TY - JOUR
T1 - Efficacy of liraglutide for weight loss among patients with type 2 diabetes
T2 - The SCALE diabetes randomized clinical trial
AU - NN8022-1922 Study Group
AU - Davies, Melanie J.
AU - Bergenstal, Richard
AU - Bode, Bruce
AU - Kushner, Robert F.
AU - Lewin, Andrew
AU - Skjøth, Trine Vang
AU - Andreasen, Arne Haahr
AU - Jensen, Christine Bjørn
AU - DeFronzo, Ralph A.
AU - Valensi, Paul
AU - Levy, Marc
AU - Benabdallah, Sonia
AU - Serusclat, Pierre
AU - Courreges, Jean Pierre
AU - Gouet, Didier
AU - Clavel, Sylvaine
AU - Cariou, Bertrand
AU - Tyler, Kerstin
AU - Hanefeld, Markolf
AU - Jordan, Ralf
AU - Milek, Karsten
AU - Rose, Ludger
AU - Sauter, Joachim
AU - Steindorf, Joerg
AU - Wendish, Ulrich
AU - Rudofsky, Gottfried
AU - Erlinger, Rudolf
AU - Harman-Boehm, Ilana
AU - Mosenzon, Ofri
AU - Cohen, Josef
AU - Karasik, Avraham
AU - Minuchin, Oscar
AU - Snyman, Hans Hendrik
AU - Komati, Stephanus M.
AU - Naiker, Puvanesveri
AU - Lombaard, Johannes Jurgens
AU - Podgorski, Gracjan
AU - Saleh, Munira Fakir
AU - Muñoz, Manuel
AU - Parreño, Luis De Teresa
AU - García, Santiago Durán
AU - Esteban, Basilio Moreno
AU - Fernández, Margarita Rivas
AU - Pérez, Angel Maria Sendón
AU - Burguera, Bartolomé
AU - Vázquez, Clotilde
AU - Hemmingsson, Joanna Uddén
AU - Eizyk, Enrique
AU - Rautio, Aslak
AU - Granda-Rodriguez, Ramona
N1 - Publisher Copyright:
Copyright © 2015 American Medical Association. All rights reserved.
PY - 2015/8/18
Y1 - 2015/8/18
N2 - Importance: Weight loss of 5% to 10% can improve type 2 diabetes and related comorbidities. Few safe, effective weight-management drugs are currently available. Objective: To investigate efficacy and safety of liraglutide vs placebo for weight management in adults with overweight or obesity and type 2 diabetes. Design, Setting, and Participants: Fifty-six-week randomized (2:1:1), double-blind, placebo-controlled, parallel-group trial with 12-week observational off-drug follow-up period. The study was conducted at 126 sites in 9 countries between June 2011 and January 2013. Of 1361 participants assessed for eligibility, 846 were randomized. Inclusion criteria were body mass index of 27.0 or greater, age 18 years or older, taking 0 to 3 oral hypoglycemic agents (metformin, thiazolidinedione, sulfonylurea) with stable body weight, and glycated hemoglobin level 7.0% to 10.0%. Interventions: Once-daily, subcutaneous liraglutide (3.0mg) (n = 423), liraglutide (1.8mg) (n = 211), or placebo (n = 212), all as adjunct to 500 kcal/d dietary deficit and increased physical activity (≥150 min/wk). Main Outcomes and Measures: Three coprimary end points: relative change inweight, proportion of participants losing 5% or more, or more than 10%, of baselineweight atweek 56. Results: Baseline weight was 105.7 kg with liraglutide (3.0-mg dose), 105.8 kg with liraglutide (1.8-mg dose), and 106.5 kg with placebo. Weight loss was 6.0% (6.4 kg) with liraglutide (3.0-mg dose), 4.7% (5.0 kg) with liraglutide (1.8-mg dose), and 2.0% (2.2 kg) with placebo (estimated difference for liraglutide [3.0mg] vs placebo, -4.00% [95% CI, -5.10% to -2.90%]; liraglutide [1.8mg] vs placebo, -2.71% [95% CI, -4.00% to -1.42%]; P < .001 for both). Weight loss of 5% or greater occurred in 54.3% with liraglutide (3.0mg) and 40.4% with liraglutide (1.8mg) vs 21.4% with placebo (estimated difference for liraglutide [3.0mg] vs placebo, 32.9% [95% CI, 24.6% to 41.2%]; for liraglutide [1.8mg] vs placebo, 19.0% [95% CI, 9.1% to 28.8%]; P < .001 for both). Weight loss greater than 10% occurred in 25.2% with liraglutide (3.0mg) and 15.9% with liraglutide (1.8mg) vs 6.7% with placebo (estimated difference for liraglutide [3.0mg] vs placebo, 18.5% [95% CI, 12.7% to 24.4%], P < .001; for liraglutide [1.8mg] vs placebo, 9.3% [95% CI, 2.7% to 15.8%], P = .006). More gastrointestinal disorders were reported with liraglutide (3.0mg) vs liraglutide (1.8mg) and placebo. No pancreatitis was reported. Conclusions and Relevance: Among overweight and obese participants with type 2 diabetes, use of subcutaneous liraglutide (3.0mg) daily, compared with placebo, resulted inweight loss over 56weeks. Further studies are needed to evaluate longer-term efficacy and safety.
AB - Importance: Weight loss of 5% to 10% can improve type 2 diabetes and related comorbidities. Few safe, effective weight-management drugs are currently available. Objective: To investigate efficacy and safety of liraglutide vs placebo for weight management in adults with overweight or obesity and type 2 diabetes. Design, Setting, and Participants: Fifty-six-week randomized (2:1:1), double-blind, placebo-controlled, parallel-group trial with 12-week observational off-drug follow-up period. The study was conducted at 126 sites in 9 countries between June 2011 and January 2013. Of 1361 participants assessed for eligibility, 846 were randomized. Inclusion criteria were body mass index of 27.0 or greater, age 18 years or older, taking 0 to 3 oral hypoglycemic agents (metformin, thiazolidinedione, sulfonylurea) with stable body weight, and glycated hemoglobin level 7.0% to 10.0%. Interventions: Once-daily, subcutaneous liraglutide (3.0mg) (n = 423), liraglutide (1.8mg) (n = 211), or placebo (n = 212), all as adjunct to 500 kcal/d dietary deficit and increased physical activity (≥150 min/wk). Main Outcomes and Measures: Three coprimary end points: relative change inweight, proportion of participants losing 5% or more, or more than 10%, of baselineweight atweek 56. Results: Baseline weight was 105.7 kg with liraglutide (3.0-mg dose), 105.8 kg with liraglutide (1.8-mg dose), and 106.5 kg with placebo. Weight loss was 6.0% (6.4 kg) with liraglutide (3.0-mg dose), 4.7% (5.0 kg) with liraglutide (1.8-mg dose), and 2.0% (2.2 kg) with placebo (estimated difference for liraglutide [3.0mg] vs placebo, -4.00% [95% CI, -5.10% to -2.90%]; liraglutide [1.8mg] vs placebo, -2.71% [95% CI, -4.00% to -1.42%]; P < .001 for both). Weight loss of 5% or greater occurred in 54.3% with liraglutide (3.0mg) and 40.4% with liraglutide (1.8mg) vs 21.4% with placebo (estimated difference for liraglutide [3.0mg] vs placebo, 32.9% [95% CI, 24.6% to 41.2%]; for liraglutide [1.8mg] vs placebo, 19.0% [95% CI, 9.1% to 28.8%]; P < .001 for both). Weight loss greater than 10% occurred in 25.2% with liraglutide (3.0mg) and 15.9% with liraglutide (1.8mg) vs 6.7% with placebo (estimated difference for liraglutide [3.0mg] vs placebo, 18.5% [95% CI, 12.7% to 24.4%], P < .001; for liraglutide [1.8mg] vs placebo, 9.3% [95% CI, 2.7% to 15.8%], P = .006). More gastrointestinal disorders were reported with liraglutide (3.0mg) vs liraglutide (1.8mg) and placebo. No pancreatitis was reported. Conclusions and Relevance: Among overweight and obese participants with type 2 diabetes, use of subcutaneous liraglutide (3.0mg) daily, compared with placebo, resulted inweight loss over 56weeks. Further studies are needed to evaluate longer-term efficacy and safety.
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U2 - 10.1001/jama.2015.9676
DO - 10.1001/jama.2015.9676
M3 - Article
C2 - 26284720
AN - SCOPUS:84940665526
SN - 0098-7484
VL - 314
SP - 687
EP - 699
JO - JAMA - Journal of the American Medical Association
JF - JAMA - Journal of the American Medical Association
IS - 7
ER -