Effect of Once-Weekly Exenatide on Clinical Outcomes According to Baseline Risk in Patients With Type 2 Diabetes Mellitus: Insights From the EXSCEL Trial.
dc.contributor.author | Mentz, Robert J | |
dc.contributor.author | Bethel, M Angelyn | |
dc.contributor.author | Merrill, Peter | |
dc.contributor.author | Lokhnygina, Yuliya | |
dc.contributor.author | Buse, John B | |
dc.contributor.author | Chan, Juliana C | |
dc.contributor.author | Felício, João S | |
dc.contributor.author | Goodman, Shaun G | |
dc.contributor.author | Choi, Jasmine | |
dc.contributor.author | Gustavson, Stephanie M | |
dc.contributor.author | Iqbal, Nayyar | |
dc.contributor.author | Lopes, Renato D | |
dc.contributor.author | Maggioni, Aldo P | |
dc.contributor.author | Öhman, Peter | |
dc.contributor.author | Pagidipati, Neha J | |
dc.contributor.author | Poulter, Neil R | |
dc.contributor.author | Ramachandran, Ambady | |
dc.contributor.author | Reicher, Barry | |
dc.contributor.author | Holman, Rury R | |
dc.contributor.author | Hernandez, Adrian F | |
dc.contributor.author | EXSCEL Study Group | |
dc.date.accessioned | 2020-01-10T19:11:09Z | |
dc.date.available | 2020-01-10T19:11:09Z | |
dc.date.issued | 2018-10 | |
dc.date.updated | 2020-01-10T19:11:07Z | |
dc.description.abstract | Background In the EXSCEL (Exenatide Study of Cardiovascular Event Lowering), exenatide once-weekly resulted in a nonsignificant reduction in major adverse cardiovascular events ( MACEs ) and a nominal 14% reduction in all-cause mortality in 14 752 patients with type 2 diabetes mellitus (T2 DM ) with and without cardiovascular disease. Whether patients at increased risk for events experienced a comparatively greater treatment benefit with exenatide is unknown. Methods and Results In the EXSCEL population, we created risk scores for MACEs and all-cause mortality using step-wise selection of baseline characteristics. A risk score was calculated for each patient, and a time-to-event model for each end point was developed including the risk score, treatment assignment, and risk-treatment interaction. Interaction P values evaluating for a differential treatment effect by baseline risk were reported. Over a median follow-up of 3.2 years (interquartile range, 2.2, 4.4), 1091 (7.4%) patients died and 1744 (11.8%) experienced a MACE . Independent predictors of MACEs and all-cause mortality included age, sex, comorbidities (eg, previous cardiovascular event), body mass index, blood pressure, hemoglobin A1c, and estimated glomerular filtration rate. The all-cause mortality and MACE risk models had modest discrimination with optimism-corrected c-indices of 0.73 and 0.71, respectively. No interaction was observed between treatment effect and risk profile for either end point (both interactions, P>0.1). Conclusions Baseline characteristics (eg, age, previous cardiovascular events) and routine laboratory values (eg, hemoglobin A1c, estimated glomerular filtration rate) provided modest prognostic value for mortality and MACEs in a broad population of patients with type 2 diabetes mellitus. Exenatide's effects on mortality and MACEs were consistent across the spectrum of baseline risk. Clinical Trial Registration URL: https://www.clinicaltrials.gov . Unique identifier: NCT 01144338. | |
dc.identifier.issn | 2047-9980 | |
dc.identifier.issn | 2047-9980 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Ovid Technologies (Wolters Kluwer Health) | |
dc.relation.ispartof | Journal of the American Heart Association | |
dc.relation.isversionof | 10.1161/JAHA.118.009304 | |
dc.subject | EXSCEL Study Group | |
dc.subject | Humans | |
dc.subject | Cardiovascular Diseases | |
dc.subject | Diabetes Mellitus, Type 2 | |
dc.subject | Hypoglycemic Agents | |
dc.subject | Treatment Outcome | |
dc.subject | Drug Administration Schedule | |
dc.subject | Incidence | |
dc.subject | Cause of Death | |
dc.subject | Survival Rate | |
dc.subject | Risk Assessment | |
dc.subject | Risk Factors | |
dc.subject | Retrospective Studies | |
dc.subject | Follow-Up Studies | |
dc.subject | Dose-Response Relationship, Drug | |
dc.subject | Time Factors | |
dc.subject | Aged | |
dc.subject | Middle Aged | |
dc.subject | United States | |
dc.subject | Female | |
dc.subject | Male | |
dc.subject | Glycated Hemoglobin A | |
dc.subject | Exenatide | |
dc.title | Effect of Once-Weekly Exenatide on Clinical Outcomes According to Baseline Risk in Patients With Type 2 Diabetes Mellitus: Insights From the EXSCEL Trial. | |
dc.type | Journal article | |
duke.contributor.orcid | Mentz, Robert J|0000-0002-3222-1719 | |
duke.contributor.orcid | Lopes, Renato D|0000-0003-2999-4961 | |
duke.contributor.orcid | Hernandez, Adrian F|0000-0003-3387-9616 | |
pubs.begin-page | e009304 | |
pubs.issue | 19 | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Clinical Research Institute | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Medicine, Cardiology | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Biostatistics & Bioinformatics | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Population Health Sciences | |
pubs.organisational-group | Neurology, Neurocritical Care | |
pubs.organisational-group | Neurology | |
pubs.publication-status | Published | |
pubs.volume | 7 |
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