Mansoor Husain
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Recent Grants
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Role of tissue-resident progenitor cells in vascular disease
Open Date: 2020-04-01
Close Date: 2021-03-01
Grant: Close
Cardiovascular effects of GLP-1(28-36): focus on heart failure
Open Date: 2019-04-01
Close Date: 2024-03-01
Grant: Close
Harmonized assessment of common disease mechanisms and biomarkers in rodent models of vascular cognitive impairment and heart failure
Open Date: 2016-07-01
Close Date: 2018-12-01
Grant: Close
Mechanisms of action of the cardioprotective metabolite GLP-1(28-36)
Open Date: 2016-07-01
Close Date: 2019-06-01
Grant: Close
Transcriptional Control of Maternal Obesity-Induced Programming of Adult Cardiac Disease
Open Date: 2016-07-01
Close Date: 2017-06-30
Articles (10)
Year:
2023
Year:
2023
Aim Glucagon‐like peptide‐1 receptor agonists improve glycaemic control: some are now available as oral and subcutaneous formulations, and some have indications for reducing cardiovascular risk. The expanded scope for these therapies warrants comprehensive safety evaluations. We report the safety/tolerability of subcutaneous and oral semaglutide from the SUSTAIN and PIONEER clinical trial programmes, respectively. Materials and methods Adverse events (AEs) from 16 randomized placebo‐ or active‐controlled phase IIIa trials in patients with type 2 diabetes (n = 11 159) including once‐weekly subcutaneous semaglutide (n = 3150; SUSTAIN trials) or once‐daily oral semaglutide (n = 4116; PIONEER trials) were analysed. Data pools were analysed for each programme, with separate analyses of cardiovascular outcomes trials (CVOTs; n = 6480). Results In the phase IIIa pools, gastrointestinal disorders were reported in 41.9%/39.1% of patients with subcutaneous/oral semaglutide, respectively (most prevalent during initiation/escalation) versus 22.0%/24.8% with comparators. Rates of kidney disorders, acute pancreatitis, malignant neoplasms, hypoglycaemia, diabetic retinopathy, heart failure and other cardiovascular events were similar for semaglutide versus comparators. Cholelithiasis incidence was higher with subcutaneous and oral semaglutide versus placebo. Diabetic retinopathy incidence was higher with subcutaneous semaglutide versus placebo in SUSTAIN 6. Small pulse rate increases occurred with both formulations; there was no increased rate of arrhythmias. Fatal AE incidence was similar between semaglutide and comparators. Versus placebo, CVOTs showed a reduced risk of major adverse cardiovascular events with subcutaneous semaglutide and non‐inferiority criteria were met with oral semaglutide. Conclusions The most common AEs with semaglutide were gastrointestinal disorders, which decreased with continued therapy. These comprehensive safety/tolerability data may better inform patient selection and guidance in care.
Year:
2023
Year:
2023
Year:
2022
Year:
2022
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2022
Year:
2021
Year:
2021
Year:
2021
Collaborators (16)
Andrew King
University of Pittsburgh
Kenneth Margulies
Professor, Clinician-Educator
University of Pennsylvania
William David Strain
-
Tina Vilsbøll
-
Senthil Selvaraj
Duke University
Anne Turner
Medical Research Institute of New Zealand
Martin James
University of Exeter
Rashan Haniffa
Professor
University of Edinburgh
john quigley
Professor of Medicine
University of Chicago
Thomas Truelsen
University of Copenhagen
James Januzzi
-
Sanjiv Shah
Northwestern University
Darren McGuire
Distinguished Teaching Professor
University of Texas Southwestern Medical School
Barry Borlaug
Professor
Mayo Clinic
Tamta Chkhikvadze
Hospitalist Scholar, Clinical Assistant Professor
NYU Langone Health
Edward Fysh
University of Western Australia
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