MTHFR genotype and differential evolution of metabolic parameters after initiation of a second generation antipsychotic: an observational study

Ruud van Winkel, Tim Moons, Odette Peerbooms, Bart Rutten, Joseph Peuskens, Stephan Claes, Jim van Os, Marc De Hert*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

39 Citations (Web of Science)

Abstract

Most second-generation antipsychotics (SGAs) induce metabolic disturbances, but large differences exist in the degree to which individual patients develop these. Little is known about genetic factors associated with differential liability. Cross-sectional studies suggested an association between polymorphisms in 5,10-methylenetetraydrofolate reductase (MTHFR) and metabolic syndrome in patients with schizophrenia. This study aimed to assess whether the C677T (rs1801133) or A1298C (rs1801131) polymorphism in the MTHFR gene predict differential evolution of metabolic parameters over the course of a 3-month follow-up period after initiation of an SGA. One hundred and four patients with schizophrenia initiated on a SGA were measured at baseline, 6 weeks and 3 months. MTHFR A1298C, but not C677T, genotype predicted pos-baseline increases in weight [beta = 2.5, standard error (SE)= 0.92, P = 0.006], waist circumference (beta = 2.0, SE = 1.0, P = 0.050), fasting glucose (beta = 2.8, SE = 1.2, P = 0.024) and glucose at 120 min during the Oral Glucose Tolerance Test (beta = 10.7, SE = 4.5, P = 0.018) following a de novo metabolic challenge with a specific SGA. A1298C allele carriers consistently displayed the most unfavorable evolution of metabolic parameters. Thus, MTHFR A1298C genotype may explain part of the individual liability to metabolic disturbances in patients with schizophrenia. Int Clin Psychopharmacol 25: 270-276
Original languageEnglish
Pages (from-to)270-276
JournalInternational Clinical Psychopharmacology
Volume25
Issue number5
DOIs
Publication statusPublished - Sep 2010

Keywords

  • antipsychotic
  • cardiovascular risk
  • diabetes
  • genetics 5, 10-methylenetetraydrofolate reductase
  • schizophrenia

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