Association between Bone-Related Physiological Substances and Oral Function in Community-Dwelling Older People

Int J Environ Res Public Health. 2022 Aug 27;19(17):10677. doi: 10.3390/ijerph191710677.

Abstract

Background: Oral dysfunction is related to long-term cares including activities of daily living. The objective of this study was to determine the association between oral function and the bone-related physiological substances osteocalcin (OC) and insulin-like growth factor-1 (IGF-1).

Methods: The study participants were 139 community-dwelling older people in Japan. Evaluation of oral dysfunction was based on subjective judgment by each participant. Blood analysis included OC, IGF-1, and albumin.

Results: Univariate and multiple logistic analyses showed that IGF-1 was significantly associated with a "decline in masticatory function" (p = 0.0074 and p = 0.0308, respectively). Receiver operating characteristic curve analysis of IGF-1 levels revealed a threshold score of 108 ng/mL (p < 0.01) for discriminating a "decline in masticatory function". Logistic regression analysis revealed that participants with an IGF-1 level ≤108 ng/mL had an odds ratio of 4.31 (p < 0.05) for a "decline in masticatory function". No significant association was found between the OC level and oral dysfunction.

Conclusions: These results suggest a possible relationship between lower serum IGF-1 levels and a decline in masticatory dysfunction in community-dwelling older people.

Keywords: IGF-1; community-dwelling; mastication; older people.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activities of Daily Living
  • Aged
  • Cross-Sectional Studies
  • Humans
  • Independent Living*
  • Insulin-Like Growth Factor I* / chemistry
  • Insulin-Like Growth Factor I* / metabolism
  • Japan
  • Mastication / physiology
  • Oral Health*
  • Osteocalcin* / chemistry
  • Osteocalcin* / metabolism

Substances

  • Osteocalcin
  • Insulin-Like Growth Factor I

Grants and funding

This research was funded by JSPS KAKENHI, grant number 18K10800 and The Research Foundation for Dementia of Osaka.