4.3 Article

Three-way interaction effects of early life stress, positive parenting and FKBP5 in the development of depressive symptoms in a general population

Journal

JOURNAL OF NEURAL TRANSMISSION
Volume 128, Issue 9, Pages 1409-1424

Publisher

SPRINGER WIEN
DOI: 10.1007/s00702-021-02405-0

Keywords

Adolescence; cG x E; Diathesis stress; Differential susceptibility; FKBP Prolyl Isomerase 5

Funding

  1. Uppsala University
  2. Soderstrom Konig Foundation [SLS-559921, SLS-655791, SLS-745221]
  3. Ake Wiberg's Foundation [M15-0239]
  4. Swedish Research Council for Health, Working Life and Welfare (FORTE) [2015-00897]
  5. Swedish Brain Foundation
  6. Swedish Alcohol Monopoly Research Council (SRA)
  7. Swedish Council for Working Life and Social Research (FAS)
  8. Uppsala and Orebro Regional Research Council
  9. Fredrik and Ingrid Thurings Foundation
  10. County Council of Vastmanland
  11. Swedish Psychiatric Foundation
  12. Svenska Spel Research Council
  13. Malardalen University

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The study showed that FKBP5 gene may play a role in the development of depressive symptoms among young adults, with significant three-way interactions found for certain SNPs with early life stress (ELS) and positive parenting style (PASCQ(pos)). Some SNPs exhibited diathesis stress patterns while others showed differential susceptibility patterns of interaction.
FKBP5 gene-environment interaction (cG x E) studies have shown diverse results, some indicating significant interaction effects between the gene and environmental stressors on depression, while others lack such results. Moreover, FKBP5 has a potential role in the diathesis stress and differential susceptibility theorem. The aim of the present study was to evaluate whether a cG x E interaction effect of FKBP5 single-nucleotide polymorphisms (SNPs) or haplotype and early life stress (ELS) on depressive symptoms among young adults was moderated by a positive parenting style (PASCQ(pos)), through the frameworks of the diathesis stress and differential susceptibility theorem. Data were obtained from the Survey of Adolescent Life in Vastmanland Cohort Study, including 1006 participants and their guardians. Data were collected during 2012, when the participants were 13 and 15 years old (Wave I: DNA), 2015, when participants were 16 and 18 years old (Wave II: PASCQ(pos), depressive symptomology and ELS) and 2018, when participants were 19 and 21 years old (Wave III: depressive symptomology). Significant three-way interactions were found for the FKBP5 SNPs rs1360780, rs4713916, rs7748266 and rs9394309, moderated by ELS and PASCQ(pos), on depressive symptoms among young adults. Diathesis stress patterns of interaction were observed for the FKBP5 SNPs rs1360780, rs4713916 and rs9394309, and differential susceptibility patterns of interaction were observed for the FKBP5 SNP rs7748266. Findings emphasize the possible role of FKBP5 in the development of depressive symptoms among young adults and contribute to the understanding of possible differential susceptibility effects of FKBP5.

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