Vestergaard Peter, Rejnmark Lars, Mosekilde Leif
Department of Endocrinology and Metabolism C, Aarhus University Hospital, Aarhus University, Aarhus, Denmark.
Calcif Tissue Int. 2008 Jan;82(1):34-43. doi: 10.1007/s00223-007-9095-0. Epub 2008 Jan 4.
To study the risk of fractures associated with anxiolytics, sedatives, and hypnotics, we conducted a case-control study. Cases were all subjects with any fracture during the year 2000 (n = 124,655). For each case, three controls (n = 373,962) matched on age and gender were randomly drawn from the background population. The exposure was use of any anxiolytic, sedative, or hypnotics. Adjustments were made for a number of potential confounders. Most anxiolytics, sedatives, and hypnotics were associated with a limited increase in the risk of fractures. There was a dose-response relationship, and drugs with a half-life longer than 24 h were associated with a trend toward a higher relative risk of fractures than drugs with a shorter half-life. Both current use (last use <1 year ago) and past use (last use more than one year ago) were associated with an increased risk of fractures. We conclude that anxiolytics, sedatives, and hypnotics are associated with a limited increase in the risk of fractures. For most drugs a dose-response relationship was present, and drugs with a half-life >24 h tended to be associated with a higher risk of fractures than drugs with a shorter half-life. This points to a dose-dependent risk of, for example, falls leading to fractures. However, the increased risk of fractures with past use may suggest an effect of the condition for which the drug was prescribed rather than the drug per se (confounding by indication).
为研究抗焦虑药、镇静药和催眠药与骨折风险之间的关系,我们开展了一项病例对照研究。病例为2000年期间发生任何骨折的所有受试者(n = 124,655)。对于每例病例,从背景人群中随机抽取三名年龄和性别相匹配的对照(n = 373,962)。暴露因素为使用任何抗焦虑药、镇静药或催眠药。对一些潜在混杂因素进行了调整。大多数抗焦虑药、镇静药和催眠药与骨折风险的有限增加相关。存在剂量反应关系,半衰期超过24小时的药物比半衰期较短的药物有骨折相对风险更高的趋势。当前使用(最后一次使用<1年前)和过去使用(最后一次使用超过1年前)均与骨折风险增加相关。我们得出结论,抗焦虑药、镇静药和催眠药与骨折风险的有限增加相关。对于大多数药物存在剂量反应关系,半衰期>24小时的药物比半衰期较短的药物往往骨折风险更高。这表明例如跌倒导致骨折存在剂量依赖性风险。然而,过去使用导致骨折风险增加可能提示是所开药治疗的疾病的影响而非药物本身的影响(指征性混杂)。