Heel bone mineral density and various oral diseases: a bidirectional Mendelian randomization

J Bone Miner Metab. 2023 Sep;41(5):673-681. doi: 10.1007/s00774-023-01443-w. Epub 2023 Jul 28.

Abstract

Introduction: Observational studies demonstrated that the relationship between bone mineral density and oral diseases is mixed. To access the association between heel bone mineral density and various oral diseases, we conducted the Mendelian randomization analysis to explore the association.

Materials and methods: Two-sample bidirectional Mendelian analysis was used to explore the relationship between heel bone mineral density and various oral diseases. The inverse-variance weighted (IVW) was used as the primary effect estimate, and various methods were applied to test the reliability and stability of the results, namely MR-Egger, weighted median, simple mode, and weighted mode.

Results: This study showed that there was a negative relationship between heel BMD and periodontitis when heel BMD was used as an exposure factor and periodontitis as an outcome factor (IVW OR = 0.85; 95% CI, 0.75-0.95; p = 0.005). Bidirectional Mendelian randomization showed that there was no statistically significant association between periodontitis and heel bone mineral density when chronic periodontitis was the exposure factor (p > 0.05). And there was no significant relationship between heel bone mineral density and other oral diseases (dental caries, diseases of pulp and periapical tissues, impacted teeth, cleft lip, and cleft palate, oral and oropharyngeal cancer) (p > 0.05).

Conclusion: This study showed that there was a negative relationship between heel bone density and periodontitis, and the decrease in heel bone density could promote the occurrence of periodontitis. In addition, there was no statistically significant relationship between heel bone density and other oral diseases.

Keywords: Chronic periodontitis; Genome-wide association studies; Heel bone mineral density; Mendelian randomization; Oral diseases.

MeSH terms

  • Bone Density / genetics
  • Dental Caries*
  • Fractures, Bone*
  • Humans
  • Mendelian Randomization Analysis
  • Polymorphism, Single Nucleotide
  • Reproducibility of Results