|Home | About | Journals | Submit | Contact Us | Français|
The role of new and emerging biomarkers in risk prediction has become a topic of significant interest and controversy in recent times. Currently, available models for risk prediction are reasonably good yet still misclassify a not insignificant portion of the population. The sheer number of new potential risk markers is daunting, and it is difficult to assess the importance of each one over and above the traditional risk factors. Endothelial function is one potential biomarker of risk that has been extensively studied. However, while it has demonstrated some utility in risk prediction, its use in daily clinical practice is yet to be clearly defined. The present review assesses the prognostic significance of measures of endothelial function.
Le rôle des biomarqueurs nouveaux et émergents sur la prédiction du risque est récemment devenu un sujet de grand intérêt et de controverse. Les modèles actuels de prédiction du risque sont raisonnablement bons, mais ils proposent la classification erronée d’une forte proportion de la population. Le nombre même de nouveaux marqueurs de risque potentiels est décourageant, et il est difficile d’évaluer l’importance de chacun d’eux en plus des facteurs de risque classiques. La fonction endothéliale est un biomarqueur potentiel de risque qui a fait l’objet de nombreuses études. Cependant, même s’il a démontré une certaine utilité de prédiction du risque, son utilisation dans la pratique clinique quotidienne n’est pas encore clairement définie. La présente analyse permet d’évaluer la signification pronostique de la fonction endothéliale.
The wealth of available epidemiological data has led to the development of many risk stratification models in cardiovascular disease, perhaps the most prominent of which is the Framingham model (1,2). However, there is no risk model that perfectly predicts cardiovascular risk at an individual level, and thus, there have been many attempts to refine existing risk models through the addition of further factors. Traditional risk scoring systems evaluating risk factors such as smoking, hypertension and diabetes are reasonably effective; however, nearly one-quarter of cardiovascular events occur in people with minimal identifiable risk (3). Furthermore, the prevalence of all of these risk factors is nearly the same in those with and without disease (4).
The potential risk modifier that has received the most attention of late is serum high-sensitivity C-reactive protein, which has demonstrated some additive value in refining risk in the Framingham and Physicians Health Study risk models (5,6). However, there are many other potential biomarkers available and under investigation for their utility in risk prediction, including coagulation markers, genetics, various lipids subfractions and, more recently, imaging modalities. Of particular interest to vascular biologists is the use of measures of endothelial function as a biomarker of risk.
Endothelial function is a major contributor to overall vascular health and plays an important role in clinical expression of significant vascular disease (7). Endothelial dysfunction has been found to be in association with many disease states, including all major Framingham risk factors, and dysfunction occurs before the development of overt cardiovascular disease (8–15). Furthermore, vascular dysfunction has been demonstrated to be predictive of adverse outcomes following vascular surgical or percutaneous coronary intervention (16,17). However, its role in risk assessment for an individual patient is yet to be defined. Before it can even be considered to be of value as a bio-marker, several questions must be answered:
These issues are addressed in more detail in the present review.
Healthy endothelium is vital as a regulator of vascular homeostasis. It sits as a monolayer of endothelial cells lining the lumen of the vasculature, extending from large conduit vessels down to the intravasculature microcirculation (19). As such, it is exposed to any and all systemic stressors, undergoing constant injury and subsequent repair (19,20), and has the ability to exert vascular control. The endothelium has myriad roles that demonstrate its centrality in the development of atherosclerosis (7). This understanding has evolved since the initial description of endothelium-derived relaxing factor (21).
The endothelium has many functions beyond simply serving as an inert, selectively permeable barrier between the circulation and the vessel wall (Figure 1). It plays a role in vasomotion (and thus responses to ischemia), platelet function (adhesion and aggregation), inflammation, coagulation and fibrinolysis, smooth muscle cell proliferation and mediating endothelial progenitor cell activity. Healthy endothelial function relies on the production of nitric oxide (NO), prostaglandin I2 and endothelium-derived hyperpolarizing factor; all of these vasoactive substances support endothelial function through their effect on vasodilation, but also by being anti-inflammatory, anti-proliferative and anticoagulatory (via heparin and protein C and S), and by promoting fibrinolysis (via tissue plasminogen activator) (22) and diminishing platelet aggregation (via NO and prostacyclin) (23). In disease, the role of endothelins, angiotensin II and free radicals become dominant, promoting vasoconstriction (via diminished NO), smooth muscle cell proliferation (via mitogenic substances such as endothelin-1) (24) and inflammation, while also resulting in platelet aggregation and coagulation. In moving from health to disease, the endothelium loses its antiatherogenic characteristics, and abnormal responses to injury develop. Perturbations in endothelial function are a very early sign of atherosclerotic disease (25,26).
The relationship between cardiovascular risk factors and endothelial dysfunction is thought to be mediated via the common pathway of increased oxidative stress, although the exact mechanisms are different for various pathologies. Diabetes, hypertension, hyperlipidemia and smoking are all known to cause increased oxidative stress, and all have been demonstrated to lead to endothelial dysfunction.
While numerous molecules play a role in endothelial function, the most prominent and central one is NO. NO bioavailability is reduced in the presence of reactive oxygen species that are generated at times of oxidative stress (27). NO bioavailability is further reduced at times of stress owing to oxidation and subsequent depletion of tetrahydrobiopterin (28). This results in the uncoupling of NO synthase, and therefore a disruption in the healthy balance of the nitroso-redox system, resulting in impaired endothelial function (28). Tetrahydrobiopterin supplementation has been demonstrated to improve endothelial function in patients with high levels of oxidative stress, such as patients with diabetes (29) or hypercholesterolemia (30–32).
There are currently no treatments directed toward primarily improving endothelial function, because its utility as a clinical end point has not been established and it is not measured outside of the research setting. However, the roles of several cardiovascular medications in improving endothelial dysfunction have been well documented. Of particular importance are 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors (statins) and angiotensin-converting enzyme inhibitors. It bas been demonstrated that low-density lipoprotein reduction with statins improves endothelial function in both the coronary and peripheral vascular beds (33–35); furthermore, this improvement has been associated with favourable cardiovascular outcomes. Angiotensin-converting enzyme inhibition has been demonstrated to have similar beneficial effects (36,37).
These medications are obviously well established to reduce cardiovascular events, which perhaps highlights the importance of endothelial function in such events. Still, there is no evidence to suggest that treatment with a goal of improving endothelial function results in an improvement in cardiovascular health and a reduction in CV events.
There are many published mechanisms by which to assess endothelial function, varying from very invasive, such as intracoronary assessment, to noninvasive, such as brachial artery flow-mediated dilation (FMD) (Table 1).
The first assessments of endothelial function were made in the coronary circulation (38,39). Using coronary angiography and intra-vascular ultrasound, the responses of the coronary circulation to endothelium-dependent stimuli (such as acetylcholine) in terms of coronary diameter and blood flow can be directly measured. This is still considered to be the gold standard in terms of endothelial function assessment. However, this method is obviously invasive, time intensive and expensive. Outside of use in patients already undergoing angiography, it is limited. It is especially impractical for any long-term study requiring serial measurement.
Atherosclerosis is not a disease limited to the coronary arteries. It is a systemic and diffuse disease, and we can therefore assess endothelial function in any vascular bed and extrapolate our findings systemically (19). Thus, methods have been established to assess endothelial function in the peripheral circulation. The relationship between coronary and peripheral measures of endothelial function is modest to good (40).
The brachial artery is one that holds particular appeal for peripheral endothelial assessment. It is easily and consistently accessible across patient populations. Initial assessments of endothelial function using the forearm were done using similar techniques as the intracoronary assessments: it involved direct cannulation of the brachial artery and infusion of vasoactive substance. The change in volume of the forearm was then assessed as a measure of forearm microvascular function. This technique of impedance plethysmography was demonstrated to be reproducible and easily taught, and was used extensively in small studies of endothelial function (41). Impairment in endothelial function demonstrated by this technique has been shown to be predictive of cardiovascular events in a small cohort of patients (14,42).
However, less invasive methods of assessing endothelial function in the forearm have been developed. Specifically, newer methods no longer require intervention at all: with the use of ultrasound imaging, dilation of the brachial artery in response to ischemic stress (FMD) can be assessed. FMD is a well-accepted and validated modality for assessing endothelial function (43,44). This technique has been used with very good reproducibility and low interobserver variability (45). In addition, recently, there has been interest in the hyperemic stimulus itself as a marker of endothelial health (46). A recent study by Huang et al (16) demonstrated that both FMD and hyperemic velocity were predictive of cardiovascular events in a cohort of patients with peripheral arterial disease referred for vascular surgery. However, this technique requires vasoactive medications to be held, as well as time and significant skill to perform.
Another noninvasive way to measure endothelial function is by using peripheral arterial tonometry (PAT) devices (47). This newly developed device resembles a pulse oximeter and is placed on the index finger tip in a similar manner. Measurements of pulse volume amplitude are thereby taken from both fingers. Similar to FMD, a blood pressure cuff is placed on the right arm, and PAT is measured before cuff inflation and subsequently following deflation. A measure of pulse amplitude is thereby obtained in a hyperemic state, which is reported as a ratio compared to the pulse volume amplitude in the nonstressed arm (PAT ratio). Impairment in hyperemic pulse response (lower PAT ratio) has been associated with impaired endothelial function. In a relatively large sample (1957 patients) of Framingham Third Generation Cohort participants, PAT ratio was shown to be affected by numerous traditional cardiovascular risk factors, including diabetes, smoking and lipid measures (48). This lends some credence to its proposed validity. An advantage of this technique includes its relative ease of use with shallow learning curve, but it is still limited by the length of time studies take as well as the need to avoid vasoactive medications and to fast prior to undergoing study.
Although the use of PAT has recently been validated in reasonably larger populations, its role in vasomotor assessments of endothelial function is not yet secure. The pathophysiology underlying impaired digital hyperemic responses to stress is not clearly defined. Furthermore, while PAT has been demonstrated to be associated with other peripheral measures of endothelial function, such as FMD, the association is modest at best (47). Further study and time are required to truly assess its utility; to that end, there are a number of very large studies underway studying patients from the Framingham study, among others, with PAT to answer some of these lingering questions.
Beyond assessing coronary vasoreactivity, FMD and PAT, there are multitudinous other methods by which to measure endothelial function. These include other methods of assessing vasomotion, imaging modalities (cardiac magnetic resonance, positron emission tomography and nuclear techniques), measures of arterial compliance (applanation tonometry), and measurement of markers of oxidative stress and inflammation (endothelin-1, NO). While each of these techniques holds particular appeal, each also has technique-specific pitfalls. At present, vasomotor assessments of endothelial function with the described techniques are the most broadly described and applied. The relative importance and utility of each of these measures is yet to be determined.
There have been a number of studies that have assessed the ability of endothelial function to predict cardiovascular risk (Table 2). While earlier studies attempting to demonstrate a relationship between endothelial dysfunction were limited to high-risk populations and involved small numbers of patients, there are newer studies looking at larger, younger populations demonstrating a similar result.
Endothelial function has been demonstrated to be predictive of poor outcomes in those with established disease. In the first study of its kind, Schachinger et al (49) demonstrated a higher incidence of cardiovascular events in patients with abnormal coronary vasomotion and mild coronary disease. This provided the first evidence of the prognostic significance of coronary vascular dysfunction. This result was confirmed by others (38).
A similar study was conducted as part of the Women’s Ischemia Syndrome Evaluation trial (50); in that study of 163 women referred for clinically indicated coronary angiogram, coronary dilation in response to acetylcholine was independently predictive of cardiovascular events during a median follow-up period of 48 months. In contrast, a Dutch study of 277 patients referred for first coronary angiogram for suspected coronary artery disease showed that there was no difference in rates of events by response to intracoronary acetylcholine infusion (39).
In a study of 136 patients with single-vessel coronary disease undergoing percutaneous coronary intervention, depressed FMD was found to be a strong predictor of in-stent restenosis (17). This effect was significant, even after adjustment for other cardiovascular risk factors, including diabetes and hypercholesterolemia. In fact, preserved endothelial function was found to have a negative predictive value of 96% for excluding restenosis.
Endothelial function has been established to predict risk in those with established cardiovascular disease – but beyond that, it has proven utility in predicting risk in those with risk factors alone. Furthermore, plasticity in endothelial function in terms of response to cardiovascular risk factor treatment has been demonstrated to be predictive of risk.
Beyond looking at FMD as a measure of endothelial function, Huang et al (16) demonstrated that lower reactive hyperemia is associated with increased cardiovascular risk in a high-risk group of 267 patients with peripheral vascular disease referred for surgery. The predictive value of reactive hyperemia was incremental beyond that of FMD alone in this population.
Postmenopausal hypertensive women have been demonstrated to have abnormal endothelial function (10,15). Based on this observation, Modena et al (10) set out to determine whether standard hypertension treatments are of any benefit at the level of the endothelium. A total of 400 hypertensive postmenopausal women were enrolled, and all were documented to have impaired FMD at baseline. FMD was reassessed after six months of antihypertensive therapy, and the majority of the women had significant improvement – with the remaining demonstrating no change. Those who had improvement in their endothelial function also had a significant reduction in clinical cardiovascular events, suggesting that improvements in endothelial function portends improved prognosis.
The real role for endothelial function in risk assessment may be in reclassifying patients who are low or medium risk and do not yet have any established cardiovascular disease. These are patients who provide a diagnostic and treatment dilemma. There are now several large studies evaluating the additive value of assessment of endothelial function over and above traditional risk factors in predicting risk. A recently published study by Yeboah et al (51) examined the relationship between FMD and subsequent cardiovascular events. A total of 2792 adults with a mean age of 78.6 years from the Cardiovascular Health Study had FMD assessed at baseline and were followed for five years. Patients with FMD greater than the sex-specific median had significantly better cardiovascular event-free survival than those with FMD at or below the median. FMD remained predictive of events, above and beyond the traditional risk factors. However, it added only approximately 1% to the prognostic accuracy of the model. Thus, while FMD is a statistically significant predictor of cardiovascular risk, it is still not apparently a clinically important predictor.
A similar study of a more diverse, younger population was conducted recently by Shimbo et al (52). For this study, 842 patients free of stroke or myocardial infarction were selected from a multiethnic prospective cohort study, the Northern Manhattan Study. While FMD was found to be predictive of cardiovascular events, this relationship was not statistically significant once multivariate analysis including all traditional risk factors was conducted.
Whether a biomarker can detect early stages of disease before any clinically overt manifestations is a question of utmost importance when assessing risk ‘prediction’. If testing can only detect an abnormality once a disease state has actually been established, it is obviously of doubtful clinical or practical importance in risk stratification. Larger studies are ongoing to determine whether these measures are practical and helpful in larger cohorts, especially those including younger patients.
One ongoing study from our institution, the Firefighters And Their Endothelium (FATE) study, is a prospective study of a relatively young population of 1585 male firefighters from Canada (53). At enrollment, none of the subjects had overt cardiovascular disease. Several measures of vascular health were taken at baseline, including serum biomarkers (CRP, homocysteine, adhesion molecules), carotid intimal medial thickness and FMD measurements. Results from this study should be available shortly; the questions we may be able to answer include the applicability of FMD in predicting outcomes in a young, healthy population, and the relative importance of different measures of vascular health in predicting outcomes. In addition, there are further ongoing epidemiological studies looking at the utility of endothelial function measurement in predicting risk in young healthy and diverse populations, including the Framingham Study (46), the National Institutes of Health-sponsored Multi-Ethnic Study of Atherosclerosis (MESA) study, the Young Finnish Study and the Uppsala Seniors study (54–56).
At present, there is insufficient evidence to suggest that endothelial function should be added to the daily clinical armamentarium for risk prediction at an individual patient level. It is clearly associated with cardiovascular disease and has been demonstrated to be dysfunctional long before the development of overt cardiovascular disease. It is also demonstrated to be modifiable through the use of medications whose place in the treatment of atherosclerotic disease has been well established. However, given the high predictive value of current models, it would be difficult to add any further predictors that would be of global significance or of much additive value. As noted, the best published study in this area demonstrated that FMD only improved risk prediction by approximately 1% (51). Ongoing studies should shortly address the utility of these measures in younger subjects at intermediate risk of atherosclerosis complications, the population in which biomarkers may play an important role.
The role of endothelial function as a biomarker may be twofold: persistence in its importance in clinical trials and research, and perhaps in helping to reclassify young patients at low or moderate risk. It has a key role as a research tool in vascular biology and has helped to further our understanding of atherosclerotic disease. It has and will be useful in the evaluation of new treatments for cardiovascular disease. Before it becomes practical for use on a more regular basis, methods for assessment need to be simplified and more widely available. Further work needs to be done to determine the utility of a measure of endothelial function in identifying patients who are in need of risk modification when traditional markers are unable to do so, analogous to how measurement of CRP has identified a new cohort of patients who may benefit from statin therapy (46). At present, there is work yet to be done to determine the clinical importance and utility of endothelial function for both patients and clinicians.
BMJ is a Clinical Research Fellow of the Alberta Heritage Foundation for Medical Research, and a Tomorrow’s Research Cardiovascular Health Professionals (TORCH) Trainee. TJA is a Senior Scholar of the Alberta Heritage Foundation for Medical Research.
CONFLICTS OF INTEREST: The authors have no conflicts of interest to declare.