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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Association between brain-derived neurotrophic factor (BDNF) levels in 2 nd trimester amniotic fluid and fetal development

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Συγγραφέας
Antonakopoulos N., Iliodromiti Z., Mastorakos G., Iavazzo C., Valsamakis G., Salakos N., Papageorghiou A., Margeli A., Kalantaridou S., Creatsas G., Deligeoroglou E., Vrachnis N.
Ημερομηνία
2018
Γλώσσα
en
DOI
10.1155/2018/8476217
Λέξη-κλειδί
brain derived neurotrophic factor
brain derived neurotrophic factor
amniocentesis
amnion fluid
Article
birth weight
clinical article
comparative study
fetus
fetus development
fetus growth
fetus weight
follow up
gestational age
human
large for gestational age
pregnancy
prenatal growth
second trimester pregnancy
small for date infant
amnion fluid
female
fetus development
genetics
metabolism
newborn
physiology
Amniotic Fluid
Birth Weight
Brain-Derived Neurotrophic Factor
Female
Fetal Development
Gestational Age
Humans
Infant, Newborn
Infant, Small for Gestational Age
Pregnancy
Pregnancy Trimesters
Hindawi Limited
Εμφάνιση Μεταδεδομένων
Επιτομή
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 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.
URI
http://hdl.handle.net/11615/70664
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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