Does Sitagliptin Affect the Rate of Osteoporotic Fractures in Type 2 Diabetes? Population-Based Cohort Study

被引:39
|
作者
Majumdar, Sumit R. [1 ,2 ]
Josse, Robert G. [3 ,4 ]
Lin, Mu [5 ]
Eurich, Dean T. [2 ,5 ]
机构
[1] Univ Alberta, Dept Med, Edmonton, AB T6G 2G3, Canada
[2] Alberta Diabet Inst, Alliance Hlth Outcomes Res Diabet, Edmonton, AB T6G 2G3, Canada
[3] Univ Toronto, Dept Med, Toronto, ON M5B 1W8, Canada
[4] St Michaels Hosp, Li Ka Shing Knowledge Inst, 30 Bond St, Toronto, ON M5B 1W8, Canada
[5] Univ Alberta, Sch Publ Hlth, Edmonton, AB T6G 2G3, Canada
来源
基金
加拿大健康研究院;
关键词
DIPEPTIDYL PEPTIDASE-4 INHIBITORS; RANDOMIZED CLINICAL-TRIALS; BONE-MINERAL DENSITY; CARDIOVASCULAR OUTCOMES; RISK; ROSIGLITAZONE; METAANALYSIS; METFORMIN; MELLITUS; DRUGS;
D O I
10.1210/jc.2015-4180
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Type 2 diabetes and osteoporosis are both common, chronic, and increase with age, whereas type 2 diabetes is also a risk factor for major osteoporotic fractures (MOFs). However, different treatments for type 2 diabetes can affect fracture risk differently, with metaanalyses showing some agents increase risk (eg, thiazolidinediones) and some reduce risk (eg, sitagliptin). Objective: To determine the independent association between new use of sitagliptin and MOF in a large population-based cohort study. Design, Setting, and Subjects: A sitagliptin new user study design employing a nationally representative Unites States claims database of 72 738 insured patients with type 2 diabetes. We used 90-daytime-varying sitagliptin exposure windows and controlled confounding by using multivariable analyses that adjusted for clinical data, comorbidities, and time-updated propensity scores. Main Outcomes: We compared the incidence of MOF (hip, clinical spine, proximal humerus, distal radius) in new users of sitagliptin vs nonusers over a median 2.2 years follow-up. Results: At baseline, the median age was 52 years, 54% were men, and median A1cwas 7.5%. There were 8894 new users of sitagliptin and 63 834 nonusers with a total 181 139 person-years of follow-up. There were 741 MOF (79 hip fractures), with 53 fractures (4.8 per 1000 person-years) among new users of sitagliptin vs 688 fractures (4.0 per 1000 person-years) among nonusers (P = .3 for difference). In multivariable analyses, sitagliptin was not associated with fracture (adjusted hazard ratio 1.1, 95% confidence interval 0.8-1.4; P = .7), although insulin (P < .001), sulfonylureas (P = .008), and thiazolidinedione (P = .019) were each independently associated with increased fracture risk. Conclusions: Even in a young population with type 2 diabetes, osteoporotic fractures were not uncommon. New use of sitagliptin was not associated with fracture, but other commonly used second-line agents for type 2 diabetes were associated with increased risk. These data should be considered when making treatment decisions forthose with type 2 diabetes at particularly high risk of fractures.
引用
收藏
页码:1963 / 1969
页数:7
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