Startseite Umbilical artery pulsatility index and half-peak systolic velocity in second- and third-trimester fetuses with trisomy 18 and 13
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Umbilical artery pulsatility index and half-peak systolic velocity in second- and third-trimester fetuses with trisomy 18 and 13

  • Juan Carlos Bustos ORCID logo , Denise Vega und Waldo Sepulveda ORCID logo EMAIL logo
Veröffentlicht/Copyright: 8. Dezember 2021

Abstract

Objectives

To analyze umbilical artery (UA) Doppler velocimetry and its possible role in placenta-mediated fetal growth restriction (FGR) in second- and third-trimester fetuses with trisomy 18 and 13.

Methods

UA pulsatility index (PI) and half-peak systolic velocity deceleration time (hPSV-DT) were measured in fetuses with trisomy 18 and 13. Correlation with gestational age, birthweight, and perinatal outcome was analyzed.

Results

A total of 80 measurements were taken from 33 fetuses with trisomy 18 and 19 with trisomy 13. Overall, there was a high prevalence of abnormal UA Doppler velocimetry. In fetuses with trisomy 18, 54% (27/50) of the UA PI values and 58% (29/50) of the UA hPSV-DT values were abnormal. In fetuses with trisomy 13, 80% (24/30) of the UA PI values and 87% (26/30) of the UA hPSV-DT values were abnormal. The prevalence of abnormal UA Doppler velocimetry increased with gestational age in both types of aneuploidy. However, this trend was only significant for trisomy 13 (p<0.05). All fetuses with trisomy 18 and 86% of fetuses with trisomy 13 were classified at birth as FGR. There were no perinatal survivors in this series.

Conclusions

A high prevalence of abnormal UA Doppler velocimetry was found in second- and third-trimester fetuses with trisomy 18 and 13, which further increased with gestational age. These results may well correlate with alterations described previously in the placenta, suggesting placental insufficiency has an important role in the development of FGR in these autosomal aneuploid fetuses.


Corresponding author: Waldo Sepulveda, MD, FETALMED–Maternal-Fetal Diagnostic Center, Fetal Imaging Unit, Estoril 50, Suite 203, Santiago 7591047, Chile, Phone: (+56 2) 2215 9630, E-mail:

Funding source: Sociedad Profesional de Medicina Fetal ‘Fetalmed’ Ltda., Chile

Award Identifier / Grant number: Unrestricted Research Grant

  1. Research funding: W.S. was supported by an Unrestricted Research Grant from the Sociedad Profesional de Medicina Fetal ‘Fetalmed’ Ltda., Chile.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: The local Institutional Review Board deemed the study exempt from review.

  6. Data availability: The data that support the findings of this study are available from the corresponding author upon reasonable request.

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Received: 2021-08-24
Accepted: 2021-11-15
Published Online: 2021-12-08
Published in Print: 2022-03-28

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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