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Altered development of fetal liver perfusion in pregnancies with pregestational diabetes

BACKGROUND: Pregestational diabetes is associated with fetal macrosomia, and umbilical perfusion of the fetal liver has a role in regulating fetal growth. We therefore hypothesized that pregestational diabetes alters fetal liver blood flow depending on degree of glycemic control. METHODS: In a prosp...

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Autores principales: Lund, Agnethe, Ebbing, Cathrine, Rasmussen, Svein, Kiserud, Torvid, Hanson, Mark, Kessler, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415794/
https://www.ncbi.nlm.nih.gov/pubmed/30865630
http://dx.doi.org/10.1371/journal.pone.0211788
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author Lund, Agnethe
Ebbing, Cathrine
Rasmussen, Svein
Kiserud, Torvid
Hanson, Mark
Kessler, Jörg
author_facet Lund, Agnethe
Ebbing, Cathrine
Rasmussen, Svein
Kiserud, Torvid
Hanson, Mark
Kessler, Jörg
author_sort Lund, Agnethe
collection PubMed
description BACKGROUND: Pregestational diabetes is associated with fetal macrosomia, and umbilical perfusion of the fetal liver has a role in regulating fetal growth. We therefore hypothesized that pregestational diabetes alters fetal liver blood flow depending on degree of glycemic control. METHODS: In a prospective study, 49 women with pregestational diabetes underwent monthly ultrasound examinations during 24–36 gestational weeks. Blood flow was determined in the umbilical vein, ductus venosus and portal vein, and blood velocity was measured in the left portal vein, the latter reflecting the watershed between splanchnic and umbilical flow. The measurements were compared with reference values by z-score statistics, and the effect of HbA(1c) assessed. RESULTS: The umbilical venous flow to the liver (z-score 0.36, p = 0.002), total venous liver flow (z-score 0.51, p<0.001) and left portal vein blood velocity (z-score 0.64, p<0.001), were higher in the study group. Normalized portal venous flow was lower (z-score -0.42, p = 0.002), and normalized total venous liver flow tended to be lower after 30 gestational weeks (z-score -0.54, p = 0.047) in the diabetic pregnancies compared with reference values from a low-risk population. The left portal vein blood velocity was positively, and the portal fraction of total venous liver flow negatively correlated with first trimester HbA(1C). CONCLUSIONS: In spite of increased umbilical blood distribution to the fetal liver, graded according to glycemic control, the total venous liver flow did not match third trimester fetal growth in pregnancies with pregestational diabetes, thus contributing towards increased perinatal risks and possibly altered liver function with long-term metabolic consequences.
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spelling pubmed-64157942019-04-02 Altered development of fetal liver perfusion in pregnancies with pregestational diabetes Lund, Agnethe Ebbing, Cathrine Rasmussen, Svein Kiserud, Torvid Hanson, Mark Kessler, Jörg PLoS One Research Article BACKGROUND: Pregestational diabetes is associated with fetal macrosomia, and umbilical perfusion of the fetal liver has a role in regulating fetal growth. We therefore hypothesized that pregestational diabetes alters fetal liver blood flow depending on degree of glycemic control. METHODS: In a prospective study, 49 women with pregestational diabetes underwent monthly ultrasound examinations during 24–36 gestational weeks. Blood flow was determined in the umbilical vein, ductus venosus and portal vein, and blood velocity was measured in the left portal vein, the latter reflecting the watershed between splanchnic and umbilical flow. The measurements were compared with reference values by z-score statistics, and the effect of HbA(1c) assessed. RESULTS: The umbilical venous flow to the liver (z-score 0.36, p = 0.002), total venous liver flow (z-score 0.51, p<0.001) and left portal vein blood velocity (z-score 0.64, p<0.001), were higher in the study group. Normalized portal venous flow was lower (z-score -0.42, p = 0.002), and normalized total venous liver flow tended to be lower after 30 gestational weeks (z-score -0.54, p = 0.047) in the diabetic pregnancies compared with reference values from a low-risk population. The left portal vein blood velocity was positively, and the portal fraction of total venous liver flow negatively correlated with first trimester HbA(1C). CONCLUSIONS: In spite of increased umbilical blood distribution to the fetal liver, graded according to glycemic control, the total venous liver flow did not match third trimester fetal growth in pregnancies with pregestational diabetes, thus contributing towards increased perinatal risks and possibly altered liver function with long-term metabolic consequences. Public Library of Science 2019-03-13 /pmc/articles/PMC6415794/ /pubmed/30865630 http://dx.doi.org/10.1371/journal.pone.0211788 Text en © 2019 Lund et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lund, Agnethe
Ebbing, Cathrine
Rasmussen, Svein
Kiserud, Torvid
Hanson, Mark
Kessler, Jörg
Altered development of fetal liver perfusion in pregnancies with pregestational diabetes
title Altered development of fetal liver perfusion in pregnancies with pregestational diabetes
title_full Altered development of fetal liver perfusion in pregnancies with pregestational diabetes
title_fullStr Altered development of fetal liver perfusion in pregnancies with pregestational diabetes
title_full_unstemmed Altered development of fetal liver perfusion in pregnancies with pregestational diabetes
title_short Altered development of fetal liver perfusion in pregnancies with pregestational diabetes
title_sort altered development of fetal liver perfusion in pregnancies with pregestational diabetes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415794/
https://www.ncbi.nlm.nih.gov/pubmed/30865630
http://dx.doi.org/10.1371/journal.pone.0211788
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