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Cardiovascular consequences of myocardial bridging: A meta-analysis and meta-regression

Scientific Reportsvolume 7, Article number: 14644 (2017) | Download Citation

Abstract

Myocardial bridging, a congenital abnormality in which a coronary artery tunnels through the myocardial fibres was usually considered a benign condition. Many studies suggested a potential hemodynamic significance of myocardial bridging and some, usually case reports, implied a possible correlation between it and various cardiovascular pathologies like acute myocardial infarction, ventricular rupture, life-threatening arrhythmias, hypertrophic cardiomyopathy, apical ballooning syndrome or sudden death. The main objective of this article is to evaluate whether myocardial bridging may be associated with significant cardiac effects or if it is strictly a benign anatomical variation. To this purpose, we performed a meta-analysis (performed using the inverse variance heterogeneity model) and meta-regression, on scientific articles selected from three main databases (Scopus, Web of Science, Pubmed). The study included 21 articles. MB was associated with major adverse cardiac events - OR = 1.52 (1.01–2.30), and myocardial ischemia OR = 3.00 (1.02–8.82) but not with acute myocardial infarction, cardiovascular death, ischemia identified using imaging techniques, or positive exercise stress testing. Overall, myocardial bridging may have significant cardiovascular consequences (MACE, myocardial ischemia). More studies are needed to reveal/refute a clear association with MI, sudden death or other cardiovascular pathologies.

Introduction

Myocardial bridging (MB) is a congenital abnormality characterised by the presence of an intramural course of a coronary artery1,2,3,4, causing a distinguishing systolic and diastolic flow disturbance5. It was usually considered a benign condition, mostly because it constricts the bridged coronary during systole, while most of the blood flow occurs during diastole. Many studies suggested a potential hemodynamic significance of MB6,7,8,9,10,11,12,13,14,15,16 and some, usually case reports, implied a possible correlation between MB and various cardiovascular pathologies including acute myocardial infarction17,18, ventricular rupture19, life-threatening arrhythmias20,21, HCM22,23,24,25, apical ballooning syndrome26,27 or sudden death28. In forensic autopsies, it is sometimes considered a cause of sudden death, and is often reported as such in scientific articles, especially in association with other congenital cardiac or coronary anomalies6,22,29,30,31,32,33,34,35,36. Hong et al. published a meta-analysis in which they showed a statistically significant correlation between MB and myocardial infarction (MI), and failed to prove a positive relationship between MB and major adverse cardiac events(MACE)37. However, they did not check for potential confounding factors, nor it did perform a detailed analysis of the heterogeneity. Also, since that meta-analysis was published, many more articles about MB were issued in the scientific literature.

The main objective of this article is to evaluate whether MB may cause significant cardiac effects or if it is strictly a benign anatomical variation.

Materials and Methods

The study was performed by following the PRISMA guidelines for reporting systematic reviews and meta-analyses38.


Selection criteria

Inclusion criteria: (1) studies in which were compared a group of subjects with myocardial bridging and a group without this condition, regarding one of the following endpoints: MACE, cardiovascular (including sudden) death (CVD), MI, myocardial ischemia,; (2) raw data regarding the number of cases from each subgroup (myocardial bridging +/− outcome, no myocardial bridging +/− outcome). We used as exclusion criteria: (1) the absence of relevant information to reconstruct the data needed for analysis; (2) studies not published in English; (3) studies with less than 30 subjects in the cases group; (4) case series/case reports; (5) articles not found in online databases. MACE was defined as composite events of cardiovascular death, myocardial infarction, target vessel revascularization, and stent thrombosis39. MI was defined serum cardiac biomarker increases with symptoms of ischemia, ECG changes suggestive for new ischemia/myocardial infarction, or the identification of myocardial infarction at the autopsy. If, in a prospective study were given data about previous MIs at baseline (such as pathological Q waves), they were also included in the analysis. Cardiovascular death was defined as any death with no known non-cardiac underlying causes; we also included in this endpoint sudden deaths and cardiac arrests. Myocardial ischemia was assessed through specific signs as assessed on ECG (ST changes), a positive stress exercise test, or positive Thallium scintigraphy for ischemia.


Search method

We analyzed the results obtained from three databases: Web of Science, Scopus, and Pubmed, by using the following keywords: “myocardial bridging”, “mural coronary”. We preferred not to use additional, restrictive criteria (e.g. article type) as other varieties (letters, case presentations, reviews) could add relevant data to the meta-analysis (discussions, finding other pertinent studies). The reference list of each appropriate item was inspected for other, potentially relevant studies, to be included in the meta-analysis. The references and abstracts (if available) were imported in Thompson Endnote software, and useful articles were downloaded for further inspection.


Data collection and analysis

For each study, two reviewers extracted the data separately and included it in Excel Datasheets. We summarised the following information: study, name, the total number of cases in each group, country, general inclusion and exclusion criteria, endpoints, covariates: depth, length, systemic hypertension, angina pectoris, diabetes mellitus, hyperlipidemia, smoking, age, gender.


Risk of bias

The risk of bias was assessed separately, for each case, by two reviewers. We analysed selection bias (inclusion and exclusion criteria, whether the study was dedicated to MB or had a more general nature), multiple publication biases, measurement bias (the method used), statistical reporting bias. Based on these elements, we separated the studies in three subgroups: high risk of bias, moderate risk of bias and low risk of bias.


Quality assessment

Quality assessment was performed with the Quality in Prognostic Studies Tool from which we removed study attrition (which was considered not relevant for a prevalence study). For each remaining subscales (study participation, prognostic factor measurement, outcome measurement, study confounding, statistical analysis and reporting), we graded each study as high quality (2 points), moderate quality (1 point) or low quality (0 points) and we summed up the results (Table 1).

Table 1 Studies included in the analysis.

Statistical analysis

We determined the effect size using inverse variance heterogeneity model computed in Microsoft Excel 2016 with the MetaXL add-on version 5.3 and used Comprehensive Meta-Analysis v3 for performing meta-regression. For each group and subgroup, we performed a forest plot. For the analysis of publication bias, we used the funnel plot and the Luis Furuya-Kanamori (LFK) index. We used a continuity correction of 0.5, and 95% confidence intervals. Forest plots were done using Microsoft Excel 2016 with the MetaXL add-on 5.3, with the effect size transformed logarithmically for better viewing.

Results

Search synthesis

During the initial database research, we obtained 7358 articles from which, after deleting 4839 duplicates, we were left with 2519, that were included in the initial analysis. From them, we screened the abstracts and removed all articles not containing clinical studies that included a group of subjects with myocardial bridging and a group without this condition, regarding the above-mentioned endpoints. 32 articles selected and further downloaded. By analysing their references, we found another 5 potentially relevant items, which were also downloaded. The next step included the analysis of the full text manuscripts, after which we selected 21 to be included in the meta-analysis, which fully respected the inclusion criteria. Details about search synthesis are presented in Fig. 1 40. We detailed the papers comprised in the analysis in Table 1.

Figure 1
Figure 1

PRISMA flow diagram (The PRISMA Statement and the PRISMA Explanation and Elaboration document are distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited)40.

Major Adverse Coronary Events (MACE)

Sixteen studies contained data about a potential correlation between MB and MACE. The presence of MB led to a significantly increased risk for MACE - OR = 1.53(1.01–2.30), p < 0.001 (Fig. 2). The publication bias was minimal, with an LFK index of 0.33. The heterogeneity of the included studies was moderate (I2 = 61%). Meta-regression analysis found a positive correlation between MACE risk and the increase in age differential between subjects with MB versus subjects without MB; gender, systemic hypertension, hyperlipidemia, previous angina, diabetes mellitus or smoking failed to generate statistically significant differences (see Table 2). By performing a subgroup analysis, based on whether the studies considered significant coronary artery disease as an either inclusion or exclusion criteria, we found that, if the presence of CAD was used as an inclusion criteria, OR was 1.60(0.79–3.23), and if it was used as an exclusion criteria – 1.54 (0.79–3). By performing a subgroup analysis, based on whether the studies were done on patients with HCM, we found that studies that were not done specifically for HCM had an OR = 1.71 (1.10–2.67), while studies that were done on subjects with HCM had an OR = 0.60(0.38–1.28). See Fig. 3.

Figure 2
Figure 2

MB and MACE. Forest plot.

Table 2 Z values for meta-regression analysis.
Figure 3
Figure 3

Subgroup analysis. MACE with/without HCM. Forest plot.

Myocardial infarction

Thirteen studies contained data about a potential correlation between MB and MI. The presence of MB did not lead to a significantly increased risk for MI - OR = 1.18(0.84–1.66), p = 0.30 (Fig. 4). The publication bias was minimal (LFK index = 0.30). The heterogeneity of the included studies was low (I2 = 27%). Meta-regression analysis did not show any significant effects on the result determined by age, gender, systemic hypertension, hyperlipidemia, previous angina, diabetes mellitus or smoking (see Table 2). By performing a subgroup analysis, based on whether the studies considered significant coronary artery disease as an either inclusion or exclusion criteria, we found that, if the presence of CAD was used as an inclusion criteria, OR for MI was 0.74(0.43–1.25), and if it was used as an exclusion criteria – 1.45 (0.87–2.39).

Figure 4
Figure 4

MB and MI. Forest plot.

Cardiovascular death

Eight studies included data about a potential correlation between MB and cardiovascular death. The presence of MB did not lead to a significant increase in the risk of cardiovascular death - OR = 2.19(0.65–7.43) (Fig. 5). The publication bias is minor (LFK index = −1.28). The heterogeneity of the included studies was moderate to high (I2 = 70%). Meta-regression analysis found a positive correlation between CVD risk and the increase in age differential between subjects with MB versus subjects without MB; (see Table 2).

Figure 5
Figure 5

MB and CVD. Forrest plot.

Myocardial ischemia

Nine studies included data about a potential correlation between MB and myocardial ischemia. Two studies contained more than one method of assessing myocardial ischemia (Xiang and Schwartz), and we took into account in both cases the outcome with the most number of positive subjects. The presence of MB was significantly associated with myocardial ischemia - OR = 3.00(1.02–8.82) (Fig. 6). The publication bias was minor (LFK index = −1.68). The heterogeneity of the included studies was high (I2 = 89%). Meta-regression analysis did not show any significant effects on the result determined by age, gender, systemic hypertension, hyperlipidemia, previous angina, diabetes mellitus or smoking (see Table 2).

Figure 6
Figure 6

Myocardial ischemia and MB. Forest plot.

Discussions

Our study revealed that, overall, MB increases the risk for MACE and myocardial ischemia, and subsequently a possible connection between it and various cardiovascular pathologies cannot be excluded. The physiological characteristics and morphological consequences of MB are still not yet fully elucidated, even if there are many studies analysing specifically with these issues.

Even if MB mainly causes a systolic narrowing of the affected coronary, both cardiac phases are affected. Intracoronary Doppler showed a finger-tip-like anterograde flow of the blood in most MB patients, characterised by a sharp increase in coronary flow velocity during early diastole, followed by a steep decrease in speed, leading to a plateau in mid-late diastole41. During systole, the anterograde flow is decreased, absent, or even reversed, due to the systolic squeezing of the bridged coronary segment41. Ge et al. showed the pressure within the segment proximal of the MB to be much higher than the pressure in the aorta and that the maximum pressure in the proximal segment is reached in mid-systole compared to normal segments is reached in the end-systole42. During end-diastole, the myocardium dilates, triggering a negative pressure in the mural segment, and an increased pressure gradient between the bridged segment and the neighbouring areas(the so-called sucking phenomenon)42. The systolic compression is usually eccentric, and only rarely concentric, leading to a half-moon like echo-lucent area neighbouring the bridge when viewed through IVUS41. Previous studies showed that systolic compression by the bridge could be either elliptical, associated with a 50% reduction of the luminal area, or concentric, associated with a 75% reduction43. Other authors showed that, if superficial and short MBs do not lead to significant hemodynamic effects, this is not the case with deep and long variants, which may cause severe ischemia or cardiovascular events44. Hostiuc et al. showed that hemodynamically significant MB is associated with increased fibrosis and interstitial edema in subjects who died suddenly and had no other apparent cause of death, suggesting that the most likely cause of death was electrical instability6, which is known to be associated with increased myocardial fibrosis45,46.

Endothelial dysfunction is an early phase of atherogenesis47. Numerous studies reported an alteration of the normal endothelial physiology associated with MB, including an abnormal response to acetylcholine (ACh) or decreased responses to NO and endothelin-1. Acetylcholine acts as an endothelium-dependent vasodilator, by stimulating the release of EDRF, if the endothelium is intact48. If however there are endothelial lesions (including atherosclerotic disease), ACh will cause smooth muscle constriction49. ACh-generated vasoconstriction was often showed to be associated with MB. For example, Kuhn revealed that vasoconstriction after the administration of ACh is higher in the coronary segment containing a MB compared to non-bridged segments50. Kim et al. showed that, after infusion with ACh, subjects with MB have a statistically significant increase in focal vasoconstriction in the mural segment, compared to similar, non-bridged coronary segments from the control group51. Teragawa showed that subjects with MB have an almost two-fold increase in the rate of coronary spasm compared with the control group52. Zoghi et al. showed, by measuring flow-mediated dilatation in the brachial artery, that the presence of MB also leads to remote vasoconstrictive effects53. Herrmann demonstrated that MB causes an increased shear stress and significant vasoconstriction after the administration of ACh without changes in the coronary blood flow16. Masuda et al. found that bridged LAD segments have a weaker immunoreaction to endothelial nitric oxide synthase (eNOS) and endothelin-1(ET-1) compared to the proximal and distal segments54. NO leads to vasodilatation, and it might be involved in the “sucking phenomenon” described by Ge42.

The segment proximal to the MB is put at a high wall shear stress due to the significant pressure gradients between the bridged area and the proximal coronary segment42, potentially causing a chronic coronary pressure overload (CCPO)16. CCPO is associated with significant endothelial changes, including intimal thickening, medial thickening, disruption of the internal elastic lamina or endothelium55, favouring the appearance of atherosclerosis.

Nakaura et al. showed that mid-LAD MB is strongly positively associated with atherosclerosis (OR = 4.99). They did not mention, however, the location of the atherosclerotic plaques (distally, intramural or proximal from the bridged area). Hong et al. found that the prevalence of lesions located distally from the MB was significantly lower compared to those located proximally (5.9% versus 62.4%). In their article age, male gender, a history of diabetes mellitus, systemic hypertension, bifurcated vascular lesions, smoking index, or hyperlipidemia increased the severity of the coronary stenosis56. Wang et al. showed that MB (both superficial and deep) is associated with non-significant stenosis proximal to the bridged area and that MB in middle LAD is positively associated with stenosis in non-bridged arteries. The most likely explanation for the latter is the fact that deep MB has hemodynamic significance, causing a disturbed flow in the other coronaries, and therefore increases the frequency of atherosclerotic deposits57. By compressing the tunnelled artery during systole, MB increases lymph drainage of the vessel wall, protecting against lipid accumulation within the bridged coronary wall57,58. Verhagen et al. suggested that the reason for the lack of atherosclerosis under the bridged coronary is represented by a lack of exposure to perivascular adipose tissue at that site, which is known to secrete pro-inflammatory adipokines and cytokines59. Saidi et al., on the other hand, showed that between the bridged muscle and the coronary is sometimes interposed an adipose layer, which they hypothesised to act as a cushion, limiting the compressing forces acting upon the bridged coronary segment60. However, this layer would, in fact, secrete pro-inflammatory adipokines and cytokines. Locally increased eNOS is known to be associated with increased atherosclerosis in coronary arteries54,61; therefore, increased eNOS levels proximally from the bridged segment might be involved in the development of proximal segment atherosclerosis. Another explanation for the distribution of atherosclerosis/around the bridged area might be represented by the shape of the endothelial cells, which are spindle-shaped under the bridge, suggesting they are under a high shear stress, while in other regions they have a polygonal distribution, suggesting they are subjected to a decreased shear stress58,62. Increased shear stress seems to decrease monocyte adhesion and lipid transfer across the vascular wall, therefore decreasing the risk for atherosclerosis59,62.

Bilen et al. showed that subjects with MB have a significantly increased mean platelet volume (MPV). Larger platelets are associated with increased reactivity and production of more prothrombotic factors63. Potential causes for this result might be a reduced production of prostacyclin and nitric oxide, impairment of endothelial-dependent vasorelaxation, increased proximal atherosclerosis, increased shear stress64. This increased thrombogenic status might favour the development of coronary thrombosis or might increase its severity.

Numerous studies suggested or proved that MB is associated with various types of physiological changes. Ge et al. showed that MB leads to a decreased coronary flow velocity reserve, which remains higher proximally compared to distally from the bridged segment; also, coronary flow velocity reserve seems to be more affected in subjects with severe coronary stenosis41. Schwartz et al. quantified the decrease in the coronary flow reserve caused by MB – they found a mean ratio of 2.0 distally from the bridged coronary artery (normally the value is above 3)7. Fractional flow reserve is often used to quantify the physiological significance of CAD. It is not influenced by heart rate or blood pressure changes65, nor by dobutamine challenge in subjects with fixed CAD66. Diefenbach et al. showed that inotropic challenge leads to a significant increase in the degree and length of MB segments, as evaluated on CAG, compared to those obtained at rest in symptomatic subjects, suggesting the presence of a specific coronary physiological response to inotropic stimuli67. Yoshino et al. proved that fractional flow reserve (FFR) to dobutamine challenge is significantly decreased in the presence of microvascular endothelial dysfunction65. Heart rate recovery is a prognostic tool for the cardiac autonomic functions68; increased heart rate recovery (HHR) was associated with decreased parasympathetic activity69, a higher susceptibility for atherosclerosis, and increased five-year mortality70. Okutucu showed the presence of MB on LAD to be a significant predictor for increased HHR at 1 minute (b = −8.524; 95% CI −14.934 to −2.113; p = 0.009), and argued that the finding was caused by silent or symptomatic myocardial ischemia. QT dispersion (QTd), defined as the minimum QT interval subtracted from the maximum, is an effective marker for electrical myocardial heterogeneity; higher values are associated with an increased risk of cardiac arrhythmias71. Aksan et al. demonstrated that subjects with MB have a significantly increased QTd during peak exercise compared with its baseline value (42.6 ms versus 36.4 ms), while in non-MB subjects the increase during peak exercise was not statistically significant (29.1 ms, versus a baseline value of 27.1 ms)72.

All these results come to confirm that, at least in some cases, MB may have various cardiovascular consequences. Our study showed that MB presence is associated with an increased risk of MACE and myocardial ischemia, but failed to show a possible positive correlation with CMH, MI, or cardiovascular death. However, even if these associations did not reach statistical significance, the variability of the confidence intervals is very high, which can be caused either by the heterogeneity of the studies included in the meta-analysis, or by a highly variable response to this condition (possibly dependent upon length, depth or the MB, its location, associated pathologies, and so on). The scientific literature analysis showed or suggested a series of associations between MB and cardiovascular pathologies, including, coronary spasm, MI, HCM, Takotsubo cardiomyopathy, arrhythmias, or sudden death.

The association between coronary artery spasm and MB was first implied by Grover et al., who reported the case of a patient who developed CAS during cardiac pacing, an association that was later on confirmed by other studies (see e.g. ref.73). Recent articles showed that patients with MB have a higher incidence of coronary vasospasm induced by ACh. Sung et al. showed that patients with MB who responded to lower doses of ACh had a more severe decrease of the luminal diameter, and had a worse cumulative clinical outcome after 12 months compared to subjects who needed larger ACh doses for a positive response. The mechanical stress caused by the systolic narrowing is known to lead to endothelial dysfunction. Subjects with variant angina are known to be hyperactive to vasoconstrictor stimuli74. Atherosclerotic epicardial vessels may present a paradoxical vasoconstriction caused by a direct stimulation of the mural smooth muscle, as a result of widespread endothelial dysfunction49. Corroborated, these results might suggest that the coronary vasospasm associated with MB might lead to the development of myocardial ischemia, especially in the presence of other coronary pathologies71,75.

De Agustin et al. showed that subjects with chest pain and without severe coronary artery stenosis are significantly more likely to have MB compared to those with severe CAD; moreover, in the MB subgroup hyperlipidemia was considerably less often found compared to the group of subjects without MB76. Tang et al. showed that, in subjects with MB, cardiac ischemia is strongly associated with the degree of mean systolic narrowing, and suggested that the degree of systolic occlusion by the MB is responsible for the appearance of myocardial ischemia77. Angelini et al. analysed the presence of MB in subjects with and without coronary artery disease, finding that its incidence is significantly lower in the group without CAD43. They also showed that there is a higher incidence of MB in men and in subjects with a systolic overload of the left ventricle.

There are two core mechanisms through which MB is thought to cause myocardial ischemia and MI - the development of atherosclerosis proximally from the bridged segment78, and a direct compression of the coronary artery by the MB79. In subjects with MI, the thickness of the MB is, on average, greater compared to the ones found in subjects without MI80. Takamura et al. studied two groups of subjects: one with MI in the area supplied by the LAD and without MB on LAD and one with MI in any myocardial area associated with MB on LAD, and found that, if the acute occlusion occurred in the LAD segment proximal from the MB, the length and thickness of the MB were significantly greater, and the distance from the ostium of the LCA to the MB was significantly shorter compared to those without an acute occlusion on the LAD proximally to the MB81.

The blood flow during systole is small compared to the one from diastole in normal conditions; this is not the case in tachycardia, when the end-diastolic volume decrease is greater compared to end-systolic volume82, potentially leading to myocardial ischemia. In this instance, the blood supply of the myocardium becomes more dependent upon the systolic blood flow, which is impaired by the bridge. There were some cases published in the scientific literature in which tachycardia was associated with MB. Feld, for example, described a patient who, during stage 5 of the Bruce protocol, developed significant flat ST depressions, followed by a complex tachycardia with a rate of 280 bpm, associated with a MB on LAD20. Den Dulk et al. presented the case of a patient with exercise-induced paroxysmal atrioventricular block21. Kracoff et al. published the case of a 35 years-old patient, with recent onset angina, who developed episodes of syncope caused by ventricular tachycardia, which was suggested to have been caused by a myocardial bridge83. Left ventricular systolic dyssynchrony or intraventricular dyssynchrony, is characterized by a delay or heterogeneity in the timing of contraction in different myocardial segments of the left ventricle. It is usually found in heart failure, and it is proven to cause a more severe myocardial disease and a poorer cardiovascular prognosis. Cai Wei et al. showed that mid-LAD MB is associated with an increased prevalence of left ventricular systolic dyssynchrony (LVSD) compared to subjects without MB; moreover, the stenosis caused by the MB and the length of the mural segment have a synergistic effect on the development of LVSD84.

Lee et al. found that MB is an independent predictor for MACE in patients with eluting drug stents (adjusted OR = 2.897)75. Similarly, Tsujita et al. found that subjects undergoing eluting drug stents for coronary artery disease in the proximal part of the LAD, and who had detectable MB distal of the stented lesion, had a significantly decreased minim stent area at the end of the procedure, and a higher target lesion vascularization rate85.

Hypertrophic cardiomyopathy, an inherited cardiovascular disease that can lead to SCD, heart failure, or stroke, is believed to be associated very often with MB86,87. Earlier studies implied a possible correlation between HCM with MB and SCD in some subgroups of patients. For example, Yetman et al. showed that MB in children with HCM is a risk factor for SCD28. However, more recent ones failed to prove a positive correlation. Tian et al. showed that, in autopsy cases, MB is not associated with SCD in HCM44. Basso et al. found that patients with HCM who died suddenly do not have a higher prevalence of MB compared to subjects with HCM who died from heart failure or other modes of death; from the analysis of their results, however, the age of the subjects with SCD was much lower (22 years, compared with 54 and 67 in the other two groups), the length and depth were higher, and the proportion of associated CAD much lower87. Sorajja et al. showed that there is no statistically significant difference regarding five-year survival between subjects with and without MB88. Our study showed that, when we excluded studies in which HCM was used as an inclusion criteria, MB increased the risk for MACE. More studies are however needed in the area before either establishing or excluding a causal link between these two pathologies.

Some studies suggested that MB is more frequent in patients with apical ballooning syndrome26,89, but not in midventricular or basal ballooning89; in these cases, MB might influence the development of Takotsubo cardiomyopathy through the generation of microvascular dysfunction and altered sympathetic activity, possibly associated with recurrent LAD segments89; more studies are needed in this area to reach definite conclusions.

Limits

A very high variability of the results, associated with a limited number of studies for testing associations between MB and various cardiovascular consequences. Many studies did not include comprehensive inclusion and exclusion criteria, or complete descriptive data, limiting the number of subgroup analyses we were able to perform. Due to the presence of highly different methodologies, and inclusion and exclusion criteria, there can be a significant selection bias, which was attempted to be minimized through subgroup analyses and meta-regression.

Conclusions

Overall, myocardial bridging may have significant cardiovascular consequences (MACE, myocardial ischemia). More studies are needed to reveal/refute a clear association with MI, sudden death or other cardiovascular pathologies.

Additional information

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References

  1. 1.

    Reymann, H. C. Dissertationem inauguralem De Vasis Cordis Propriis. Ed. Vandenhoeck, Goettingen, NL (1737).

  2. 2.

    Crainicianu, A. Anatomische Studien über die Coronararterien und experimentelle Untersuchungen über ihre Durchgängigkeit. Virchows Archiv für pathologische Anatomie und Physiologie und für klinische Medizin 238, 1–75 (1922).

  3. 3.

    Geiringer, E. The mural coronary. American heart journal 41, 359–368 (1951).

  4. 4.

    Edwards, J., Burnside, C., Swarm, R. & Lansing, A. Arteriolosclerosis in the intramural and extramural portions of coronary arteries in the human heart. Circulation 13, 235–241 (1956).

  5. 5.

    Alegria, J. R., Herrmann, J., Holmes, D. R., Lerman, A. & Rihal, C. S. Myocardial bridging. European Heart Journal 26, 1159–1168 (2005).

  6. 6.

    Hostiuc, S. et al. Morphological Changes Associated with Hemodynamically Significant Myocardial Bridges in Sudden Cardiac Death. Thoracic and cardiovascular surgeon 59, 393–398, https://doi.org/10.1055/s0030-1270703 (2011).

  7. 7.

    Schwarz, E. R. et al. Functional, angiographic and intracoronary Doppler flow characteristics in symptomatic patients with myocardial bridging: effect of short-term intravenous beta-blocker medication. Journal of the American College of Cardiology 27, 1637–1645 (1996).

  8. 8.

    Pichard, A. D., Casanegra, P., Marchant, E. & Rodriguez, J. Abnormal regional myocardial flow in myocardial bridging of the left anterior descending coronary artery. The American journal of cardiology 47, 978–982 (1981).

  9. 9.

    Aydar, Y. et al. Gender differences in the types and frequency of coronary artery anomalies. The Tohoku journal of experimental medicine 225, 239–247 (2011).

  10. 10.

    Barutcu, I. et al. Effect of treadmill exercise testing on P wave duration and dispersion in patients with isolated myocardial bridging. The international journal of cardiovascular imaging 25, 465–470 (2009).

  11. 11.

    Baryalei, M. M. et al. Off-pump supraarterial decompression myotomy for myocardial bridging. The heart surgery forum. Carden Jennings Publishing Co. 8(1), E49-E54. (2005 Feb 1).

  12. 12.

    Carvalho, V. B. et al. Hemodynamic determinants of coronary constriction in human myocardial bridges. American heart journal 108, 73–80 (1984).

  13. 13.

    Ferreira, A. et al. Myocardial bridges: morphological and functional aspects. British heart journal 66, 364–367 (1991).

  14. 14.

    Gawor, R. et al. Myocardial perfusion GSPECT imaging in patients with myocardial bridging. Journal of Nuclear Cardiology 18, 1059–1065 (2011).

  15. 15.

    Hazirolan, T. et al. Myocardial bridging on MDCT. Am J Roentgenol 188, 1074–1080 (2007).

  16. 16.

    Herrmann, J., Higano, S. T., Lenon, R. J., Rihal, C. S. & Lerman, A. Myocardial bridging is associated with alteration in coronary vasoreactivity. European heart journal 25, 2134–2142 (2004).

  17. 17.

    Tauth, J. & Sullebarger, J. T. Myocardial infarction associated with myocardial bridging: case history and review of the literature. Catheterization and cardiovascular diagnosis 40, 364–367 (1997).

  18. 18.

    Arjomand, H., AlSalman, J., Azain, J. & Amin, D. Myocardial bridging of left circumflex coronary artery associated with acute myocardial infarction. The Journal of invasive cardiology 12, 431 (2000).

  19. 19.

    Tio, R. A. & Ebels, T. Ventricular septal rupture caused by myocardial bridging. The Annals of thoracic surgery 72, 1369–1370 (2001).

  20. 20.

    Feld, H. et al. Exercise-induced ventricular tachycardia in association with a myocardial bridge. CHEST Journal 99, 1295–1296 (1991).

  21. 21.

    Den Dulk, K., Brugada, P., Braat, S., Heddle, B. & Wellens, H. J. Myocardial bridging as a cause of paroxysmal atrioventricular block. Journal of the American College of Cardiology 1, 965–969 (1983).

  22. 22.

    Dermengiu, D. et al. Sudden death associated with borderline Hypertrophic Cardiomyopathy and multiple coronary anomalies. Case report and literature review. Rom J Leg Med 1, 3–12 (2010).

  23. 23.

    Ceausu, M. et al. Sudden cardiac death due to triple myocardial bridging associated with atypical coronary topography. Rom J Morphol Embryol 54, 833–837 (2013).

  24. 24.

    Shotar, A. & Busuttil, A. Myocardial bars and bridges and sudden death. Forensic Sci Int 68, 143–147 (1994).

  25. 25.

    Dettmeyer, R. B. In Forensic Histopathology 241–282 (Springer, 2011).

  26. 26.

    Migliore, F. et al. LAD coronary artery myocardial bridging and apical ballooning syndrome. JACC: Cardiovascular Imaging 6, 32–41 (2013).

  27. 27.

    Andò, G., Trio, O. & de Gregorio, C. Coronary spasm and myocardial bridging: an elusive pathophysiological mechanism leading to apical ballooning syndrome? European Heart Journal: Acute Cardiovascular Care 5, 501–504 (2016).

  28. 28.

    Yetman, A. T., McCrindle, B. W., MacDonald, C., Freedom, R. M. & Gow, R. Myocardial bridging in children with hypertrophic cardiomyopathy—a risk factor for sudden death. New England Journal of Medicine 339, 1201–1209 (1998).

  29. 29.

    Schyma, C., Doberentz, E., Morshuis, M. & Madea, B. Fatal case of a patient with cardiac assist system. Rechtsmedizin 23, 410–414, https://doi.org/10.1007/s00194-013-0889-2 (2013).

  30. 30.

    Quaranta, F. et al. Myocarditis in athlete and myocardial bridge: An innocent bystander? World Journal of Cardiology 7, 293–298, https://doi.org/10.4330/wjc.v7.i5.293 (2015).

  31. 31.

    Eren, B. & Turkmen, N. Myocardial bridging as a possible cause of unexplained sudden death: A case report. Zdravniski Vestnik-Slovenian Medical Journal 82, 357–360 (2013).

  32. 32.

    Cutler, D. & Wallace, J. M. Myocardial bridging in a young patient with sudden death. Clinical Cardiology 20, 581–583 (1997).

  33. 33.

    Curca, G. C., Drugescu, N., Ardeleanu, C. & Ceausu, M. Investigative protocole of sudden cardiac death in young adults. Romanian Journal of Legal Medicine 16, 57–66 (2008).

  34. 34.

    Sunnassee, A., Shaohua, Z., Liang, R. & Liang, L. Unexpected death of a young woman: is myocardial bridging significant?-A case report and review of literature. Forensic Sci Med Pat 7, 42–46, https://doi.org/10.1007/s12024-010-9175-8 (2011).

  35. 35.

    Monroe, D. J., Meehan, J. T. & Schandl, C. A. Sudden Cardiac Death in a Young Man with Migraine-associated Arrhythmia. Journal of Forensic Sciences 60, 1633–1636, https://doi.org/10.1111/1556-4029.12836 (2015).

  36. 36.

    Shotar, A. & Busuttil, A. Myocardial bars and bridges and sudden-death. Forensic Sci Int 68, 143–147, https://doi.org/10.1016/0379-0738(94)90353-0 (1994).

  37. 37.

    Hong, L., Liu, J., Luo, S. & Li, J. Chinese Medical Journal 127(5), 945–950 (2014).

  38. 38.

    Moher, D., Liberati, A., Tetzlaff, J., Altman, D. G. & Group, P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS medicine 6, e1000097 (2009).

  39. 39.

    Chen, Y., Zhang, Y., Tang, Y., Huang, X. & Xie, Y. High-maintenance-dose clopidogrel in patients undergoing percutaneous coronary intervention: a systematic review and meta-analysis. PloS one 8, e78549 (2013).

  40. 40.

    Moher, D., Liberati, A., Tetzlaff, J., Altman, D. G. & Group, P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg 8, 336–341 (2010).

  41. 41.

    Ge, J. et al. New signs characteristic of myocardial bridging demonstrated by intracoronary ultrasound and Doppler. European Heart Journal 20, 1707–1716 (1999).

  42. 42.

    Ge, J., Erbel, R., Görge, G., Haude, M. & Meyer, J. High wall shear stress proximal to myocardial bridging and atherosclerosis: intracoronary ultrasound and pressure measurements. British heart journal 73, 462–465 (1995).

  43. 43.

    Angelini, P., Trivellato, M., Donis, J. & Leachman, R. D. Myocardial bridges: a review. Progress in cardiovascular diseases 26, 75–88 (1983).

  44. 44.

    Tian, T. et al. Myocardial Bridging as a Common Phenotype of Hypertrophic Cardiomyopathy Has No Effect on Prognosis. The American journal of the medical sciences 347, 429–433 (2014).

  45. 45.

    Barr, C. S., Naas, A., Freeman, M., Lang, C. C. & Struthers, A. D. QT dispersion and sudden unexpected death in chronic heart failure. The Lancet 343, 327–329 (1994).

  46. 46.

    Marra, M. P. et al. Impact of the presence and amount of myocardial fibrosis by cardiac magnetic resonance on arrhythmic outcome and sudden cardiac death in nonischemic dilated cardiomyopathy. Heart Rhythm 11, 856–863 (2014).

  47. 47.

    Zeiher, A. M., Drexler, H., Wollschläger, H. & Just, H. Modulation of coronary vasomotor tone in humans. Progressive endothelial dysfunction with different early stages of coronary atherosclerosis. Circulation 83, 391–401 (1991).

  48. 48.

    Vita, J. A. et al. Coronary vasomotor response to acetylcholine relates to risk factors for coronary artery disease. Circulation 81, 491–497 (1990).

  49. 49.

    Ludmer, P. L. et al. Paradoxical vasoconstriction induced by acetylcholine in atherosclerotic coronary arteries. New England Journal of Medicine 315, 1046–1051 (1986).

  50. 50.

    Kuhn, F. E. et al. Evidence for endothelial dysfunction and enhanced vasoconstriction in myocardial bridges. American heart journal 122, 1764–1766 (1991).

  51. 51.

    Kim, J. W. et al. Myocardial bridging is related to endothelial dysfunction but not to plaque as assessed by intracoronary ultrasound. Heart 94, 765–769 (2008).

  52. 52.

    Teragawa, H. et al. Myocardial bridging increases the risk of coronary spasm. Clinical cardiology 26, 377–383 (2003).

  53. 53.

    Zoghi, M. et al. Impaired endothelial function in patients with myocardial bridge. Echocardiography 23, 577–581 (2006).

  54. 54.

    Masuda, T. et al. The effect of myocardial bridging of the coronary artery on vasoactive agents and atherosclerosis localization. The Journal of pathology 193, 408–414 (2001).

  55. 55.

    Ghaleh, B. et al. Selective large coronary endothelial dysfunction in conscious dogs with chronic coronary pressure overload. Am J Physiol-Heart C 274, H539–H551 (1998).

  56. 56.

    Hong, H. et al. Angiographically evident atherosclerotic stenosis associated with myocardial bridging and risk factors for the artery stenosis located proximally to myocardial bridging. Anadulu Kardiyoloji Dergisi: AKD 14, 40 (2014).

  57. 57.

    Wang, Y. et al. Intramural coronary arterial course is associated with coronary arterial stenosis and prognosis of major cardiac events. Arteriosclerosis, thrombosis, and vascular biology 33, 439–444 (2013).

  58. 58.

    Ishii, T. et al. The significance of myocardial bridge upon atherosclerosis in the left anterior descending coronary artery. The Journal of pathology 148, 279–291 (1986).

  59. 59.

    Verhagen, S. N. et al. Relationship between myocardial bridges and reduced coronary atherosclerosis in patients with angina pectoris. Int J Cardiol 167, 883–888 (2013).

  60. 60.

    Saidi, H., Ongeti, W. & Ogeng’o, J. Morphology of human myocardial bridges and association with coronary artery disease. African health sciences 10 (2010).

  61. 61.

    Wilcox, J. N. et al. Expression of multiple isoforms of nitric oxide synthase in normal and atherosclerotic vessels. Arteriosclerosis, thrombosis, and vascular biology 17, 2479–2488 (1997).

  62. 62.

    Scher, A. M. Absence of atherosclerosis in human intramyocardial coronary arteries: a neglected phenomenon. Atherosclerosis 149, 1–3 (2000).

  63. 63.

    Bilen, E. et al. Increase in mean platelet volume in patients with myocardial bridge. Clinical and Applied Thrombosis/Hemostasis 19, 437–440 (2013).

  64. 64.

    Yuri Gasparyan, A., Ayvazyan, L., P Mikhailidis, D. & Kitas, D. G. Mean platelet volume: a link between thrombosis and inflammation? Curr Pharm Design 17, 47–58 (2011).

  65. 65.

    Yoshino, S. et al. Fractional flow reserve with dobutamine challenge and coronary microvascular endothelial dysfunction in symptomatic myocardial bridging. Circulation Journal 78, 685–692 (2014).

  66. 66.

    Bartunek, J., Wijns, W., Heyndrickx, G. R. & de Bruyne, B. Effects of dobutamine on coronary stenosis physiology and morphology. Circulation 100, 243–249 (1999).

  67. 67.

    Diefenbach, C., Erbel, R., Treese, N., Bollenbach, E. & Meyer, J. Incidence of myocardial bridges after adrenergic stimulation and decreasing afterload in patients with angina pectoris, but normal coronary arteries. Zeitschrift fur Kardiologie 83, 809–815 (1994).

  68. 68.

    Okutucu, S. et al. Assessment of cardiac autonomic functions by heart rate recovery indices in patients with myocardial bridge. Cardiology journal 23, 524–531, https://doi.org/10.5603/CJ.a2016.0046 (2016).

  69. 69.

    Tang, Y.-D., Dewland, T. A., Wencker, D. & Katz, S. D. Post-exercise heart rate recovery independently predicts mortality risk in patients with chronic heart failure. J Card Fail 15, 850–855 (2009).

  70. 70.

    Nishime, E. O., Cole, C. R., Blackstone, E. H., Pashkow, F. J. & Lauer, M. S. Heart rate recovery and treadmill exercise score as predictors of mortality in patients referred for exercise ECG. Jama 284, 1392–1398 (2000).

  71. 71.

    Aksan, G. et al. Exercise-Induced Repolarization Changes in Patients with Isolated Myocardial Bridging. Med Sci Monitor 21, 2116–2124 (2015).

  72. 72.

    Aksakal, A., Urumdas, M., Yaman, M., Ates, A. H. & Arslan, U. Prevalence and three-year follow-up of patients with isolated myocardial bridge in the mid-Black Sea region: a retrospective single-center study. Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology 44, 203–206, https://doi.org/10.5543/tkda.2015.32754 (2016).

  73. 73.

    Ciampricotti, R. & El Gamal, M. Vasospastic coronary occlusion associated with a myocardial bridge. Catheterization and Cardiovascular Interventions 14, 118–120 (1988).

  74. 74.

    Kaski, J. C. et al. Local coronary supersensitivity to diverse vasoconstrictive stimuli in patients with variant angina. Circulation 74, 1255–1265 (1986).

  75. 75.

    Lee, C.-H., Kim, U., Park, J.-S. & Kim, Y.-J. Impact of Myocardial Bridging on the Long-term Clinical Outcomes of Patients with Left Anterior Descending Coronary Artery Disease Treated with a Drug-Eluting Stent. Heart, Lung and Circulation 23, 758–763 (2014).

  76. 76.

    de Agustín, J. A. et al. Myocardial bridging assessed by multidetector computed tomography: likely cause of chest pain in younger patients with low prevalence of dyslipidemia. Revista Española de Cardiología (English Edition) 65, 885–890 (2012).

  77. 77.

    Tang, K. et al. The role of myocardial perfusion imaging in evaluating patients with myocardial bridging. Journal of Nuclear Cardiology 18, 117–122 (2011).

  78. 78.

    Ishikawa, Y. et al. Anatomic properties of myocardial bridge predisposing to myocardial infarction. Circulation 120, 376–383 (2009).

  79. 79.

    Möhlenkamp, S., Hort, W., Ge, J. & Erbel, R. Update on myocardial bridging. Circulation 106, 2616–2622 (2002).

  80. 80.

    Ishikawa, Y. et al. Histopathologic profiles of coronary atherosclerosis by myocardial bridge underlying myocardial infarction. Atherosclerosis 226, 118–123 (2013).

  81. 81.

    Takamura, K. et al. Anatomical characteristics of myocardial bridge in patients with myocardial infarction by multi-detector computed tomography. Circulation Journal 75, 642–648 (2011).

  82. 82.

    Hunt, D., Burdeshaw, J. & Baxley, W. Left ventricular volumes during ventricular tachycardia, first post-tachycardia beat, and subsequent beats in normal rhythm. British heart journal 36, 148 (1974).

  83. 83.

    Kracoff, O. H., Ovsyshcher, I. & Gueron, M. Malignant course of a benign anomaly: Myocardial bridging. Chest 92, 1113–1115, https://doi.org/10.1378/chest.92.6.1113 (1987).

  84. 84.

    Cai, W. et al. Left ventricular systolic dyssynchrony in patients with isolated symptomatic myocardial bridge. Scandinavian Cardiovascular Journal 47, 11–19 (2013).

  85. 85.

    Tsujita, K. et al. Impact of myocardial bridge on clinical outcome after coronary stent placement. The American journal of cardiology 103, 1344–1348 (2009).

  86. 86.

    Maron, B. J., Wolfson, J. K., Epstein, S. E. & Roberts, W. C. Intramural (“small vessel”) coronary artery disease in hypertrophic cardiomyopathy. Journal of the American College of Cardiology 8, 545–557 (1986).

  87. 87.

    Basso, C. et al. Myocardial bridging, a frequent component of the hypertrophic cardiomyopathy phenotype, lacks systematic association with sudden cardiac death. European heart journal 30, 1627–1634 (2009).

  88. 88.

    Sorajja, P. et al. Myocardial bridging in adult patients with hypertrophic cardiomyopathy. Journal of the American College of Cardiology 42, 889–894 (2003).

  89. 89.

    Stiermaier, T. et al. Frequency and significance of myocardial bridging and recurrent segment of the left anterior descending coronary artery in patients with takotsubo cardiomyopathy. The American journal of cardiology 114, 1204–1209 (2014).

  90. 90.

    Brolin, E. B. et al. Prevalence of Myocardial Bridging in Patients With Myocardial Infarction and Nonobstructed Coronary Arteries. American Journal of Cardiology 116, 1833–1839, https://doi.org/10.1016/j.amjcard.2015.09.017 (2015).

  91. 91.

    Canyigit, M. et al. Myocardial bridging as evaluated by 16 row MDCT. European journal of radiology 69, 156–164 (2009).

  92. 92.

    Kim, S.-S. et al. Long-term clinical course of patients with isolated myocardial bridge. Circulation Journal 74, 538–543 (2010).

  93. 93.

    Kim, J. W. et al. Comparison of frequency of coronary spasm in Korean patients with versus without myocardial bridging. The American journal of cardiology 100, 1083–1086 (2007).

  94. 94.

    Kitazume, H. et al. Myocardial bridges in obstructive hypertrophic cardiomyopathy. American heart journal 106, 131–135 (1983).

  95. 95.

    La Grutta, L. et al. Atherosclerotic pattern of coronary myocardial bridging assessed with CT coronary angiography. The international journal of cardiovascular imaging 28, 405–414 (2012).

  96. 96.

    Marcos-Alberca, P. et al. Clinical outcomes of patients with intramyocardial bridging diagnosed by multi-detector cardiac computed tomography. Int J Cardiol 148, 123–125, https://doi.org/10.1016/j.ijcard.2011.01.068 (2011).

  97. 97.

    Mohiddin, S. A., Begley, D., Shih, J. & Fananapazir, L. Myocardial bridging does not predict sudden death in children with hypertrophic cardiomyopathy but is associated with more severe cardiac disease. Journal of the American College of Cardiology 36, 2270–2278 (2000).

  98. 98.

    Rha, S. et al. Association of myocardial bridge and acetylcholine induced coroanry artery spasm and 12-months clinical outcomes. Eur Heart J 33, 792–793 (2012).

  99. 99.

    Rubinshtein, R. et al. Long-term prognosis and outcome in patients with a chest pain syndrome and myocardial bridging: a 64-slice coronary computed tomography angiography study. European Heart Journal-Cardiovascular Imaging, jet010 (2013).

  100. 100.

    Schwarz, E. R. et al. Myocardial bridging in absence of coronary artery disease: proposal of a new classification based on clinical-angiographic data and long-term follow-up. Cardiology 112, 13–21 (2008).

  101. 101.

    Sheu, M.-H. et al. Myocardial bridging in Taiwanese: Noninvasive assessment by 64-detector row coronary computed tomographic angiography. Journal of the Chinese Medical Association 74, 164–168 (2011).

  102. 102.

    Wang, M.-H. et al. Myocardial bridging detection by non-invasive multislice spiral computed tomography: comparison with intravascular ultrasound. Chinese medical journal 121, 17–21 (2008).

  103. 103.

    Xiang, D.-C., Gong, Z.-H., He, J.-X., Ruan, Y.-J. & Xie, Z.-H. Characteristics of stress tests and symptoms in patients with myocardial bridge and coronary artery spasm. Coronary artery disease 20, 27–31 (2009).

  104. 104.

    Yan, H.-b et al. Frequency of infarct-related artery with myocardial bridging in patients with ST-elevation myocardial infarction and its impact upon percutaneous coronary intervention. Chinese medical journal 119, 539–543 (2006).

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Acknowledgements

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Affiliations

  1. Department of Legal Medicine and Bioethics, Department 2 Morphological Sciences, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania

    • Sorin Hostiuc
  2. Division of Anatomy, Faculty of Dental Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania

    • Mugurel Constantin Rusu
  3. MEDCENTER, Centre of Excellence in Laboratory Medicine and Pathology, Bucharest, Romania

    • Mugurel Constantin Rusu
  4. Department of Internal Medicine and Gastroenterology, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania

    • Mihaela Hostiuc
  5. Department of Anatomy, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania

    • Ruxandra Irina Negoi
  6. Department of Surgery, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania

    • Ionuț Negoi

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Contributions

S.H. and I.N. done the statistical analysis, M.C.R. and M.H. performed the database research, R.I.N. reviewed the conflicts in the databases obtained by M.C.R. and M.S.H. wrote the first draft of the manuscript; M.C.R., M.H., R.I.N., I.N. reviewed the manuscript critically for contents. S.H., M.C.R., M.H., R.I.N., I.N. agreed to the final version of the manuscript.

Competing Interests

The authors declare that they have no competing interests.

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Correspondence to Sorin Hostiuc.

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