Methylation Patterns of the FKBP5 Gene in Association with Childhood Maltreatment and Depressive Disorders

Author:

Großmann Nora L.1,Weihs Antoine12ORCID,Kühn Luise1ORCID,Sauer Susann3,Röh Simone3,Wiechmann Tobias3,Rex-Haffner Monika3,Völzke Henry45,Völker Uwe56ORCID,Binder Elisabeth B.37,Teumer Alexander15ORCID,Homuth Georg6ORCID,Klinger-König Johanna1ORCID,Grabe Hans J.12

Affiliation:

1. Department of Psychiatry and Psychotherapy, University Medicine Greifswald, 17475 Greifswald, Germany

2. German Center for Neurodegenerative Diseases (DZNE), Site Rostock/Greifswald, 17489 Greifswald, Germany

3. Department Genes and Environment, Max Planck Institute of Psychiatry, 80804 Munich, Germany

4. Institute for Community Medicine, University Medicine Greifswald, 17475 Greifswald, Germany

5. German Centre for Cardiovascular Research (DZHK), Partner Site Greifswald, University Medicine Greifswald, 17475 Greifswald, Germany

6. Interfaculty Institute of Genetics and Functional Genomics, University Medicine Greifswald, 17475 Greifswald, Germany

7. Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA 30322, USA

Abstract

Childhood maltreatment is an important risk factor for adult depression and has been associated with changes in the hypothalamic pituitary adrenal (HPA) axis, including cortisol secretion and methylation of the FKBP5 gene. Furthermore, associations between depression and HPA changes have been reported. This study investigated the associations of whole-blood FKBP5 mRNA levels, serum cortisol levels, childhood maltreatment, and depressive symptoms with the whole-blood methylation status (assessed via target bisulfite sequencing) of 105 CpGs at the FKBP5 locus using data from the general population-based Study of Health in Pomerania (SHIP) (N = 203). Both direct and interaction effects with the rs1360780 single-nucleotide polymorphism were investigated. Nominally significant associations of main effects on methylation of a single CpG site were observed at intron 3, intron 7, and the 3′-end of the gene. Additionally, methylation at two clusters at the 3′-end and intron 7 were nominally associated with childhood maltreatment × rs1360780 and depressive symptoms × rs1360780, respectively. The results add to the understanding of molecular mechanisms underlying the emergence of depression and could aid the development of personalised depression therapy and drug development.

Funder

German Federal State of Mecklenburg-West Pomerania

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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