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  Genetic Variants in the Genes of the Stress Hormone Signalling Pathway and Depressive Symptoms during and after Pregnancy

Schneider, M., Engel, A., Fasching, P. A., Haeberle, L., Binder, E. B., Voigt, F., et al. (2014). Genetic Variants in the Genes of the Stress Hormone Signalling Pathway and Depressive Symptoms during and after Pregnancy. BIOMED RESEARCH INTERNATIONAL, 469278. doi:10.1155/2014/469278.

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 Creators:
Schneider, Michael1, Author
Engel, Anne1, Author
Fasching, Peter A.1, Author
Haeberle, Lothar1, Author
Binder, Elisabeth B.2, Author           
Voigt, Franziska1, Author
Grimm, Jennifer1, Author
Faschingbauer, Florian1, Author
Eichler, Anna1, Author
Dammer, Ulf1, Author
Rebhan, Dirk1, Author
Amann, Manuela1, Author
Raabe, Eva1, Author
Goecke, Tamme W.1, Author
Quast, Carina2, Author           
Beckmann, MatthiasW.1, Author
Kornhuber, Johannes1, Author
Seifert, Anna3, Author           
Burghaus, Stefanie1, Author
Affiliations:
1external, ou_persistent22              
2Dept. Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035295              
3Max Planck Institute of Psychiatry, Max Planck Society, ou_1607137              

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 Abstract: Purpose. The aim of this study was to investigate whether single nucleotide polymorphisms (SNPs) in genes of the stress hormone signaling pathway, specifically FKBP5, NR3C1, and CRHR1, are associated with depressive symptoms during and after pregnancy. Methods. The Franconian Maternal Health Evaluation Study (FRAMES) recruited healthy pregnant women prospectively for the assessment of maternal and fetal health including the assessment of depressiveness. The German version of the 10-item Edinburgh Postnatal Depression Scale (EPDS) was completed at three time points in this prospective cohort study. Visit 1 was at study entry in the third trimester of the pregnancy, visit 2 was shortly after birth, and visit 3 was 6-8 months after birth. Germline DNA was collected from 361 pregnant women. Nine SNPs in the above mentioned genes were genotyped. After construction of haplotypes for each gene, a multifactorial linear mixed model was performed to analyse the depression values over time. Results. EPDS values were within expected ranges and comparable to previously published studies. Neither did the depression scores differ for comparisons among haplotypes at fixed time points nor did the change over time differ among haplotypes for the examined genes. No haplotype showed significant associations with depressive symptoms severity during pregnancy or the postpartum period. Conclusion. The analysed candidate haplotypes in FKBP5, NR3C1, and CRHR1 did not show an association with depression scores as assessed by EPDS in this cohort of healthy unselected pregnant women.

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Language(s): eng - English
 Dates: 2014-03
 Publication Status: Published online
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 Identifiers: ISI: 000333344900001
DOI: 10.1155/2014/469278
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Title: BIOMED RESEARCH INTERNATIONAL
Source Genre: Journal
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Publ. Info: New York, NY, USA : Hindawi Publishing Corporation
Pages: - Volume / Issue: - Sequence Number: 469278 Start / End Page: - Identifier: ISSN: 2314-6133