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Obesity (Silver Spring) ; 24(11): 2278-2288, 2016 11.
Article in English | MEDLINE | ID: mdl-27804269

ABSTRACT

OBJECTIVE: To identify an early response criterion for predicting ≥5% weight loss with liraglutide 3.0 mg at week 56 and to compare efficacy outcomes in early responders (ERs) and early nonresponders (ENRs). METHODS: Using pooled data from the SCALE Obesity and Prediabetes and SCALE Diabetes trials, weight loss of ≥4% at 16 weeks best predicted ≥5% weight loss after 56 weeks. Weight loss and changes in cardiometabolic risk factors and health-related quality of life were evaluated in ERs (≥4% weight loss at week 16) and ENRs (<4% weight loss at week 16) completing 56 weeks' treatment. RESULTS: Proportions of ERs/ENRs to liraglutide 3.0 mg were 77.3%/22.7% (individuals without type 2 diabetes, T2D) and 62.7%/37.3% (those with T2D). Greater mean weight loss was observed in ERs versus ENRs: 10.8% versus 3.0% (without T2D) and 8.5% versus 3.1% (T2D). In both trials, greater proportions of ERs versus ENRs achieved ≥5%, >10%, and >15% weight loss at week 56 with liraglutide 3.0 mg. Greater improvements in cardiometabolic risk factors and health-related quality of life scores were observed in ERs versus ENRs. CONCLUSIONS: The early response criterion was clinically useful to identify individuals who would achieve clinically meaningful weight loss at 56 weeks.


Subject(s)
Anti-Obesity Agents/pharmacology , Biomarkers/blood , Liraglutide/pharmacology , Weight Loss/drug effects , Adult , Body Mass Index , Body Weight , Cardiovascular System/drug effects , Dose-Response Relationship, Drug , Double-Blind Method , Endpoint Determination , Exercise , Female , Humans , Male , Middle Aged , Obesity/blood , Prediabetic State/blood , Quality of Life , Respiratory System/drug effects , Risk Factors , Treatment Outcome
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