Effect of dipeptidyl peptidase-4 inhibitors on heart failure: A meta-analysis of randomized clinical trials

© 2016 Elsevier Ireland Ltd. All rights reserved. Background: Recent studies have suggested that dipeptidyl peptidase-4 inhibitors (DPP-4 inhibitors) may be associated with increased risk of heart failure (HF), but evidence was inconclusive. We aimed to determine the effects of DPP-4 inhibitors on r...

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Main Authors: J. Kongwatcharapong, P. Dilokthornsakul, S. Nathisuwan, A. Phrommintikul, N. Chaiyakunapruk
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/56148
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spelling th-cmuir.6653943832-561482018-09-05T03:09:39Z Effect of dipeptidyl peptidase-4 inhibitors on heart failure: A meta-analysis of randomized clinical trials J. Kongwatcharapong P. Dilokthornsakul S. Nathisuwan A. Phrommintikul N. Chaiyakunapruk Medicine © 2016 Elsevier Ireland Ltd. All rights reserved. Background: Recent studies have suggested that dipeptidyl peptidase-4 inhibitors (DPP-4 inhibitors) may be associated with increased risk of heart failure (HF), but evidence was inconclusive. We aimed to determine the effects of DPP-4 inhibitors on risk of HF. Methods: An extensive search in PubMed, EMBASE, CINAHL, IPA, Cochrane, ClinicalTrial.gov and the manufacturers' websites for randomized controlled trials (RCT) of all DPP-4 inhibitors was performed up to June 2015. All RCTs comparing DPP-4 inhibitors to any comparators with minimum follow-up of 12 weeks were included. The primary outcome was the occurrence of HF. Results: A total of 54 studies with 74,737 participants were included for analysis. Overall, DPP-4 inhibitors were not associated with an increased risk of HF compared to comparators (relative risk (RR) 1.106; 95% CI 0.995-1.228; p = 0.062). When analyzed individually, saxagliptin was significantly associated with the increased risk of HF (RR 1.215; 95% CI, 1.028-1.437; p = 0.022), while others were not. Age ≥ 65 years, diabetes duration of ≥ 10 years and BMI ≥ 30 kg/m2were associated with an increased risk of HF among patients using saxagliptin. Conclusions: Our meta-analysis suggested a differential effect of each DPP-4 inhibitor on the risk of HF. Use of saxagliptin significantly increases the risk of HF by 21% especially among patients with high CV risk while no signals were detected with other agents. This information should be taken into consideration when prescribing DDP-4 inhibitors. 2018-09-05T03:09:39Z 2018-09-05T03:09:39Z 2016-05-15 Journal 18741754 01675273 2-s2.0-84962810190 10.1016/j.ijcard.2016.02.146 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84962810190&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/56148
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Medicine
spellingShingle Medicine
J. Kongwatcharapong
P. Dilokthornsakul
S. Nathisuwan
A. Phrommintikul
N. Chaiyakunapruk
Effect of dipeptidyl peptidase-4 inhibitors on heart failure: A meta-analysis of randomized clinical trials
description © 2016 Elsevier Ireland Ltd. All rights reserved. Background: Recent studies have suggested that dipeptidyl peptidase-4 inhibitors (DPP-4 inhibitors) may be associated with increased risk of heart failure (HF), but evidence was inconclusive. We aimed to determine the effects of DPP-4 inhibitors on risk of HF. Methods: An extensive search in PubMed, EMBASE, CINAHL, IPA, Cochrane, ClinicalTrial.gov and the manufacturers' websites for randomized controlled trials (RCT) of all DPP-4 inhibitors was performed up to June 2015. All RCTs comparing DPP-4 inhibitors to any comparators with minimum follow-up of 12 weeks were included. The primary outcome was the occurrence of HF. Results: A total of 54 studies with 74,737 participants were included for analysis. Overall, DPP-4 inhibitors were not associated with an increased risk of HF compared to comparators (relative risk (RR) 1.106; 95% CI 0.995-1.228; p = 0.062). When analyzed individually, saxagliptin was significantly associated with the increased risk of HF (RR 1.215; 95% CI, 1.028-1.437; p = 0.022), while others were not. Age ≥ 65 years, diabetes duration of ≥ 10 years and BMI ≥ 30 kg/m2were associated with an increased risk of HF among patients using saxagliptin. Conclusions: Our meta-analysis suggested a differential effect of each DPP-4 inhibitor on the risk of HF. Use of saxagliptin significantly increases the risk of HF by 21% especially among patients with high CV risk while no signals were detected with other agents. This information should be taken into consideration when prescribing DDP-4 inhibitors.
format Journal
author J. Kongwatcharapong
P. Dilokthornsakul
S. Nathisuwan
A. Phrommintikul
N. Chaiyakunapruk
author_facet J. Kongwatcharapong
P. Dilokthornsakul
S. Nathisuwan
A. Phrommintikul
N. Chaiyakunapruk
author_sort J. Kongwatcharapong
title Effect of dipeptidyl peptidase-4 inhibitors on heart failure: A meta-analysis of randomized clinical trials
title_short Effect of dipeptidyl peptidase-4 inhibitors on heart failure: A meta-analysis of randomized clinical trials
title_full Effect of dipeptidyl peptidase-4 inhibitors on heart failure: A meta-analysis of randomized clinical trials
title_fullStr Effect of dipeptidyl peptidase-4 inhibitors on heart failure: A meta-analysis of randomized clinical trials
title_full_unstemmed Effect of dipeptidyl peptidase-4 inhibitors on heart failure: A meta-analysis of randomized clinical trials
title_sort effect of dipeptidyl peptidase-4 inhibitors on heart failure: a meta-analysis of randomized clinical trials
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84962810190&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/56148
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