Literature DB >> 24955870

Levels of brain derived neurotrophic factors across gestation in women with preeclampsia.

Vandita D'Souza1, Vidya Patil1, Hemlata Pisal1, Karuna Randhir1, Asmita Joshi1, Savita Mehendale2, Girija Wagh2, Sanjay Gupte3, Sadhana Joshi4.   

Abstract

Preeclampsia (PE) is a major pregnancy complication of placental origin which leads to adverse pregnancy outcome. Brain derived neurotrophic factor (BDNF) is suggested to promote trophoblast growth and regulate placental and fetal development. This study for the first time examines the levels of maternal plasma BDNF at various time points during gestation, cord plasma and placental BDNF levels and their association with birth outcome in women with PE. Normotensive control (NC) women (n=89) and women with PE (n=61) were followed at three different time points [16-20 weeks (T1), 26-30 weeks (T2) and at delivery (T3)]. Maternal blood at all time points and cord blood was collected. Results indicate that maternal BDNF levels at T1 (p=0.050) and T3 (p=0.025) were lower in women with PE than in NC women. Cord BDNF levels at delivery in women with PE were lower (p=0.032) than those in NC women. Placental BDNF gene expression was also lower (p=0.0082) in women with PE than in NC women. Our data suggests that BDNF plays an important role in the development of the materno-fetal-placental unit during pregnancy. Alteration in the levels of BDNF during pregnancy may be associated with an abnormal development of the placenta resulting in PE.
Copyright © 2014. Published by Elsevier Ltd.

Entities:  

Keywords:  Brain derived neurotrophic factor; Placental development; Preeclampsia; Pregnancy

Mesh:

Substances:

Year:  2014        PMID: 24955870     DOI: 10.1016/j.ijdevneu.2014.06.008

Source DB:  PubMed          Journal:  Int J Dev Neurosci        ISSN: 0736-5748            Impact factor:   2.457


  8 in total

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7.  Placental CpG methylation of HPA-axis genes is associated with cognitive impairment at age 10 among children born extremely preterm.

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  8 in total

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