DOI:
10.37988/1811-153X_2023_4_140Evaluation of the influence of connective tissue dysplasia on morphologic and biochemical rearrangements in the organic and mineral matrix of lower third molars at different stages of eruption
Downloads
Abstract
Purpose of the work is to evaluate the maturity of the hard tissues of the lower third molars at different stages of eruption in connective tissue dysplasia, based on the results of microscopic and biochemical methods.Material and methods.
The study involved 84 women in the age groups 14—17, 18—21, 22—26, 27—31, 32—36 years with and without connective tissue dysplasia who had teeth 38, 48, which were at different stages of eruption, extracted for orthodontic or emergency indications. After preparation of dentin, enamel and enamel-dentin junction samples according to our own methods, microscopic examination was carried out using a scanning electron microscope Jeol JCM-5700, the morphology of dental hard tissues was evaluated on a longitudinal section, as well as biochemical examination by IR spectroscopy, the position and intensity of absorption bands (AB) were determined at all stages.
Results.
Statistically significant differences between age groups in CTD were found in the superficial section: in the age group 22—26 years at the stages of rudiment (p=0.0001), up to the gingival level (p=0.02), up to the level of the crown of the second molar (p=0.002); in the age group 14—17 years at the stage of eruption up to the level of the crown of the second molar (p=0.0200). In the deep section, differences were established only at the age of 14—17 years at the stage up to the level of the crown of the second molar (p=0.0200). The intensity of AB phosphate (967 cm−1) decreases in CTD at all stages of eruption except for the rudimentary stage, but it is at this stage that the intensity of AB 1050 cm−1 also decreases, which generally indicates a decrease in the mineral content of dental hard tissues in CTD. The AB intensity of collagen (1202 and 1249 cm−1) in CTD increases in dentin and decreases in enamel.
Conclusions.
The results of microscopic and biochemical examination of the hard tissues of lower third molars show that the presence of collagen fibers in dentin affects the biochemical and mechanical properties of enamel through enamel-dentin junction, due to strong adhesion and proper packing of collagen fibrils.
Key words:
teething disorder, lower third molar, scanning electron microscopy, spectroscopy, collagen fibers, enamel, dentin, enamel-dentin junctionFor Citation
[1]
Korshunov A.S., Vagner V.D., Belskaya L.V., Kuryatnikov K.N., Serov D.O., Krasnov V.A., Shulmeyster D.D., Bondar I.A. Evaluation of the influence of connective tissue dysplasia on morphologic and biochemical rearrangements in the organic and mineral matrix of lower third molars at different stages of eruption. Clinical Dentistry (Russia). 2024; 26 (4): 140—150. DOI: 10.37988/1811-153X_2023_4_140
References
- Bankole O.O., Lawal F.B. Teething. Int Q Community Health Educ. 2017; 37 (2): 99—106. PMID: 28511599
- Choukroune C. Tooth eruption disorders associated with systemic and genetic diseases: clinical guide. Journal of Dentofacial Anomalies and Orthodontics. 2017; 20 (4): 402. DOI: 10.1051/odfen/2018129
- Yu Y., Cui C., Guan S.Y., Xu R.S., Zheng L.W., Zhou X.D., Fan Y. Function of orofacial stem cells in tooth eruption: An evolving perspective. Chin J Dent Res. 2021; 24 (3): 143—152. PMID: 34491008
- Wise G.E., King G.J. Mechanisms of tooth eruption and orthodontic tooth movement. J Dent Res. 2008; 87 (5): 414—34. PMID: 18434571
- Kjær I. Mechanism of human tooth eruption: review article including a new theory for future studies on the eruption process. Scientifica (Cairo). 2014; 2014: 341905. PMID: 24688798
- Ippolitov Yu.A., Ippolitov I.Yu., Seredin P.V. Morphology of the human dental enamel. Indian Journal of Dentistry. 2014; 5: 135—139. DOI: 10.1016/j.ijd.2014.03.004
- Korshunov A., Vagner V., Konev V., Moskovskiy S., Kuryatnikov K., Skurikhina A., Yakovlev V., Nurakhmetova A. Research of connective tissue dysplasia influence on teething. Saudi Dent J. 2022; 34 (5): 385—389. PMID: 35814839
- Leontev V.K. Dental enamel as biocybernetic system. Moscow: GEOTAR-Media, 2016. 72 p. (In Russian). eLIBRARY ID: 26074164
- Shumilovich B.R., Vorob'yeva Yu.B., Malykhina I.E., Chertovskikh A.V. Modern views on the crystal structure of hydroxyapatite and processes age-related changes of tooth enamel (in vitro study). Journal of Anatomy and Histopatology. 2015; 1: 77—86 (In Russian). eLIBRARY ID: 23570153
- Lacruz R.S., Habelitz S., Wright J.T., Paine M.L. Dental enamel formation and implications for oral health and disease. Physiol Rev. 2017; 97 (3): 939—993. PMID: 28468833
- Jussila M., Thesleff I. Signaling networks regulating tooth organogenesis and regeneration, and the specification of dental mesenchymal and epithelial cell lineages. Cold Spring Harb Perspect Biol. 2012; 4 (4): a008425. PMID: 22415375
- McGuire J.D., Walker M.P., Mousa A., Wang Y., Gorski J.P. Type VII collagen is enriched in the enamel organic matrix associated with the dentin-enamel junction of mature human teeth. Bone. 2014; 63: 29—35. PMID: 24594343
- Korshunov A.S., Konev V.P., Vagner V.D., Kuryatnikov K.N., Skurikhina A.P., Gafner L.V., Bondar A.A., Sergeev V.I. Facial and dental status of a human with connective tissue dysplasia. Medical and pharmaceutical journal Pulse. 2020; 11: 95—99 (In Russian). eLIBRARY ID: 44335839
- Kalmin O.V., Zyulkina L.A., Ivanov P.V., Malanyin I.V.Sex difference in craniofacial, odontometrical indices and peculiarities of masticatory apparatus reduction at penza and penza region inhabitants. Journal of New Medical Technologies. 2010; 17 (2): 298—300 (In Russian). eLIBRARY ID: 16459674
- Monalisa W., Kokila G., Sharma H.D., Gopinathan P.A., Singh O.M., Kumaraswamy S. Sexual dimorphism of enamel area, coronal dentin area, bicervical diameter and dentinoenamel junction scallop area in longitudinal ground section. J Oral Maxillofac Pathol. 2018; 22 (3): 423—429. PMID: 30651693
- Shaweesh A.I. Duration and rate of clinical eruption of third molars. Dental Oral Biology and Craniofacial Research. 2019; 2 (1): 1—5. DOI: 10.31487/j.DOBCR.2019.01.002
- Korshunov A.S., Vagner V.D., Kuryatnikov K.N., Serov D.O., Torohov A.L., Shykhalieva D.D., Sarf E.A., Bel’skaya L.V. Infrared Spectroscopy to Analyze Sexual Dimorphism of Hard Dental Tissue Maturation at Eruption in Patients with Connective Tissue Dysplasia. Appl Spectrosc. 2023; 77 (5): 457—469. PMID: 36765457
- Korshunov A.S., Vagner V.D., Kuryatnikov K.N., Meloyan A.D., Kasiy M.N., Sarf E.A., Bel’skaya L.V. IR-spectroscopic analysis of hard tissues of lower “wisdom” teeth at the eruption stage of connective tissue dysplasia. Journal of Applied Spectroscopy. 2022; 89 (4): 689—697. DOI: 10.1007/s10812-022-01410-9
- Vagner V.D., Korshunov A.S., Kuryatnikov K.N., Rogachev E.A., Belskaya L.V., Sarf E.A., Maksimenko K.A. The nature of metabolic processes in human dental hard tissues depending on their morphological structure. Stomatology. 2022; 6: 7—13 (In Russian). eLIBRARY ID: 50005723
- Risnes S., Li C. Aspects of the final phase of enamel formation as evidenced by observations of superficial enamel of human third molars using scanning electron microscopy. Arch Oral Biol. 2018; 86: 72—79. PMID: 29190456
- Iijima M., Moradian-Oldak J. Interactions of amelogenins with octacalcium phosphate crystal faces are dose dependent. Calcif Tissue Int. 2004; 74 (6): 522—31. PMID: 15354860
- Du C., Falini G., Fermani S., Abbott C., Moradian-Oldak J. Supramolecular assembly of amelogenin nanospheres into birefringent microribbons. Science. 2005; 307 (5714): 1450—4. PMID: 15746422
- Silin A.V., Terekhov A.Yu., Andreevskaya M.V., Maryanovich A.T. Proteins of mineralized dental tissues. Russian Biomedical Research. 2022; 7 (2): 53—68. DOI: 10.56871/1744.2022.70.82.005
Downloads
Received
September 21, 2023
Accepted
November 21, 2023
Published on
January 16, 2024