TY - JOUR
T1 - Effects of commonly used medications on bone tissue mineralisation in SaOS-2 human bone cell line
T2 - An in vitro study
AU - Salai, M.
AU - Somjen, D.
AU - Gigi, R.
AU - Yakobson, O.
AU - Katzburg, S.
AU - Dolkart, O.
PY - 2013
Y1 - 2013
N2 - 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 medicationinduced osteoporosis.
AB - 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 medicationinduced osteoporosis.
UR - http://www.scopus.com/inward/record.url?scp=84888342566&partnerID=8YFLogxK
U2 - 10.1302/0301-620X.95B11.31158
DO - 10.1302/0301-620X.95B11.31158
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AN - SCOPUS:84888342566
SN - 2049-4394
VL - 95 B
SP - 1575
EP - 1580
JO - Bone and Joint Journal
JF - Bone and Joint Journal
IS - 11
ER -