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Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide
OBJECTIVE: Having demonstrated short-term weight loss with liraglutide in this group of obese adults, we now evaluate safety/tolerability (primary outcome) and long-term efficacy for sustaining weight loss (secondary outcome) over 2 years. DESIGN: A randomized, double-blind, placebo-controlled 20-we...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374073/ https://www.ncbi.nlm.nih.gov/pubmed/21844879 http://dx.doi.org/10.1038/ijo.2011.158 |
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author | Astrup, A Carraro, R Finer, N Harper, A Kunesova, M Lean, M E J Niskanen, L Rasmussen, M F Rissanen, A Rössner, S Savolainen, M J Van Gaal, L |
author_facet | Astrup, A Carraro, R Finer, N Harper, A Kunesova, M Lean, M E J Niskanen, L Rasmussen, M F Rissanen, A Rössner, S Savolainen, M J Van Gaal, L |
author_sort | Astrup, A |
collection | PubMed |
description | OBJECTIVE: Having demonstrated short-term weight loss with liraglutide in this group of obese adults, we now evaluate safety/tolerability (primary outcome) and long-term efficacy for sustaining weight loss (secondary outcome) over 2 years. DESIGN: A randomized, double-blind, placebo-controlled 20-week study with 2-year extension (sponsor unblinded at 20 weeks, participants/investigators at 1 year) in 19 European clinical research centers. SUBJECTS: A total of 564 adults (n=90–98 per group; body mass index 30–40 kg m(−2)) enrolled, 398 entered the extension and 268 completed the 2-year trial. Participants received diet (500 kcal deficit per day) and exercise counseling during 2-week run-in, before being randomly assigned (with a telephone or web-based system) to once-daily subcutaneous liraglutide (1.2, 1.8, 2.4 or 3.0 mg, n=90–95), placebo (n=98) or open-label orlistat (120 mg × 3, n=95). After 1 year, liraglutide/placebo recipients switched to liraglutide 2.4 mg, then 3.0 mg (based on 20-week and 1-year results, respectively). The trial ran from January 2007–April 2009 and is registered with Clinicaltrials.gov, number NCT00480909. RESULTS: From randomization to year 1, liraglutide 3.0 mg recipients lost 5.8 kg (95% confidence interval 3.7–8.0) more weight than those on placebo and 3.8 kg (1.6–6.0) more than those on orlistat (P⩽0.0001; intention-to-treat, last-observation-carried-forward). At year 2, participants on liraglutide 2.4/3.0 mg for the full 2 years (pooled group, n=184) lost 3.0 kg (1.3–4.7) more weight than those on orlistat (n=95; P<0.001). Completers on liraglutide 2.4/3.0 mg (n=92) maintained a 2-year weight loss of 7.8 kg from screening. With liraglutide 3.0 mg, 20-week body fat decreased by 15.4% and lean tissue by 2.0%. The most frequent drug-related side effects were mild to moderate, transient nausea and vomiting. With liraglutide 2.4/3.0 mg, the 2-year prevalence of prediabetes and metabolic syndrome decreased by 52 and 59%, with improvements in blood pressure and lipids. CONCLUSION: Liraglutide is well tolerated, sustains weight loss over 2 years and improves cardiovascular risk factors. |
format | Online Article Text |
id | pubmed-3374073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33740732012-06-13 Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide Astrup, A Carraro, R Finer, N Harper, A Kunesova, M Lean, M E J Niskanen, L Rasmussen, M F Rissanen, A Rössner, S Savolainen, M J Van Gaal, L Int J Obes (Lond) Original Article OBJECTIVE: Having demonstrated short-term weight loss with liraglutide in this group of obese adults, we now evaluate safety/tolerability (primary outcome) and long-term efficacy for sustaining weight loss (secondary outcome) over 2 years. DESIGN: A randomized, double-blind, placebo-controlled 20-week study with 2-year extension (sponsor unblinded at 20 weeks, participants/investigators at 1 year) in 19 European clinical research centers. SUBJECTS: A total of 564 adults (n=90–98 per group; body mass index 30–40 kg m(−2)) enrolled, 398 entered the extension and 268 completed the 2-year trial. Participants received diet (500 kcal deficit per day) and exercise counseling during 2-week run-in, before being randomly assigned (with a telephone or web-based system) to once-daily subcutaneous liraglutide (1.2, 1.8, 2.4 or 3.0 mg, n=90–95), placebo (n=98) or open-label orlistat (120 mg × 3, n=95). After 1 year, liraglutide/placebo recipients switched to liraglutide 2.4 mg, then 3.0 mg (based on 20-week and 1-year results, respectively). The trial ran from January 2007–April 2009 and is registered with Clinicaltrials.gov, number NCT00480909. RESULTS: From randomization to year 1, liraglutide 3.0 mg recipients lost 5.8 kg (95% confidence interval 3.7–8.0) more weight than those on placebo and 3.8 kg (1.6–6.0) more than those on orlistat (P⩽0.0001; intention-to-treat, last-observation-carried-forward). At year 2, participants on liraglutide 2.4/3.0 mg for the full 2 years (pooled group, n=184) lost 3.0 kg (1.3–4.7) more weight than those on orlistat (n=95; P<0.001). Completers on liraglutide 2.4/3.0 mg (n=92) maintained a 2-year weight loss of 7.8 kg from screening. With liraglutide 3.0 mg, 20-week body fat decreased by 15.4% and lean tissue by 2.0%. The most frequent drug-related side effects were mild to moderate, transient nausea and vomiting. With liraglutide 2.4/3.0 mg, the 2-year prevalence of prediabetes and metabolic syndrome decreased by 52 and 59%, with improvements in blood pressure and lipids. CONCLUSION: Liraglutide is well tolerated, sustains weight loss over 2 years and improves cardiovascular risk factors. Nature Publishing Group 2012-06 2011-08-16 /pmc/articles/PMC3374073/ /pubmed/21844879 http://dx.doi.org/10.1038/ijo.2011.158 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Astrup, A Carraro, R Finer, N Harper, A Kunesova, M Lean, M E J Niskanen, L Rasmussen, M F Rissanen, A Rössner, S Savolainen, M J Van Gaal, L Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide |
title | Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide |
title_full | Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide |
title_fullStr | Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide |
title_full_unstemmed | Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide |
title_short | Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide |
title_sort | safety, tolerability and sustained weight loss over 2 years with the once-daily human glp-1 analog, liraglutide |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374073/ https://www.ncbi.nlm.nih.gov/pubmed/21844879 http://dx.doi.org/10.1038/ijo.2011.158 |
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