Javier Vázquez-Bourgon1,2,3, Rocío Pérez-Iglesias4,5, Víctor Ortiz-García de la Foz6,4, Paula Suárez Pinilla6,4,7, Álvaro Díaz Martínez4,7,8, Benedicto Crespo-Facorro6,4,7. 1. Department of Psychiatry, University Hospital Marqués de Valdecilla-IDIVAL, Avda.Valdecilla s/n, 39008, Santander, Spain. javazquez@humv.es. 2. CIBERSAM: Centro de Investigación Biomédica en Red en Salud Mental, Madrid, Spain. javazquez@humv.es. 3. School of Medicine, University of Cantabria, Santander, Spain. javazquez@humv.es. 4. CIBERSAM: Centro de Investigación Biomédica en Red en Salud Mental, Madrid, Spain. 5. Psychosis Studies Department, Institute of Psychiatry, Psychology and Neuroscience, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK. 6. Department of Psychiatry, University Hospital Marqués de Valdecilla-IDIVAL, Avda.Valdecilla s/n, 39008, Santander, Spain. 7. School of Medicine, University of Cantabria, Santander, Spain. 8. IBBTEC: Instituto de Biomedicina y Biotecnología de Cantabria, Santander, Spain.
Abstract
INTRODUCTION: The use of second-generation antipsychotics (SGA) has been associated with metabolic changes. However, there are differences in the metabolic profile between SGAs. We have previously observed that ziprasidone had a more benign early metabolic profile compared to aripiprazole and quetiapine. However, a long-term follow-up is preferred to detect clinically relevant impairment in metabolic parameters. We aimed to compare the effect of aripiprazole, ziprasidone, and quetiapine on metabolic measures in first-episode non-affective psychosis patients after 1 year of treatment. MATERIAL AND METHODS: One hundred and sixty-five drug-naïve patients, suffering from a first episode of non-affective psychosis, were randomly assigned to receive quetiapine, ziprasidone, or aripiprazole. Weight and glycemic/lipid parameters were recorded at baseline and after 1 year of treatment. RESULTS: After 1 year of antipsychotic treatment, we found significant increments in weight, BMI, total cholesterol, LDL-cholesterol, triglycerides, and the triglyceride/HDL index in the sample as a whole. These changes produced a significant rise in the percentage of patients with obesity, hypercholesterolemia, and hypertriglyceridemia. However, when comparing the differential effect of each antipsychotic medication, we found no significant differences in any of the metabolic parameters between antipsychotics groups after 1 year of treatment. CONCLUSION: We concluded that the antipsychotics studied present similar metabolic profiles. However, the primary exposure to SGAs during the first year of psychosis was associated with significant increases in weight and metabolic parameters, leading to increments in obesity, hypertriglyceridemia, and hypercholesterolemia.
RCT Entities:
INTRODUCTION: The use of second-generation antipsychotics (SGA) has been associated with metabolic changes. However, there are differences in the metabolic profile between SGAs. We have previously observed that ziprasidone had a more benign early metabolic profile compared to aripiprazole and quetiapine. However, a long-term follow-up is preferred to detect clinically relevant impairment in metabolic parameters. We aimed to compare the effect of aripiprazole, ziprasidone, and quetiapine on metabolic measures in first-episode non-affective psychosispatients after 1 year of treatment. MATERIAL AND METHODS: One hundred and sixty-five drug-naïve patients, suffering from a first episode of non-affective psychosis, were randomly assigned to receive quetiapine, ziprasidone, or aripiprazole. Weight and glycemic/lipid parameters were recorded at baseline and after 1 year of treatment. RESULTS: After 1 year of antipsychotic treatment, we found significant increments in weight, BMI, total cholesterol, LDL-cholesterol, triglycerides, and the triglyceride/HDL index in the sample as a whole. These changes produced a significant rise in the percentage of patients with obesity, hypercholesterolemia, and hypertriglyceridemia. However, when comparing the differential effect of each antipsychotic medication, we found no significant differences in any of the metabolic parameters between antipsychotics groups after 1 year of treatment. CONCLUSION: We concluded that the antipsychotics studied present similar metabolic profiles. However, the primary exposure to SGAs during the first year of psychosis was associated with significant increases in weight and metabolic parameters, leading to increments in obesity, hypertriglyceridemia, and hypercholesterolemia.
Entities:
Keywords:
Cholesterol; Glucose; Medication-naïve; Second-generation antipsychotic; Triglycerides; Weight gain
Authors: T Scott Stroup; Joseph P McEvoy; Kimberly D Ring; Robert H Hamer; Lisa M LaVange; Marvin S Swartz; Robert A Rosenheck; Diana O Perkins; Abraham M Nussbaum; Jeffrey A Lieberman Journal: Am J Psychiatry Date: 2011-07-18 Impact factor: 18.112
Authors: Robert Kerwin; Bruno Millet; Erik Herman; Csaba M Banki; Henrik Lublin; Miranda Pans; Linda Hanssens; Gilbert L'Italien; Robert D McQuade; Jean-Noël Beuzen Journal: Eur Psychiatry Date: 2007-06-07 Impact factor: 5.361
Authors: Rocio Perez-Iglesias; Benedicto Crespo-Facorro; Jose Antonio Amado; Maria Teresa Garcia-Unzueta; Maria Luz Ramirez-Bonilla; Cesar Gonzalez-Blanch; Obdulia Martinez-Garcia; Jose Luis Vazquez-Barquero Journal: J Clin Psychiatry Date: 2007-11 Impact factor: 4.384
Authors: Marcos Gómez-Revuelta; José María Pelayo-Terán; María Juncal-Ruiz; Víctor Ortiz-García de la Foz; Javier Vázquez-Bourgon; Ana González-Pinto; Benedicto Crespo-Facorro Journal: Int J Neuropsychopharmacol Date: 2018-12-01 Impact factor: 5.176
Authors: J Vázquez-Bourgon; M Gómez-Revuelta; J Mayoral-van Son; J Labad; V Ortiz-García de la Foz; E Setién-Suero; R Ayesa-Arriola; D Tordesillas-Gutiérrez; M Juncal-Ruiz; B Crespo-Facorro Journal: Eur Psychiatry Date: 2022-08-16 Impact factor: 7.156
Authors: Danielle A Chipchura; Zachary Freyberg; Corey Edwards; Susan G Leckband; Michael J McCarthy Journal: Front Psychiatry Date: 2018-10-11 Impact factor: 4.157
Authors: Marcos Gómez-Revuelta; José María Pelayo-Terán; María Juncal-Ruiz; Javier Vázquez-Bourgon; Paula Suárez-Pinilla; Rodrigo Romero-Jiménez; Esther Setién Suero; Rosa Ayesa-Arriola; Benedicto Crespo-Facorro Journal: Int J Neuropsychopharmacol Date: 2020-04-23 Impact factor: 5.176