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dc.creatorAntonakopoulos N., Iliodromiti Z., Mastorakos G., Iavazzo C., Valsamakis G., Salakos N., Papageorghiou A., Margeli A., Kalantaridou S., Creatsas G., Deligeoroglou E., Vrachnis N.en
dc.date.accessioned2023-01-31T07:32:06Z
dc.date.available2023-01-31T07:32:06Z
dc.date.issued2018
dc.identifier10.1155/2018/8476217
dc.identifier.issn09629351
dc.identifier.urihttp://hdl.handle.net/11615/70664
dc.description.abstractThe 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 2 nd 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 2 nd 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. © 2018 Nikolaos Antonakopoulos et al.en
dc.language.isoenen
dc.sourceMediators of Inflammationen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85059797992&doi=10.1155%2f2018%2f8476217&partnerID=40&md5=ef029c1f9f3fcd313ac07232cd2a155c
dc.subjectbrain derived neurotrophic factoren
dc.subjectbrain derived neurotrophic factoren
dc.subjectamniocentesisen
dc.subjectamnion fluiden
dc.subjectArticleen
dc.subjectbirth weighten
dc.subjectclinical articleen
dc.subjectcomparative studyen
dc.subjectfetusen
dc.subjectfetus developmenten
dc.subjectfetus growthen
dc.subjectfetus weighten
dc.subjectfollow upen
dc.subjectgestational ageen
dc.subjecthumanen
dc.subjectlarge for gestational ageen
dc.subjectpregnancyen
dc.subjectprenatal growthen
dc.subjectsecond trimester pregnancyen
dc.subjectsmall for date infanten
dc.subjectamnion fluiden
dc.subjectfemaleen
dc.subjectfetus developmenten
dc.subjectgeneticsen
dc.subjectmetabolismen
dc.subjectnewbornen
dc.subjectphysiologyen
dc.subjectAmniotic Fluiden
dc.subjectBirth Weighten
dc.subjectBrain-Derived Neurotrophic Factoren
dc.subjectFemaleen
dc.subjectFetal Developmenten
dc.subjectGestational Ageen
dc.subjectHumansen
dc.subjectInfant, Newbornen
dc.subjectInfant, Small for Gestational Ageen
dc.subjectPregnancyen
dc.subjectPregnancy Trimestersen
dc.subjectHindawi Limiteden
dc.titleAssociation between brain-derived neurotrophic factor (BDNF) levels in 2 nd trimester amniotic fluid and fetal developmenten
dc.typejournalArticleen


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