Cancer Res Treat.  2021 Jan;53(1):252-260. 10.4143/crt.2020.275.

The Broad Variability in Dental Age Observed among Childhood Survivors Is Cancer Specific

Affiliations
  • 1Department of Pediatric Dentistry, Medical University of Lodz, Lodz, Poland
  • 2Department of Pediatrics, Diabetology, Endocrinology and Nephrology, Medical University of Lodz, Lodz, Poland
  • 3Department of Pediatrics, Oncology and Hematology, Medical University of Lodz, Lodz, Poland

Abstract

Purpose
The study aimed to assess the differences in dental maturation between childhood cancer survivors and healthy children.
Materials and Methods
Fifty-nine cancer patients including 16 (27.1%) girls and 43 (72.8%) boys, aged between 4 and 16 years, underwent dental and radiographic examinations. The mean duration of anticancer therapy was 16.8 months (range, 1 to 47 months), and 4.6 years (range, 8 to 123 months) had passed since the termination of disease. The control group consisted of 177 panoramic radiographs of age- and sex-matched healthy individuals. Dental age (DA) was estimated with Demirjian’s scale and delta age, i.e., DA–chronological age (CA), was used to compare groups.
Results
The DA of cancer survivors was accelerated by almost 1 year compared to their CA (9.9±3.1 vs. 8.9±2.8, p=0.040). The greatest difference was observed among patients with brain tumor: delta (DA–CA) was 2.2±1.1 years. Among all cancer patients, only children with familial adenomatous polyposis (FAP)-associated hepatoblastoma (HP) demonstrated delayed DA, with regard to both other cancer survivors (p=0.011) and healthy patients (p=0.037). All four patients with HP suffered from FAP, and three of them had documented adenomatous polyposis coli (APC) genes mutation. The DA of cancer patients having teeth with short roots was significantly greater than that of the cancer survivors without this anomaly (12.8±3.2 vs. 9.0±2.4, p < 0.001).
Conclusion
DA in children may be altered by cancer disease.

Keyword

Cancer survivors; Dental age estimation; Hepatoblastoma; APC genes

Figure

  • Fig. 1. Diagram of Demirjian’s classification. Stage description (Demirjian et al. Hum Biol. 1973;45:211-27 [7]). (A) In both radicular and multiradicular teeth, a beginning of calcification is seen at the superior level of the crypt in the form of an inverted cone or cones. There is no fusion of these calcified points. (B) Fusion of the calcified points forms one or several cusps which unite to give a regularly outlined occlusal surface. (C) Enamel formation is complete at the occlusal surface. Its extension and convergence towards the cervical region is seen. The beginning of a dentinal deposit is seen. The outline of the pulp chamber has a curved shape at the occlusal border. (D) The crown formations completed down to the cemento-enamel junction. The superior border of the pulp chamber in the uniradicular teeth has a definite curved form, being concave towards the cervical region. The projection of the pulp horns if present, gives an outline shaped like an umbrella top. In molars the pulp chamber has a trapezoidal form. Beginning of root formation is seen in the form of a spicule. (E) Uniradicular teeth: The walls of the pulp chamber now form straight lines, whose continuity is broken by the presence of the pulp horn, which is larger than in the previous stage. The root length is less than the crown height. Molars: Initial formation of the radicular bifurcation is seen in the form of either a calcified point or a semi-lunar shape. The root length is still less than the crown height. (F) Uniradicular teeth: The walls of the pulp chamber now form a more or less isosceles triangle. The apex ends in a funnel shape. The root length is equal to or greater than the crown height. Molars: The calcified region of the bifurcation has developed further down from its semi-lunar stage to give the roots a more definite and distinct outline with funnel shaped endings. The roots length is equal to or greater than the crow height. (G) The walls of the root canal are now parallel and its apical end is still partially open (distal root in molars). (H) The apical end of the root canal is completely closed (distal root in molars). The periodontal membrane has a uniform width around the root and the apex.

  • Fig. 2. Differences in dental age to chronological age between cancer survivors and control patients.

  • Fig. 3. Values of delta dental age to chronological age in patients with different types of cancer (A) and hepatoblastoma compared to the healthy patients and other cancer patients (B). Gray zone represents interquartile range for healthy controls.

  • Fig. 4. Differences in dental age to chronological age in cancer patients according to tooth abnormalities: short roots (A), microdontic teeth (B), and hypodontia (C).


Reference

References

1. Zubowska M, Wyka K, Fendler W, Mlynarski W, Zalewska-Szewczyk B. Interleukin 18 as a marker of chronic nephropathy in children after anticancer treatment. Dis Markers. 2013; 35:811–8.
Article
2. Kang CM, Hahn SM, Kim HS, Lyu CJ, Lee JH, Lee J, et al. Clinical risk factors influencing dental developmental disturbances in childhood cancer survivors. Cancer Res Treat. 2018; 50:926–35.
Article
3. Proc P, Szczepanska J, Skiba A, Zubowska M, Fendler W, Mlynarski W. Dental anomalies as late sdverse rffect among young children treated for cancer. Cancer Res Treat. 2016; 48:658–67.
4. Kawakami T, Nakamura Y, Karibe H. Cyclophosphamide-induced morphological changes in dental root development of ICR mice. PLoS One. 2015; 10:e0133256.
Article
5. Kaste SC, Goodman P, Leisenring W, Stovall M, Hayashi RJ, Yeazel M, et al. Impact of radiation and chemotherapy on risk of dental abnormalities: a report from the Childhood Cancer Survivor Study. Cancer. 2009; 115:5817–27.
6. Avery JK, Steele PF, Avery N. Oral development and histology. 3rd ed. Stuttgart: Thieme;2002.
7. Demirjian A, Goldstein H, Tanner JM. A new system of dental age assessment. Hum Biol. 1973; 45:211–27.
8. Holtta P, Alaluusua S, Saarinen-Pihkala UM, Peltola J, Hovi L. Agenesis and microdontia of permanent teeth as late adverse effects after stem cell transplantation in young children. Cancer. 2005; 103:181–90.
Article
9. Holtta P, Hovi L, Saarinen-Pihkala UM, Peltola J, Alaluusua S. Disturbed root development of permanent teeth after pediatric stem cell transplantation. Dental root development after SCT. Cancer. 2005; 103:1484–93.
10. Martin MB, Li CS, Rowland CC, Howard SC, Kaste SC. Correlation of bone age, dental age, and chronological age in survivors of childhood acute lymphoblastic leukaemia. Int J Paediatr Dent. 2008; 18:217–23.
Article
11. van der Pas-van Voskuilen IG, Veerkamp JS, Raber-Durlacher JE, Bresters D, van Wijk AJ, Barasch A, et al. Long-term adverse effects of hematopoietic stem cell transplantation on dental development in children. Support Care Cancer. 2009; 17:1169–75.
Article
12. Flores AP, Monti CF, Brunotto M. Dental and chronological age in children under oncological treatment. J Forensic Sci. 2015; 60:453–6.
Article
13. Tomas LF, Monico LS, Tomas I, Varela-Patino P, Martin-Biedma B. The accuracy of estimating chronological age from Demirjian and Nolla methods in a Portuguese and Spanish sample. BMC Oral Health. 2014; 14:160.
Article
14. Rozylo-Kalinowska I, Kiworkowa-Raczkowska E, Kalinowski P. Dental age in Central Poland. Forensic Sci Int. 2008; 174:207–16.
15. Sobieska E, Fester A, Nieborak M, Zadurska M. Assessment of the dental age of children in the Polish population with comparison of the Demirjian and the Willems methods. Med Sci Monit. 2018; 24:8315–21.
Article
16. Chudasama PN, Roberts GJ, Lucas VS. Dental age assessment (DAA): a study of a Caucasian population at the 13 year threshold. J Forensic Leg Med. 2012; 19:22–8.
Article
17. Esan TA, Schepartz LA. The timing of permanent tooth development in a Black Southern African population using the Demirjian method. Int J Legal Med. 2019; 133:257–68.
Article
18. Wang J, Bai X, Wang M, Zhou Z, Bian X, Qiu C, et al. Applicability and accuracy of Demirjian and Willems methods in a population of Eastern Chinese subadults. Forensic Sci Int. 2018; 292:90–6.
Article
19. Jayaraman J, Roberts GJ. Comparison of dental maturation in Hong Kong Chinese and United Kingdom Caucasian populations. Forensic Sci Int. 2018; 292:61–70.
Article
20. Chehab DA, Tanbonliong T, Peyser J, Udin R. Association between body mass index and dental age in Hispanic children. Gen Dent. 2017; 65:54–8.
21. Hashim HA, Mansoor H, Mohamed MH. Assessment of skeletal age using hand-wrist radiographs following Bjork system. J Int Soc Prev Community Dent. 2018; 8:482–7.
22. Ferrandez A, Carrascosa A, Audi L, Baguer L, Rueda C, Bosch-Castane J, et al. Longitudinal pubertal growth according to age at pubertal growth spurt onset: data from a Spanish study including 458 children (223 boys and 235 girls). J Pediatr Endocrinol Metab. 2009; 22:715–26.
Article
23. Brinksma A, Roodbol PF, Sulkers E, Kamps WA, de Bont ES, Boot AM, et al. Changes in nutritional status in childhood cancer patients: a prospective cohort study. Clin Nutr. 2015; 34:66–73.
Article
24. Paulsson L, Arvini S, Bergstrom N, Klingberg G, Lindh C. The impact of premature birth on dental maturation in the permanent dentition. Clin Oral Investig. 2019; 23:855–61.
Article
25. Giardiello FM, Petersen GM, Brensinger JD, Luce MC, Cayouette MC, Bacon J, et al. Hepatoblastoma and APC gene mutation in familial adenomatous polyposis. Gut. 1996; 39:867–9.
Article
26. Lubinsky M, Kantaputra PN. Syndromes with supernumerary teeth. Am J Med Genet A. 2016; 170:2611–6.
Article
27. Basaran G, Erkan M. One of the rarest syndromes in dentistry: gardner syndrome. Eur J Dent. 2008; 2:208–12.
Article
28. Ruiz-Mealin EV, Parekh S, Jones SP, Moles DR, Gill DS. Radiographic study of delayed tooth development in patients with dental agenesis. Am J Orthod Dentofacial Orthop. 2012; 141:307–14.
Article
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