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DOI 10.1002/jor.22030

Медицинская библиотека · Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2011

Effect of atorvastatin on the cortical bones of corticosteroid treated rabbits.

Handal John A, John Thomas K, Goldstein Daniel T, Khurana Jasvir S, Saing Minn, Braitman Leonard E, Samuel Solomon P

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Osteoporosis ("secondary" osteoporosis) and avascular necrosis (AVN) of the femoral head are well-known adverse effects of corticosteroid therapy. Statins have been reputed to increase bone strength and bone density. In this study, we evaluated the effect of atorvastatin calcium on the flexural properties (3-point bending strength and modulus) of corticosteroid (methylprednisolone acetate) treated rabbit femurs and tibias. Our study hypothesis was that the use of statins would counteract the loss of bone strength caused by corticosteroid treatment. The 40 rabbits were divided into 5 groups: control, corticosteroid alone and corticosteroid combined with oral doses of atorvastatin calcium (2, 10, or 20 mg/day). A daily oral dose of atorvastatin calcium treatment for 70 days weakened the long bones of methylprednisolone acetate treated rabbits irrespective of the dosage (2, 10, or 20 mg). Cortical bone strength was assessed using the 3-point bending test at the end of the study period. A daily oral dose of atorvastatin calcium did not attenuate the loss of cortical bone strength caused by corticosteroid treatment in rabbits. It appeared to decrease that bone strength. If these results hold true in humans, they would have wide applicability given the frequent combined use of corticosteroids and statins in many patients.

Для цитирования: Handal John A, John Thomas K, Goldstein Daniel T, Khurana Jasvir S, Saing Minn, Braitman Leonard E, Samuel Solomon P. Effect of atorvastatin on the cortical bones of corticosteroid treated rabbits.. Journal of orthopaedic research : official publication of the Orthopaedic Research Society. 2011. DOI: 10.1002/jor.22030.

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