Stomatologist № 4 (35) – 2019, pp. 20-25 Scientific publications
Dental pathology as a polymorbidity cluster, caused by disturbance
of iron metabolism in patients with β-thalassemia
R.V. Shadlinskaya
MD, PhD, Associate professor, Azerbaijan Medical University, Baku, Azerbaijan
https://doi.org/10.32993/stomatologist.2019.4(35).1
ABSTRACT
The aim of study. This study aimed to determine the dental status during disturbance of iron metabolism in patients with β-thalassemia.
Objects and methods. İron metabolism indicators and dental status were investigated in 58 patients with
homozygous and 17 patients with heterozygous β-thalassemia. The control group consisted of 16 people, without any hereditary and somatic pathology. Excessive amount of iron in the form of ferritin, high level of hepcidin and low level of total iron binding capacity (p < 0.001) were found in homozygous patients. All examined patients with a homozygous β-thalassemia form had progressive dental lesions: chronic and acute stages of periodontal diseases, multiple caries and its complications, characteristic dental-maxillary anomalies (Angle class 2 malocclusions).
Results and discussion. In patients with homozygous β-thalassemia, the accumulation of iron compounds in the form of ferritin increased, and iron binding capacity decreased. The accumulation of excess iron was accompanied by an increasing of hepcidin level in the blood, which was a protective reaction, allowing to reduce the presence of microbes in the focus of inflammation.
Conclusions.. Dental pathology is an equal cluster of polymorbidity, caused by impaired iron metabolism in the homozygous form of β-thalassemia. The dental care is the most important aspect of monitoring of patients with β-thalassemia.
Keywords: dental morbidity, thalassemia, comorbidity, iron metabolism, periodontal disease
References
- De Sanctis V., Kattamis C., Canatan D., et al. β-Thalassemia Distribution in the Old World: an Ancient Disease Seen from a Historical Standpoint. The Mediterranean Journal of Hematology and Infectious Diseases, 2017, vol. 9, no. 1, e2017018, doi:10.4084/MJHID.2017.018
- Thein S.L. The molecular basis of β-thalassemia. Cold Spring Harb Perspect Med., 2013, vol. 1, no. 3, 5 a011700, doi: 10.1101/cshperspect.a011700
- Mosca A., Paleari R., Leone D., Ivaldi G. The relevance of hemoglobin F measurement in the diagnosis of thalassemias and related hemoglobinopathies. ClinBiochem, 2009, vol. 42, no. 18, pp. 1797–1801.
- Weatherall J.D., Clegg J.B. The ThalassaemiaSyndroms // The Thalassaemia Syndroms, 3-rd Edition, Oxford: Blackwell, 2001, р. 132–174.
- Asadov Ch.D. Immunologic Abnormalities in β-Thalassemia. J Blood Disorders Transf., 2014, vol. 5, 224 p.
- Gozzelli R., Arosio P. Iron homeostasis in health and disease. Int. J. Mol. Sci., 2016, vol. 17, no. 1, pp. 130–144, doi: 10.3390/ijms17010130
- Gulieva R.D., Ragimova Je. F., Zejnalova A.A. Vlijanie gemotransfuzij u bolnyh bolshoj ß-talassemiej na obmen zheleza. [Influence of hemotransfusions in patients with large ß-thalassemia on iron metabolism]. Materialy 1-j Respublikanskoj nauchno-prakticheskoj konferencii po sluzhbe krovi, Baku–1996. – Materials of the 1st Republican Scientific and Practical Conference on Blood Service, Baku, 1996, p. 71.
- Liu L., Huang M. Essential role of the iron-sulfur cluster binding domain of the primase regulatory subunit Pri2 in DNA replication initiation. Protein Cell., 2001, vol. 6, no. 3, pp. 194–210, doi:10.1007/s13238-015-0134-8
- Kell Douglas, Pretorius Etheresia. Serum ferritin is an important inflammatory disease marker, as it is mainly a leakage product from damaged cells. Metallomics, 2014, vol. 6, no. 4, pp. 748–753, doi: 10.1039/c3mt00347g.
- Stiban J1., So M., Kaguni L.S. Iron-Sulfur Clusters in Mitochondrial Metabolism: Multifaceted Roles of a Simple Cofactor. Biochemistry (Moscow), 2016, vol. 81, no. 10, pp. 1066–1080, doi: 10.1134/S0006297916100059
- Wessting-Kesnick M. Iron homeostasis and the inflammatory response. AnnuRer. Nutr., 2010, vol. 30, pp. 105–122, doi:10.1146/012809.104804
- McLellan S.A., Walsh T.S. Oxygen delivery and haemoglobin. Continuing Education in Anaesthesia Critical Care & Pain, 2004, vol. 4, no. 4, pp. 123–126, doi: 10.1093/bjaceaccp/mkh033
- Shadlinskaja R.V. Osobennosti stomatologicheskoj zabolevaemosti bolnykh s β-talassemiej. [Oral and dental disease in patients with β-thalassemia]. Parodontologija, Sankt-Peterburg. – Periodontology, St. Petersburg, 2016, vol. 21, no. 1, pp. 22–25.
- Yousif A. Al-Raheem, Mohammed Abdul Hussein, RaadSalih Al-ani, Mehdi Abdul Hadi Al-Rubayee. The Impact of Thalassemia Major on Dental Integrity and Development. MDJ, 2009, vol. 6, No. 4, p. 394.
- Dev S., Babitt J.L. Overview of iron metabolism in health and disease. Hemodialysis International, 2017, vol. 21, no. 1, pp. 6–20.
- Gorbacheva I.A., Kirsanov A.I. Patogeneticheskaja rol sistemnyh mehanizmov svobodnoradikalnogo okislenija pri sochetannyh zabolevanijah vnutrennih organov i parodonta. [Pathogenetic role of systemic mechanisms of free radical oxidation in combined diseases of internal logos and periodontium]. Vestn. Sankt-Peterburg. gos. med. akad. im. I.I. Mechnikova. – Vestnik of the St. Petersburg State Medical Academy I.I. Mechnikov, 2003, no. 3, pp. 135–138.
- Dedova L.N., Denisova Ju.L., Solomevich A.S. Podderzhivajushhaja terapija u pacientov s boleznjami periodontal. [Maintenance therapy of periodontal diseases]. Stomatolog. Minsk. – Stomatologist, Minsk, 2015, no. 4 (19), pp. 75−81.
Correspondence to: E-mail: r.shadlinskaya@yahoo.com