Ghosh Mahua, Majumdar Sumit R
Division of General Internal Medicine, Department of Medicine, University of Alberta, Edmonton, AB, Canada.
Endocrine. 2014 Aug;46(3):397-405. doi: 10.1007/s12020-014-0167-4. Epub 2014 Feb 7.
Osteoporosis is increasing in prevalence and importance as society's age, with the clinical consequence of fractures of the hip, spine, and upper extremity, leading to impaired quality of life, loss of function and independence, and increased morbidity and mortality. A major risk factor for osteoporosis is older age, and cardiovascular diseases also share this risk factor; therefore, osteoporosis and cardiovascular disease often coexist and share risk factors. Medications used for the treatment of cardiovascular diseases, in particular antihypertensive drugs, have been shown in a variety of studies of varying designs to modulate bone health in both a positive or negative manner. In this article, we reviewed the pharmacology, potential mechanisms, and possible effects on bone mineral density and fracture risk of commonly prescribed antihypertensive medications, including thiazide and non-thiazide diuretics, beta-blockers, calcium channel blockers, renin-angiotensin-aldosterone system agents, and nitrates.
随着社会老龄化,骨质疏松症的患病率和重要性日益增加,其临床后果是髋部、脊柱和上肢骨折,导致生活质量受损、功能丧失和独立性丧失,以及发病率和死亡率增加。骨质疏松症的一个主要危险因素是年龄较大,心血管疾病也存在这一危险因素;因此,骨质疏松症和心血管疾病常并存且有共同的危险因素。在各种设计各异的研究中,用于治疗心血管疾病的药物,尤其是抗高血压药物,已显示出对骨骼健康有正面或负面的调节作用。在本文中,我们综述了常用抗高血压药物(包括噻嗪类和非噻嗪类利尿剂、β受体阻滞剂、钙通道阻滞剂、肾素 - 血管紧张素 - 醛固酮系统药物和硝酸盐)的药理学、潜在机制以及对骨密度和骨折风险的可能影响。