Does the Time of Drug Administration Alter the Metabolic Risk of Aripiprazole

Antipsychotic drugs cause metabolic abnormalities through a mechanism that involves antagonism of D 2 dopamine receptors (D 2 R). Under healthy conditions, insulin release follows a circadian rhythm and is low at night, and in pancreatic beta-cells, D 2 Rs negatively regulate insulin release. Since they are sedating, many antipsychotics are dosed at night. However, the resulting reduction in overnight D 2 R activity may disrupt 24 h rhythms in insulin release, potentially exacerbating metabolic dysfunction. We examined retrospective clinical data from patients treated over approximately 1 year with the antipsychotic drug aripiprazole (ARPZ), a D2R partial agonist. To identify effects of timing on metabolic risk, we found cases treated with ARPZ either in the morning ( n = 90) or at bedtime ( n = 53), and compared hemoglobin A1c, and six secondary metabolic parameters across the two groups. After controlling for demographic and clinical factors, patients treated with ARPZ at night had a significant decrease in HDL cholesterol, while in patients who took ARPZ in the morning had no change. There was a non-significant trend toward higher serum triglycerides in the patients treated with ARPZ at night vs. morning. There were no group differences in hemoglobin A1c, BMI, total cholesterol, LDL cholesterol, or blood pressure. Patients taking APPZ at night developed a worse lipid profile, with lower HDL cholesterol and a trend toward higher triglycerides. These changes may pose additional metabolic risk factors compared to those who take ARPZ in the morning. Interventions based on drug timing may reduce some of the adverse metabolic consequences of antipsychotic drugs

Aripiprazole · Drug · Psychiatry · Schizophrenia (object-oriented programming · Circadian rhythm and melatonin · Medicine · Schizophrenia research and treatment · Sleep and related disorders · Pharmacology

• Effectiveness of Antipsychotic Drugs in Patients with Chronic Schizophrenia

  Jeffrey A Lieberman, T Scott Stroup et al.•New England Journal of Medicine•2005

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