@article{5257e66d0d6f4d72a908b96c55f5358d,
title = "Causes of death in a contemporary cohort of patients with type 2 diabetes and atherosclerotic cardiovascular disease: Insights from the TECOS trial",
abstract = "Objective: We evaluated the specific causes of death and their associated risk factors in a contemporary cohort of patients with type 2 diabetes and atherosclerotic cardiovascular disease (ASCVD). Research Design and Methods: We used data from the Trial Evaluating Cardiovascular Outcomes with Sitagliptin (TECOS) study (n = 14,671), a cardiovascular (CV) safety trial adding sitagliptin versus placebo to usual care in patients with type 2 diabetes and ASCVD (median follow-up 3 years). An independent committee blinded to treatment assignment adjudicated each cause of death. Cox proportional hazards models were used to identify risk factors associated with each outcome. Results: A total of 1,084 deaths were adjudicated as the following: 530 CV (1.2/100 patientyears [PY], 49% of deaths), 338 non-CV (0.77/100 PY, 31% of deaths), and 216 unknown (0.49/100 PY, 20% of deaths). Themost common CV death was sudden death (n = 145, 27% of CV death) followed by acute myocardial infarction (MI)/stroke (n = 113 [MI n = 48, stroke n = 65], 21% of CV death) and heart failure (HF) (n = 63, 12% of CV death). Themost common non-CV deathwas malignancy (n = 154, 46% of non-CV death). The risk of specific CV death subcategories was lower among patients with no baseline history of HF, including sudden death (hazard ratio [HR] 0.4; P = 0.0036), MI/stroke death (HR 0.47; P = 0.049), and HF death (HR 0.29; P = 0.0057). Conclusions: In this analysis of a contemporary cohort of patients with diabetes and ASCVD, sudden death was the most common subcategory of CV death. HF prevention may represent an avenue to reduce the risk of specific CV death subcategories.",
author = "{TECOS Study Group} and Abhinav Sharma and Green, {Jennifer B.} and Allison Dunning and Yuliya Lokhnygina and Al-Khatib, {Sana M.} and Lopes, {Renato D.} and Buse, {John B.} and Lachin, {John M.} and {Van De Werf}, Frans and Armstrong, {Paul W.} and Kaufman, {Keith D.} and Eberhard Standl and Chan, {Juliana C.N.} and Distiller, {Larry A.} and Russell Scott and Peterson, {Eric D.} and Holman, {Rury R.}",
note = "Funding Information: Funding. This study was funded by Merck & Co., Inc., Kenilworth, NJ. Duality of Interest. A.S. reports receiving support from Canadian Cardiovascular Society-Bayer, Alberta Innovates, Roche Diagnostics, and Takeda Pharmaceuticals. J.B.G. has received grants from Merck, AstraZeneca, and GlaxoSmithKline; grants and personal fees from Merck; other support from Boehringer Ingelheim; and personal fees from Bioscientifica and the Endocrine Society. Y.L. has received grants from Merck, Janssen Research & Development, AstraZeneca, GlaxoSmithKline, and Bayer HealthCare AG. R.D.L. has received research support from Bristol-Myers Squibb and GlaxoSmithKline and personal fees from Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, GlaxoSmithKline, Pfizer, and Portola Pharmaceuticals. J.B.B. has received consulting fees from PhaseBio and research support from AstraZeneca, Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, Eli Lilly, GI Dynamics, GlaxoSmithKline, Intarcia Therapeutics, Johnson & Johnson, Lexicon, Medtronic MiniMed, National Institutes of Health, Novo Nordisk, Orexigen Therapeutics, Sanofi, Scion NeuroStim, Takeda Pharmaceuticals, and Thera-cos; owns stocks/shares in PhaseBio; has served as an advisor under contract with his employer for AstraZeneca, Dance Biopharm, Eli Lilly, Elcelex, GI Dynamics, Lexicon, Merck, Metavention, Novo Nordisk, Orexigen Therapeutics, vTv Therapeutics; and has received other support from ADOCIA, Insulin Algorithms, Dexcom, Fractyl, NovaTarg, and Shenzhen HighTide. J.M.L. has received personal fees from AstraZeneca, Boehringer Ingelheim, Eli Lilly, Gilead Sciences, Janssen Pharmaceuticals, Merck through Oxford University, and Novartis. F.V.d.W. has received study grants and personal fees from Merck, AstraZeneca, and Boehringer Ingelheim. P.W.A. has received grants, personal fees, and nonfinancial support from Merck and grants from AstraZeneca. K.D.K. is an employee of Merck & Co., Inc., the manufacturer of sitagliptin, and owns stock and stock options in Merck & Co., Inc. E.S. has received personal fees from Oxford Diabetes Trials Unit, AstraZeneca, Bayer, Boehringer Ingelheim, Merck Serono, EXCEMED, Novartis, Novo Nordisk, and Sanofi. J.C.N.C. has received an honorarium while serving as consultant or speaker for Merck Sharp & Dohme, and her affiliated institutions have received research and educational grants from Merck Sharp & Dohme. 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 Squibb; personal fees from Amgen, Bayer, Intarcia Therapeutics, Novartis, and Novo Nordisk; and other support from GlaxoSmithKline, Janssen, and Takeda Pharmaceuticals. No other potential conflicts of interest relevant to this article were reported. Author Contributions. A.S. contributed to the study design and data analysis and interpretation, and drafted the manuscript. J.B.G., S.M.A.-K., R.D.L., J.B.B., J.M.L., F.V.d.W., P.W.A., K.D.K., E.S., J.C.N.C., L.A.D., and R.S. edited the manuscript. A.D. and Y.L. performed the statistical analyses. E.D.P. and R.R.H. contributed to the study design and data analysis and interpretation, and edited the manuscript. A.S. and R.R.H. are the guarantors of this work and, as such, had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Publisher Copyright: {\textcopyright} 2017 by the American Diabetes Association.",
year = "2017",
month = dec,
day = "1",
doi = "10.2337/dc17-1091",
language = "English (US)",
volume = "40",
pages = "1763--1770",
journal = "Diabetes Care",
issn = "1935-5548",
publisher = "American Diabetes Association Inc.",
number = "12",
}