A randomized, open‐label, active comparator trial assessing the effects of 26 weeks of liraglutide or sitagliptin on cardiovascular function in young obese adults with type 2 diabetes. Issue 7 (1st April 2020)
- Record Type:
- Journal Article
- Title:
- A randomized, open‐label, active comparator trial assessing the effects of 26 weeks of liraglutide or sitagliptin on cardiovascular function in young obese adults with type 2 diabetes. Issue 7 (1st April 2020)
- Main Title:
- A randomized, open‐label, active comparator trial assessing the effects of 26 weeks of liraglutide or sitagliptin on cardiovascular function in young obese adults with type 2 diabetes
- Authors:
- Webb, David R.
Htike, Zin Zin
Swarbrick, Daniel J.
Brady, Emer M.
Gray, Laura J.
Biglands, John
Gulsin, Gaurav S.
Henson, Joseph
Khunti, Kamlesh
McCann, Gerry P.
Waller, Helen L.
Webb, M'Balu A.
Sargeant, Jack A.
Yates, Thomas
Zaccardi, Francesco
Davies, Melanie J. - Abstract:
- Abstract: Aim: To compare the effects of a glucagon‐like peptide‐1 receptor agonist and a dipeptidyl peptidase‐4 inhibitor on magnetic resonance imaging‐derived measures of cardiovascular function. Materials and methods: In a prospective, randomized, open‐label, blinded endpoint trial liraglutide (1.8 mg) and sitagliptin (100 mg) were compared in asymptomatic, non‐insulin treated young (aged 18‐50 years) adults with obesity and type 2 diabetes. The primary outcome was difference in circumferential peak early diastolic strain rate change (PEDSR), a biomarker of cardiac diastolic dysfunction 26 weeks after randomization. Secondary outcomes included other indices of cardiac structure and function, HbA1c and body weight. Results: Seventy‐six participants were randomized (54% female, mean ± SD age 44 ± 6 years, diabetes duration 4.4 years, body mass index 35.3 ± 6.1 kg m −2 ), of whom 65% had ≥1 cardiovascular risk factor. Sixty‐one participants had primary outcome data available. There were no statistically significant between‐group differences (intention‐to‐treat; mean [95% confidence interval]) in PEDSR change (−0.01 [−0.07, +0.06] s −1 ), left ventricular ejection fraction (−1.98 [−4.90, +0.94]%), left ventricular mass (+1.14 [−5.23, +7.50] g) or aortic distensibility (−0.35 [−0.98, +0.28] mmHg −1 × 10 −3 ) after 26 weeks. Reductions in HbA1c (−4.57 [−9.10, −0.37] mmol mol −1 ) and body weight (−3.88 [−5.74, −2.01] kg) were greater with liraglutide. Conclusion: There were noAbstract: Aim: To compare the effects of a glucagon‐like peptide‐1 receptor agonist and a dipeptidyl peptidase‐4 inhibitor on magnetic resonance imaging‐derived measures of cardiovascular function. Materials and methods: In a prospective, randomized, open‐label, blinded endpoint trial liraglutide (1.8 mg) and sitagliptin (100 mg) were compared in asymptomatic, non‐insulin treated young (aged 18‐50 years) adults with obesity and type 2 diabetes. The primary outcome was difference in circumferential peak early diastolic strain rate change (PEDSR), a biomarker of cardiac diastolic dysfunction 26 weeks after randomization. Secondary outcomes included other indices of cardiac structure and function, HbA1c and body weight. Results: Seventy‐six participants were randomized (54% female, mean ± SD age 44 ± 6 years, diabetes duration 4.4 years, body mass index 35.3 ± 6.1 kg m −2 ), of whom 65% had ≥1 cardiovascular risk factor. Sixty‐one participants had primary outcome data available. There were no statistically significant between‐group differences (intention‐to‐treat; mean [95% confidence interval]) in PEDSR change (−0.01 [−0.07, +0.06] s −1 ), left ventricular ejection fraction (−1.98 [−4.90, +0.94]%), left ventricular mass (+1.14 [−5.23, +7.50] g) or aortic distensibility (−0.35 [−0.98, +0.28] mmHg −1 × 10 −3 ) after 26 weeks. Reductions in HbA1c (−4.57 [−9.10, −0.37] mmol mol −1 ) and body weight (−3.88 [−5.74, −2.01] kg) were greater with liraglutide. Conclusion: There were no differences in cardiovascular structure or function after short‐term use of liraglutide and sitagliptin in younger adults with obesity and type 2 diabetes. Longer studies in patients with more severe cardiac dysfunction may be necessary before definitive conclusions can be made about putative pleiotropic properties of incretin‐based therapies. … (more)
- Is Part Of:
- Diabetes, obesity & metabolism. Volume 22:Issue 7(2020)
- Journal:
- Diabetes, obesity & metabolism
- Issue:
- Volume 22:Issue 7(2020)
- Issue Display:
- Volume 22, Issue 7 (2020)
- Year:
- 2020
- Volume:
- 22
- Issue:
- 7
- Issue Sort Value:
- 2020-0022-0007-0000
- Page Start:
- 1187
- Page End:
- 1196
- Publication Date:
- 2020-04-01
- Subjects:
- cardiac magnetic resonance -- diastolic dysfunction -- liraglutide -- obesity -- peak early diastolic strain rate -- randomized controlled trial -- sitagliptin -- type 2 diabetes -- young adults
Diabetes -- Periodicals
Obesity -- Periodicals
Metabolism -- Disorders -- Periodicals
Clinical pharmacology -- Periodicals
616.462 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=1462-8902&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1463-1326 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/dom.14023 ↗
- Languages:
- English
- ISSNs:
- 1462-8902
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 3579.601970
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