith N, Lespérance F, Talajic M. Depression and 18-month prognosis after myocardial infarction. Circulation 1995; 91(4): 999-1005.

136. Strik JJ, Honig A, Maes M. Depression and myocardial infarction: relationship between heart and mind. Prog Neuro-Psychopharmacology Biol Psychiatry 2001; 25(4): 879-92.

137. Naqvi TZ, Naqvi SSA, Merz CNB. Gender differences in the link between depression and cardiovascular disease. Psychosom Med 2005; 67 Suppl 1(SUPPL. 1): S15–8.

138. Olson MB, Kelsey SF, Matthews K, et al. Symptoms, myocardial ischaemia and quality of life in women: results from the NHLBI-sponsored WISE Study. Eur Heart J 2003; 24(16): 1506-14.

139. Bjerkeset O, Nordahl HM, Mykletun A, Holmen J, Dahl AA. Anxiety and depression following myocardial infarction: gender differences in a 5-year prospective study. J Psychosom Res 2005; 58(2): 153-61.

140. van Elderen T, Maes S, Dusseldorp E. Coping with coronary heart disease: a longitudinal study. J Psychosom Res 1999; 47(2): 175-83.

141. Hobfoll SE, Dunahoo CL, Ben-Porath Y, Monnier J. Gender and coping: The dual-axis model of coping. Am J Community Psychol 1994; 22(1): 49-82.

142. Norris CM, Ghali WA, Galbraith PD, et al. Women with coronary artery disease report worse health-related quality of life outcomes compared to men. Health Qual Life Outcomes 2004; 2(1): 21.

143. Gijsberts CM, Agostoni P, Hoefer IE, et al. Gender differences in health-related quality of life in patients undergoing coronary angiography. Open Heart 2015; 2(1): e000231.

144. Zaninotto P, Sacker A, Breeze E, McMunn A, Steptoe A. Gender-specific changes in well-being in older people with coronary heart disease: evidence from the English Longitudinal Study of Ageing. Aging Ment Health 2016; 20(4): 432-40.

145. Schweikert B, Hunger M, Meisinger C, König H-H, Gapp O, Holle R. Quality of life several years after myocardial infarction: comparing the MONICA/KORA registry to the general population. Eur Heart J 2009; 30(4): 436–43.

146. Feola M, Garnero S, Daniele B, et al. Gender differences in the efficacy of cardiovascular rehabilitation in patients after cardiac surgery procedures. J Geriatr Cardiol 2015; 12(5):575-9.

147. Newman AB, Fitzpatrick AL, Lopez O, et al. Dementia and Alzheimer’s disease incidence in relationship to cardiovascular disease in the Cardiovascular Health Study cohort. J Am Geriatr Soc 2005; 53(7):1101-7.

148. Aronson MK, Ooi WL, Morgenstern H, et al. Women, myocardial infarction, and dementia in the very old. Neurology 1990; 40(7): 1102-6.

149. Phan HM, Alpert JS, Fain M. Frailty, inflammation, and cardiovascular disease: evidence of a connection. Am J Geriatr Cardiol 2008; 17(2): 101-7.

150. Fried LP, Tangen CM, Walston J, et al. Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci 2001; 56(3): M146-56.

151. Ekerstad N, Swahn E, Janzon M, et al. Frailty is independently associated with short-term outcomes for elderly patients with non-ST-segment elevation myocardial infarction. Circulation 2011; 124(22): 2397-404.

152. Afilalo J. Frailty in patients with cardiovascular disease: why, when, and how to measure. Curr Cardiovasc Risk Rep 2011; 5(5): 467-72.

153. Sergi G, Veronese N, Fontana L, et al. Pre-frailty and risk of cardiovascular disease in elderly men and women: the Pro.V.A. study. J Am Coll Cardiol 2015; 65(10): 976-83.

154. von Haehling S, Anker SD, Doehner W, Morley JE, Vellas B. Frailty and heart disease. Int J Cardiol 2013; 168: 1745-7.

155. Afilalo J, Karunananthan S, Eisenberg MJ, Alexander KP, Bergman H. Role of frailty in patients with cardiovascular disease. Am J Cardiol 2009; 103(11): 1616-21.

Conflict of interest statement: the Authors declare no potential conflits of interest or any financial or personal relationships with other people or organizations that could inappropriately bias conduct and findings of this study.