Literature DB >> 29627109

Myocardial Infarction Subtypes in Patients With Type 2 Diabetes Mellitus and the Effect of Liraglutide Therapy (from the LEADER Trial).

Steven P Marso1, Michael A Nauck2, Tea Monk Fries3, Søren Rasmussen3, Marianne Bach Treppendahl3, John B Buse4.   

Abstract

Diabetes mellitus (DM) is a known risk factor for myocardial infarction (MI); however, data regarding MI subtypes in people with diabetes are limited. In the Liraglutide Effect and Action in Diabetes: Evaluation of Cardiovascular Outcome Results (LEADER) trial (n = 9,340), liraglutide significantly reduced the risk of major adverse cardiovascular (CV) events (composite of CV death, nonfatal MI, or nonfatal stroke) versus placebo in patients with type 2 DM and high CV risk. Liraglutide also reduced risk of first MI (292 events with liraglutide vs 339 with placebo). This post hoc analysis characterized MIs (first and recurrent) occurring in LEADER, by treatment arm and regarding incidence, outcome, subtype, and troponin levels. A total of 780 MIs (first and recurrent) were reported, with fewer in the liraglutide-treatment group than in the placebo-treatment group (359 vs 421, p = 0.022). Numerically fewer MIs were associated with CV death with liraglutide than with placebo (17 vs 28 fatal MIs, p = 0.28). Symptomatic MIs in both arms were mainly non-ST-segment elevation MI (555/641) and spontaneous MI (518/641). Numerically greater proportions of symptomatic MIs were associated with troponin levels ≤5× or ≤10× the upper reference limit with liraglutide versus placebo (p = 0.16 and p = 0.42, respectively). At baseline, more liraglutide-treated patients than placebo-treated patients with MI during the trial had a history of coronary artery bypass graft (p = 0.008), and fewer had peripheral arterial disease in the lower extremities (p = 0.005) and >50% stenosis of the coronary artery, the carotid artery, or other arteries (p = 0.044). In conclusion, this analysis showed that liraglutide reduces the incidence of MIs in patients with type 2 DM at high CV risk and may impact the clinical outcomes of MI.
Copyright © 2018 The Author(s). Published by Elsevier Inc. All rights reserved.

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Year:  2018        PMID: 29627109     DOI: 10.1016/j.amjcard.2018.02.030

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  5 in total

1.  Health-related quality of life in people with type 2 diabetes participating in the LEADER trial.

Authors:  Michael A Nauck; John B Buse; Johannes F E Mann; Stuart Pocock; Heidrun Bosch-Traberg; Helle Frimer-Larsen; Qing Ye; Alastair Gray
Journal:  Diabetes Obes Metab       Date:  2018-10-25       Impact factor: 6.577

Review 2.  GLP-1 receptor agonists (GLP-1RAs): cardiovascular actions and therapeutic potential.

Authors:  Xiaoxuan Ma; Zhenghong Liu; Iqra Ilyas; Peter J Little; Danielle Kamato; Amirhossein Sahebka; Zhengfang Chen; Sihui Luo; Xueying Zheng; Jianping Weng; Suowen Xu
Journal:  Int J Biol Sci       Date:  2021-05-11       Impact factor: 6.580

3.  Impact of daily glucose fluctuations on cardiovascular outcomes after percutaneous coronary intervention for patients with stable coronary artery disease undergoing lipid-lowering therapy.

Authors:  Hiroyuki Yamamoto; Toshiro Shinke; Hiromasa Otake; Hiroyuki Kawamori; Takayoshi Toba; Masaru Kuroda; Yushi Hirota; Kazuhiko Sakaguchi; Wataru Ogawa; Ken-Ichi Hirata
Journal:  J Diabetes Investig       Date:  2020-12-18       Impact factor: 4.232

4.  Nonglycemic Outcomes of Antidiabetic Medications.

Authors:  Christopher Morse; David Sze; Dhiren Patel; Jennifer Goldman
Journal:  Clin Diabetes       Date:  2019-04

Review 5.  Effects of GLP-1 receptor agonists and SGLT-2 inhibitors on cardiac structure and function: a narrative review of clinical evidence.

Authors:  Andrea Natali; Lorenzo Nesti; Domenico Tricò; Ele Ferrannini
Journal:  Cardiovasc Diabetol       Date:  2021-09-28       Impact factor: 9.951

  5 in total

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