[Current views on the interaction between the treatment of osteoporosis and cardiovascular diseases]

Tomasz Zapolski1, Andrzej Wysokiński2

  • 1Katedra i Klinika Kardiologii, Uniwersytet Medyczny, Lublin,

Wiadomosci Lekarskie (Warsaw, Poland : 1960)
|December 13, 2016
PubMed

Insights

Menopause increases risks for osteoporosis and cardiovascular disease. This study explores their potential link and how treatments for one condition may affect the other, impacting drug choices.

Area of Science:

  • Gerontology
  • Cardiology
  • Endocrinology

Background:

  • Osteoporosis and atherosclerotic disease are common post-menopause, often viewed as independent age-related conditions.
  • Emerging evidence suggests a potential link between cardiovascular disease and osteoporosis.
  • Understanding this connection is crucial for managing patient health effectively.

Purpose of the Study:

  • To investigate the association between cardiovascular disease and osteoporosis.
  • To analyze the mutual beneficial and adverse effects of drugs used for these conditions.
  • To evaluate drug interactions between osteoporosis treatments and cardiovascular medications.

Main Methods:

  • Review of current literature on drug interactions between cardiovascular and osteoporosis therapies.
  • Analysis of side effects of cardiological drugs on bone health.
  • Evaluation of potential benefits of cardiovascular drugs for osteoporosis prevention.
  • Examination of adverse cardiovascular effects of osteoporosis drugs.
  • Review of bisphosphonates, strontium ranelate, hormone replacement therapy (HRT), and selective estrogen receptor modulators (SERMs).
  • Discussion of cardiac effects of calcium and related metabolic drugs (vitamin D, parathormone, calcitonin).

Main Results:

  • Osteoporosis treatments can have adverse effects on the cardiovascular system.
  • Cardiovascular drugs may impact bone health, both positively and negatively.
  • Specific drug classes like bisphosphonates and SERMs require careful consideration regarding cardiovascular and bone health.
  • Calcium and vitamin D supplementation require monitoring for cardiac effects.

Conclusions:

  • The interplay between osteoporosis and cardiovascular disease necessitates a comprehensive approach to treatment.
  • Clinicians must consider potential drug interactions and side effects when managing patients with both conditions.
  • Further research is needed to optimize therapeutic strategies for post-menopausal women at risk for both osteoporosis and cardiovascular disease.

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