Biochemical Markers Linking Osteoporosis and Cardiovascular Risk in Older Adults: A Retrospective Analysis

Preeti Nigotia1, Uditkumar Agrawal2, Ashish Sharma3

  • 1Department of Medicine, SRVS Medical College, Shivpuri, Madhya Pradesh, India.

Insights

Osteoporosis is linked to unhealthy cholesterol and homocysteine levels, impacting bone mineral density (BMD) and increasing cardiovascular disease (CVD) risk. Lower BMD significantly elevates this risk, suggesting BMD as a potential CVD biomarker.

Area of Science:

  • Metabolic bone disorders
  • Cardiovascular disease research
  • Biochemical marker analysis

Background:

  • Osteoporosis is a common metabolic bone disorder, especially in the elderly, often co-occurring with cardiovascular morbidity.
  • Existing research suggests a potential link between osteoporosis and cardiovascular disease (CVD).

Purpose of the Study:

  • To investigate the associations between osteoporosis, key biochemical markers, bone mineral density (BMD), and cardiovascular disease (CVD).
  • To evaluate the predictive potential of BMD for CVD risk.

Main Methods:

  • Cross-sectional analysis of 280 osteoporosis patients and 182 controls.
  • Assessed serum levels of triglycerides, total cholesterol (TC), LDL, HDL, and homocysteine (HCY).
  • Evaluated correlations between biochemical indices and BMD; compared CVD prevalence and used ROC analysis for BMD's predictive value.

Main Results:

  • Positive associations found between osteoporosis and higher triglyceride, TC, and LDL levels.
  • Inverse associations observed between osteoporosis and elevated HDL and HCY levels.
  • Lower BMD and higher CVD incidence in osteoporosis patients; reduced BMD significantly increased cardiovascular risk.

Conclusions:

  • Significant associations exist among osteoporosis, lipid profiles, HCY levels, BMD, and CVD.
  • Dyslipidemia and altered HCY metabolism may contribute to bone loss and cardiovascular pathology.
  • BMD shows potential as a biomarker for identifying individuals at increased cardiovascular risk.
Abstract

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