Chan Ding-Cheng, Yang Rong-Sen, Ho Chung-Han, Tsai Yau-Sheng, Wang Jhi-Joung, Tsai Kang-Ting
Department of Gerontology and Geriatrics, National Taiwan University Hospital, Taipei, Taiwan; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Superintendent Office, National Taiwan University Hospital JinShan Branch, New Taipei City, Taiwan.
Department of Orthopedics, National Taiwan University Hospital, Taipei, Taiwan.
PLoS One. 2015 Apr 13;10(4):e0123279. doi: 10.1371/journal.pone.0123279. eCollection 2015.
Bone remodeling has been linked to glucose metabolism in animal studies, but the results of human trials were inconclusive. Bisphosphonates may play a role in glucose metabolism through their impacts on bone remodeling enzymes. In this study, we aimed to examine the influence of alendronate usage on the incidence of type 2 diabetes mellitus (DM) among osteoporotic patients.
A retrospective cohort study was designed to include osteoporotic patients without DM from a population-based cohort containing 1,000,000 subjects. Patients treated with alendronate (exposed group, N=1,011) were compared with those who received no treatment (age and gender matched non-exposed group, N=3,033). Newly diagnosed DM was identified from medical records by International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9CM) code. The incidence of DM in both groups was calculated for comparison.
The non-exposed group had a significantly higher incidence of DM (Odds ratio 1.21, 95% confidence interval 1.03~1.41) when compared with the exposed group. In subgroup analysis, the DM risk reduction in exposed group was only significant among those younger than 65 years and those without hypertension or dyslipidemia. Patients who were prescribed alendronate more than or equal to 3 times had demonstrated a significant reduction in DM risk.
Our study showed alendronate might yield a protective effect for incident DM. This effect became insignificant in patients with older age, dyslipidemia or hypertension. The underlying mechanism needs further exploration with prospective data for confirmation of the observed findings.
在动物研究中,骨重塑与葡萄糖代谢相关,但人体试验结果尚无定论。双膦酸盐可能通过影响骨重塑酶在葡萄糖代谢中发挥作用。在本研究中,我们旨在探讨阿仑膦酸钠的使用对骨质疏松患者2型糖尿病(DM)发病率的影响。
一项回顾性队列研究纳入了来自一个包含100万受试者的人群队列中的无DM的骨质疏松患者。将接受阿仑膦酸钠治疗的患者(暴露组,N = 1,011)与未接受治疗的患者(年龄和性别匹配的非暴露组,N = 3,033)进行比较。通过国际疾病分类第九版临床修订本(ICD - 9CM)编码从医疗记录中识别新诊断的DM。计算两组DM的发病率以进行比较。
与暴露组相比,非暴露组的DM发病率显著更高(优势比1.21,95%置信区间1.03~1.41)。在亚组分析中,暴露组中DM风险降低仅在年龄小于65岁且无高血压或血脂异常的人群中显著。服用阿仑膦酸钠≥3次的患者DM风险显著降低。
我们的研究表明阿仑膦酸钠可能对新发DM产生保护作用。在老年、血脂异常或高血压患者中这种作用不明显。潜在机制需要前瞻性数据进一步探索以证实观察结果。