Preview

Medical alphabet

Advanced search
Open Access Open Access  Restricted Access Subscription or Fee Access

Assessment of the state of mineral metabolism in patients with tooth loss during dental implantation against the background of vitamin D deficiency

https://doi.org/10.33667/2078-5631-2024-28-60-64

Abstract

   Background. The widespread occurrence of mineral metabolism disorders in the modern world, including those due to vitamin D deficiency, affects the results of patient rehabilitation performed by dental surgeons using dental implants.

   The aim of the study was to assess the state of mineral metabolism during dental implantation in young and middle-aged patients with tooth loss due to vitamin D deficiency.

   Materials and methods. From 2011 to 2024, 450 patients aged 25–50 years with tooth loss due to identified vitamin D deficiency in the absence of other somatic pathology were examined and treated at Sechenov University and a private clinic. All patients underwent laboratory examination, including assessment of mineral metabolism indicators – the level of total calcium, vitamin D (25 (OH) D), parathyroid hormone, thyroid stimulating hormone. Also, 30 randomly selected patients underwent assessment of osteogenesis markers (bone matrix formation marker P1NP, serum cross-linked C-telopeptide of type I collagen CTX). Patients were referred to an endocrinologist due to detected vitamin D deficiency, therapy was prescribed. All patients underwent dental implantation and concomitant surgeries to increase bone volume, if necessary, considering the study group: in group 1 – until reference values of vitamin D were achieved, in group 2 – after. Comparison of parameters before and after drug therapy was performed using Student’s T-test or Mann-Whitney, the results were considered statistically significant at p < 0.05.

   Results. In the examined sample, 2.1 % of patients had a pronounced deficiency of (25(OH)D) (< 10 ng/ml), 60.4 % had a deficiency (< 20 ng/ml), and 37.5 % had insufficiency (20–30 ng/ml), with the initial level of vitamin D in both study groups not statistically different (< 20 ng/ml, p < 0.05). After the treatment, the level of (25(OH)D) in all patients reached the reference values (30–60 ng/ml, p < 0.05) also without statistically significant difference when compared by groups (median 1 = 42.75 and median 2 = 43.65, respectively, p > 0.05), but was significantly higher when assessed dynamically within each
group (p < 0.05). No deviations from reference values for osteogenesis markers were found over time, although a statistically significant slight decrease in both parameters within the normal range was noted after treatment compared to the initial level (p < 0.05).

   Conclusion. In young and middle-aged patients with tooth loss due to vitamin D deficiency, no significant changes in laboratory parameters (blood calcium levels, parathyroid hormone, and osteogenesis markers over time) were found during dental implantation and concomitant surgeries.

About the Authors

E. Yu. Diachkova
I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Ekaterina Yuryevna Diachkova, Candidate of Medical Sciences, Associate Professor

E.V. Borovsky Institute of Dentistry; Surgical Dentistry of Department

Moscow



M. M. Skachkova
I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Marina Mikhailovna Skachkova, 5th year student

E.V. Borovsky Institute of Dentistry

Moscow



S. V. Tarasenko
I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Svetlana V. Tarasenko, MD, Professor, Head of the Department

E.V. Borovsky Institute of Dentistry; Department of Surgical Dentistry

Moscow

AuthorID: 701143



K. Yu. Zharova
REAVIZ Medical University
Russian Federation

Karina Yusufovna Zharova, student

medical faculty

Moscow



E. N. Kytko
I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Elizaveta Nikolaevna Kytko, 1st year student

F.F. Erisman Institute of Public Health

Moscow



References

1. Gun’ko, M. V. Osteoporosis and dental implantation / M. V. Gun’ko // Stomatology. – 2009. – Vol. 88, No. 6. – P. 73–78. – EDN: LFTRAR.

2. Yanushevich O., Kozlova M., Kozlova L., Belyakova A. Comparative evaluation of cone-beam computed tomography and histological studies of bone tissue of jaws. Endodontics Today. 2014;12(3):49–53.

3. Mashchenko E.A., Khesin R.A., Malichenko S.B., Kozlova M.V. Efficacy of the comprehensive antiresorptive therapy at different stages of surgical rehabilitation in dentition defects in female patients with postmenopausal osteoporosis. Mediko-sotsyal’naya ekspertiza i reabilitatsiya (Medical and Social Expert Evaluation and Rehabilitation, Russian Journal). 2016; 19(2):71–79. (In Russ.) DOI: 10.18821/1560-9537-2016-19-2-71-79.

4. Tsolaki I. N., Madianos P. N., Vrotsos J. A. Outcomes of Dental Implants in Osteoporotic Patients. A Literature Review // Journal of Prosthodontics on Dental Implants. – 2015. – P. 235–253.

5. Merheb, J., Temmerman, A., Rasmusson, L. et al. Influence of Skeletal and Local Bone Density on Dental Implant Stability in Patients with Osteoporosis // Clinical implant dentistry and related research. – 2016. – Vol. 18. – №. 2. – P. 253–260.

6. Camargo W. A. Takemoto, S., Hoekstra, J. W. et al. Effect of surface alkali-based treatment of titanium implants on ability to promote in vitro mineralization and in vivo bone formation // Acta biomaterialia. – 2017. – Vol. 57. – P. 511–523.

7. De Medeiros F., Kudo GAH, Leme BG et al. Dental implants in patients with osteoporosis : a systematic review with meta-analysis // International journal of oral and maxillofacial surgery. – 2018. – Vol. 47. – №. 4. – P. 480–491.

8. Osteodensitometry: methodological recommendations // Godzenko AV et al. // M.: NPC medical radiology – 2017.

9. Osteoporosis / A. T. Andreeva, I. A. Baranova, J. E. Belaya [et al.]. – 2<sup>nd</sup> edition, revised and supplemented. – Moscow : Limited Liability Company Publishing Group GEOTAR-Media, 2023. – 752 p. – ISBN 978-5-9704-7145-6. – EDN: NTJNKM.

10. Alsulaimani L, Alqarni A, Almarghlani A, et al. The relationship between low serum vitamin D level and early dental implant failure : a systematic review // Cureus. – 2022. – Vol. 14. – №. 1.

11. Schwarz F., Derks J., Monje A., & Wang, H. L. Peri-implantitis. Journal of clinical periodontology. 2018; 45: S246–S266.

12. Dalago HR, Schuldt Filho G, Rodrigues MA et al. Risk indicators for peri-implantitis. A cross-sectional study with 916 implants. Clin Oral Implants Res. 2017;28:144–150.

13. Dvorak G, Arnhart C, Heuberer S, et al. Peri-implantitis and late implant failures in postmenopausal women: a cross-sectional study. J Clin Periodontol. 2011;38:950–955.

14. Kozlova M.V. Atrophy of the alveolar part and process of the jaws in osteopenic syndrome in patients with thyroid pathology and hypogonadism: modern methods of diagnosis and treatment : abstract of the dissertation of the Doctor of Medical Sciences: 14.00.21, 14.00.03; [Place of protection: Moscow State Medical Dentist. un-t]. – Moscow, 2009. – 46 p.

15. Diachkova E.Yu., Tarasenko S.V., Do Phan Ngoc Minh et al. Surgical treatment of patient with secondary partly absence of the teeth on the background of disturbances of bone mineral metabolism with dental implants // Endodontics Today. – 2019. – Vol. 17, № 2. – P. 65-70. – DOI: 10.33925/1683-2981-2019-17-2-65-70 – EDN: SYVIRD.

16. Diachkova E.Yu., Tarasenko S.V., Fadeev V.V. et al. Analysis of the dental implantation results according to the dentists’ questionnaire data on the example of the russian federation separate subject. Head and neck. Russian Journal. 2022; 10 (2, Suppl. 2): 46–49. – DOI: 10.37988/1811-153X_2022_3_32 – EDN: LPEPIZ. (In Russian).

17. Morozova E.A. The use of a neodymium laser in surgical dentistry : dis. Doctor of Medical Sciences; Moscow, 2022: I.M. Sechenov First Moscow State Medical University (Sechenov University) – 341 page.

18. Trybek G, Aniko-Wlodarczyk M, Kwiatek J et al. The effect of vitamin D3 on the osteointegration of dental implants. Balt J Health Phys Act. 2018;10(4):25–33. doi: 10.29359/BJHPA.10.4.02.

19. Salari N., Ghasemi H, Mohammadi L, et al. The global prevalence of osteoporosis in the world : a comprehensive systematic review and meta-analysis // Journal of orthopedic surgery and research. – 2021. – Vol. 16. – P. 1–20.

20. Marcucci G., Brandi M. L. Rare causes of osteoporosis // Clinical cases in mineral and bone metabolism. – 2015. – Vol. 12. – № 2. – P. 151.

21. Kwiatek J., Jaroń A., Trybek G. Impact of the 25-hydroxycholecalciferol concentration and vitamin D deficiency treatment on changes in the bone level at the implant site during the process of osseointegration: A prospective, randomized, controlled clinical trial // Journal of Clinical Medicine. – 2021. – Vol. 10. – №. 3. – P. 526.

22. Mangano F.G., Oskouei S.G., Paz A. et al. Low serum vitamin D and early dental implant failure: Is there a connection? A retrospective clinical study on 1740 implants placed in 885 patients. Journal of dental research, dental clinics, dental prospects. 2018; 12(3):174. doi: 10.15171/joddd.2018.027

23. Werny J. G., Sagheb K, Diaz L, et al. Does vitamin D have an effect on osseointegration of dental implants? A systematic review // International Journal of Implant Dentistry. – 2022. – Vol. 8. – № 1. – P. 16.

24. Pimentel S. P., Casarin R. C., Ribeiro F. V. et al. Impact of micronutrients supplementation on bone repair around implants: microCT and counter-torque analysis in rats // Journal of Applied Oral Science. – 2016. – Vol. 24. – P. 45–51.

25. Mahdavi, R., Belgheisi, G., Haghbin-Nazarpak, M. et al. Bone tissue engineering gelatin–hydroxyapatite/graphene oxide scaffolds with the ability to release vitamin D: Fabrication, characterization, and in vitro study // Journal of Materials Science: Materials in Medicine. – 2020. – Vol. 31. – P. 1–14.

26. Nastri, L., Moretti, A., Migliaccio S. et al. Do dietary supplements and nutraceuticals have effects on dental implant osseointegration? A scoping review // Nutrients. – 2020. – Vol. 12. – №. 1. – P. 268.

27. Muresan, G. C., Hedesiu, M., Lucaciu, O. et al. Effect of vitamin D on bone regeneration : a review //Medicina. – 2022. – Vol. 58. – №. 10. – P. 1337.

28. Garg, P., Ghalaut, P., Dahiya, K. et al. Comparative evaluation of crestal bone level in patients having low level of Vitamin D treated with dental implant with or without Vitamin D3 supplements // National Journal of Maxillofacial Surgery. – 2020. – Vol. 11. – №. 2. – P. 199.

29. Chang S. W., Lee H. C. Vitamin D and health-The missing vitamin in humans // Pediatrics & Neonatology. – 2019. – Vol. 60. – № 3. – P. 237}244.

30. Fischer, V., Haffner-Luntzer, M., Prystaz, K. et al. Calcium and vitamin-D deficiency marginally impairs fracture healing but aggravates posttraumatic bone loss in osteoporotic mice // Scientific reports. – 2017. – Vol. 7. – № 1. – P. 7223.


Review

For citations:


Diachkova E.Yu., Skachkova M.M., Tarasenko S.V., Zharova K.Yu., Kytko E.N. Assessment of the state of mineral metabolism in patients with tooth loss during dental implantation against the background of vitamin D deficiency. Medical alphabet. 2024;(28):60-64. (In Russ.) https://doi.org/10.33667/2078-5631-2024-28-60-64

Views: 114


ISSN 2078-5631 (Print)
ISSN 2949-2807 (Online)