Pharmacogenetic study of second-generation antipsychotic long-term treatment metabolic side effects (the SLiM Study): rationale, objectives, design and sample description

Rev Psiquiatr Salud Ment. 2014 Oct-Dec;7(4):166-78. doi: 10.1016/j.rpsm.2014.05.004. Epub 2014 Oct 19.
[Article in English, Spanish]

Abstract

Aim: Weight gain is an important and common side effect of second generation antipsychotics (SGAs). Furthermore, these drugs can induce other side effects associated with higher cardiovascular morbidity and mortality, such as insulin resistance, diabetes or metabolic syndrome. Preliminary studies show that inter-individual genetic differences produce varying degrees of vulnerability to the different SGA-induced side effects. The Second-generation antipsychotic Long-term treatment Metabolic side effects (SLiM) study aims to identify clinical, environmental and genetic factors that explain inter-individual differences in weight gain and metabolic changes in drug-naïve patients after six months of treatment with SGAs.

Materials and methods: The SLIM study is a multicenter, observational, six-month pharmacogenetic study where a cohort of 307 drug-naïve paediatric and adult patients (age range 8.8-90.1 years) and a cohort of 150 age- and sex- matched healthy controls (7.8-73.2 years) were recruited.

Results: This paper describes the rationale, objectives and design of the study and provides a description of the sample at baseline.

Conclusions: Results from the SLiM study will provide a better understanding of the clinical, environmental, and genetic factors involved in weight gain and metabolic disturbances associated with SGA treatment.

Keywords: Agentes antipsicóticos; Antipsychotic Agents; Aumento de peso; Drug-Related Side Effects and Adverse Reactions; Efectos secundarios y reacciones adversas a medicamentos; Farmacogenética; Metabolic Syndrome; Pharmacogenetics; Síndrome metabólico; Weight Gain.

Publication types

  • Multicenter Study
  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Case-Control Studies
  • Child
  • Clinical Protocols
  • Female
  • Humans
  • Longitudinal Studies
  • Male
  • Metabolic Diseases / chemically induced*
  • Metabolic Diseases / genetics*
  • Middle Aged
  • Pharmacogenetics
  • Polymorphism, Single Nucleotide*
  • Prospective Studies
  • Psychotropic Drugs / adverse effects*
  • Research Design
  • Weight Gain / drug effects*
  • Weight Gain / genetics*
  • Young Adult

Substances

  • Psychotropic Drugs