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http://purl.uniprot.org/citations/24685985http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/24685985http://www.w3.org/2000/01/rdf-schema#comment"

Background/aims

Cortisol plays an important role during pregnancy. It controls maternal glucose metabolism and fetal development. Cortisol metabolism is partially controlled by the 11b-HSD2. This enzyme is expressed in the kidney and human placenta. The activity of the enzyme is partially controlled by functional polymorphisms: the HSD11B2[CA]n microsatellite polymorphism. The impact of this functional gene polymorphism on cortisol metabolism and potential effects on the newborn's is unknown so far.

Methods

In the current prospective birth cohort study in southern Asia, we analyzed the association of the HSD11B2[CA]n microsatellite polymorphisms in 187 mothers and their newborn's on maternal and newborn's serum cortisol concentrations.

Results

Using multivariable regression analyses considering known confounding (gestational age, newborn's gender, the labor uterine contraction states and the timing during the day of blood taking), we showed that the fetal HSD11B2[CA]n microsatellite polymorphisms in the first intron was related to maternal cortisol concentration (R2=0.26, B=96.27, p=0.007), whereas as the newborn's cortisol concentrations were independent of fetal and maternal HSD11B2[CA]n microsatellite polymorphism.

Conclusions

Our study showed for the first time that the fetal HSD11B2[CA]n microsatellite polymorphism of the HSD11B2 gene in healthy uncomplicated human pregnancy is associated with maternal cortisol concentration. This indicates that fetal genes controlling cortisol metabolism may affect maternal cortisol concentration and hence physiology in healthy pregnant women."xsd:string
http://purl.uniprot.org/citations/24685985http://purl.org/dc/terms/identifier"doi:10.1159/000355761"xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/author"Chen D."xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/author"Li J."xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/author"Chen Y.P."xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/author"Liu T.B."xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/author"Wang Z.N."xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/author"Dong Y.P."xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/author"Hocher B."xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/name"Kidney Blood Press Res"xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/pages"132-141"xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/title"A functional fetal HSD11B2[CA]n microsatellite polymorphism is associated with maternal serum cortisol concentrations in pregnant women."xsd:string
http://purl.uniprot.org/citations/24685985http://purl.uniprot.org/core/volume"38"xsd:string
http://purl.uniprot.org/citations/24685985http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/24685985
http://purl.uniprot.org/citations/24685985http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/24685985
http://purl.uniprot.org/uniprot/#_P80365-mappedCitation-24685985http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24685985
http://purl.uniprot.org/uniprot/P80365http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/24685985