DNA methylation, insulin resistance and second-generation antipsychotics in bipolar disorder

Author:

Burghardt Kyle J1,Goodrich Jacyln M2,Dolinoy Dana C2,Ellingrod Vicki L34

Affiliation:

1. Department of Pharmacy Practice, Wayne State University Eugene Applebaum College of Pharmacy & Health Sciences, 259 Mack Avenue, Suite 2190, Detroit, MI 48201, USA

2. Department of Environmental Sciences, University of Michigan School of Public Health, 6638 SPH Tower, 1415 Washington Heights, Ann Arbor, MI 48109, USA

3. Department of Clinical Social & Administrative Sciences, College of Pharmacy, University of Michigan, 428 Church Street, Ann Arbor, MI 48109, USA

4. Department of Psychiatry, School of Medicine, University of Michigan, 1301 Catherine, Ann Arbor, MI 48109, USA

Abstract

Aims: This study aimed to assess the effect of second-generation antipsychotic (SGA) use and insulin resistance on a global measure of DNA methylation in patients diagnosed with bipolar disorder. Materials & Methods: Subjects stable on medication (either mood stabilizer monotherapy or adjuvant SGAs) were assessed for insulin resistance. Global methylation levels were assessed in leukocyte DNA from whole blood using the Luminometric Methylation Assay. Multivariable linear regression was used to investigate the effect of insulin resistance and SGA use on DNA methylation. Results: A total of 115 bipolar I subjects were included in this study. The average age was 43.1 ±12.2 years and 73% were on SGAs. Average% global methylation was 77.0 ± 3.26 and was significantly influenced by insulin resistance, SGA use and smoking. Conclusion: This is the first study to show a relationship between SGA use, insulin resistance and global DNA methylation. Further work will be needed to identify tissue- and gene-specific methylation changes.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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