Article (Scientific journals)
Increased risk of severe hypoglycemic events before and after cardiovascular outcomes in TECOSSuggests an at-risk type 2 diabetes frail patient phenotype
Standl, E.; Stevens, S. R.; Armstrong, P. W. et al.
2018In Diabetes Care, 41 (3), p. 596-603
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Keywords :
Article; Aged; Body Weight; Cardiovascular Diseases; Diabetes Mellitus, Type 2; Double-Blind Method; Endpoint Determination; Female; Glomerular Filtration Rate; Hospitalization; Humans; Hypoglycemia; Incidence; Insulin; Male; Proportional Hazards Models; Risk Factors; Sitagliptin Phosphate; Treatment Outcome
Abstract :
[en] OBJECTIVE Severe hypoglycemic events (SHEs) in type 2 diabetes are associated with subsequent cardiovascular (CV) event risk.We examined whether CV events were associated with subsequent SHE risk. RESEARCH DESIGN AND METHODS Time-dependent associations between SHEs and a composite CV end point (fatal/ nonfatal myocardial infarction or stroke, hospitalization for unstable angina, hospitalization for heart failure [hHF]) were examined post hoc in 14,671 TECOS (Trial Evaluating Cardiovascular Outcomes With Sitagliptin) participants with type 2 diabetes and CV disease followed for a median of 3.0 years. RESULTS SHEs were uncommon and unassociated with sitagliptin therapy (N = 160 [2.2%], 0.78/100 patient-years vs. N = 143 [1.9%], 0.70/100 patient-years for placebo; hazard ratio [HR] 1.12 [95%CI 0.89, 1.40], P = 0.33). Patientswith (versus without) SHEswere older with longer diabetes duration, lower body weight, and lower estimated glomerular filtration rate;weremore frequentlywomen, nonwhite, and insulin treated; and more often had microalbuminuria or macroalbuminuria. Analyses adjusted for clinical factors showed SHEs were associated with increased risk of the primary composite CV end point (1.55 [1.06, 2.28], P = 0.025), all-cause death (1.83 [1.22, 2.75], P = 0.004), and CV death (1.72 [1.02, 2.87], P = 0.040). Conversely, nonfatal myocardial infarction (3.02 [1.83, 4.96], P < 0.001), nonfatal stroke (2.77 [1.36, 5.63], P = 0.005), and hHF (3.68 [2.13, 6.36], P < 0.001) were associated with increased risk of SHEs. Fully adjusted models showed no association between SHEs and subsequent CV or hHF events, but the association between CV events and subsequent SHEs remained robust. CONCLUSIONS These findings, showing greater risk of SHEs after CV events and greater risk of CV events after SHEs, suggest a common at-risk type 2 diabetes frail patient phenotype. © 2017 by The American Diabetes Association.
Disciplines :
Cardiovascular & respiratory systems
Endocrinology, metabolism & nutrition
Author, co-author :
Standl, E.;  Munich Diabetes Research Group E.V. at Helmholtz Centre, Neuherberg, Germany
Stevens, S. R.;  Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, United States
Armstrong, P. W.;  Canadian VIGOUR Centre, University of Alberta, Edmonton, AL, Canada
Buse, J. B.;  University of North Carolina School of Medicine, Chapel Hill, NC, United States
Chan, J. C. N.;  Department of Medicine and Therapeutics, Chinese University of Hong Kong, Shatin, Hong Kong
Green, J. B.;  Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, United States
Lachin, J. M.;  George Washington University Biostatistics Center, Rockville, MD, United States
Scheen, André  ;  Université de Liège - ULiège > Département des sciences cliniques > Département des sciences cliniques
Travert, F.;  Paris 7 University, Bichat-Claude Bernard Hospital, Paris, France
Van De Werf, F.;  University of Leuven, Leuven, Belgium
Peterson, E. D.;  Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, United States
Holman, R. R.;  Oxford Centre for Diabetes, Endocrinology and Metabolism, Diabetes Trials Unit, University of Oxford, Oxford, United Kingdom
Language :
English
Title :
Increased risk of severe hypoglycemic events before and after cardiovascular outcomes in TECOSSuggests an at-risk type 2 diabetes frail patient phenotype
Publication date :
2018
Journal title :
Diabetes Care
ISSN :
0149-5992
eISSN :
1935-5548
Publisher :
American Diabetes Association Inc.
Volume :
41
Issue :
3
Pages :
596-603
Peer reviewed :
Peer Reviewed verified by ORBi
Funders :
NIMH - National Institute of Mental Health [US-MD]
MSD - Merck Sharp and Dohme [BE]
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