TY - JOUR
T1 - Long-term effect of CB1 blockade with rimonabant on cardiometabolic risk factors
T2 - two year results from the RIO-Europe Study
AU - RIO-Europe Study Group
AU - Van Gaal, Luc F
AU - Scheen, André J
AU - Rissanen, Aila M
AU - Rössner, Stephan
AU - Hanotin, Corinne
AU - Ziegler, Olivier
PY - 2008/7
Y1 - 2008/7
N2 - AIMS: Rimonabant, the first selective cannabinoid type 1 receptor blocker, has been shown to produce weight loss and improvements in several cardiometabolic risk factors over 1 year. We report the 2 year efficacy and tolerability data of rimonabant.METHODS AND RESULTS: Patients with a body mass index > or =30 or >27 kg/m(2) with treated/untreated hypertension, dyslipidaemia, or both, were randomized to double-blind treatment with placebo, rimonabant 5 or 20 mg once daily plus a calorie-restricted diet for 2 years. Weight loss from baseline to 2 years in the intention-to-treat population was significantly greater with rimonabant 20 mg (mean +/- SD: -5.5 +/- 7.7 kg; P < 0.001) and 5 mg (-2.9 +/- 6.5 kg; P = 0.002) than placebo (-1.2 +/- 6.8 kg). Rimonabant 20 mg produced significantly greater improvements than placebo in waist circumference, high-density lipoprotein cholesterol, triglycerides, fasting glucose and insulin levels, insulin resistance, and metabolic syndrome prevalence. Rimonabant 20 mg produced clinically meaningful improvements in all Impact of Weight on Quality of Life-Lite questionnaire domain scores at 2 years. Rimonabant was generally well tolerated and rates of adverse events, including depressed mood disorders and disturbances were similar to placebo during year 2. Proportions of patients with clinically significant depression (Hospital Anxiety and Depression Scale score >11) were similar in all treatment groups.CONCLUSION: Rimonabant 20 mg over 2 years promoted clinically relevant and durable weight loss and improvements in cardiometabolic risk factors.
AB - AIMS: Rimonabant, the first selective cannabinoid type 1 receptor blocker, has been shown to produce weight loss and improvements in several cardiometabolic risk factors over 1 year. We report the 2 year efficacy and tolerability data of rimonabant.METHODS AND RESULTS: Patients with a body mass index > or =30 or >27 kg/m(2) with treated/untreated hypertension, dyslipidaemia, or both, were randomized to double-blind treatment with placebo, rimonabant 5 or 20 mg once daily plus a calorie-restricted diet for 2 years. Weight loss from baseline to 2 years in the intention-to-treat population was significantly greater with rimonabant 20 mg (mean +/- SD: -5.5 +/- 7.7 kg; P < 0.001) and 5 mg (-2.9 +/- 6.5 kg; P = 0.002) than placebo (-1.2 +/- 6.8 kg). Rimonabant 20 mg produced significantly greater improvements than placebo in waist circumference, high-density lipoprotein cholesterol, triglycerides, fasting glucose and insulin levels, insulin resistance, and metabolic syndrome prevalence. Rimonabant 20 mg produced clinically meaningful improvements in all Impact of Weight on Quality of Life-Lite questionnaire domain scores at 2 years. Rimonabant was generally well tolerated and rates of adverse events, including depressed mood disorders and disturbances were similar to placebo during year 2. Proportions of patients with clinically significant depression (Hospital Anxiety and Depression Scale score >11) were similar in all treatment groups.CONCLUSION: Rimonabant 20 mg over 2 years promoted clinically relevant and durable weight loss and improvements in cardiometabolic risk factors.
KW - Adult
KW - Anti-Obesity Agents/adverse effects
KW - Blood Glucose/metabolism
KW - Body Mass Index
KW - Cannabinoid Receptor Antagonists
KW - Cardiovascular Diseases/etiology
KW - Cholesterol, HDL/blood
KW - Dose-Response Relationship, Drug
KW - Epidemiologic Methods
KW - Female
KW - Humans
KW - Insulin/blood
KW - Male
KW - Metabolic Syndrome/prevention & control
KW - Middle Aged
KW - Obesity/blood
KW - Piperidines/adverse effects
KW - Pyrazoles/adverse effects
KW - Rimonabant
KW - Treatment Outcome
KW - Triglycerides/blood
KW - Weight Loss/drug effects
U2 - 10.1093/eurheartj/ehn076
DO - 10.1093/eurheartj/ehn076
M3 - Article
C2 - 18417461
SN - 0195-668X
VL - 29
SP - 1761
EP - 1771
JO - European Heart Journal
JF - European Heart Journal
IS - 14
ER -