TY - JOUR
T1 - Mechanical characterization of human umbilical and chorionic plate arteries affected by fetal growth restriction
AU - Arenas, Germán A.
AU - Navarrete, Álvaro
AU - Gonzalez, José Miguel
AU - Utrera, Andrés
AU - García-Herrera, Claudio
AU - Krause, Bernardo J.
N1 - Publisher Copyright:
© The Author(s) 2026. Published by Oxford University Press on behalf of National Academy of Sciences. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
PY - 2026/11
Y1 - 2026/11
N2 - Fetal growth restriction (FGR) is a pregnancy complication associated with increased perinatal morbidity and mortality in the short term, along with an elevated risk of developing cardiometabolic diseases in the long term. FGR is also associated with vascular dysfunction in the fetoplacental unit. In this work, we develop a clinical study of the fetoplacental circulation (encompassing umbilical and chorionic arteries) under the FGR condition, utilizing a combination of numerical and experimental approaches to quantify biomechanical and morphological characteristics. Placental samples from normal (n = 5) and FGR pregnancies (n = 5) underwent biomechanical testing (ring-opening and ring-tensile tests) under physiological conditions. Biomechanical behavior, including material properties and residual stress, was characterized via numerical analysis using a hyperelastic model and a simulation of the ring-closure process. Morphological analysis, including wall thickness and layer area measurements, was performed to relate structural features to biomechanical behavior. The umbilical and chorionic arteries exhibit distinct responses to FGR: the umbilical artery undergoes both morphological remodeling and changes in biomechanical properties, whereas the chorionic artery primarily shows biomechanical alterations. Overall, this study provides novel biomechanical evidence of the impact of FGR on placental vasculature, highlighting the complex interplay between morphology and mechanics in fetoplacental blood vessels.
AB - Fetal growth restriction (FGR) is a pregnancy complication associated with increased perinatal morbidity and mortality in the short term, along with an elevated risk of developing cardiometabolic diseases in the long term. FGR is also associated with vascular dysfunction in the fetoplacental unit. In this work, we develop a clinical study of the fetoplacental circulation (encompassing umbilical and chorionic arteries) under the FGR condition, utilizing a combination of numerical and experimental approaches to quantify biomechanical and morphological characteristics. Placental samples from normal (n = 5) and FGR pregnancies (n = 5) underwent biomechanical testing (ring-opening and ring-tensile tests) under physiological conditions. Biomechanical behavior, including material properties and residual stress, was characterized via numerical analysis using a hyperelastic model and a simulation of the ring-closure process. Morphological analysis, including wall thickness and layer area measurements, was performed to relate structural features to biomechanical behavior. The umbilical and chorionic arteries exhibit distinct responses to FGR: the umbilical artery undergoes both morphological remodeling and changes in biomechanical properties, whereas the chorionic artery primarily shows biomechanical alterations. Overall, this study provides novel biomechanical evidence of the impact of FGR on placental vasculature, highlighting the complex interplay between morphology and mechanics in fetoplacental blood vessels.
KW - biomechanical characterization
KW - fetoplacental arteries
KW - finite element method
KW - ring-opening test
KW - ring-tensile test
UR - https://www.scopus.com/pages/publications/105039527456
U2 - 10.1093/pnasnexus/pgag158
DO - 10.1093/pnasnexus/pgag158
M3 - Article
AN - SCOPUS:105039527456
SN - 2752-6542
VL - 5
JO - PNAS Nexus
JF - PNAS Nexus
IS - 5
M1 - pgag158
ER -