Josse Robert G, Majumdar Sumit R, Zheng Yinggan, Adler Amanda, Bethel M Angelyn, Buse John B, Green Jennifer B, Kaufman Keith D, Rodbard Helena W, Tankova Tsvetalina, Westerhout Cynthia M, Peterson Eric D, Holman Rury R, Armstrong Paul W
St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Diabetes Obes Metab. 2017 Jan;19(1):78-86. doi: 10.1111/dom.12786. Epub 2016 Oct 6.
To examine fracture incidence among participants in the Trial Evaluating Cardiovascular Outcomes with Sitagliptin (TECOS).
We used data from 14 671 participants in the TECOS study who were randomized double-blind to sitagliptin (n = 7332) or placebo (n = 7339). Cumulative fracture incidence rates were calculated and their association with study treatment assignment was examined using multivariable Cox proportional hazards regression.
The baseline mean (standard deviation) participant age was 65.5 (8.0) years, diabetes duration was 11.6 (8.1) years and glycated haemoglobin level was 7.2 (0.5)% [55.2 (5.5) mmol/mol], and 29.3% of participants were women and 32.1% were non-white. During 43 222 person-years' follow-up, 375 (2.6%; 8.7 per 1000 person-years) had a fracture; 146 were major osteoporotic fractures (hip, n = 34; upper extremity, n = 81; and clinical spine, n = 31). Adjusted analyses showed fracture risk increased independently with older age (P < .001), female sex (P < .001), white race (P < .001), lower diastolic blood pressure (P < .001) and diabetic neuropathy (P = .003). Sitagliptin, compared with placebo, was not associated with a higher fracture risk [189 vs 186 incident fractures: unadjusted hazard ratio (HR) 1.01, 95% confidence interval (CI) 0.82 to 1.23, P = .944; adjusted HR 1.03, P = .745], major osteoporotic fractures (P = .673) or hip fractures (P = .761). Insulin therapy was associated with a higher fracture risk (HR 1.40, 95% CI 1.02-1.91; P = .035), and metformin with a lower risk (HR 0.76, 95% CI 0.59-0.98; P = .035).
Fractures were common among people with diabetes in the TECOS study, but were not related to sitagliptin therapy. Insulin and metformin treatment were associated with higher and lower fracture risks, respectively.
研究西他列汀评估心血管结局试验(TECOS)参与者的骨折发生率。
我们使用了TECOS研究中14671名参与者的数据,这些参与者被随机双盲分配至西他列汀组(n = 7332)或安慰剂组(n = 7339)。计算累积骨折发生率,并使用多变量Cox比例风险回归分析其与研究治疗分配的关联。
参与者的基线平均(标准差)年龄为65.5(8.0)岁,糖尿病病程为11.6(8.1)年,糖化血红蛋白水平为7.2(0.5)% [55.2(5.5)mmol/mol],29.3%的参与者为女性,32.1%为非白人。在43222人年的随访期间,375人(2.6%;每1000人年8.7例)发生骨折;146例为严重骨质疏松性骨折(髋部,n = 34;上肢,n = 81;临床脊柱,n = 31)。校正分析显示,骨折风险随年龄增长(P <.001)、女性(P <.001)、白人种族(P <.001)、较低的舒张压(P <.001)和糖尿病神经病变(P =.003)而独立增加。与安慰剂相比,西他列汀与较高的骨折风险无关[189例与186例新发骨折:未校正风险比(HR)1.01,95%置信区间(CI)0.82至1.23,P =.944;校正HR 1.03,P =.745],严重骨质疏松性骨折(P =.673)或髋部骨折(P =.761)。胰岛素治疗与较高的骨折风险相关(HR 1.40,95%CI 1.02 - 1.91;P =.035),而二甲双胍与较低的风险相关(HR 0.76,95%CI 0.59 - 0.98;P =.035)。
在TECOS研究中,糖尿病患者骨折很常见,但与西他列汀治疗无关。胰岛素和二甲双胍治疗分别与较高和较低的骨折风险相关。