A comparative study on the effectiveness of application of different types of biological matrixes on mandibular alveolar mucosa lesion healing
DOI:
https://doi.org/10.12775/JEHS.2020.10.06.040Keywords
amniotic membrane, PRP growth factors, hyaluronic acid, epithelization, wound healingAbstract
Periodontal diseases is one of the most relevant and important problem in modern dentistry due to their increasing prevalence in population, association with the occurrence of focus of chronic infection, progressive development and irreversibility which, in case of severe damage of periodontal tissues, eventually leads to a loss of the number of teeth. All of the named factors eventually lead to the development of irreversible inflammatory-dystrophic and destructive changes in periodontal tissues. During the recent years the method of guided tissue regeneration that uses membranes is being successfully used for the treatment of periodontal diseases.
A comparative study on the mandibular alveolar mucosa lesion healing during application of different types of biological matrixes containing decellularized amniotic membrane, decellularized amniotic membrane in combination with platelet-rich plasma (PRP) growth factors, and decellularized amniotic membrane in combination with PRP growth factors and hyaluronic acid was performed. The study proved the acceleration of the processes of wound area reduction. Under experimental conditions, the wound healing lasted from day 3 to day 5 of the study; however, the rate of reduction of the wound area was slower, which indicates an alterative stage of the acute inflammatory process. During days 5 – 7 (stage of regeneration, the 2nd phase of wound process) the wound area reduced rapidly and by day14 a complete epithelization of the surgical wound was observed in all groups using decellularized amniotic membrane. In the group using the combination of PRP growth factors and hyaluronic acid the epithelization of wound was already observed on the day5. In the control group healing occurres with scar formation.
References
Jiménez-Sánchez M.C., Cabanillas-Balsera D., Areal-Quecuty V., Velasco-Ortega E., Martín-González J., Segura-Egea J.J. Cardiovascular diseases and apical periodontitis: association not always implies causality. Med. Oral Patol. Oral Cir. Bucal. 2020; 25(5): 652-659.
Pietropaoli D., Monaco A., D'Aiuto F., Muñoz Aguilera E., Ortu E., Giannoni M., Czesnikiewicz-Guzik M., Guzik T.J., Ferri C., Del Pinto R. Active gingival inflammation is linked to hypertension. J. Hypertens. 2020; 38(10): 2018-2027.
Scannapieco F.A., Gershovich E. The prevention of periodontal disease - An overview. Periodontol. 2000. 2020; 84(1): 9-13.
Sczepanik F.S.C., Grossi M.L., Casati M., Goldberg M., Glogauer M., Fine N., Tenenbaum H.C. Periodontitis is an inflammatory disease of oxidative stress: We should treat it that way. Periodontol 2000. 2020; 84(1): 45-68.
Du Q., Ma X. Research progress of correlation between periodontal pathogens and systemic diseases. Nan Fang Yi Ke Da Xue Xue Bao. 2020; 40(5): 759-764.
Wang M., Xie J., Wang C., Zhong D., Xie L., Fang H. Immunomodulatory Properties of Stem Cells in Periodontitis: Current Status and Future Prospective. Stem Cells Int. 2020; 2020: 9836518. doi: 10.1155/2020/9836518. eCollection 2020.
Wang J., Yang X., Zou X., Zhang Y., Wang J., Wang Y. Relationship between periodontal disease and lung cancer: A systematic review and meta-analysis. J. Periodontal Res. 2020; 55(5): 581-593.
Kushkevych I., Coufalová M., Vítězová M., Rittmann S.K.R. Sulfate-Reducing Bacteria of the Oral Cavity and Their Relation with Periodontitis-Recent Advances. J. Clin. Med. 2020; 9(8): 2347. doi: 10.3390/jcm9082347.
Möller B., Kollert F., Sculean A., Villiger P.M. Infectious Triggers in Periodontitis and the Gut in Rheumatoid Arthritis (RA): A Complex Story About Association and Causality. Front Immunol. 2020 ; 11: 1108. doi: 10.3389/fimmu.2020.01108. eCollection 2020.
Foz A.M., Artese H.P., Horliana A.C., Pannuti C.M., Romito G.A. Occlusal adjustment associated with periodontal therapy--a systematic review. J. Dent. 2012; 40(12):1025-1035.
Beck J.D., Papapanou P.N., Philips K.H., Offenbacher S. Periodontal Medicine: 100 Years of Progress. J. Dent. Res. 2019; 98(10): 1053-1062
Krawiec M., Dominiak M. The role of vitamin D in the human body with a special emphasis on dental issues: Literature review. Dent. Med. Probl. 2018; 55(4): 419-424
Woelber J.P., Tennert C. Chapter 13: Diet and Periodontal Diseases. Monogr. Oral Sci. 2020; 28: 125-133.
Gruber R. Osteoimmunology: Inflammatory osteolysis and regeneration of the alveolar bone. J. Clin. Periodontol. 2019; 46(21): 52-69
Omar O., Elgali I., Dahlin C., Thomsen P. Barrier membranes: More than the barrier effect? J. Clin. Periodontol. 2019; 46 (Suppl Suppl 21): 103-123.
Zhuang Y., Lin K., Yu H. Advance of Nano-Composite Electrospun Fibers in Periodontal Regeneration. Front. Chem. 2019; 7: 495. doi: 10.3389/fchem.2019.00495. eCollection 2019.
Al-Khateeb R., Prpic J. Hyaluronic acid: the reason for its variety of physiological and biochemical functional properties. Appl. Clin. Res. Clin. Trials Regul. Aff. 2019;6:112–159.
El Sheshtawy A.S., Nazzal H., El Shahawy O.I., El Baz A.A., Ismail S.M., Kang J., Ezzat K.M. The effect of platelet-rich plasma as a scaffold in regeneration/revitalisation endodontics of immature permanent teeth assessed using 2-dimensional radiographs and Cone Beam Computed Tomography: A randomised controlled trial. Int. Endod. J. 2020; 53(7): 905-921.
Wilshaw S.P., Kearney J.N., Fisher J., Ingham E. Production of an acellular amniotic membrane matrix for use in tissue engineering. Tissue Eng. 2006; 12: 2117-2129.
Alagl A., Bedi S., Hassan K., Al Humaid J. Use of platelet-rich plasma for regeneration in non-vital immature permanent teeth: clinical and cone-beam computed tomography evaluation. J. Int. Med. Res. 2017; 45, 583-593.
Bezgin T., Yilmaz A.D., Celik B.N., Kolsuz M.E., Sonmez H. Efficacy of platelet-rich plasma as a scaffold in regenerative endodontic treatment. J. Endodontics. 2015; 41: 36-44.
Anitua E., Sanchez M., Merayo-Lloves J., De la Fuente M., Muruzabal F., Orive G. Plasma rich in growth factors (PRGF-Endoret) stimulates proliferation and migration of primary keratocytes and conjunctival fibroblasts and inhibits and reverts TGF-beta1-Induced myodifferentiation. Invest. Ophthalmol. Vis. Sci. 2011; 52(9): 6066-6073.
Holmes H.L., Wilson B., Goerger J.P., Silverberg J.L., Cohen I., Zipfel W.R., Fortier L.A. Facilitated recruitment of mesenchymal stromal cells by bone marrow concentrate and platelet rich plasma. PLoS One. 2018; 3(3): e0194567. doi: 10.1371/journal.pone.0194567. eCollection 2018.
Castillo-Cardiel G., Medina-Quintana V.M., Lomelí-Enríquez M., Medrano-Muñoz F., Guerrero-Velázquez C., Contreras-López C.K., Fuentes-Orozco C., Irusteta-Jiménez L., Michel-Espinoza L.R., González-Ojeda A. Platelet-rich plasma and its effect in bone regeneration in mandibular fractures. Controlled clinical trial. Gac. Med. Mex. 2017; 153(4): 459-465.
Popova L.N. How the boundaries of the formed epidermis change during wound healing. PhD (Med) Thesis. Voronezh. 1942: 14 p [In Russian].
Kuzin M.I., Kostyuchenok B.A. Wounds and Wound Infection: A Guide for Physicians. Medicine: Moscow, 1990: 592 p [In Russian].
Downloads
Published
How to Cite
Issue
Section
License
The periodical offers access to content in the Open Access system under the Creative Commons Attribution-NonCommercial-ShareAlike 4.0
Stats
Number of views and downloads: 432
Number of citations: 0