Rafael Violante Ortiz
Mexican Social Security Institute
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Featured researches published by Rafael Violante Ortiz.
The New England Journal of Medicine | 2015
Xavier Pi-Sunyer; Arne Astrup; Ken Fujioka; Frank L. Greenway; Alfredo Halpern; Michel Krempf; David C.W. Lau; Carel W. le Roux; Rafael Violante Ortiz; Christine B. Jensen; John Wilding
BACKGROUND Obesity is a chronic disease with serious health consequences, but weight loss is difficult to maintain through lifestyle intervention alone. Liraglutide, a glucagon-like peptide-1 analogue, has been shown to have potential benefit for weight management at a once-daily dose of 3.0 mg, injected subcutaneously. METHODS We conducted a 56-week, double-blind trial involving 3731 patients who did not have type 2 diabetes and who had a body-mass index (BMI; the weight in kilograms divided by the square of the height in meters) of at least 30 or a BMI of at least 27 if they had treated or untreated dyslipidemia or hypertension. We randomly assigned patients in a 2:1 ratio to receive once-daily subcutaneous injections of liraglutide at a dose of 3.0 mg (2487 patients) or placebo (1244 patients); both groups received counseling on lifestyle modification. The coprimary end points were the change in body weight and the proportions of patients losing at least 5% and more than 10% of their initial body weight. RESULTS At baseline, the mean (±SD) age of the patients was 45.1±12.0 years, the mean weight was 106.2±21.4 kg, and the mean BMI was 38.3±6.4; a total of 78.5% of the patients were women and 61.2% had prediabetes. At week 56, patients in the liraglutide group had lost a mean of 8.4±7.3 kg of body weight, and those in the placebo group had lost a mean of 2.8±6.5 kg (a difference of -5.6 kg; 95% confidence interval, -6.0 to -5.1; P<0.001, with last-observation-carried-forward imputation). A total of 63.2% of the patients in the liraglutide group as compared with 27.1% in the placebo group lost at least 5% of their body weight (P<0.001), and 33.1% and 10.6%, respectively, lost more than 10% of their body weight (P<0.001). The most frequently reported adverse events with liraglutide were mild or moderate nausea and diarrhea. Serious events occurred in 6.2% of the patients in the liraglutide group and in 5.0% of the patients in the placebo group. CONCLUSIONS In this study, 3.0 mg of liraglutide, as an adjunct to diet and exercise, was associated with reduced body weight and improved metabolic control. (Funded by Novo Nordisk; SCALE Obesity and Prediabetes NN8022-1839 ClinicalTrials.gov number, NCT01272219.).
Endocrine Practice | 2016
Patrick M. O'Neil; W. Timothy Garvey; J. Michael Gonzalez-Campoy; Pablo Mora; Rafael Violante Ortiz; German Guerrero; Birgitte Claudius; Xavier Pi-Sunyer
OBJECTIVE Scarce data exist on pharmacotherapy for obesity in Hispanic individuals. This post hoc analysis of pooled data from 4 phase 3a trials compared the efficacy and safety of liraglutide 3.0 mg versus placebo, as adjunct to a reduced-calorie diet and physical activity, in Hispanic versus non-Hispanic subgroups. METHODS We conducted the double-blind randomized, placebo-controlled trials in adults with a minimum body mass index (BMI) of 27 kg/m2 with at least 1 comorbidity, or a minimum BMI of 30 kg/m2, at clinical research sites worldwide. In this analysis, we investigated possible differences in treatment effects between 534 Hispanics (10.4% of the population) and 4,597 non-Hispanics (89.6%) through statistical tests of interaction between subgroups and treatment. Variables examined included mean and categorical weight change, cardiovascular risk markers, and safety data. RESULTS Both subgroups achieved clinically significant mean weight loss at end-of-treatment with liraglutide 3.0 mg versus placebo: Hispanics 7.0% versus 1.5%, treatment difference -5.1% (95% CI, -6.2 to -4.0); non-Hispanics 7.5% versus 2.3%, -5.2% (95% CI, -5.5 to -4.8). More individuals in both subgroups lost ≥5%, >10%, and >15% of their baseline weight with liraglutide 3.0 mg than with placebo. Efficacy endpoints generally did not vary with ethnicity (P>.05). Adverse events were comparable between ethnic subgroups, with more gastrointestinal disorders reported with liraglutide 3.0 mg than placebo. CONCLUSION Efficacy and safety were largely similar between Hispanic and non-Hispanic subgroups. Results support that liraglutide 3.0 mg, used with a reduced-calorie diet and physical activity, can facilitate weight loss in Hispanic individuals. ABBREVIATIONS A1c = glycated hemoglobin BMI = body mass index CI = confidence interval FPG = fasting plasma glucose GLP-1 = glucagon-like peptide-1 hsCRP = high-sensitivity C-reactive protein SCALE = Satiety and Clinical Adiposity - Liraglutide Evidence in individuals with and without diabetes T2DM = type 2 diabetes mellitus.
Canadian Journal of Diabetes | 2015
David C.W. Lau; Michel Krempf; Arne Astrup; Carel W. le Roux; Ken Fujioka; Frank L. Greenway; Alfredo Halpern; Rafael Violante Ortiz; John Wilding; Damir Boras; Søren Kruse Lilleøre; Xavier Pi-Sunyer
Obesity Research & Clinical Practice | 2014
Joseph Proietto; Carel W. le Roux; Xavier Pi-Sunyer; Arne Astrup; Ken Fujioka; Frank L. Greenway; Alfredo Halpern; David C.W. Lau; Rafael Violante Ortiz; Alana Philips; Søren Kruse Lilleøre; John Wilding
Canadian Journal of Diabetes | 2016
David C.W. Lau; Arne Astrup; Ken Fujioka; Frank L. Greenway; Carel W. le Roux; Lucv An Gaal; Rafael Violante Ortiz; John Wilding; Trine Skjoth; Linda Shapiro Manning; Jelena Vukmirica; Xavier Pi-Sunyer
Obesity Research & Clinical Practice | 2014
Gary A. Wittert; Carel W. le Roux; Arne Astrup; Ken Fujioka; Frank L. Greenway; Alfredo Halpern; David C.W. Lau; Rafael Violante Ortiz; John Wilding; Sabina Furber; Søren Kruse Lilleøre; Xavier Pi-Sunyer
Canadian Journal of Diabetes | 2015
Joanne Liutkus; Ken Fujioka; Arne Astrup; Frank L. Greenway; Alfredo Halpern; Michel Krempf; David C.W. Lau; Carel W. le Roux; Rafael Violante Ortiz; John Wilding; Michael Lyng Wolden; Damir Boras; Xavier Pi-Sunyer
Canadian Journal of Diabetes | 2015
David C.W. Lau; Frank L. Greenway; Ken Fujioka; Arne Astrup; Alfredo Halpern; Michel Krempf; Carel W. le Roux; Rafael Violante Ortiz; John Wilding; Søren Kruse Lilleøre; Damir Boras; Xavier Pi-Sunyer
Society for Endocrinology Endocrine Update 2017 | 2017
Barbara McGowan; Carel W. le Roux; Arne Astrup; Ken Fujioka; Frank L. Greenway; David C.W. Lau; Gaal Luc Van; Rafael Violante Ortiz; John Wilding; Trine Skjoth; Xavier Pi-Sunyer
Diabetologie Und Stoffwechsel | 2015
Frank L. Greenway; C le Roux; David C.W. Lau; Arne Astrup; Ken Fujioka; Alfredo Halpern; Michel Krempf; Rafael Violante Ortiz; John Wilding; Cb Svendsen; Christine B. Jensen; Xavier Pi-Sunyer; J Kienhöfer; A Segner