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

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Bethel, M Angelyn

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Merrill, Peter

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Lokhnygina, Yuliya

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Buse, John B

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Chan, Juliana C

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Felício, João S

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Goodman, Shaun G

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Choi, Jasmine

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Gustavson, Stephanie M

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Iqbal, Nayyar

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Lopes, Renato D

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Maggioni, Aldo P

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Öhman, Peter

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Pagidipati, Neha J

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Poulter, Neil R

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Ramachandran, Ambady

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Reicher, Barry

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Holman, Rury R

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Hernandez, Adrian F

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EXSCEL Study Group

dc.date.accessioned

2020-01-10T19:11:09Z

dc.date.available

2020-01-10T19:11:09Z

dc.date.issued

2018-10

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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

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2047-9980

dc.identifier.uri

https://hdl.handle.net/10161/19763

dc.language

eng

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Ovid Technologies (Wolters Kluwer Health)

dc.relation.ispartof

Journal of the American Heart Association

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10.1161/JAHA.118.009304

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EXSCEL Study Group

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Humans

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Cardiovascular Diseases

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Diabetes Mellitus, Type 2

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Hypoglycemic Agents

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Treatment Outcome

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Drug Administration Schedule

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Incidence

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Cause of Death

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Survival Rate

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Risk Assessment

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Risk Factors

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Retrospective Studies

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Follow-Up Studies

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Dose-Response Relationship, Drug

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Time Factors

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Aged

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Middle Aged

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United States

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Female

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Male

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Glycated Hemoglobin A

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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

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School of Medicine

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Duke

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Duke Clinical Research Institute

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Institutes and Centers

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Medicine, Cardiology

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Medicine

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Clinical Science Departments

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Biostatistics & Bioinformatics

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Basic Science Departments

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Population Health Sciences

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Neurology, Neurocritical Care

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Neurology

pubs.publication-status

Published

pubs.volume

7

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