Several studies have evaluated the traditional cardiovascular risk factors in patients with CAE and compared them in those with CAD. Giannoglu et al. [32] have reported a male dominance in patients with CAE. This gender difference has been reported previously [38, 81] and supposed due to the lower incidence of CAD in women, although the relation between CAE and CAD is not fully understood [32]. Moreover, the higher likelihood of males having CAE compared with women is generally consistent with a study in Spain in which male gender was demonstrated as an independent factor that increased the hazard of CAE [11]. Age has been shown to constitute a significant factor that is inversely associated with the presence of CAE [32]. A similar finding of significantly younger age among patients with CAE compared to those without CAE has previously been reported [11, 21, 82]. On the other hand, Markis et al. [53] have reported comparable sex and mean age in patients with CAE and patients with CAD. Although contradictory results were reported [21], hypertension and dyslipidemia were also reported to be implicated in the pathogenesis of CAE [10, 31, 53]. Smoking was found to be more common in patients with CAE than in those with CAD [11]. Cocain use was also found to be an independent predictor of CAE in which smoking was excluded from the model [67].

Among cardiovascular risk factors, diabetes mellitus has taken our attention by independently and inversely associating with CAE. Diabetes mellitus is a well known risk factor positively associated with coronary atherosclerosis and its complications, i.e. cardiovascular events [7, 29, 45]. Effects of diabetes mellitus on progression of atherosclerosis have been shown by the demonstration of increased carotid artery intima-media thickness [64, 95]. Androulakis et al. [5] and Bermudez et al. [11] have reported significant independent and inverse association between CAE and diabetes mellitus. Supporting this inverse association, relative demographic data have already been provided in many studies referring to patients with CAE, in whom a low prevalence of diabetes was noticed [81, 94]. Diabetes mellitus is known to promote negative remodeling in the arterial wall and impairs compensatory arterial enlargement during the course of the atherosclerotic process [47, 91]. It is reasonable to expect such an inverse association between diabetes mellitus and CAE. On the other hand, this makes a contradictory situation being positively associated with atherosclerosis and negatively associated with CAE. This contradiction also suggests that the pathogenesis underlying CAE is not simply a variant of coronary atherosclerosis. In accordance with these observations, increased prevalence of abdominal aortic aneurysm (AAA) has been reported in patients without diabetes mellitus [13, 44]. Blanchard et al. [13] have reported that neither clinical hypercholesterolemia nor serum levels of total cholesterol, low density lipoprotein cholesterol, and high density lipoprotein cholesterol is associated with AAA. However they have reported an inverse association between diabetes mellitus and abdominal aortic aneurysm. The results of this study suggest that the risk factors for AAA may differ from those for atherosclerosis and that atherosclerosis per se is not an adequate explanation as the cause of AAA [13].

A rare variant of CAE can be found as a congenital anomaly, independent of any cardiovascular risk factor. Congenital CAE is frequently associated with other cardiac anomalies such as bicuspid aortic valve, aortic root dilatation, ventricular septal defect or pulmonary stenosis [17, 90]. In addition, CAE have been well documented in patients with cyanotic congenital heart disease. These necropsy specimens of dilated and tortuous coronary arteries showed medial smooth muscle cell loss, increased medial collagen and disrupted internal elastic lamina [17].

CAE has a high coexistence with CAD. Approximately 85% of patients with CAE also have concomitant stenosing CAD [21, 27, 77, 82]. In patients with concomitant CAD, the right coronary artery is most frequently involved in the ectatic process, followed by the left anterior descending artery and the circumflex artery [21, 82]. The right coronary artery is also the most commonly involved coronary artery in patients with isolated CAE ranging from 45% to 75% [10, 14, 21, 50, 82].

However, with regard to CAD, the LAD is most commonly affected, followed by the right coronary and left circumflex artery [32]. Furthermore involvement of the right coronary artery by the stenotic lesion is the least compared to left anterior descending and left circumflex artery in Demopoulos’s report [21]. In patients with CAD coexisting with CAE, 34% of the stenotic lesions were in the vessels affected by the ectatic process, while 65% were in the non-ectatic vessels [21]. p ]It has also been demonstrated that total CAD severity, expressed as the number of coronary stenotic lesions per patient, is found to be equivalent in patients with CAD coexisting with and without CAE. The two patient groups have a similar incidence of one vessel, two vessel, and three vessel disease [21]. Patients with coronary ectasia and coronary obstructive disease are similar in any respect to those with similar coronary obstructive disease, but without ectasia [53]. On the other hand, Giannoglou et al. found that patients with CAE exhibited higher rates of CAD than those without CAE, a difference that was statistically significant [32]. However, over the 9 year study period, burden of CAD increased markedly in the same study in contrast to CAE whose prevalence remained the same [32].

The frequent coexistence of CAE with CAD and histopathological findings resembling those of atherosclerosis have led to the conclusion that the mechanism underlying the pathogenesis of CAE is a variant of atherosclerosis. However, there are some differences in the proven association with CAE compared to CAD. These issues are summarized in Table 2.

Histological examination has been performed in only a minority of studies [19, 53, 81, 94] typically revealing marked destruction and reduction of the medial elastic fibers with disruption of the internal and external elastic laminae, usually out of proportion to the degree of the intimal involvement. However, as the histopathological characteristics are similar to coronary atherosclerosis, there are obvious similarities between the pathogenesis of CAE and CAD. On the other hand, the loss of musculoelastic arterial wall components in CAE was noticed to be unrelated to local atheromatous burden [10, 94]. Nonatherosclerotic forms of CEA have been described with an intact vessel intima, but with extensive media degeneration (smooth muscle cell replacement by hyalinized collagen) [55, 65]. Thus, a functional loss of the musculoelastic components of the coronary artery media is considered to be the predominant aspect in the pathogenesis of CAE [10, 53, 81].

Celik et al. [14] have shown an association between increased carotid intima-media-thickness and isolated CAE, suggesting that atherosclerosis may be involved in the pathogenesis of isolated CAE. However, they did not study patients with concomitant CAE and CAD. Another ultrasonographic study has shown that patients with CAE coexisting with CAD have a significantly lower carotid intima-media thickness compared those with CAD and without CAE indicating that the mechanism underlying CAE might differ from the ones observed in atherosclerosis [99]. Interestingly, decreased endothelium-independent vasodilatation has been shown in patients with CAE and CAD compared to those with CAD alone [3].

Some authors have suggested NO to play a role in the formation of CAE, which is distinct from atherogenesis. England [24, 25] has reported an increased frequency of CAE in individuals who had been exposed to herbicide sprays. A herbicide containing acetylcholinesterase inhibitor directly stimulates NO production by increasing acetylcholine. It has been proposed that chronic nitrite exposure may cause hyaline degeneration of the coronary artery intimamedia resulting in abnormal coronary dilatation. Johanning et al. [43] and Fukuda et al. [30] have experimentally shown that NO production plays a major role in inflammation and aneurysm pathogenesis. The overexpression of iNOS has been shown in varicose veins together with an increased expression of TGF-β ₁ and the presence of macrophages [41]. It is therefore interesting to note that the association of peripheral varicose veins with CAE and varicocele has been documented recently [46, 100].

NO production by iNOS occurs primarily by inflammatory cells resulting in high NO levels and toxic products that degrade elastin and disrupt the extracellular matrix [9, 60]. Inhibition of NO has been shown to limit aneurysmal dilatation of the aorta [43].

In accordance with these findings, Turhan et al. have reported increased levels of C-reactive protein and adhesion molecules indicating an increased inflammatory process in patients with isolated CAE compared with both patients with and patients without CAD [87, 88]. Furthermore, regarding the extracellular matrix, Lamblin et al. [50] found that MMP-3 5A/5A genotype was significantly more frequent in patients with CAE than in the control group of CAD patients. Increased MMP-3 activity is known to be associated with structural alterations in the vessel wall through the degradation of extracellular matrix proteins such as proteoglycans, laminin, fibronectin and collagen types III, IV, V and IX [23, 97]. Additionally, MMP-3 activity is increased in the wall of aortic aneurysms [57, 100]. Finally, the recent observation that high circulating levels of MMP-3 are associated with coronary lesions in Kawasaki disease, which is one of the underlying potential etiologies of CAE [73], also supports an important role for MMP-3 in the pathogenesis of CAE.

Regarding the high coexistence of CAE and CAD, positive remodeling described as enlargement of the area within the external elastic membrane [34] may play a role in the pathogenesis of CAE. Atherosclerotic coronary arteries undergo expansive remodeling to accommodate an increasing plaque burden, especially during early stages of plaque accumulation and following plaque rupture [34, 69]. One can regard CAE as a consequence of extensive positive remodeling. However, this hypothesis remains to be proven.

Williams and Stewart [96] have suggested that, in most patients, coronary ectasia is a diffuse disease of the coronary arteries rather than a localized abnormality of a single arterial segment. Increased ‘thrombolysis in myocardial infarction’ (TIMI) frame count, which is an angiographic definition describing the number of cineangiographic frames from initial contrast opacification of the proximal coronary artery segment to opacification of distal arterial landmarks [33], has been shown in both ectatic and nonectatic coronary arteries [62, 72]. A similar finding has also been reported using magnetic resonance flow velocity [56]. Angiographic signs of turbulent and stagnant flow include delayed antegrade dye filling, a segmental back flow phenomenon and local deposition of dye (stasis) in the dilated coronary segment [48, 53]. Slow flow has also been demonstrated in the non-ectatic vessels of the same patients with CAE. Additionally, Akyurek et al. [4] have demonstrated lower resting blood flow velocity and coronary flow reserve by using the Doppler wire (Flowire) in patients with isolated CAE. Following intracoronary administration of papaverine, a potent hyperemic stimulus, the coronary flow reserve was 1.51 in CAE compared with 2.67 in control arteries (p<0.001), suggesting a combination of epicardial flow disturbances and microvascular dysfunction as the cause of myocardial ischaemia.

A generalized deficit of the wall of the entire arterial system has already been assumed, as associations have been found between CAE and ectasias or aneurysms in other parts of the arterial tree including the abdominal aorta and peripheral arteries [51, 66, 76, 85]. Papadakis et al. [61] reported an association between CAE and aneurysm of the ascending aorta. They have found increased incidence of CAE in patients with aneurysm of ascending aorta (26%) compared to age-matched control group (5%). On the contrary the incidence of CAD is significantly lower in patients with aneurysm of ascending aorta (26%) than in control group (73%). Additionally, Stajduhar et al. [70] reported that all patients with CAE and abdominal aneurysms had obstructive CAD, whereas Papadakis et al. found this in only 38% of patients (8 out of 21) with CAE and ascending aortic aneurysms. A possible explanation for this discrepancy may be that aneurysms of the ascending aorta most often result from the process of cystic medial degeneration, whereas atherosclerotic aneurysms occur infrequently in this segment of the aorta [61].

Coexistence of CAE with venous dilatation has been described, including varicosities of the coronary venous tree [10] and of the leg veins [85]. Recently, increased prevalence of peripheral varicous vein has been reported by Androulakis et al. [6] in patients with CAE compared to those with CAD. Histological examination of the varicosities usually shows degeneration, fragmentation and loss of the medial elastic tissue, fragmentation and reshape of the collagen fiber network, accumulation of extracellular matrix widely separating the hypertrophied medial VSMC and thickening of the intima [58, 68, 84]. Recently, we have shown increased prevalence of varicocele, which is pathologic dilatation of pampiniform plexus in patients with CAE compared to patients with CAD [99]. These findings have also suggested that the mechanism underlying CAE might affect not only the arterial system, but also the venous system in the body. Although some preexisting intimal hyperplasia has been shown in the saphenous veins of the patients who underwent coronary bypass surgery [28], atherosclerosis is known to be a disease of elastic arteries and medium and large size muscular arteries [35]. The coexistence of CAE and venous system dilatation raises the possibility that there might be different pathogenic mechanism or mechanisms between the pathogenesis of CAE and atherosclerosis.

The clinical course of CAE mainly depends on whether it is isolated or coexisted with CAD. No significant differences existed between the patients with CAD coexisting with CAE during a follow-up of 5 years [82]. Patients with coronary ectasia and coronary obstructive disease are similar in every respect to those with similar coronary obstructive disease but without ectasia. Demopoulos et al. [21] have reported comparable 2-year survival in patients with and without CAE (96.7% vs 94.8%). Although there is a measurable incidence of previous myocardial infarction, patients with pure ectasia have a good prognosis [21].

Pure ectasia is not completely innocuous, since there is an appreciable incidence of a previous myocardial infarction and angina [21]. On the other hand Baman et al. [8] used more stringent criteria for identifying patients with CAE, reported a significant adverse outcome among 276 patients they studied, with a 5-year survival of 71%.

Treatment modalities of CAE have been well reviewed by Manginas and Cokkinos [52]. Coronary artery bypass grafting has been used for many years for the treatment of significant CAD co-existing with ectatic coronary segments. The presence of thrombus within the CAE and the question of the necessity to remove large aneurysms have led to the introduction of a variety of operative procedures, including proximal and distal ligation, aneurysmorrhectomy and even aneurysm resection [1, 92]. The post-operative outcome, however, was uniformly good [37]. Autologous venous graft-covered stent was applied in a patient with an aneurysm in the right coronary artery. Although the immediate and long-term angiographic evaluation after the covered stent implantation showed complete sealing of the aneurysm without restenosis [79], long-term benefits have not been confirmed by trials.

Unlike the concomitant CAD and CAE, medical treatment for isolated CAE is not readily described. Since patients with isolated CAE or dilated coronaropathy have considerable risk of myocardial infarction due to microemboli and thrombotic occlusion [65], the application of platelet inhibitors as prophylaxis against ischemic syndromes is indispensable in all forms of CEA [48, 89]. Although some authors previously suggested use of anticoagulant drugs in patients with CAE, there is no available data to date [52]. Concerning the medical treatment of CAE, nitroglycerin should be discussed in details. In contrast to the NTG effect in stenotic CAD, where the drug had been proven to restore myocardial ischemia in coronary sinus studies [78], nitroglycerin can lead to aggravation of myocardial ischemia in patients with CAE and without obstructive lesions [48]. Kruger et al. demonstrated that nitroglycerin (0.8 mg) provoked a further significant deterioration of myocardial ischemia and a frank cardiac lactate production. The results of their study strongly suggest that nitroglycerin has no therapeutic benefit in “dilated coronaropathy,” but it may lower the ischemic threshold [48]. Consequently, the administration of nitrates in “dilated coronaropathy” should be avoided. Myocardial ischemia development in patients with isolated CAE has been shown to be depended on heart rate; therefore, a reasonable therapeutic approach might be the administration of beta-blockers due to their negative chronotropic effect and reduction of myocardial oxygen consumption in the absence of vasodilation [40, 48].