Effects of commonly used medications on bone tissue mineralisation in SaOS-2 human bone cell line: an in vitro study.

Bone Joint J

Tel-Aviv Sourasky Medical Center, Division of Orthopedic Surgery, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Published: November 2013

AI Article Synopsis

  • The study examined how common medications affect the activity of bone-forming cells (osteoblasts) in lab tests, focusing on their growth and ability to mineralize tissue.
  • A list of medications was taken from older patients' records, and the effects of rosuvastatin, metformin, metoprolol, citalopram, and omeprazole were specifically analyzed.
  • Results showed that all drugs promoted DNA synthesis in osteoblasts, with rosuvastatin being the most effective, while some medications like metformin and metoprolol inhibited mineralization, suggesting a need for careful evaluation of these drugs to prevent osteoporosis.

Article Abstract

We analysed the effects of commonly used medications on human osteoblastic cell activity in vitro, specifically proliferation and tissue mineralisation. A list of medications was retrieved from the records of patients aged > 65 years filed in the database of the largest health maintenance organisation in our country (> two million members). Proliferation and mineralisation assays were performed on the following drugs: rosuvastatin (statin), metformin (antidiabetic), metoprolol (β-blocker), citalopram (selective serotonin reuptake inhibitor [SSRI]), and omeprazole (proton pump inhibitor (PPI)). All tested drugs significantly stimulated DNA synthesis to varying degrees, with rosuvastatin 5 µg/ml being the most effective among them (mean 225% (SD 20)), compared with metformin 10 µg/ml (185% (SD 10)), metoprolol 0.25 µg/ml (190% (SD 20)), citalopram 0.05 µg/ml (150% (sd 10)) and omeprazole 0.001 µg/ml (145% (SD 5)). Metformin and metoprolol (to a small extent) and rosuvastatin (to a much higher extent) inhibited cell mineralisation (85% (SD 5)). Our results indicate the need to evaluate the medications prescribed to patients in terms of their potential action on osteoblasts. Appropriate evaluation and prophylactic treatment (when necessary) might lower the incidence and costs associated with potential medication-induced osteoporosis.

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Source
http://dx.doi.org/10.1302/0301-620X.95B11.31158DOI Listing

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