Year : 2020 Month : October Volume : 9 Issue : 42 Page : 3102-3106

Morpho-Histological Study of Myocardial Bridges and Their Association with Atherosclerosis

Jaya Raghu Ram Chodimella1, Pavitra Kondety2

1Department of Pathology, Maharaja s Institute of Medical Sciences, Vizianagaram, Andhra Pradesh, India.
2Department of Pathology, Gitam Institute of Medical Sciences and Research, Visakhapatnam, Andhra Pradesh, India.

CORRESPONDING AUTHOR

Dr. Pavitra Kondety, Assistant Professor, Department of Pathology, Gitam Institute of Medical Sciences and Research, Visakhapatnam, Andhra Pradesh, India
Email : kondetypavitra@gmail.com

ABSTRACT

BACKGROUND

Coronary arteries supply blood to the heart. They run through the epicardial adipose tissue during their course. Occasionally a band of myocardial tissue overlies a segment of the coronary arteries. This band of myocardium overlying the coronary artery is named as Myocardial Bridge (MB). There have been numerous instances of sudden and unexpected cardiac death where the presentation of myocardial bridging was the main clinically pertinent finding post-mortem. We wanted to study the distinct morphological aspects of MBs along with the structural composition of the coronary vessel present beneath, in front of and past the myocardial bridge.

 

METHODS

Microscopy and morphometry were utilized to detail the distinct morphological characteristics of myocardial bridges as well as to take a closer look at the structural composition of the coronary vessel present beneath, in front of and past the myocardial bridge being evaluated. Three segments of the left anterior descending artery (LAD) were utilized to glean testable samples. These samples are as follows: (A) located proximally to the bridge at a distance of 8 mm, (B) alongside the bridge and (C) located distally from the bridge at a distance of 8 mm.

 

RESULTS

Prevalence of MB was found to be 40 %. Male to female ratio was 7:1. 87.5 % of the hearts have single MB, 10 % have double MB, 2.5 % have triple MB. Most common vessel affected is LAD. The MBs ranged in length from 4.4 mm to 45 mm with a length of 12.67 mm being the quantifiable mean. Thickness of MB ranged from 0.4 to 1.9 mm with mean thickness of 1.11 mm. The component of the coronary artery that was bridged often showed a diminished tunica intima compared to similar segments taken from proximal and distal sites. It should be noted that the proximal segment is predisposed to atherosclerotic presentation on account of myocardial bridging.

 

CONCLUSIONS

A myocardial bridge leads to detrimental changes in the vessel which in turn leads to early presentation of atherosclerosis, arrhythmias, myocardial infarctions and in severe cases, sudden death. Myocardial bridging is frequently localized in the LAD. It can have significant effects on the overall health.

 

KEY WORDS

Myocardial Bridging, Coronary Atherosclerosis, Coronary Artery Disease, Myocardial Infarction

BACKGROUND

There have been numerous instances of sudden and unexpected cardiac death where the presentation of myocardial bridging was the main clinically pertinent finding post-mortem. Numerous studies have been done to establish the association between the presence of MB and cardiovascular disease, arrhythmias and sudden cardiac death.

The coronary arteries supply blood to the heart. They run through the epicardial adipose tissue during their course. Occasionally a band of myocardial tissue overlies a segment of the coronary arteries. This band of myocardium overlying the coronary artery is named as Myocardial Bridge (MB).1,2 Myocardial bridges have been  reported to exist exclusively in the mid portion  of left anterior descending artery (LAD) by  few a studies.3,4 Many authors considered MB as a benign anatomical variant rather than a congenital anomaly.4,5,6 But this was challenged by other studies. These studies found that there was significant correlation between presence of myocardial bridging and the presentation of cardiovascular heart disease, arrhythmias and sudden cardiac death.2,3,4,7-12

MB are often localized to the middle segment of the LAD. Branches that split away in a diagonal fashion showcase 18 % involvement while marginal branches showcase a higher degree of involvement at 40 %. Myocardial bridging can present either in single or multiple formats with multiple MBs occurring within the same coronary artery and its corresponding branches or another by its side.7 Ferreira et al.13 divided the myocardial bridging into two types: superficial and deep muscle. The superficial type presents with no coronary flow constriction during systole; while the deep type has the possibility of coronary artery compression, resulting in reduced blood flow and potential induction of myocardial ischemia.

There have been incidences of sudden death due to cardiac causes where myocardial bridging was the only significant finding on autopsy. Few reports show atheromatous changes in the coronary artery proximal to the MB with absence of atheromatous changes in the tunnelled coronary artry.14 Occasionally myocardial bridges are reported to cause angina or myocardial infarction.15 The autopsy of  these patients (6 % of patients with myocardial infarction) did not reveal the presence of atherosclerosis. This left only myocardial bridges as the causative factor.16 Although post-mortem detection of myocardial bridges is seen in 30 - 40 % of cases, only 5 % of the general population is reported to have narrowing of coronary vessels.17 Myocardial akinesia alongside a myocardial infarction could potentially decrease the rate at which MB are detected.16

A majority of MB are silent clinically. But the longest and deepest ones may exert significant pressure in the underlying coronary vessels to reduce myocardial blood supply. The pressure applied by the MB during the cardiac systole and deceleration in the development of coronary atherosclerosis may reduce heart diseases. The haemodynamic stress applied by the presence of t MB contraction may be the important factors in  the occurrence of coronary heart disease (CHD) where MB are existent.7,18,19 Several studies have recorded the correlation of MB with CHD such as myocardial ischemia, arrhythmia, acute coronary syndromes or sudden death.18,19 From a histopathological and clinical point of view, the presence of MB protects the tunnelled segment of coronary artery from the development of atherosclerosis by 3 main mechanisms, including: low tensile stress, high shear stress and decrease tension of the coronary wall.20 Therefore, the MB maybe considered as a protective factor from atherosclerosis through the surrounding myocardium that acts as haemodynamic microenvironment within the bridges.19

A distinct link between myocardial bridging and the development of atherosclerosis proximal to a tunnelled artery have been demonstrated pathologically.4,21-23 However, as catheter coronary angiography cannot detect the presence of myocardial bridging, it does not allow for a causal relationship to be established  between myocardial bridging and coronary atherosclerosis in vivo.24

 

Objectives

The primary goal of this study was to detail the distinct morphological aspects of MBs as well as to take an in depth look at the structural composition of the coronary vessel present beneath, in front of and past the myocardial bridge being evaluated.

METHODS

A descriptive cross-sectional study was carried out with non-random convenient sampling. One hundred preserved hearts were scrutinized. These adult hearts were sourced from Department of Anatomy, Maharaja’s Institute of Medical Sciences (MIMS), Vizianagaram, Andhra Pradesh. The ethics review committee of MIMS cleared the study when contacted for approval. The perivascular adipose tissue was vivisected to reveal the coronary vessels. These vessels were traced from the sinus of Valsalva to their distal points. Intramyocardial segments (coronary tunnelling) were identified, traced, and recorded. Measurements were taken of the length and the thickness (at the intermediate zone) of each bridge. Their distances from the sinus of Valsalva were measured as well using a digital Vernier (0.1 mm precision).

The hearts were harvested within 72 hours from death. They were closely observed for any degradative changes and autolytic components. These hearts were then subjected to morphometry. Light microscopy was employed to confirm the existence of significant bridging.

Three components of the tunnelled artery were taken for sampling. First one was taken 8 mm proximal to the bridge second one was taken containing the bridge and the third on was taken 8 mm distal to the bridge. All samples were removed en block. They were dehydrated using alcohol solutions of increasing grades and embedded in paraffin wax. 7 µm thick sections (on slides) were taken from representative areas. Haematoxylin and Eosin and Verhoff-Van-Gieson stains were done on the sections. Masons trichrome staining was also utilized to demonstrate structural details. Morphometry was done with point counting was done to measure the thickness of the tunica intima, media and luminal area. The stained segments were observed under an eye piece with the morphometer. The grid points that fell on the tunica, intima, media and lumen were counted and recorded.

 

Statistical Analysis

The means and variances were investigated and analyzed utilizing the Statistical Package for Social Sciences (SPSS) for Windows version 11.5.0 Chicago, Illinois 2002. Analysis of variance was used to compare the mean thickness of the intimae of the pre, juxta and post-bridged segments of the LAD. A recorded p value that was < 0.05 was considered statistically significant.

RESULTS

In the present study the prevalence was found to be 40 %. Male to female ratio was 7:1. Age group in the study was from 45 - 79 years with mean age of 69.14 years. 87.5 % have single MB, 10 % have double MB, 2.85 % have triple MB. Most common vessel effected is LAD, 100 %. Most common site of LAD affected is middle 1 / 3rd in 70 %, with proximal 1 / 3rd in 20 %, and distal 1 / 3rd in 10 % of cases.

Length of MB ranged from 4.4 mm to 45 mm with mean of 12.67 mm. Thickness of MB ranged from 0.4 to 1.9 mm with mean thickness of 1.11 mm. Distance of MB from coronary ostia is from 22.5 to 54.5 mm with mean distance of 32.15 mm.

 

DISCUSSION

Findings in this particular study are homogenous with gathered literature from prior necropsy studies. The study done by Loukas M et al25 on 200 hearts showed a total of 81 bridges with MBs being found in 69 hearts (34.5 %). A singular bridge was found in 59 of the gathered while 10 showed multiple bridging (8 with double bridges and 2 with triple bridges). Ferreira AG et al13 found that single and multiple MB were seen in 50 (55.6 %) out of 90 hearts. The LAD was consistently the most commonly affected artery.

In our study prevalence was found to be 40 %. The middle LAD coronary artery was the site where myocardial bridges frequently consolidated in the current study.

Polacek et al26 showcased that the muscular bridges organized by ventricular myocardium were regularly 10 to 20 mm long, up to 5 mm. thick, and frequently localized in the proximal half of the anterior descending branch (60 %). They also reported that the stretch of the artery before the bridge normally corresponds to the site at which occlusions most frequently occur. The intima of the artery under the bridge was usually thin, whereas before the bridge it is strongly hyperplastic. This presentation can be sometimes be seen behind the bridge as well.

We were able to note that bridged segments of the coronary artery tended to exhibit a constricted and limited tunica in contrast to the proximal and distal segments of the same vessel.

Based on the findings detailed previously in the course of the study, assertions have been made that the myocardial bridge can be held accountable for predisposition of the proximal segment of the artery to atherosclerosis.6

In contrast, the tunneled segment is protected by the bridge from atherosclerosis. It presents with a reduced intima when compared to the distal segment. Compression of the segment underlying the MB can potentially be associated with an increased resistance to blood flow. This corresponds to reduced mural tension for any given tension as surmised by the Laplace principle.27,28

       The perivascular spaces contain adipose tissue around the bridged CA. This can be recognized as a cushion of sorts which mitigates the constricting forces on the affected vessels during systole.

CONCLUSIONS

Presence of MB results in modification of the pre-bridge section of the coronary segment that is comparable to early atherosclerotic presentation. Prevalence of myocardial bridging is around 40 % in the general population. They are more common in males. Myocardial bridging is frequently localized in the left anterior descending coronary artery. A significant number of the gathered hearts show only one MB, although multiple MB are known to occur. Presentations of MB can be associated with several concerning cardiovascular events, such as arrhythmias, myocardial infarctions, and in severe cases, sudden death.

Symptomatic patients should be subjected to conservative treatment with the plan progressing to surgical intervention depending on the individual condition of the patient in question. Recognition and general awareness of the morphological characteristics and pathological effects of myocardial bridging on the epicardial coronary branches allow clinicians and cardiologists to formulate better treatment modalities and surgical interventions.

REFERENCES

1

Reyman HC. Dissertatio de vasis cordis propriis. Bibl Anat 1737;2:359-78.

2

Geiringer E. The mural coronary. Am Heart J 1951;41(3):359-68.                                      

CrossRef | Google Scholar | PubMed
3

Angelini P, Trivellato M, Donis J, et al. Myocardial bridges: a review. Prog Cardiovasc Dis 1983;26(1):75-88.                       

CrossRef | Google Scholar | PubMed
4

Ishii T, Asuwa N, Masuda S, et al. The effects of a myocardial bridge on coronary atherosclerosis and ischaemia. J Pathol 1998;185(1):4-9.          

CrossRef | Google Scholar | PubMed
5

Konen E, Goitein O, Di Segni E. Myocardial bridging, a common anatomical variant rather than a congenital anomaly. Semin Ultrasound CT MR 2008;29(3):195-203                                    

CrossRef | Google Scholar | PubMed
6

Ripa C, Melatini MC, Olivieri F, et al. Myocardial bridging: a forgotten cause of acute coronary syndrome- a case report. Int J Angiol 2007;16(3):115-8.      

CrossRef | Google Scholar | PubMed
7

Möhlenkamp S, Hort W, Ge J, et al. Update on myocardial bridging. Circulation 2002;106(20):2616-22.                 

CrossRef | Google Scholar | PubMed
8

Kim SY, Lee YS, Lee JB, et al. Evaluation of myocardial bridge with multidetector computed tomography. Circ J 2010;74(1):137-41.          

CrossRef | Google Scholar | PubMed
9

Kalaria VG, Koradia N, Breall JA. Myocardial bridge: a clinical review. Catheter Cardiovasc Interv 2002;57(4):552-6.                 

CrossRef | Google Scholar | PubMed
10

Gow RM. Myocardial bridging: does it cause sudden death? Card Electrophysiol Rev 2002;6(1-2): 112-4.                      

CrossRef | Google Scholar | PubMed
11

Morales AR, Romanelli R, Tate LG, et al. Intramural left anterior descending coronary artery: significance of the depth of the muscular tunnel. Hum Pathol 1993;24(7):693-701.                              

CrossRef | Google Scholar | PubMed
12

Corrado D, Thiene G, Cocco P, et al. Non-atherosclerotic coronary artery disease and sudden death in the young. Br Heart J 1992;68(6):601-7.             

CrossRef | Google Scholar | PubMed
13

Ferreira AG, Trotter SE, Konig B, et al. Myocardial bridges: morphological and functional aspects. Br Heart J 1991;66(5):364-7.          

CrossRef | Google Scholar | PubMed
14

Saidi HS, Olumbe AO, Kalebi A. Anatomy and pathology of coronary artery in adult black kenyans. East Afr Med J 2002;79(6):323-7.            

CrossRef | Google Scholar | PubMed
15

Burnsides C, Edwards JC, Lansing AI, et al. Artherosclerosis in intramural and extramural portions of coronary arteries in human heart. Circulation 1956;13(2):235-41. 

CrossRef | Google Scholar | PubMed
16

Widmann JD, Cox SL, Roongsritong C. Unappreciable myocardial bridge causing anterior myocardial infarction and postinfarction angina. South Med J 2003;96(4):400-402.

CrossRef | Google Scholar | PubMed
17

Resar JR, Brinker JA. Bridge work. Cathet Cardiovasc Diagn 1997;41(4);421-2.                     

CrossRef | Google Scholar | PubMed
18

Bourassa MG, Butnaru A, Lesperance J, et al. Symptomatic myocardial bridges: overview of ischemic mechanisms and current diagnostic and treatment strategies. J Am Coll Cardiol 2003;41(3):351-9.               

CrossRef | Google Scholar | PubMed
19

Ishikawa Y, Akasaka Y, Suzuki K, et al. Anatomic properties of myocardial bridge predisposing to myocardial infarction. Circulation 2009;120(5):376-3.               

CrossRef | Google Scholar | PubMed
20

Chatzizisis YS, Giannoglou GD. Myocardial bridges spared from atherosclerosis: overview of the underlying mechanisms. Can J Cardiol 2009;25(4):219-22.    

CrossRef | Google Scholar | PubMed
21

Ge J, Erbel R, Gorge G, et al. High wall shear stress proximal to myocardial bridging and atherosclerosis: intracoronary ultrasound and pressure measurements. Br Heart J 1995;73(5):462-5.              

CrossRef | Google Scholar | PubMed
22

Ishikawa Y, Akasaka Y, Ito K, et al. Significance of anatomical properties of myocardial bridge on atherosclerosis evolution in the left anterior descending coronary artery. Atherosclerosis 2006;186(2):380-9.              

CrossRef | Google Scholar | PubMed
23

Ishii T, Hosoda Y, Osaka T, et al. The significance of myocardial bridge upon atherosclerosis in the left anterior descending coronary artery. J Pathol 1986;148(4):279-91.               

CrossRef | Google Scholar | PubMed
24

Nakaura T, Nagayoshi Y, Awai K, et al. Myocardial bridging is associated with coronary atherosclerosis in the segment proximal to the site of bridging. J Cardiol 2014;63(2):134-9.          

CrossRef | Google Scholar | PubMed
25

Loukas M, Curry B, Bowers M, et al. The relationship of myocardial bridges to coronary artery dominance in the adult human heart. J Anat 2006;209(1):43-50.

CrossRef | Google Scholar | PubMed
26

Polacek P. Relation of myocardial bridges and loops on the coronary arteries to coronary occlusions. Am Heart J 1961;61(1):44-52.            

CrossRef | Google Scholar | PubMed
27

Shotar A, Busuttil A. Myocardial bars and bridges and sudden death. Forensic Sci Int 1994;68(3):143-7.              

CrossRef | Google Scholar | PubMed
28

Bandyopandhyay B, Kulkarni S, Mody R, et al. Extrinsic obstruction of the main coronary arteries in a child with hypertrophic cardiomyopathy. Indian Heart J 2002;54(2):202-5. 

Google Scholar | PubMed

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How to cite this article

histological study of myocardial bridges and their association with atherosclerosis. J Evolution Med Dent Sci 2020;9(42): 3102-3106, DOI: 10.14260/jemds/2020/681

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