Skip to main content

Advertisement

Log in

Influence of metabolic-linked early life factors on the eruption timing of the first primary tooth

  • Original Article
  • Published:
Clinical Oral Investigations Aims and scope Submit manuscript

Abstract

Aim

Early eruption of permanent teeth has been associated with childhood obesity and diabetes mellitus, suggesting links between tooth eruption and metabolic conditions. This longitudinal study aimed to identify pre-, peri- and postnatal factors with metabolic consequences during infancy that may affect the eruption timing of the first primary tooth (ETFT) in children from an ethnically heterogeneous population residing within the same community.

Material and methods

Participants were recruited (n = 1033) through the GUSTO (Growing Up in Singapore Towards healthy Outcomes) birth cohort (n = 1237). Oral examinations were performed at 3-month intervals from 6 to 18 months of age. Crude and adjusted analyses, with generalized linear modelling, were conducted to link ETFT to potential determinants occurring during pregnancy, delivery/birth and early infancy.

Results

Overall mean eruption age of the first primary tooth was 8.5 (SD 2.6) months. Earlier tooth eruption was significantly associated with infant’s rate of weight gain during the first 3 months of life and increased maternal childbearing age. Compared to their Chinese counterparts, Malay and Indian children experienced significantly delayed tooth eruption by 1.2 and 1.7 months, respectively.

Conclusions

Infant weight gain from birth to 3 months, ethnicity and maternal childbearing age were significant determinants of first tooth eruption timing. Early life influences can affect primary tooth development, possibly via metabolic pathways.

Clinical relevance

Timing of tooth eruption is linked to general growth and metabolic function. Therefore, it has potential in forecasting oral and systemic conditions such as caries and obesity.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Wise GE, Frazier-Bowers S, D’Souza RN (2002) Cellular, molecular, and genetic determinants of tooth eruption. Crit Rev Oral Biol Med 13(4):323–334

    Article  PubMed  Google Scholar 

  2. Kiran K et al (2011) Prevalence of systemic and local disturbances in infants during primary teeth eruption: a clinical study. Eur J Paediatr Dent 12(4):249–252

    PubMed  Google Scholar 

  3. Noor-Mohammed R, Basha S (2012) Teething disturbances; prevalence of objective manifestations in children under age 4 months to 36 months. Med Oral Patol Oral Cir Bucal 17(3):e491–e494

  4. Thesleff I (2006) The genetic basis of tooth development and dental defects. Am J Med Genet A 140(23):2530–2535

    Article  PubMed  Google Scholar 

  5. Koch G, Kreiborg S, Andreasen JO (2009) Eruption and shedding of teeth. In: Koch G, Poulsen S (Eds) Pediatric dentistry: a clinical approach. Wiley-Blackwell, United Kingdom, p 197–211

  6. Seow WK et al (1988) Dental eruption in low birth-weight prematurely born children: a controlled study. Pediatr Dent 10(1):39–42

    PubMed  Google Scholar 

  7. Marks Jr SC, Cahill DR (1987) Regional control by the dental follicle of alterations in alveolar bone metabolism during tooth eruption. J Oral Pathol 16(4):164–169

    PubMed  Google Scholar 

  8. Philbrick WM et al (1998) Parathyroid hormone-related protein is required for tooth eruption. Proc Natl Acad Sci U S A 95(20):11846–11851

    Article  PubMed  PubMed Central  Google Scholar 

  9. Young ER (1989) The thyroid gland and the dental practitioner. J Can Dent Assoc 55(11):903–907

    PubMed  Google Scholar 

  10. Sanchez-Perez L, Irigoyen ME, Zepeda M (2010) Dental caries, tooth eruption timing and obesity: a longitudinal study in a group of Mexican schoolchildren. Acta Odontol Scand 68(1):57–64

    Article  PubMed  Google Scholar 

  11. Must A et al (2012) The association between childhood obesity and tooth eruption. Obesity (Silver Spring) 20(10):2070–2074

  12. Lal S et al (2008) Accelerated tooth eruption in children with diabetes mellitus. Pediatrics 121(5):e1139–e1143

    Article  PubMed  Google Scholar 

  13. Morales E et al (2015) Deficit of vitamin D in pregnancy and growth and overweight in the offspring. Int J Obes (Lond) 39(1):61–68

  14. Kalk P et al (2009) Impact of maternal body mass index on neonatal outcome. Eur J Med Res 14(5):216–222

    PubMed  PubMed Central  Google Scholar 

  15. Boney CM et al (2005) Metabolic syndrome in childhood: association with birth weight, maternal obesity, and gestational diabetes mellitus. Pediatrics 115(3):e290–e296

    Article  PubMed  Google Scholar 

  16. Autti-Ramo I (2000) Twelve-year follow-up of children exposed to alcohol in utero. Dev Med Child Neurol 42(6):406–411

    Article  PubMed  Google Scholar 

  17. Bergmann KE et al (2003) Early determinants of childhood overweight and adiposity in a birth cohort study: role of breast-feeding. Int J Obes Relat Metab Disord 27(2):162–172

    Article  PubMed  Google Scholar 

  18. Vehik K, Dabelea D (2012) Why are C-section deliveries linked to childhood type 1 diabetes? Diabetes 61(1):36–37

  19. Goldani MZ et al (2013) Cesarean section and increased body mass index in school children: two cohort studies from distinct socioeconomic background areas in Brazil. Nutr J 12:104

  20. Low JA, Lindsay BG, Derrick EJ (1997) Threshold of metabolic acidosis associated with newborn complications. Am J Obstet Gynecol 177(6):1391–1394

    Article  PubMed  Google Scholar 

  21. Hernandez MI, Mericq V (2011) Metabolic syndrome in children born small-for-gestational age. Arq Bras Endocrinol Metabol 55(8):583–589

    Article  PubMed  Google Scholar 

  22. de Jong M et al (2014) Components of the metabolic syndrome in early childhood in very-low-birth-weight infants. Horm Res Paediatr 81(1):43–49

    Article  PubMed  Google Scholar 

  23. Stuebe A (2009) The risks of not breastfeeding for mothers and infants. Rev Obstet Gynecol 2(4):222–231

    PubMed  PubMed Central  Google Scholar 

  24. Shaweesh AI, Al-Omiri MK, Alsoleihat FD (2011) Variation in time of emergence of permanent teeth among urban and rural Jordanian school children. Saudi Med J 32(10):1066–1072

    PubMed  Google Scholar 

  25. Thongprasom K (1991) The eruptive period of deciduous dentition of normal Thai children in Bangkok. J Dent Assoc Thai 5:207–213

    Google Scholar 

  26. Thitasomakul S et al (2006) A longitudinal study of early childhood caries in 9- to 18-month-old Thai infants. Community Dent Oral Epidemiol 34(6):429–436

    Article  PubMed  Google Scholar 

  27. Hughes TE et al (2007) Strong genetic control of emergence of human primary incisors. J Dent Res 86(12):1160–1165

    Article  PubMed  Google Scholar 

  28. Soh SE et al (2014) Cohort profile: Growing Up in Singapore Towards healthy Outcomes (GUSTO) birth cohort study. Int J Epidemiol 43(5):1401–1409

    Article  PubMed  Google Scholar 

  29. Alberti KG, Zimmet PZ (1998) Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med 15(7):539–553

    Article  PubMed  Google Scholar 

  30. WHO (2004) Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet 363(9403):157–163

    Article  Google Scholar 

  31. Mikolajczyk RT et al (2011) A global reference for fetal-weight and birthweight percentiles. Lancet 377(9780):1855–1861

  32. Swami D et al (1992) Age estimation from eruption of temporary teeth in Himachal Pradesh. J Forensic Med Toxicol 9(3–4):3–7

    Google Scholar 

  33. Pahkala R, Pahkala A, Laine T (1991) Eruption pattern of permanent teeth in a rural community in northeastern Finland. Acta Odontol Scand 49(6):341–349

    Article  PubMed  Google Scholar 

  34. Arvystas MG (1976) Familial generalized delayed eruption of the dentition with short stature. Oral Surg Oral Med Oral Pathol 41(2):235–243

    Article  PubMed  Google Scholar 

  35. Rami Reddy V, Vijayalakshmi PB, Chndrasekhar BK (1986) Reddy, deciduous tooth emergence and physique of Velama children of southeastern Andhra Pradesh, India. Acta Odontol Pediatr 7(1):1–5

    PubMed  Google Scholar 

  36. Viscardi RM, Romberg E, Abrams RG (1994) Delayed primary tooth eruption in premature infants: relationship to neonatal factors. Pediatr Dent 16(1):23–28

    PubMed  Google Scholar 

  37. Alvarez JO et al (1988) Chronic malnutrition, dental caries, and tooth exfoliation in Peruvian children aged 3–9 years. Am J Clin Nutr 48(2):368–372

    PubMed  Google Scholar 

  38. Alvarez JO et al (1990) The effect of nutritional status on the age distribution of dental caries in the primary teeth. J Dent Res 69(9):1564–1566

    Article  PubMed  Google Scholar 

  39. Symonds ME (2007) Integration of physiological and molecular mechanisms of the developmental origins of adult disease: new concepts and insights. Proc Nutr Soc 66(3):442–450

    Article  PubMed  Google Scholar 

  40. Billewicz WZ et al (1973) The development of primary teeth in Chinese (Hong Kong) children. Hum Biol 45(2):229–241

    PubMed  Google Scholar 

  41. McGill Jr HC et al (1996) Early determinants of adult metabolic regulation: effects of infant nutrition on adult lipid and lipoprotein metabolism. Nutr Rev 54(2 Pt 2):S31–S40

    PubMed  Google Scholar 

  42. Symonds ME et al (2009) Nutritional programming of the metabolic syndrome. Nat Rev Endocrinol 5(11):604–610

    Article  PubMed  Google Scholar 

  43. Low WD et al (1973) Eruption of the deciduous dentition in Chinese children in Hong Kong. Z Morphol Anthropol 65(2):129–142

    PubMed  Google Scholar 

  44. Holman DJ, Jones RE (1991) Longitudinal analysis of deciduous tooth emergence in Indonesian children. I. Life table methodology. Am J Hum Biol 3:389–403

    Article  Google Scholar 

  45. GunaShekhar M, Tenny J (2010) Longitudinal study of age and order of eruption of primary teeth in Indian children. J Clin Exp Dent 2(3):e113–e116

    Article  Google Scholar 

  46. Psoter WJ et al (2003) Median ages of eruption of the primary teeth in white and Hispanic children from Arizona. Pediatr Dent 25(3):257–261

    PubMed  Google Scholar 

  47. Zhang YD et al (2005) Making a tooth: growth factors, transcription factors, and stem cells. Cell Res 15(5):301–316

    Article  PubMed  Google Scholar 

  48. Fatemifar G et al (2013) Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances. Hum Mol Genet 22(18):3807–3817

    Article  PubMed  PubMed Central  Google Scholar 

  49. Vainio S et al (1993) Identification of BMP-4 as a signal mediating secondary induction between epithelial and mesenchymal tissues during early tooth development. Cell 75(1):45–58

    Article  PubMed  Google Scholar 

  50. Kere J et al (1996) X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet 13(4):409–416

    Article  PubMed  Google Scholar 

  51. Savage T et al (2013) Increasing maternal age is associated with taller stature and reduced abdominal fat in their children. PLoS One 8(3):e58869

    Article  PubMed  PubMed Central  Google Scholar 

  52. Garn SM, Lewis AB, Polacheck DL (1960) Interrelations in dental development. I. Interrelationships within the dentition. J Dent Res 39:1049–1055

    Article  PubMed  Google Scholar 

  53. Barker DJP (1998) Mother, babies and health in later life. Churchill Livingstone, Edinburgh

    Google Scholar 

Download references

Acknowledgments

This study was funded by Singapore’s National Medical Research Council (NMRC/CIRG/1341/2012: R-221-000-059-511) and supported by the Singapore National Research Foundation under its TCR Flagship Programme on Developmental Pathways to Metabolic Disease (NMRC/TCR/004-NUS/2008 and NMRC/TCR/012-NUHS/2014). A special thanks is extended to the GUSTO sub-domains for their great support; Professor Michael Kramer for his important advice and input; and Pang Wei Wei, Izzuddin Bin Mohd Aris, Tan Pei Ting and Priyangi Alwis for their valuable contributions. The continuous and skilful help of the home visitors and the clinical team from the National University Hospital and the KK Women’s and Children’s Hospital, as well as the database and biostatistics teams, is deeply appreciated.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Chin-Ying Stephen Hsu.

Ethics declarations

Ethical Approval

All work involving human participants was approved by the National Healthcare Group Domain Specific Review Board (NHG DSRB Ref: 2009/00021) and SingHealth Centralized Institutional Review Board (CIRB Ref: 2009/280/D).

Informed Consent

Written informed consent was obtained from all participants prior to their inclusion in the study.

Conflict of interest

The authors declare that they have no competing interests.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Un Lam, C., Hsu, CY.S., Yee, R. et al. Influence of metabolic-linked early life factors on the eruption timing of the first primary tooth. Clin Oral Invest 20, 1871–1879 (2016). https://doi.org/10.1007/s00784-015-1670-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00784-015-1670-6

Keywords

Navigation