Predominant location of coronary artery atherosclerosis in the left anterior descending artery. The impact of septal perforators and the myocardial bridging effect

Abstract

Introduction

Coronary artery atherosclerosis presents characteristic patterns of plaque distribution despite systemic exposure to risk factors. We hypothesized that local hemodynamic forces induced by the systolic compression of intramuscular septal perforators could be involved in atherosclerotic processes in the left anterior descending artery (LAD) adjacent to the septal perforators’ origin. Therefore we studied the spatial distribution of atherosclerosis in coronary arteries, especially in relation to the septal perforators’ origin.

Material and methods

64-slice computed tomography angiography was performed in 309 consecutive patients (92 male and 217 female) with a mean age of 59.9 years. Spatial plaque distribution in the LAD was analyzed in relation to the septal perforators’ origin. Additionally, plaque distribution throughout the coronary artery tree is discussed.

Results

The coronary calcium score (CCS) was positive in 164 patients (53.1%). In subjects with a CCS > 0, calcifications were more frequent in the LAD (n = 150, 91.5%) compared with the right coronary artery (RCA) (n = 94, 57.3%), circumflex branch (CX) (n = 76, 46.3%) or the left main stem (n = 42, 25.6%) (p < 0.001). Total CCS was higher in the LAD at 46.1 (IQR: 104.2) and RCA at 34.1 (IQR: 90.7) than in the CX at 16.8 (IQR: 61.3) (p = 0.007). In patients with calcifications restricted to a single vessel (n = 54), the most frequently affected artery was the LAD (n = 42, 77.8%). In patients with lesions limited to the LAD, the plaque was located mostly (n = 37, 88.1%) adjacent to the septal perforators’ origin.

Conclusions

We demonstrated that coronary calcifications are most frequently located in the LAD in proximity to the septal branch origin. A possible explanation for this phenomenon could be the dynamic compression of the tunneled septal branches, which may result in disturbed blood flow in the adjacent LAD segment (milking effect).

Introduction

Atherosclerotic processes involve endothelial dysfunction and local infiltration of fatty deposits with a subsequent intimal calcification resembling osteogenesis [1, 2]. Coronary artery calcifications occur almost exclusively in atherosclerotic plaques. Moreover, the amount of calcium correlates with the overall magnitude of atherosclerotic plaque burden [2, 3].

Despite the fact that risk factors are systemic, atherosclerotic plaques develop in a non-random manner. Preferred locations are lateral walls of the bifurcations, areas near to the side branches and branch ostia. Atherosclerotic plaques, particularly at the early stage, are eccentric, and in segments where vessels have no side branches, they emerge from the inner curvature. Plaque distribution in the “risk points” indicates the influence of blood flow conditions on the initiation and development of atherosclerosis [4, 5].

Atherosclerotic plaques are not uniformly distributed throughout the coronary artery tree. Lesions are predominantly located in the left coronary artery [6–9]. Necropsy studies and cardiac computed tomography angiography (CCTA) have demonstrated the highest plaque and calcium deposit burden in the left anterior descending artery (LAD) followed by the right coronary artery (RCA), circumflex branch (CX) and left main stem (LM) [10–15]. The distribution of calcifications tends to cluster within the proximal third of the LAD and CX, except in the RCA, where plaques are more uniformly distributed [16, 17].

The purpose of the present study was to demonstrate the spatial distribution of coronary calcifications and plaque locations using a coronary calcium score (CCS) and coronary CCTA evaluation. We hypothesized that the predominant location of coronary atherosclerosis in the proximal LAD may be linked to septal perforators (SP). Septal branches run within the heart muscle; therefore systolic compressions of SP may induce retrograde blood flow in the adjacent LAD segment, especially in patients with left ventricular hypertrophy, which has been demonstrated in patients with hypertrophic cardiomyopathy [18, 19]. Therefore, similarly to myocardial bridging, septal perforators may be considered a predisposing factor for coronary atherosclerosis at least in patients with left ventricular hypertrophy.

Material and methods

Study population

We prospectively recruited 309 consecutive patients (92 male and 217 female; mean age 59.9 years) who underwent a CCTA and concomitant coronary calcium scoring (64-slice CT scanner; Siemens Somatom Sensation, Germany) because of a definite or suspected coronary artery disease in our department (Silesian Center for Heart Diseases, Poland) between January and December 2012. Patients with history of a previous percutaneous coronary intervention and/or coronary artery bypass grafting, myocardial bridging or coronary vascular anomalies were excluded from the study. The following cardiac risk factors were recorded in the database: hypertension (history of hypertension or antihypertensive therapy), diabetes mellitus (fasting blood glucose level > 7 mmol/l or use of oral antidiabetic therapy or insulin), smoking (defined as current smoker or previous smoker within the last year) and a positive family history (presence of CAD in first-degree relatives < 55 years of age if male and < 65 years of age if female). Laboratory tests were performed for total cholesterol, fasting glucose, full blood count, C-reactive protein (CRP) and estimated glomerular filtration rate. The study has been approved by the local Ethics Committee.

Coronary artery calcium score analysis

Coronary calcium score (CCS) was assessed by a non-contrast CT scan with a 3.0 mm slice using the following acquisition: 24 x 1.2 mm, gantry rotation time of 330 ms, pitch of 0.2, maximum effective tube current of 190 mAs, tube voltage of 120 kV with an automated dose modulation. Calcified foci were defined as regions of opacification with a density of > 130 Hounsfield units and an area of ≥ 3 contiguous pixels (1.0 mm²) based on the scoring algorithm of Agatston et al. [20]. The images for the CCS were analyzed with a commercially available software package (Siemens Calcium Score, Siemens, Germany). The number of calcium deposits and total coronary calcium score were separately evaluated in the LAD, CX branches, LM and RCA. Calcifications located in the intermediate artery were classified as CX lesions.

Cardiac computed tomography angiography imaging protocol

In patients with heart rate > 60 beats/min, metoprolol (2.5 mg to 10 mg) was administered intravenously to reduce the heart rate. For coronary vasodilatation, all patients with systolic blood pressure ≥ 110 mmHg received nitroglycerin sublingually. Contrast timing was tested using an initial bolus-timing scan with an acquisition of 64 mm × 0.6 mm, gantry rotation time of 330 ms, pitch of 0.2, slices of 0.6 mm, tube voltage of 120 kV and maximum effective tube current of 900 mAs. An electrocardiography-gated tube current modulation was used in patients with stable sinus rhythm to reduce radiation exposure. In the whole studied group CCTA data were recorded using an offline workstation (Leonardo, Siemens, Germany). Images were reconstructed in mid-diastole with an individually optimized position of the reconstruction window. Plaques were identified as obstructive if diameter stenosis was 50% or greater. Coronary artery segments were classified according to the 15-segment AHA classification [21].

Statistics

A Shapiro-Wilk goodness-of-fit test was used for normality testing. The results are shown as mean ± SD or median with (interquartile range – IQR). Group comparisons were tested by the unpaired Student's t-test and the one-way ANOVA for continuous variables and the Mann-Whitney or the Kruskal-Wallis test for non-parametric testing. Qualitative variables are expressed as number of patients (n) and percentage (%) and were compared using the χ² test. P values < 0.05 were considered statistically significant. All calculations were performed using the commercially available statistical package Statistica 10 (StatSoft Inc., Tulsa, Oklahoma).

Results

The CCS computed by the Agatston method was positive in 164 patients (53.1%). Patients with a positive CCS were older than subjects with a CCS = 0 (64 years [IQR 13] vs. 57 years [IQR 11]; p < 0.001). Hypertension was more common in patients with a CCS > 0 (77% vs. 41%; p < 0.001). There was a significant difference in fasting blood glucose, diabetes prevalence and CRP concentrations, but there was no difference in total cholesterol and its fractions (Table I).

Tab. I.

Baseline characteristics

	Whole population, n = 309	CS = 0, n = 145	CS > 0, n = 164	P
Sex – female, n/%	217/70	116/80	101/62	0.005*
Age (years)	60 (13)	57 (11)	64 (13)	< 0.001†
BMI (kg/m2)	27.7 (6.6)	27.3 (7.7)	28.1 (6.4)	0.26†
Waist (cm)	91 ± 13	89 ± 12	93 ± 13	0.07‡
Hip (cm)	105 ± 10	105 ± 9	106 ± 11	0.7‡
Heart rate (1/min)	67 ± 9	67 ± 7	67 ± 10	0.9‡
SBP (mmHg)	142 ± 18	139 ± 18	146 ± 18	0.09‡
DBP (mmHg)	84 ± 9	84 ± 10	84 ± 9	0.9‡
Hypertension (%)	60	41	77	< 0.001*
Diabetes type 2 (%)	13	6	19	0.005*
Smoking (%)	19	18	19	0.86*
Family history (%)	52	53	52	0.89*
Hb (mmol/l)	8.6 ± 0.7	8.6 ± 0.7	8.6 ± 0.7	0.8‡
PLT (x 103/mm3)	217 (76)	233 (80)	205 (68)	0.3†
Fasting glucose (mmol/l)	5.4 (1.0)	5.3 (0.8)	5.7 (1.2)	0.008†
Total cholesterol (mmol/l)	5.3 ± 1.1	5.4 ± 1.1	5.1 ± 1.1	0.3‡
LDL (mmol/l)	3.1 ± 1.0	3.1 ± 1.0	3.1 ± 1.1	0.7‡
HDL (mmol/l)	1.5 ± 0.4	1.5 ± 0.3	1.5 ± 0.4	0.6‡
Triglycerides (mmol/l)	1.4 ± 0.7	1.5 ± 0.8	1.3 ± 0.5	0.1‡
CRP (mg/dl)	1.3 (1.7)	0.9 (1.4)	1.6 (1.7)	0.025†
eGFR (ml/min x 1.73 m2)	95 (32)	95 (39)	93 (30)	0.6†

^*– χ² test

^†– Mann-Whitney test

^‡– Student's t-test

BMI – body mass index, SBP – systolic blood pressure, DBP – diastolic blood pressure, PLT – platelet count, CRP – C-reactive protein, eGFR – estimated glomerular filtration rate (Cockcroft-Gault), LDL – low-density lipoprotein, HDL – high-density lipoprotein

Among the subjects with a CCS > 0, the predominant location of calcifications was the LAD (91.5%), followed by the RCA (57.3%), CX (46.3%) and LM stem (25.6%) (p < 0.001). The number of coronary calcified deposits followed the same pattern (397 vs. 226 vs. 157 vs. 49; p < 0.001). Total CCS was higher in the LAD at 46.1 (IQR: 104.2) and RCA at 34.1 (IQR: 90.7) compared to the CX at 16.8 (IQR: 61.3) (p = 0.007). In patients with a single vessel calcification (n = 54), the most frequently affected artery was the LAD (n = 42, 77.8%) (Table II). Obstructive plaques were also more common in the LAD. In patients with calcifications limited to the LAD only, plaques were located in segments 6 and/or 7 adjacent to the septal perforators’ origin in 37 subjects (88.1%) (Fig. 1, panels A and B).

Tab. II.

Comparison of calcium deposition and plaque distribution in coronary artery segments in 164 patients with coronary calcium score > 0

	LAD, n = 150	RCA, n = 94	CX, n = 76	LM, n = 42	p
Number of calcium deposits (n)	397	226	157	49	< 0.001†
Total calcium score (median [IQR])	46.1 (104.2)	34.1 (90.7)	16.8 (61.3)	35.1 (77.2)	0.007*
Localization of calcium calcifications (%)	91.5	57.3	46.3	25.6	< 0.001†
Stenosis > 50% (n/%)	37/24.6	14/14.9	7/9.2	3/7.1	< 0.001†
Patients (n = 54) with single vessel calcifications (n/%)	42/77.8	4/7.4	5/9.3	3/5.6	< 0.001†

^*– Kruskal-Wallis test

^†– χ² test

Fig. 1.

Panel A and B. Multiplanar reconstructed images of the left anterior descending artery (LAD) and the septal branch. Diagram illustrating plaque location in the proximal segment of the LAD artery. Note the anatomy of the septal branch and its intramyocardial course. In proximity to the septal branch ostium, the LAD endothelial cells are exposed to atherogenic low oscillatory shear stress, which leads to plaque formation (left panel). On the right, the corresponding region of the plaque location (myocardial bridging effect)

LAD – left anterior descending artery, OSS – oscillatory shear stress, SB – septal branch

Discussion

Plaque distribution patterns in the coronary artery tree

According to a retrospective analysis of the largest coronary angiographic database, in 34.7% of a total of 13,305 patients plaques were observed only in the left coronary artery compared with 6.5% exclusively in the right coronary artery [9]. Necropsy and CCTA studies revealed that the highest average amounts of atherosclerosis and calcified lesions accumulate in the proximal segments of the LAD, followed by the RCA, CX and LM stem [6, 10, 11]. Our results are in agreement with previous findings from necropsy protocols and angiographic studies. They confirm the predominance of atherosclerosis in the LAD artery over the RCA, CX and LM stem [5–9, 17] (Table II). Enrico et al. demonstrated in a group of 73 patients with a total of 282 plaques detected by CCTA that 46.3% of the atherosclerotic lesions were located in the LAD, 25.9% in the RCA, 18.3% in the CX and 8.1% in the LM [14]. The same pattern of highest CCS in the LAD and lower CCS in the RCA, CX and LM stem was reported by Erciyes et al. [15]. Saur et al. [22] and Ehara et al. [17] demonstrated a non-uniform distribution of plaques not only throughout the coronary vasculature but also along segments of the same vessel, with a predominance of atherosclerosis in the proximal LAD. Our results extend previous observations, and we revealed that coronary plaques are most frequently located not only in the LAD but also in proximity to the septal branch origin.

Wall shear stress and atherosclerosis

Blood vessels are constantly subjected to various types of hemodynamic forces, including wall shear stress (WSS) induced by blood flow. Wall shear stress is the tangential drag force of circulating blood onto the endothelial surface of the artery. The pathophysiology of the wall shear stress and its role in the genesis of atherosclerosis have been extensively studied [23]. It is hypothesized that the accumulation of atheromatous material in the artery “risk points” is the result of prolonged residence time of circulating pro-atherogenic particles in the disturbed flow field. Prolonged residence time may promote mass transport into the vessel wall, especially in cases of increased wall permeability due to an abnormal WSS. Additionally, it is well established that the initiation and development of atherosclerosis are also attributed to complex mechanotransduction pathways regulated by WSS, including the activation of numerous pro-atherogenic genes and up-regulation of pro-inflammatory mediators that are engaged in osteogenic signaling and differentiation of vascular cells [24, 25].

Myocardial bridging and atherosclerosis

Myocardial bridging (MB) is a congenital abnormality and most often involves the LAD. The intramural and distal segments of the bridged vessels remain free from atherosclerosis, contrary to the proximal segments, which are more susceptible to the development of atherosclerotic lesions (Fig. 2) [26, 27]. Retrograde blood flow observed in a segment proximal to MB is the result of intramural vessel compression during systole. It may lead to time-varying bidirectional flow formations generating atherogenic low oscillatory WSS [26–29]. Advanced atherosclerosis in the segment proximal to MB occurs when a myocardial bridge is longer and thicker, which may affect the hemodynamics of the blood flow during systolic vessel compressions [26, 30–32]. Non-tortuous, non-branching arteries are exposed to uniform unidirectional flow and are exposed to a relatively high WSS. Thus, wall shear stress within a normal range is atheroprotective, which may explain the absence of atherosclerosis in the bridged coronary artery segments and septal perforators. However, plaques can occasionally be found in the septal branch ostium before its entry to the myocardium [33–35].

Fig. 2.

Multiplanar reconstructed image of the left anterior descending artery (LAD). Diagram illustrating plaque location in the LAD in patient with myocardial bridge. At the segment adjacent to the myocardial bridge, retrograde coronary blood flow occurs at the systole and the endothelial cells are exposed to atherogenic low oscillatory shear stress (left panel). On the right, the corresponding region of the plaque location (myocardial bridging effect). The intramyocardial segment of the coronary artery is free of plaques

LAD – left anterior descending artery, OSS – oscillatory shear stress, MB – myocardial bridge

The anatomy of the septal perforating arteries

The interventricular septum is the most densely vascularized part of the heart. It receives two-thirds of its blood supply from penetrating septal branches originating from the proximal part of the LAD. The remaining one-third of the inferior portion of the septum is irrigated by relatively short septal branches from the posterior descending artery [36–38]. Infrequently, septal perforators arise from the diagonal branch, RCA or LM [39–42]. The first septal perforator is usually the largest [43]. The length of the septal perforators ranges from 40 to 80 mm and tends to become shorter as they reach the apex [44]. Generally, intramuscular septal branches are resistant to atherosclerosis [33, 34]. Ultrasound studies evaluating plaque distribution in the LAD have shown that in the LAD segments adjacent to the first septal perforator, mean atheroma area and mean intimal thickness were substantially greater on the septal than the antiseptal side [45].

Left ventricular hypertrophy

Left ventricular hypertrophy is an important risk factor for subclinical atherosclerosis and calcifications [46]. In a study of 2,724 young adult subjects positive for coronary artery calcium, left ventricular mass and wall thickness were associated with an increased CCS [47]. On the other hand, absence of left ventricular hypertrophy was a prerequisite for a CCS of zero [48]. According to Erciyes et al., CCS of the LAD has been found to be higher in hypertensive patients compared with normotensive subjects [15]. Abnormal patterns of coronary flow velocity and flow reversal in the LAD have been observed in patients with left ventricular hypertrophy in conditions such as aortic stenosis and systemic hypertension [49]. Using a Doppler catheter to assess flow pattern, Akasaka et al. noticed a flow reversal in the LAD in subjects with asymmetric left ventricular hypertrophy [18]. Transthoracic color flow and pulsed Doppler echocardiography revealed that abnormal flow in the LAD simply reflected the systolic flow reversal in a septal perforator in the hypertrophied muscle [19].

Conclusions

The data from our study demonstrate non-uniform calcium deposits and plaque distribution in the coronary tree. The most common location for plaques is the proximal LAD, followed by the RCA, CX and LM. Bearing in mind that a hemodynamic milieu could be involved in the genesis of atherosclerosis, we conclude that the proximal LAD segment susceptibility to atherosclerosis can be attributed to the milking effect of septal perforators. In our opinion, systolic compression of the septal intramural branch segment can lead to disturbed flow in the adjacent LAD segment at the side of the septal origin [50]. To confirm our findings, further research, including blood flow simulation by computed fluid dynamics analysis and in vitro ultrasound measurements, is warranted to visualize the flow pattern in the LAD segment adjacent to the septal perforator.

Disclosure

Authors report no conflict of interests.