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

Grossmann, N. L., Weihs, A., Kuehn, L., Sauer, S., Roeh, S., Wiechmann, T., et al. (2024). Methylation Patterns of the FKBP5 Gene in Association with Childhood Maltreatment and Depressive Disorders. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 25(3): 1485. doi:10.3390/ijms25031485.

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Grossmann, Nora L., Author
Weihs, Antoine, Author
Kuehn, Luise, Author
Sauer, Susann1, Author           
Roeh, Simone1, Author           
Wiechmann, Tobias1, Author           
Rex-Haffner, Monika1, Author           
Voelzke, Henry, Author
Voelker, Uwe, Author
Binder, Elisabeth B.1, Author           
Teumer, Alexander, Author
Homuth, Georg, Author
Klinger-Koenig, Johanna, Author
Grabe, Hans J., Author
Affiliations:
1Dept. Genes and Environment, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035295              

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 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 x rs1360780 and depressive symptoms x 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.

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 Dates: 2024
 Publication Status: Published online
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 Identifiers: ISI: 001160255800001
DOI: 10.3390/ijms25031485
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Title: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Source Genre: Journal
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Pages: - Volume / Issue: 25 (3) Sequence Number: 1485 Start / End Page: - Identifier: ISSN: 1661-6596