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

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2023

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2022

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2022

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2022

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2021

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2021

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2021

Collaborators (16)

Andrew King

University of Pittsburgh

UNITED STATES
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Kenneth Margulies

Professor, Clinician-Educator

University of Pennsylvania

UNITED STATES
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William David Strain

-

UNITED KINGDOM
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Tina Vilsbøll

-

DENMARK
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Senthil Selvaraj

Duke University

UNITED STATES
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Anne Turner

Medical Research Institute of New Zealand

NEW ZEALAND
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Martin James

University of Exeter

UNITED KINGDOM
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Rashan Haniffa

Professor

University of Edinburgh

UNITED KINGDOM
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john quigley

Professor of Medicine

University of Chicago

UNITED STATES
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Thomas Truelsen

University of Copenhagen

DENMARK
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James Januzzi

-

UNITED STATES
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Sanjiv Shah

Northwestern University

UNITED STATES
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Darren McGuire

Distinguished Teaching Professor

University of Texas Southwestern Medical School

UNITED STATES
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Barry Borlaug

Professor

Mayo Clinic

UNITED STATES
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Tamta Chkhikvadze

Hospitalist Scholar, Clinical Assistant Professor

NYU Langone Health

UNITED STATES
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Edward Fysh

University of Western Australia

AUSTRALIA
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