Associations between bone mineral density and coronary artery calcification: a systematic review and meta-analysis

Peiyu Zhang1, Liu Yang2, Qingwen Xu1

  • 1School of Integrative Medicine, Hunan University of Chinese Medicine, Changsha, China.

Insights

Low bone mineral density (BMD) is linked to a higher prevalence of coronary arterial calcification (CAC). However, this association becomes insignificant when adjusting for age and other factors, suggesting independent aging processes.

Area of Science:

  • Cardiovascular Health
  • Bone Metabolism
  • Gerontology

Background:

  • The relationship between bone mineral density (BMD) and coronary arterial calcification (CAC) remains a subject of ongoing scientific debate.
  • Existing studies present conflicting findings regarding the correlation between BMD and CAC.

Purpose of the Study:

  • To conduct a comprehensive meta-analysis to clarify the association between BMD and CAC.
  • To evaluate the prevalence and severity of CAC in individuals with varying BMD levels.

Main Methods:

  • Systematic literature search across major databases (PubMed, Embase, Google Scholar, Cochrane Library).
  • Inclusion of observational studies, pooling odds ratios (OR) and correlation coefficients with 95% confidence intervals (CI).
  • Sub-group analysis and funnel plots were employed to assess heterogeneity and publication bias.

Main Results:

  • Seventeen studies met the inclusion criteria.
  • Low BMD was associated with a significantly higher prevalence of CAC (OR = 2.11, P=0.02) and increased CAC scores (MD = 33.77, P=0.000).
  • However, multivariate logistic regression showed no significant association after adjusting for confounders (age-adjusted OR = 1.00, P=0.95; multivariable-adjusted OR = 0.95, P=0.33).

Conclusions:

  • Low BMD is linked to increased prevalence and severity of CAC, particularly in postmenopausal women.
  • The association loses statistical significance when accounting for age and other confounding variables.
  • Low BMD and CAC may represent independent aging processes, necessitating further high-quality research.
Abstract

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