Research Article


Ultra-structural changes of coronary arterial endothelium with myocardial bridge in human

Sann Lin Ko1
,  
Thin Thin Win2
,  
Khine Zaw Oo3
,  
Tun Tun Win4
,  
Aye Moe Moe Kyaw5

1 Assistant Lecturer, Department of Anatomy, Defence Services Medical Academy, Mingalardon, Postal Code 11021, Yangon, Myanmar

2 Associate Professor, Department of Anatomy, Defence Services Institute of Nursing and Paramedical Sciences (DSINP), Mingalardon, Postal Code 11021, Yangon, Myanmar

3 Head of Department, Department of Nuclear Medical Research, Defence Services Medical Research Center, Tatkon-Nay Pyi Taw, Postal Code 100603, Myanmar

4 Lecturer, Department of Preventive and Social Medicine, Defence Services Medical Academy, Mingalardon, Postal Code 11021, Yangon, Myanmar

5 Professor, Department of Anatomy, Defence Services Medical Academy, Mingalardon, Postal Code 11021, Yangon, Myanmar

Address correspondence to:

Sann Lin Ko

Department of Anatomy, Defence Services Medical Academy, Mingalardon, Postal Code 11021, 100A, War Oo Street, Phaw-kan Qurter, Insein Township, Postal Code 11012, Yangon,

Myanmar

Access full text article on other devices

Access PDF of article on other devices

Article ID: 100027A04SK2020

doi: 10.5348/100027A04SK2020RA

How to cite this article

Ko SL, Win TT, Oo KZ, Win TT, Kyaw AMM. Ultra-structural changes of coronary arterial endothelium with myocardial bridge in human. Edorium J Anat Embryo 2020;7:100027A04SK2020.

ABSTRACT

Aims: The study aimed to compare the scanning electron microscopic gradings of the endothelium and calcium depositions between proximal, under-bridging, distal, and control segments of the coronary artery with myocardial bridge (MB).

Methods: The autopsy of 45 adult hearts with MB among the 243 cases was collected from North Okkalapa General and Teaching Hospital, Yangon. Then, the length and thickness of the MB were measured. The endothelial gradings and elements composition of each specimen was examined by a scanning electron microscope (Phenom Pro X) with energy dispersion X-ray spectrometry (EDS) operated at 15 kV.

Results: In the present study, 45 bridges (18.5%) were observed among the 243 hearts. They were located on the left anterior descending artery (LAD) in all cases (100%). The mean length of the MB was 18.3 ± 11.7 mm (range 1.5–59 mm). The mean thickness of the MB was 2.8 ± 1.5 mm (range 1–6.3 mm). In comparing endothelial cell gradings and calcium deposition of four segments, the proximal segment was significantly different from the under-bridging segment, distal segment, and control segment. The under-bridging segment was significantly different gradings from the distal segment (p < 0.05).

Conclusion: The proximal segment was the most endothelial damage site due to hemodynamic effect of the MB. The under-bridging segment was the least endothelial damage site which might be due to the atheroprotective effect of the MB in under segment.

Keywords: Calcium, Coronary artery, Endothelium, Myocardial bridge, Ultra-structural

Introduction


The myocardial muscle fiber over the segment of the coronary artery was known as a “myocardial bridge” (MB). The common affected location of MB was the middle parts of the left anterior descending artery (LAD) [1],[2],[3],[4]. In autopsy studies, the frequency of MB was 4.7–86% [5],[6].

The proximal segment of MB was more prone to arteriosclerosis [7]. Angiographic studies assumed that MB was not associated with atherosclerosis changes of the coronary artery. There was a complex relationship between MB and major cardiovascular events that depended on the anatomical properties of MBs [6]. Meta-analysis review suggested that more studies need to find out the association between myocardial bridging and myocardial infarct, and sudden death [8].

Many researchers concluded that hemodynamic changes occurred in the different segments of the coronary artery with MB. Endothelial dysfunctions more occurred in the proximal LAD but less in the middle or under-bridging segment of LAD due to different effect of wall shear stress (WSS) and local tensile stress (TS) [9],[10],[11],[12],[13]. Jain et al. [14] described that the different blood flow velocities of the LAD were both systole and diastole. In recent years, there had been an increasing amount of literature with regard to the histopathology, pathophysiology, electron microscopic study, and element analysis of MB. Tohno et al. [15] described that the accumulation of the elements was different in the proximal segment of MBs and under-bridging segments of the LAD. In the experimental study, abnormal hemodynamic effect appeared in the proximal segment of the myocardial segment during high-pressure compression [16].

Theore, the findings of the present study provided information for incidence, location, length, and thickness of the bridging segments as well as the ultra-structural findings and intimal calcification of the endothelium of the coronary artery with or without MB.

MATERIALS AND METHODS


In this cross-sectional analytic study, 45 hearts with myocardial bridging, males 30 (67%) and females 15 (33%), the age ranged from 24 to 85 years (mean 52 years), were collected from North Okkalapa General and Teaching Hospital during December 2017 to December 2019. Ethical approval for this study was obtained from the Institutional Review Board of Defence Services Medical Academy and Defence Services Medical Research Center (FWA-00023030, IORG-0009413, IRB-00011205). The length and thickness of MB were measured with the aid of Vernier Callipers, with 0.01 mm precision. Then, the four pieces of the coronary artery were taken in proximal (segment 1), under (segment 2) and distal segments (segment 3) of the coronary artery with MB, and segment from a coronary artery without MB in the same autopsy hearts to be used as control (segment 4).

 

Scanning electron microscopy (SEM) and energy dispersion X-ray spectrometry (EDS) analysis

The sample coronary arterial tissues were fixed in a 2.5% glutaraldehyde solution with Na-phosphate at pH 7.2. Dehydration was done with a graded ethanol series and a critical-point dryer (Quorum K850). The sample was coated with 5 nm of gold by using a sputter coater (Quorum Q150R ES). The entire endothelial surface of four segments of each specimen was examined with a scanning electron microscope (Phenom Pro X) operated at 15 kV. Energy dispersion X-ray spectrometry (EDS) examined the element deposition of each specimen. The specimens were observed by researchers and blinded the data of manipulation group.

 

Statistical analysis

Data were composed in Microsoft Excel. Data analysis was carried out by Wilcoxon signed-rank test. P value of less than 0.05 was considered to be significant.

 

Scanning electron microscopic endothelium gradings (SEM grading)

Grading “0”—This grading included normal endothelial cells and there was no defect in endothelial cell junction.

Grading “1”—In this grading, no defect was found in endothelial cell junction but the cells were unusually raised above the normal endothelium surface. Leucocytes more frequently adhered to the surface membrane. Leucocytes transition may present or not.

Grading “2”—The two endothelial cells that had wider cell junction and everted cell margin.

Grading “3”—An endothelial lesion that had isolated detachment of endothelial cells. Most of the area had a normal endothelial cell but some focal surfaces exposed subendothelial connective tissue.

Grading “4”—Most of the area (two or more focal area) was covered by subendothelial tissue.

RESULTS


The location, length, and thickness of MBs in human adult autopsied hearts

In the present study, 45 bridges (18.5%) were observed among the 243 autopsy hearts. There were located on the LAD in all cases (100%). Myocardial bridge was observed in males 30 (67%) and females 15 (33%), the age ranged from 24 to 85 years (mean 52 years). There were no double MBs in LAD. All MBs were located in the middle part of the LAD (Figure 1). The presence of a collateral branch was found in the LAD of three autopsied hearts. The collateral branch arose before the LAD entered to the myocardial bridging segment. The mean length of the MB was 18.3 ± 11.7 mm (range 1.5–59 mm). The mean thickness of the MB was 2.8 ±1.5 mm (range 1–6.3 mm). The length of the MB is described in detail in Table 1.

 

Scanning electron microscopic findings of endothelium at proximal, under, distal, and control segments

The scanning electron microscopic features of endothelial cells were varied in proximal, under, distal, and control segments. The mean and sum of endothelial grading scores of proximal segments were 2.02 and 91, respectively. In the case of advanced endothelial grading (endothelial gradings “3” and “4”), the subendothelial connective tissue was exposed at the detached area of the coronary arterial endothelium. The subendothelial connective tissue with the huge calcified plaque was covered at the proximal segment of the MB (Figure 2). These types of severe endothelial damage (endothelial gradings “3” and “4”) were found in the proximal segment (38%), distal segment (11%), and control segment (7%). There was no endothelial grading 3 and grading 4 in under bridging segment (segment 2).

In the endothelium of under bridging segment (segment 2), the range of endothelial grading score was “0–2.” The mean and sum of endothelial grading scores were 0.42 and 19, respectively. In the endothelium of the distal segment, the mean and sum of endothelial grading scores were 0.96 and 43, respectively. In the endothelium of the control segment (segment 4), the range of endothelial grading score was “0–4.” The mean and the sum of endothelial grading score was 0.67 and 30, respectively.

In the case of lower endothelial grading (endothelial gradings 1 and 2), the shape of endothelial cells was dehiscent endothelial junction or everted cell margin. There were leucocytes, probably monocytic, adherent to an intact endothelial surface. There was increased cellularity such as platelets. Most of the cells aligned along the main axis of blood flow (Figure 2).

 

The energy dispersion X-ray spectrometry analysis of proximal, under, distal, and control segments

In the energy dispersion X-ray spectrometry analysis, the Calcium element was found six cases in the proximal segment (segment 1), one case in segments 2 and 3, and three cases in segment 4, respectively. Iron (Fe) was detected in four cases in segment 1 and one in segment 2. The other elements such as sodium (Na), phosphorus (P), copper (Cu), and sulfur (S) were detected. In energy dispersion X-ray spectrometry analysis of case number 37, energy dispersion X-ray spectrometry (EDS) spikes showed carbon (C), calcium (Ca), oxygen (O), nitrogen (N), and phosphorus (P). The energy dispersion X-ray spectrometry for calcium (Ca) was 1.27% atomic concentration (3.66% weight concentration) and phosphorus (P) was 0.84% atomic concentration (1.88 % weight concentration) (Figure 3).

 

Comparing the scanning electron microscopic gradings and the energy dispersion X-ray spectrometry analysis of endothelium between four segments

Comparing to scanning electron micrographic endothelial gradings of four segments, segment 1 was significantly different from segment 2, segment 3, and segment 4. Segment 2 was significantly different from segment 3. Segment 4 was not significantly different from both segment 2 and segment 3 (p 0.05) (Figure 4).

Comparing to the energy dispersion X-ray spectrometry findings of four segments, calcium deposition in segment 1 was significantly different from segment 2, segment 3, and segment 4. Segment 2 was a similar deposition of calcium in segments 3 and 4. Segment 3 was not significantly different from segment 4 (p 0.05).

Figure 1: Long myocardial bridging on the left anterior descending artery. MB length (10 mm) and thickness (2 mm).
Table 1: Length of myocardial bridge among the collected human adult autopsy hearts (mm)
Figure 2: Scanning electron micrograph of proximal, under-bridging, distal, and control segments of case number 37. The subendothelial connective tissue with the huge calcified plaque (Black arrow).
Figure 3: Histogram of energy dispersion X-ray spectrometry analysis of proximal segments (A) and under segment (B) (C: carbon, Ca: calcium, N: nitrogen, O: oxygen, and P: phosphorus).
Figure 4: Scanning electron microscopic endothelial gradings of four segments of the coronary artery with myocardial bridge.

Discussion


The results of the present study were consistent with the reviews of Möhlenkamp et al. [5] and Ishikawa et al. [6] demonstrated that the frequency of MB was 4.7–86%. In the present study, MBs were found over the left anterior descending branch of the left coronary artery (100%) and no MB on other coronaries arteries. These results were in keeping with previous studies [1],[2],[3],[4]. In this study, the collateral branch arose before the LAD entered to the myocardial bridging segment. There might be collateral circulation for the MB.

The present study compared the data from the meta-analysis review on MB of Hostiuc [17] who reviewed the thickness of the MB of 39 studies (11 autopsy and 28 computed tomography (CT) studies). The overall mean MB thickness of the meta-analysis review was 2.63 mm (2.48–2.85). The present study was consistent with meta-analysis review on autopsy studies which was 2.80 mm (2.39–3.22). The present study was thicker MB than 2.57 mm (2.31–2.83) in CT studies. The range of MB thickness in the present study was from 1 to 6.3 mm which was wider than the previous researches which were the range of MB, from 1 to 4 mm [18],[19],[20],[21],[22]. This study had a narrower range of MB thickness than 0.5 to 9.1 mm [4] and ranged from 5 to 27 mm observed by Loukas et al. [23]. In the previous autopsy and angiography studies reported the length of the MB were varied from 0.5 to 69 mm [1],[18],[21],[22],[24],[25],[26]. The range of length of the present study was 1.5–59 mm. The findings of the present study supported the results of previous studies.

The severe endothelial damage (SEM grades 3 and 4) of the coronary artery with MB in the present study lected SEM grading of Davies et al. [27] and Hangler et al. [28] who described as subendothelial connective tissue covered all luminal surface of the coronary artery. Most cases of the proximal segment (38%) of the present study lected those of Ding et al. [16] who verified the effect of the MB led to irregular hemodynamics at the proximal end of the under bridging segment of the coronary artery. The present study confirmed the severity or higher grading of endothelial injury which lected the degree of compression of MB over the coronary artery.

The results of the present study also supported the findings of many previous works. The previous researches described that the hemodynamic changes simulated WSS alteration in the different segments of the vessel including proximal, middle, and distal segments in patients with MB. Endothelial dysfunctions of the proximal LAD were associated with the site of lower WSS. There was nonendothelial dysfunction in the middle segment of LAD at greater WSS [9],[10],[11],[12]. The present study confirmed the report of Jain et al. [14] in which the blood flow velocity could be increased under bridging segment of LAD at both systole and diastole. According to the pathophysiology review, it might be due to structural and functional changes of endothelial cells and smooth muscle cells induced by higher local TS described by Haga et al. [13].

The mean and sum grading scores of segment 1 were higher than segments 2–4. The endothelial grading scores of segment 2 were “0–2.” There was no advanced endothelial grading (grades 3 and 4) in under segment. Most of the distal and control segments of MB cases were grade 2. Some of the distal and control segments had a major defect in endothelial integrity. The SEM findings of the present study lected the work of Ishikawa et al. [29], who stated that the quantity of intimal thickening of the coronary artery segments was depending on the thickness and length of MB. The SEM findings of the present study matched the findings of Davies et al. [27] and Hangler et al. [28] who described the SEM features of endothelial injury.

This study supported the work of Tohno et al. [15] who described that the calcium (Ca), phosphorus (P), zinc (Zn), and sodium (Na) were not uniform coronary artery with myocardial bridging cases. The elements accumulation was higher in the proximal part of MB than in the distal part of MB in comparison with under bridging segment of the LAD artery but there was no detailed description of element deposition of under segment. The present study was also agreed with the findings of Ge et al. [30] who described that calcium deposit with an eccentric plaque located at the proximal segment to the bridge especially in the systolic phase. In the animal study, calcium elements were not deposited in an early stage of lesions but they were found in the advance stage of the lesion as hydroxyapatite [31]. Theore, the calcium elements were not found in all advance endothelial grading cases of the present study. They would depend on the type of calcification and method of analysis. In the present study, all iron (Fe) detected cases were SEM grade 4. This study is consistent with that of Salonen et al. [32] who reported iron might be involved in the atherogenesis process and a possible risk factor in coronary heart disease.

The present study confirmed the experiment of Ding et al. [16] who revealed that oscillatory shear stress which was significantly greater in the proximal segment of MB than the distal segment of MB under the 50% compression on the coronary artery. There were higher WSS at the distal segment of MB than the proximal segment of MB. The proximal end of MB was higher the oscillatory stress than other segments, at experimental 80% compression pressure [33]. The solid mechanical forces induced stresses which caused plaque growth and fissure at the proximal segments of MB [30]. These hemodynamic mechanisms played an important role in endothelium damage of the MB.

Conclusion


The under-bridging segment was the least endothelial damage site which might be due to the atheroprotective effect of the MB in under segment. The proximal segment was the most endothelial damage site. The distal segment had lower endothelial grading than the proximal segment and higher endothelial grading than both of the under bridging segment and control segment. It might be the different blood flow and shear stress in these segments.

REFERENCES


1.

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] [Pubmed] Back to citation no. 1  

2.

Bezerra AJ, Prates JC, DiDio LJ. Incidence and clinical significance of bridges of myocardium over the coronary arteries and their branches. Surg Radiol Anat 1987;9(4):273–80. [CrossRef] [Pubmed] Back to citation no. 1  

3.

Baptista CA, DiDio LJ. The relationship between the directions of myocardial bridges and of the branches of the coronary arteries in the human heart. Surg Radiol Anat 1992;14(2):137–40. [CrossRef] [Pubmed] Back to citation no. 1  

4.

Chen YD, Wu MH, Sheu MH, Chang CY. Myocardial bridging in Taiwan: Depiction by multidetector computed tomography coronary angiography. J Formos Med Assoc 2009;108(6):469–74. [CrossRef] [Pubmed] Back to citation no. 1  

5.

Möhlenkamp S, Hort W, Ge J, Erbel R. Update on myocardial bridging. Circulation 2002;106(20):2616–22. [CrossRef] [Pubmed] Back to citation no. 1  

6.

Ishikawa Y, Kawawa Y, Kohda E, Shimada K, Ishii T. Significance of the anatomical properties of a myocardial bridge in coronary heart disease. Cir J 2011;75(7):1559–66. [CrossRef] [Pubmed] Back to citation no. 1  

7.

Li W, Zhang M, Yuan D, Cai P. Ultrastructure and hemodynamic changes of endothelial cells from myocardial bridge mural coronary artery. Cuangzhou: 2011 IEEE International Symposium on IT in Medicine and Education; 2011. p. 101–5. [CrossRef] Back to citation no. 1  

8.

Hostiuc S, Rusu MC, Hostiuc M, Negoi RI, Negoi I. Cardiovascular consequences of myocardial bridging: A meta-analysis and meta-regression. Sci Rep 2017;7(1):14644. [CrossRef] [Pubmed] Back to citation no. 1  

9.

Walpola PL, Gotlieb AI, Cybulsky MI, Langille BL. Expression of ICAM-1 and VCAM-1 and monocyte adherence in arteries exposed to altered shear stress. Arteriosclerosis, Thrombosis, and Vascular Biology 1995;15(1):2–10. [CrossRef] Back to citation no. 1  

10.

Malek AM, Alper SL, Izumo S. Hemodynamic shear stress and its role in atherosclerosis. JAMA 1999;282(21):2035–42. [CrossRef] [Pubmed] Back to citation no. 1  

11.

McNally JS, Davis ME, Giddens DP, et al. Role of xanthine oxidoreductase and NAD(P)H oxidase in endothelial superoxide production in response to oscillatory shear stress. Am J Physiol Heart Circ Physiol 2003;285(6):H2290–7. [CrossRef] [Pubmed] Back to citation no. 1  

12.

Javadzadegan A, Moshfegh A, Qian Y, Kritharides L, Yong ASC. Myocardial bridging and endothelial dysfunction – Computational fluid dynamics study. J Biomech 2019;85:92–100. [CrossRef] [Pubmed] Back to citation no. 1  

13.

Haga JH, Li YSJ, Chien S. Molecular basis of the effects of mechanical stretch on vascular smooth muscle cells. J Biomech 2007;40(5):947–60. [CrossRef] [Pubmed] Back to citation no. 1  

14.

Jain SP, White CJ, Ventura HO. De novo appearance of a myocardial bridge in heart transplant: Assessment by intravascular ultrasonography, Doppler, and angioscopy. Am Heart J 1993;126(2):453–6. [CrossRef] [Pubmed] Back to citation no. 1  

15.

Tohno Y, Tohno S, Minami T, Pakdeewong-Ongkana N, Suwannahoy P, Quiggins R. Different accumulation of elements in proximal and distal parts of the left anterior descending artery beneath the myocardial bridge. Biol Trace Elem Res 2016;171(1):17–25. [CrossRef] [Pubmed] Back to citation no. 1  

16.

Ding H, Yang Q, Shang K, et al. Estimation of shear stress by using a myocardial bridge-mural coronary artery simulating device. Cardiol J 2017;24(5):530–8. [CrossRef] [Pubmed] Back to citation no. 1  

17.

Hostiuc S, Negoi I, Rusu MC, Hostiuc M. Myocardial bridging: A meta-analysis of prevalence. J Forensic Sci 2018;63(4):1176–85. [CrossRef] [Pubmed] Back to citation no. 1  

18.

Polacek P, Kralove H. Relation of myocardial bridges and loops on the coronary arteries to coronary occulsions. Am Heart J 1961;61:44–52. [CrossRef] [Pubmed] Back to citation no. 1  

19.

Stolte M, Weis P, Prestele H. Muscle bridges over the left anterior descending coronary artery: Their influence on arterial disease (author’s transl). [Article in German]. Virchows Arch A Pathol Anat Histol 1977;375(1):23–36. [CrossRef] [Pubmed] Back to citation no. 1  

20.

Reig J, Loncan MP, Martin S, Binia M, Petit M, Domenech JM. Myocardial bridges. Incidence and relation to some certain coronary variables. [Article in French]. Arch Anat Histol Embryol 1986;69:101–10. [Pubmed] Back to citation no. 1  

21.

Ferreira AG Jr, Trotter SE, König B Jr, Décourt LV, Fox K, Olsen EG. Myocardial bridges: Morphological and functional aspects. Br Heart J 1991;66(5):364–7. [CrossRef] [Pubmed] Back to citation no. 1  

22.

Bourassa MG, Butnaru A, Lespérance J, Tardif JC. Symptomatic myocardial bridges: Overview of ischemic mechanisms and current diagnostic and treatment strategies. J Am Coll Cardiol 2003;41(3):351–9. [CrossRef] [Pubmed] Back to citation no. 1  

23.

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] [Pubmed] Back to citation no. 1  

24.

Noble J, Bourassa MG, Petitclerc R, Dyrda I. Myocardial bridging and milking effect of the left anterior descending coronary artery: Normal variant or obstruction? Am J Cardiol 1976;37(7):993–9. [CrossRef] [Pubmed] Back to citation no. 1  

25.

Kramer JR, Kitazume H, Proudfit WL, Sones FM Jr. Clinical significance of isolated coronary bridges: Benign and frequent condition involving the left anterior descending artery. Am Heart J 1982;103(2):283–8. [CrossRef] [Pubmed] Back to citation no. 1  

26.

Angelini P, Trivellato M, Donis J, Leachman RD. Myocardial bridges: A review. Prog Cardiovasc Dis 1983;26(1):75–88. [CrossRef] [Pubmed] Back to citation no. 1  

27.

Davies MJ, Woolf N, Rowles PM, Pepper J. Morphology of the endothelium over atherosclerotic plaques in human coronary arteries. Br Heart J 1988;60(6):459–64. [CrossRef] [Pubmed] Back to citation no. 1  

28.

Hangler HB, Pfaller K, Ruttmann E, et al. Effects of intracoronary shunts on coronary endothelial coating in the human beating heart. Ann Thorac Surg 2004;77(3):776–80. [CrossRef] [Pubmed] Back to citation no. 1  

29.

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] [Pubmed] Back to citation no. 1  

30.

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. Br Heart J 1995;73(5):462–5. [CrossRef] [Pubmed] Back to citation no. 1  

31.

Watt F, Rajendran R, Ren MQ, Halliwell B, Tan BKH. A nuclear microscopy study of trace elements Ca, Fe, Zn and Cu in atherosclerosis. Nuclear Instruments and Methods in Physics Research section B: Beam Interactions with Materials and Atoms 2006;249(1–2):646–52. [CrossRef] Back to citation no. 1  

32.

Salonen JT, Nyyssönen K, Korpela H, Tuomilehto J, Seppänen R, Salonen R. High stored iron levels are associated with excess risk of myocardial infarction in eastern Finnish men. Circulation 1992;86(3):803–11. [CrossRef] [Pubmed] Back to citation no. 1  

33.

Cheng C, Tempel D, van Haperen R, et al. Atherosclerotic lesion size and vulnerability are determined by patterns of fluid shear stress. Circulation 2006;113(23):2744–53. [CrossRef] [Pubmed] Back to citation no. 1  

SUPPORTING INFORMATION


Acknowledgments

We are grateful to Brigadier General Tin Maung Hlaing, Commandant (Retried), Defence Services Medical Research Center, Nay Pyi Taw for providing the Scanning Electron Microscopy unit and Professor Aung Soe, Head of Department of Forensic Medicine, University of Medicine (2), Yangon for giving opportunity to sample collection and gross anatomy dissection. We would like to acknowledge Dr. Thiha Nyunt, Nanova-scientific Company, for providing technical support for electron microscopy.

Author Contributions

Sann Lin Ko - Substantial contributions to conception and design, Analysis of data, Interpretation of data, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published

Thin Thin Win - Substantial contributions to conception and design, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published

Khine Zaw Oo - Acquisition of data, Interpretation of data, Revising it critically for important intellectual content, Final approval of the version to be published

Tun Tun Win - Analysis of data, Revising it critically for important intellectual content, Final approval of the version to be published

Aye Moe Moe Kyaw - Revising it critically for important intellectual content, Final approval of the version to be published

Data Availability Statement

The corresponding author is the guarantor of submission.

Consent For Publication

Written informed consent was obtained from the patient for publication of this article.

Data Availability

All relevant data are within the paper and its Supporting Information files.

Competing Interests

Authors declare no conflict of interest.

Copyright

© 2020 Sann Lin Ko et al. This article is distributed under the terms of Creative Commons Attribution License which permits unrestricted use, distribution and reproduction in any medium provided the original author(s) and original publisher are properly credited. Please see the copyright policy on the journal website for more information.