Association between Brain-Derived Neurotrophic Factor (BDNF) Levels in 2nd Trimester Amniotic Fluid and Fetal Development

The development of the fetal nervous system mirrors general fetal development, comprising a combination of genetic resources and effects of the intrauterine environment. Our aim was to assess the 2nd trimester amniotic fluid levels of brain-derived neurotrophic factor (BDNF) and to investigate its a...

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Main Authors: Nikolaos Antonakopoulos, Zoe Iliodromiti, George Mastorakos, Christos Iavazzo, Georgios Valsamakis, Nikolaos Salakos, Aris Papageorghiou, Alexandra Margeli, Sophia Kalantaridou, George Creatsas, Efthymios Deligeoroglou, Nikolaos Vrachnis
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2018/8476217
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spelling doaj-b9c91022b4c548eebdb7be0d143a14ea2020-11-24T21:45:40ZengHindawi LimitedMediators of Inflammation0962-93511466-18612018-01-01201810.1155/2018/84762178476217Association between Brain-Derived Neurotrophic Factor (BDNF) Levels in 2nd Trimester Amniotic Fluid and Fetal DevelopmentNikolaos Antonakopoulos0Zoe Iliodromiti1George Mastorakos2Christos Iavazzo3Georgios Valsamakis4Nikolaos Salakos5Aris Papageorghiou6Alexandra Margeli7Sophia Kalantaridou8George Creatsas9Efthymios Deligeoroglou10Nikolaos Vrachnis11Second Department of Obstetrics and Gynecology, National and Kapodistrian University of Athens Medical School, Aretaieio Hospital, Athens, GreeceSecond Department of Obstetrics and Gynecology, National and Kapodistrian University of Athens Medical School, Aretaieio Hospital, Athens, GreeceSecond Department of Obstetrics and Gynecology, National and Kapodistrian University of Athens Medical School, Aretaieio Hospital, Athens, GreeceGynecological Oncology Department, Metaxa Cancer Hospital, Piraeus, GreeceDepartment of Endocrinology and Metabolic Disorders, University of Thessaly Medical School, Larissa University Hospital, Larissa, GreeceSecond Department of Obstetrics and Gynecology, National and Kapodistrian University of Athens Medical School, Aretaieio Hospital, Athens, GreeceSt George’s University of London Medical School and St George’s University Hospitals NHS Foundation Trust, London, UKDepartment of Clinical Biochemistry, “Aghia Sophia” Children’s Hospital, Athens, GreeceSecond Department of Obstetrics and Gynecology, National and Kapodistrian University of Athens Medical School, Aretaieio Hospital, Athens, GreeceSecond Department of Obstetrics and Gynecology, National and Kapodistrian University of Athens Medical School, Aretaieio Hospital, Athens, GreeceSecond Department of Obstetrics and Gynecology, National and Kapodistrian University of Athens Medical School, Aretaieio Hospital, Athens, GreeceSecond Department of Obstetrics and Gynecology, National and Kapodistrian University of Athens Medical School, Aretaieio Hospital, Athens, GreeceThe development of the fetal nervous system mirrors general fetal development, comprising a combination of genetic resources and effects of the intrauterine environment. Our aim was to assess the 2nd trimester amniotic fluid levels of brain-derived neurotrophic factor (BDNF) and to investigate its association with fetal growth. In accordance with our study design, samples of amniotic fluid were collected from women who had undergone amniocentesis early in the 2nd trimester. All pregnancies were followed up until delivery and fetal growth patterns and birth weights were recorded, following which pregnancies were divided into three groups based on fetal weight: (1) AGA (appropriate for gestational age), (2) SGA (small for gestational age), and (3) LGA (large for gestational age). We focused on these three groups representing a reflection of the intrauterine growth spectrum. Our results revealed the presence of notably higher BDNF levels in the amniotic fluid of impaired growth fetuses by comparison with those of normal growth. Both SGA and macrosomic fetuses are characterized by notably higher amniotic fluid levels of BDNF (mean values of 36,300 pg/ml and 35,700 pg/ml, respectively) compared to normal-growth fetuses (mean value of 32,700 pg/ml). Though apparently small, this difference is, nevertheless, statistically significant (p value < 0.05) in SGA fetuses in the extremes of the distribution, i.e., below the 3rd centile. In conclusion, there is clear evidence that severe impairment of fetal growth induces the increased production of fetal brain growth factor as an adaptive mechanism in reaction to a hostile intrauterine environment, thereby accelerating fetal brain development and maturation.http://dx.doi.org/10.1155/2018/8476217
collection DOAJ
language English
format Article
sources DOAJ
author Nikolaos Antonakopoulos
Zoe Iliodromiti
George Mastorakos
Christos Iavazzo
Georgios Valsamakis
Nikolaos Salakos
Aris Papageorghiou
Alexandra Margeli
Sophia Kalantaridou
George Creatsas
Efthymios Deligeoroglou
Nikolaos Vrachnis
spellingShingle Nikolaos Antonakopoulos
Zoe Iliodromiti
George Mastorakos
Christos Iavazzo
Georgios Valsamakis
Nikolaos Salakos
Aris Papageorghiou
Alexandra Margeli
Sophia Kalantaridou
George Creatsas
Efthymios Deligeoroglou
Nikolaos Vrachnis
Association between Brain-Derived Neurotrophic Factor (BDNF) Levels in 2nd Trimester Amniotic Fluid and Fetal Development
Mediators of Inflammation
author_facet Nikolaos Antonakopoulos
Zoe Iliodromiti
George Mastorakos
Christos Iavazzo
Georgios Valsamakis
Nikolaos Salakos
Aris Papageorghiou
Alexandra Margeli
Sophia Kalantaridou
George Creatsas
Efthymios Deligeoroglou
Nikolaos Vrachnis
author_sort Nikolaos Antonakopoulos
title Association between Brain-Derived Neurotrophic Factor (BDNF) Levels in 2nd Trimester Amniotic Fluid and Fetal Development
title_short Association between Brain-Derived Neurotrophic Factor (BDNF) Levels in 2nd Trimester Amniotic Fluid and Fetal Development
title_full Association between Brain-Derived Neurotrophic Factor (BDNF) Levels in 2nd Trimester Amniotic Fluid and Fetal Development
title_fullStr Association between Brain-Derived Neurotrophic Factor (BDNF) Levels in 2nd Trimester Amniotic Fluid and Fetal Development
title_full_unstemmed Association between Brain-Derived Neurotrophic Factor (BDNF) Levels in 2nd Trimester Amniotic Fluid and Fetal Development
title_sort association between brain-derived neurotrophic factor (bdnf) levels in 2nd trimester amniotic fluid and fetal development
publisher Hindawi Limited
series Mediators of Inflammation
issn 0962-9351
1466-1861
publishDate 2018-01-01
description The development of the fetal nervous system mirrors general fetal development, comprising a combination of genetic resources and effects of the intrauterine environment. Our aim was to assess the 2nd trimester amniotic fluid levels of brain-derived neurotrophic factor (BDNF) and to investigate its association with fetal growth. In accordance with our study design, samples of amniotic fluid were collected from women who had undergone amniocentesis early in the 2nd trimester. All pregnancies were followed up until delivery and fetal growth patterns and birth weights were recorded, following which pregnancies were divided into three groups based on fetal weight: (1) AGA (appropriate for gestational age), (2) SGA (small for gestational age), and (3) LGA (large for gestational age). We focused on these three groups representing a reflection of the intrauterine growth spectrum. Our results revealed the presence of notably higher BDNF levels in the amniotic fluid of impaired growth fetuses by comparison with those of normal growth. Both SGA and macrosomic fetuses are characterized by notably higher amniotic fluid levels of BDNF (mean values of 36,300 pg/ml and 35,700 pg/ml, respectively) compared to normal-growth fetuses (mean value of 32,700 pg/ml). Though apparently small, this difference is, nevertheless, statistically significant (p value < 0.05) in SGA fetuses in the extremes of the distribution, i.e., below the 3rd centile. In conclusion, there is clear evidence that severe impairment of fetal growth induces the increased production of fetal brain growth factor as an adaptive mechanism in reaction to a hostile intrauterine environment, thereby accelerating fetal brain development and maturation.
url http://dx.doi.org/10.1155/2018/8476217
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