TY - JOUR
T1 - Sitagliptin and risk of fractures in type 2 diabetes
T2 - Results from the TECOS trial
AU - On behalf of the TECOS Study Group
AU - Josse, Robert G.
AU - Majumdar, Sumit R.
AU - Zheng, Yinggan
AU - Adler, Amanda
AU - Bethel, M. Angelyn
AU - Buse, John B.
AU - Green, Jennifer B.
AU - Kaufman, Keith D.
AU - Rodbard, Helena W.
AU - Tankova, Tsvetalina
AU - Westerhout, Cynthia M.
AU - Peterson, Eric D.
AU - Holman, Rury R.
AU - Armstrong, Paul W.
N1 - Funding Information:
The authors wish to thank the investigators, staff, and participants in the TECOS study, without whose efforts and collaboration this work would not have been possible. We thank the following academic partners and contract research organizations for their assistance: Parexel International; Jubilant Clinsys; Clinogent; Canadian VIGOUR Centre; Green Lane Coordinating Centre; and South Australian Health and Medical Research Institute. S.R.M. holds the Endowed Chair in Patient Health Management supported by the Faculties of Medicine and Dentistry and Pharmacy and Pharmaceutical Sciences at the University of Alberta. R.R.H. is an NIHR Senior Investigator. We acknowledge permission from the authors of reference 13 to use a similarly designed diagram to display fracture location. R. G. J. has received grants or personal fees from Amgen, AstraZeneca, Boehringer-Ingelheim, Eli Lilly, Janssen and Merck. M. A. B. has received grants, personal fees, and other support from Merck, Sharp & Dohme, other support from Boehringer-Ingelheim, Novo Nordisk, Glaxo and Smith Kline, and non-financial support from Bayer. J. B. B. has served as a consultant for PhaseBio, has received research support from AstraZeneca, Boehringer-Ingelheim, Bristol-Myers Squibb, Eli Lilly, GI Dynamics, J&J, Lexicon, Novo Nordisk and Orexigen, is a shareholder in PhaseBio, and has been an advisor under contract with employer for AstraZeneca, Dance Biopharm, Eli Lilly, Elycylex, GI Dynamics, Lexicon, Merck, Metavention, Novo Nordisk, Orexigen and vTv Therapeutics. J. B. G. has received grants from Merck Sharp & Dohme, AstraZeneca and GlaxoSmithKline, grants and personal fees from Merck Sharp & Dohme, other support from Boehringer-Ingelheim, and personal fees from Bioscientifica and The Endocrine Society. K. D. K. is an employee of Merck & Co., Inc., the manufacturer of sitagliptin, and owns stock and stock options in Merck & Co., Inc. H. W. R. has received research support and consulting fees from Astra Zeneca, BI, Janssen, Lilly, Merck, NovoNoridsk, Sanofi and Regeneron. T. T. has received grants and personal fees from Merck, Sharp & Dohme, Boehringer-Ingelheim, Novo Nordisk, Sanofi, Eli Lilly, Novartis, Servier and AstraZeneca. E. D. P. has received grants and personal fees from Janssen, grants from Eli Lilly, and personal fees from AstraZeneca, Bayer and Sanofi. R. R. H. has received grants and personal fees from Merck, grants from Bayer, AstraZeneca, and Bristol-Myers Squib, personal fees from Amgen, Bayer, Intarcia, Novartis, Novo Nordisk, and other support from GlaxoSmithKline, Janssen and Takeda. P. W. A. has received grants, personal fees and non-financial support from Merck and grants from AstraZeneca. S. R. M., Y. Z., A. A. and C. M. W. have no disclosures. R. G. J., S. R. M. and Y. Z. designed the study, performed the statistical analysis and interpretation, and drafted, reviewed, and approved the final manuscript. A. A., M. A. B., J. B. B., J. B. G., K. D. K., H. W. R., T. T., C. M. W. and E. D. P. reviewed, revised and approved the final manuscript. P. W. A. and R. R. H. were contributors to the study design and critically reviewed, edited and approved the final manuscript. R. G. J., R. R. H. and P. W. A. are the guarantors of this work and, as such, had full access to all of the data in the study and take full responsibility for the work as a whole, including the study design and integrity of the data. Parts of this work were presented at the American Diabetes Association meeting in 2016.
Publisher Copyright:
© 2016 John Wiley & Sons Ltd
PY - 2017/1/1
Y1 - 2017/1/1
N2 - Aim: To examine fracture incidence among participants in the Trial Evaluating Cardiovascular Outcomes with Sitagliptin (TECOS). Research design and methods: 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. Results: 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). Conclusion: 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.
AB - Aim: To examine fracture incidence among participants in the Trial Evaluating Cardiovascular Outcomes with Sitagliptin (TECOS). Research design and methods: 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. Results: 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). Conclusion: 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.
KW - DPP-4 inhibitors
KW - diabetes
KW - fractures
KW - sitagliptin
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U2 - 10.1111/dom.12786
DO - 10.1111/dom.12786
M3 - Article
C2 - 27607571
AN - SCOPUS:84995596092
SN - 1462-8902
VL - 19
SP - 78
EP - 86
JO - Diabetes, Obesity and Metabolism
JF - Diabetes, Obesity and Metabolism
IS - 1
ER -