Effect of liraglutide on physical performance in type 2 diabetes (LIPER2): A randomised, double-blind, controlled trial

被引:4
作者
Maria Waegner, Ana [1 ,2 ]
Miranda-Calderin, Guillermo
Arantza Ugarte-Lopetegui, Miren [3 ]
Marrero-Santiago, Hector [4 ]
Suarez-Castellano, Laura [4 ]
del Pino Alberiche-Ruano, Maria [1 ,2 ]
Castillo-Garcia, Nuria [3 ]
Jose Lopez-Madrazo, Maria [1 ]
Aleman, Carolina [3 ]
Martinez-Mancebo, Carla [6 ]
Lopez-Rios, Laura [1 ,2 ]
Diez del Pino, Alicia [5 ]
Javier Novoa-Mogollon, Francisco [1 ,2 ]
机构
[1] Complejo Hosp Univ Insular Materno Infant, Endocrinol & Nutr Dept, Av Maritima S-N, Las Palmas Gran Canaria 35016, Spain
[2] Univ Palmas Gran Canaria, IUIBS, Las Palmas Gran Canaria, Spain
[3] Complejo Hosp Univ Insular Materno Infant, Phys Med & Rehabil Dept, Av Maritima S-N, La Palmas Gran Canaria 35016, Spain
[4] Complejo Hosp Univ Insular Materno Infant, Dept Cardiol, Av Maritima S-N, Las Palmas Gran Canaria 35016, Spain
[5] Complejo Hosp Univ Insular Materno Infant, Hosp Pharm, Av Maritima S-N, Las Palmas Gran Canaria 35016, Spain
[6] Ctr Salud Maspalomas, Gerencia Atenc Primaria, Gran Canaria, Spain
关键词
Randomised controlled trial; Ergometry; Maximal oxygen consumption; Ventricular function; Diabetes; GLP1-agonist;
D O I
10.1016/j.conctc.2016.06.007
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Preclinical studies and small clinical trials suggest that glucagon-like peptide 1 (GLP1) may have a positive effect on ventricular function. Liraglutide is a GLP1-analogue used in the treatment of type 2 diabetes. LIPER2 is a phase IV, randomised, double-blind, placebo-controlled, parallel-design trial, assessing the effect of 6 months' liraglutide 1.8 mg/d on measures of cardiac function and physical performance in patients with type 2 diabetes. A total of 30 patients with type 2 diabetes will be included, if their HbA1c is between 7 and 10% while on oral agents (including metformin if tolerated and not contraindicated), a maximum of 2 intermediate or long-acting insulin injections per day or a combination of both. After their baseline examinations, patients are randomised to receive a daily subcutaneous liraglutide or placebo injection (titrated to 1.8 mg/d if tolerated) for 6 months. The primary end-point is the maximal oxygen consumption during cycle ergometry at the end of the study period. Other end-points include distance covered during a 6-min walk test, left ventricular ejection fraction and other measures of ventricular systolic and diastolic functions assessed by echocardiography, heart rate, blood pressure, pro-brain natriuretic peptide, C-reactive protein, HbA1c, lipids, apolipoprotein B, body weight and waist girth. Safety end-points include adverse event reporting, blood count, kidney and liver function, amylase, lipase, electrolytes, calcitonin, CA19.9 and pregnancy test for fertile women. At the time of this report, recruitment is still ongoing. Results are expected to be reported in December 2016. (C) 2016 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license
引用
收藏
页码:46 / 51
页数:6
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