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Tympanosclerosis and atherosclerosis plaques: a comparative analytical study on some new microbiological and immunohistochemical aspects

  • Otology
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Abstract

Purpose

The aim of this study was to compare chemical contents, expression of BMP-8a, and the presence of Mycoplasma and ExoS-ExoU exotoxins producing Pseudomonas aeruginosa in tympanosclerosis (TS) and atherosclerosis (AS) plaques.

Methods

Thirty-six cases with TS and AS plaques (18 each) were selected and examined for chemical, immunohistochemical, and microbial analysis. SPSS ver. 21 and t test analysis were used for comparing the findings, and the level of significance was considered as p < 0.05.

Results

TS plaques showed lower carbon, higher calcium, and phosphorous contents compared to AS plaques (p value < 0.05). Chlorine was detected in AS plaques (1.8 w%) which could probably be due to the presence of myeloperoxidase (MPO) in atherosclerotic artery. Contrary to spherical shape of the surface of TS plaques, AS plaques were needle shaped. BMP-8a expression in TS plaques (59.5%) was significantly higher (p value < 0.0001) than AS plaques (20%). Of the 18 TS specimens, 12, 14, and 3 were positive for ExoS, ExoU Pseudomonas aeruginosa, and Mycoplasma genes, respectively, while of the 18 AS specimens, 2, 2, and 3 were positive for ExoS, ExoU Pseudomonas aeruginosa, and Mycoplasma genes, respectively.

Conclusion

TS plaques are different from AS plaques in terms of elemental components, surface morphology, and BMP-8a expression. Therefore, different calcification process and pathogenesis may be responsible for these two diseases. The results of our study showed that both TS and AS plaques have genetic footprint of Mycoplasma, but the level of calcium concentration-dependent exotoxins genes was found only in TS plaques.

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References

  1. Mansour S, Magnan J, Nicolas K et al (2018) Tympanosclerosis. Middle ear diseases. Springer; New York, USA, pp 161–204

    Chapter  Google Scholar 

  2. Chole RA, Sharon JD, Chronic Otitis Media, Mastoiditis, and Petrositis (2020). In: Cummings Flint PW, Haughey BH, Robbins KT et al (eds) Otolaryngology-head and neck surgery, 7th edn. Elsevier Health Sciences; Amsterdam, Netherlands, pp 28–31

    Google Scholar 

  3. Dinç AE, Cömert F, Damar M et al (2016) Role of Chlamydia pneumoniae and Helicobacteria pylori in the development of tympanosclerosis. Eur Arch Otorhinolaryngol 273:889–892

    Article  PubMed  Google Scholar 

  4. Gibb A, Pang Y (1994) Current considerations in the etiology and diagnosis of tympanosclerosis. Eur Arch Otorhinolaryngol 251:439–451

    Article  CAS  PubMed  Google Scholar 

  5. Kattoor AJ, Pothineni NVK, Palagiri D et al (2017) Oxidative stress in atherosclerosis. Curr Atheroscler Rep 19:42–52

    Article  PubMed  CAS  Google Scholar 

  6. Çiçek D, Vayisoğlu Y, Görür K et al (2010) Is there any relation between coronary atherosclerosis and tympanosclerosis? Anatol J Cardiol 10:121–125

    Article  Google Scholar 

  7. Koç A, Üneri C (2005a) Ultrastructural comparison between tympanosclerosis and atherosclerosis. Türk Otolarengoloji Arşivi 43:137–144

    Google Scholar 

  8. Ashtari F, Saberi A, Shaigannezhad V et al (2007) Association between Chlamydia pneumoniae infection and carotid atherosclerotic plaques. J Res Med Sci 12:165–171

    Google Scholar 

  9. Iriz A, Eryilmaz A, Gocer C et al (2011) Could Helicobacter pylori play a role in the aetiopathogenesis of tympanosclerosis? J Laryngol Otol 125:1121–1124

    Article  CAS  PubMed  Google Scholar 

  10. Pirodda A, Bruzzi C, Ferri G et al (2010) Otoscopic findings in hypercholesterolemic subjects. B-ENT 6:123–126

    CAS  PubMed  Google Scholar 

  11. Pirodda A, Ferri GG, Bruzzi C et al (2004) Possible relationship between tympanosclerosis and atherosclerosis. Acta Oto-laryngol 124:574–576

    Article  Google Scholar 

  12. Doluoglu S, Gocer C, Toprak U et al (2015) Increased carotid artery intima-media thickness in patients with tympanosclerosis: common risk factors with atherosclerosis? Kaohsiung J Med Sci 31:199–202

    Article  PubMed  Google Scholar 

  13. Acar A, Eryilmaz A, Gocer C et al (2009) Is tympanosclerosis effected by risk factors for atherosclerosis? J Int Adv Otol 5:166–170

    Google Scholar 

  14. Russell JD, Giles J (2002) Tympanosclerosis in the rat tympanic membrane: an experimental study. Laryngoscope 112:1663–1666

    Article  PubMed  Google Scholar 

  15. Da Costa SS, Paparella MM, Schachern PA et al (1992) Temporal bone histopathology in chronically infected ears with intact and perforated tympanic membranes. Laryngoscope 102:1229–1236

    Article  PubMed  Google Scholar 

  16. Karldağ T, İlhan N, Kaygusuz İ et al (2004) Comparison of free radicals and antioxidant enzymes in chronic otitis media with and without tympanosclerosis. Laryngoscope 114:85–89

    Article  Google Scholar 

  17. Mattsson C, Magnuson K, Hellström S (1995) Myringosclerosis caused by increased oxygen concentration in traumatized tympanic membranes experimental study. Ann Otol Rhinol Laryngol 104:625–632

    Article  CAS  PubMed  Google Scholar 

  18. Guo W, Bai X, Han Y et al (2012) Expressions of TGF-β1 and MMP-9 in a guinea pig model of tympanosclerosis: possible role in the pathogenesis of this disorder. Laryngoscope 122:2037–2042

    Article  CAS  PubMed  Google Scholar 

  19. Li MO, Flavell RA (2008) TGF-β: a master of all T cell trades. Cell 134:392–404

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Pelkonen T, Sarajuuri A et al (2017) Meningoencephalitis and otitis media in a child with Mycoplasma pneumoniae infection. Acta Otolaryngol Case Reports 2:1–4

    Article  Google Scholar 

  21. Momiyama Y, Ohmori R et al (2004) Association of Mycoplasma pneumoniae infection with coronary artery disease and its interaction with chlamydial infection. Atherosclerosis 176:139–144

    Article  CAS  PubMed  Google Scholar 

  22. Mittal R, Lisi CV, Gerring R et al (2015) Current concepts in the pathogenesis and treatment of chronic suppurative otitis media. J Med Microbiol 64:1103

    Article  PubMed  PubMed Central  Google Scholar 

  23. Park M-H, Kim SY, Roh EY et al (2017) Difference of Type 3 secretion system (T3SS) effector gene genotypes (exoU and exoS) and its implication to antibiotics resistances in isolates of Pseudomonas aeruginosa from chronic otitis media. Auris Nasus Larynx 44:258–265

    Article  PubMed  Google Scholar 

  24. Katagiri T, Watabe T (2016) Bone morphogenetic proteins. Cold Spring Harb Perspect Biol 8(6):a021899

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  25. Hruska KA, Mathew S, Saab G (2005) Bone morphogenetic proteins in vascular calcification. Circ Res 97:105–114

    Article  CAS  PubMed  Google Scholar 

  26. Kaden JJ, Bickelhaupt S, Grobholz R et al (2004) Expression of bone sialoprotein and bone morphogenetic protein-2 in calcific aortic stenosis. J Heart Valve Dis 13:560–566

    PubMed  Google Scholar 

  27. Liu X, Li Y, Zheng Y et al (2009) Expression and localization of macrophages and BMP2 in mucosa of tympanosclerosis. J Clin Otorhinol Head Neck Surg 23:298–301

    Google Scholar 

  28. Cho TJ, Gerstenfeld LC, Einhorn TA (2002) Differential temporal expression of members of the transforming growth factor β superfamily during murine fracture healing. J Bone Miner Res 17:513–520

    Article  CAS  PubMed  Google Scholar 

  29. Sulzbacher I, Birner P, Trieb K et al (2002) The expression of bone morphogenetic proteins in osteosarcoma and its relevance as a prognostic parameter. J Clin Pathol 55:381–385

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Aslan H, Basoglu MS, Ilknur AE et al (2012) Analysis of tympanosclerotic plaques via atomic force microscope and scanning electron microscope. ENT Updates 2:89

    Google Scholar 

  31. Koç A, Üneri C (2005b) Ultrasctuctural comparison between tympanosclerosis and atherosclerosis. Tǘrk Otolarengoloji Arşivi 43:137–144

    Google Scholar 

  32. Hussl B, Lim DJ (1984) Fine morphology of tympanosclerosis. Recent advances in otitis media with effusion Toronto, Canada: Decker, pp 348–353

    Google Scholar 

  33. Wielinga E, Kuijpers W, Tonnaer E et al (1988) An experimental model for tympanosclerosis: a preliminary report. Acta Otolaryngol 105:537–542

    Article  CAS  PubMed  Google Scholar 

  34. Saki N, Zadeh ARS, Jonaky RS et al (2014) The prevalence rate of Helicobacter pylori infection in, chronic otitis media with effusion patients. Jundishapur J Microbiol 7:1–4

    Article  Google Scholar 

  35. Saki N, Jahani M, Samarbaf A et al (2015) Correlation between tympanosclerosis and Helicobacter pylori. Jundishapur J Microbiol 8:1–5

    Google Scholar 

  36. Schiff M, Catanzaro A, Poliquin JF et al (1980) Tympanosclerosis: a theory of pathogenesis. Ann Otol Rhinol Laryngol 89:1–16

    Article  CAS  Google Scholar 

  37. Spickett CM (2007) Chlorinated lipids and fatty acids: an emerging role in pathology. Pharmacol Ther 115:400–409

    Article  CAS  PubMed  Google Scholar 

  38. Malle E, Marsche G, Arnhold J et al (2006) Modification of low-density lipoprotein by myeloperoxidase-derived oxidants and reagent hypochlorous acid. BBA-Mol Cell Biol L 1761:392–415

    CAS  Google Scholar 

  39. Zhao G-Q, Liaw L, Hogan B (1998) Bone morphogenetic protein 8A plays a role in the maintenance of spermatogenesis and the integrity of the epididymis. Devel 125:1103–1112

    CAS  Google Scholar 

  40. Zhao G-Q, Hogan BL (1996) Evidence that mouse Bmp8a (Op2) and Bmp8b are duplicated genes that play a role in spermatogenesis and placental development. Mech Devel 57:159–168

    Article  CAS  Google Scholar 

  41. Hu M, Hu J-W, He L et al (2016) Expression of bone modeling markers and formation of bacterial biofilm in middle ear of rats with chronic suppurative otitis media induced by Pseudomonas aeruginosa. Int J Clin Exp Pathol 9:10002–10010

    CAS  Google Scholar 

  42. Csiszar A, Ahmad M, Smith KE et al (2006) Bone morphogenetic protein-2 induces proinflammatory endothelial phenotype. Am J Pathol 168:629–638

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Sorescu GP, Song H, Tressel SL et al (2004) Bone morphogenic protein 4 produced in endothelial cells by oscillatory shear stress induces monocyte adhesion by stimulating reactive oxygen species production from a nox1-based NADPH oxidase. Circ Res 95:773–779

    Article  CAS  PubMed  Google Scholar 

  44. Horsman SR, Moore RA, Lewenza S (2012) Calcium chelation by alginate activates the type III secretion system in mucoid Pseudomonas aeruginosa biofilms. PLoS ONE 7:1–11

    Article  CAS  Google Scholar 

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Funding

The project was supported by deputy of research and technology of Guilan University of Medical Sciences.

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Authors and Affiliations

Authors

Contributions

Shadman Nemati: designed and supervised the research, performed the surgery and provided tympanosclerosis plaques, analyzed data, and co-wrote the paper. Alia Saberi: analyzed data, contributed to the interpretation of the results, and co-wrote the paper. Ali Faghih Habibi: performed surgery and provided tympanosclerosis plaques. Hossein Hemmati: performed surgery and provided atherosclerosis plaques. Reza Jafari Shakib: performed experiments, analyzed data, and co-wrote the paper. Mojtaba Hedayati Ch: performed experiments, analyzed data, and co-wrote the paper. Elahe Bozorgzadeh: designed and supervised the research, performed experiments, analyzed data, and co-wrote the paper.

Corresponding author

Correspondence to Elahe Bozorgzadeh.

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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

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Nemati, S., Saberi, A., Faghih Habibi, A. et al. Tympanosclerosis and atherosclerosis plaques: a comparative analytical study on some new microbiological and immunohistochemical aspects. Eur Arch Otorhinolaryngol 278, 3743–3752 (2021). https://doi.org/10.1007/s00405-020-06451-4

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  • DOI: https://doi.org/10.1007/s00405-020-06451-4

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