Santos Leyna L, Cavalcanti Taciana B, Bandeira Francisco A
Division of Endocrinology and Diabetes, Agamenon Magalhães Hospital, Ministry of Health, University of Pernambuco Medical School, Recife, Brazil.
Clin Med Insights Endocrinol Diabetes. 2012;5:47-54. doi: 10.4137/CMED.S10007. Epub 2012 Oct 25.
Osteoporosis and cardiovascular disease are interconnected entities with pathophysiological similarities. Bisphosphonates are therapeutic options available for resorptive bone diseases; however, experimental evidence has demonstrated a role for bisphosphonates in the inhibition of atherogenesis.
A systematic review of the vascular effects of bisphosphonates on atherosclerosis was performed. Vascular effects were evaluated by the thickening of the intima-media of carotid arteries and calcification of the coronary and aorta arteries. Electronic databases PubMed, The Cochrane Library, and Embase from January 1980 to May 2011 were searched.
Of 169 potentially relevant articles, 9 clinical trials were selected. Two articles showed the benefit of the use of etidronate (-0.038 mm, P < 0.005) and alendronate (-0.025 mm, P < 0.05) on carotid artery intima-media thickening (CIMT) after one year. One article found no changes associated with the use of alendronate. The use of risedronate was associated with a reduction of plaque score on the carotid arteries (decrease of 1% at 1 year, P = 0.015). Of those studies that evaluated the effect on coronary artery calcification (CAC), the results are conflicting: one study showed no changes with use of etidronate and in another, etidronate resulted in inhibition of the process of CAC after 1 year of follow-up (-372 mm(3) in CAC score, P < 0.01). Three studies showed positive effects of etidronate on the aortic calcificaton (AC) score, showing no effect with use of ibandronate, and another showed a inhibition in the progression of the abdominal AC score with use of risendronate (P = 0.043).
Bisphosphonates seem to have an inhibitory effect on the atherosclerotic process; however, larger placebo-controlled studies are needed to better clarify this issue.
骨质疏松症和心血管疾病是具有病理生理相似性的相互关联的实体。双膦酸盐是可用于治疗吸收性骨疾病的药物;然而,实验证据表明双膦酸盐在抑制动脉粥样硬化形成中发挥作用。
对双膦酸盐对动脉粥样硬化的血管效应进行了系统评价。通过颈动脉内膜中层增厚以及冠状动脉和主动脉钙化来评估血管效应。检索了1980年1月至2011年5月的电子数据库PubMed、Cochrane图书馆和Embase。
在169篇可能相关的文章中,选择了9项临床试验。两篇文章显示,依替膦酸盐(-0.038mm,P<0.005)和阿仑膦酸盐(-0.025mm,P<0.05)在使用一年后对颈动脉内膜中层增厚(CIMT)有益。一篇文章发现使用阿仑膦酸盐没有相关变化。利塞膦酸盐的使用与颈动脉斑块评分降低相关(1年后降低1%,P=0.015)。在那些评估对冠状动脉钙化(CAC)影响的研究中,结果相互矛盾:一项研究显示使用依替膦酸盐没有变化,而在另一项研究中,依替膦酸盐在随访1年后导致CAC进程受到抑制(CAC评分降低372mm³,P<0.01)。三项研究显示依替膦酸盐对主动脉钙化(AC)评分有积极影响,显示使用伊班膦酸盐无影响,另一项研究显示使用利塞膦酸盐可抑制腹部AC评分进展(P=0.043)。
双膦酸盐似乎对动脉粥样硬化进程有抑制作用;然而,需要更大规模的安慰剂对照研究来更好地阐明这一问题。