Relationship between Serum Nutritional Factors and Bone Mineral Density: A Mendelian Randomization Study

J Clin Endocrinol Metab. 2021 May 13;106(6):e2434-e2443. doi: 10.1210/clinem/dgab085.

Abstract

Purpose: Multiple risk factors have been implicated in the development of osteoporosis. This study examined potential associations between serum nutritional factors and bone mineral density (BMD).

Methods: Six nutritional factors were selected as exposures. Outcomes included total body BMD (n = 66 945); BMD at the forearm (FA), femoral neck (FN) and lumbar spine (LS) (n = 8143, n = 32 735, and n = 28 498, respectively); estimated heel BMD (HL eBMD) (n = 394 929); and HL eBMD stratified by sex (n = 206 496). A 2-sample Mendelian randomization approach was adopted to estimate the association between serum nutritional factors and BMD. The threshold for adjusted P value was 1.39 × 10-3.

Results: Serum calcium levels were inversely associated with LS BMD (effect = -0.55; 95% CI, -0.86 to -0.24; P = 0.001), whereas serum selenium levels were positively correlated with HL eBMD (effect = 0.22; 95% CI, 0.10 to 0.33; P = 1.70 × 10-4). Regarding nominal significance, there was a positive association between serum selenium levels and FA BMD. Nominally significant results were also obtained for serum retinol as well as vitamin E levels and HL eBMD. Moreover, sex-specific effects of serum retinol and vitamin E levels on BMD were observed in men.

Conclusion: Serum calcium and selenium levels influence BMD at specific skeletal sites. This implies that these nutritional factors play crucial roles in bone metabolism.

Keywords: Bone mineral density; Mendelian randomization; calcium; nutritional factor; selenium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Density / genetics*
  • Calcium / blood
  • Female
  • Gene-Environment Interaction
  • Genome-Wide Association Study
  • Humans
  • Male
  • Mendelian Randomization Analysis
  • Multifactorial Inheritance
  • Nutrients / blood*
  • Osteoporosis / blood
  • Osteoporosis / epidemiology
  • Osteoporosis / etiology
  • Osteoporosis / genetics
  • Polymorphism, Single Nucleotide
  • Risk Factors
  • White People / genetics

Substances

  • Calcium