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Intrauterine growth restriction is associated with persistent aortic wall thickening and glomerular proteinuria during infancy
Low birth weight, caused either by preterm birth or by intrauterine growth restriction, has recently been associated with increased rates of adult renal and cardiovascular disease. Since aortic intima–media thickening is a noninvasive marker of preclinical vascular disease, we compared abdominal aor...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257045/ https://www.ncbi.nlm.nih.gov/pubmed/21490588 http://dx.doi.org/10.1038/ki.2011.99 |
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author | Zanardo, Vincenzo Fanelli, Tiziana Weiner, Gary Fanos, Vassilios Zaninotto, Martina Visentin, Silvia Cavallin, Francesco Trevisanuto, Daniele Cosmi, Erich |
author_facet | Zanardo, Vincenzo Fanelli, Tiziana Weiner, Gary Fanos, Vassilios Zaninotto, Martina Visentin, Silvia Cavallin, Francesco Trevisanuto, Daniele Cosmi, Erich |
author_sort | Zanardo, Vincenzo |
collection | PubMed |
description | Low birth weight, caused either by preterm birth or by intrauterine growth restriction, has recently been associated with increased rates of adult renal and cardiovascular disease. Since aortic intima–media thickening is a noninvasive marker of preclinical vascular disease, we compared abdominal aortic intima–media thickness among intrauterine growth restricted and equivalent gestational age fetuses in utero and at 18 months of age. The relationship between intrauterine growth restriction, fetal aortic thickening, and glomerular function during infancy was measured by enrolling 44 mothers with single-fetus pregnancies at 32 weeks gestation: 23 growth restricted and 21 of appropriate gestational age as controls. Abdominal aortic intima–media thickness was measured by ultrasound at enrollment and again at 18 months of age. Fetuses with intrauterine growth restriction had significantly higher abdominal aortic intima–media thickness compared with age controls when measured both in utero and at 18 months. At 18 months, the median urinary microalbumin and median albumin–creatinine ratio were significantly higher in those infants who experienced intrauterine growth restriction compared to the controls. Our results show that intrauterine growth restriction is associated with persistent aortic wall thickening and significantly higher microalbuminuria during infancy. |
format | Online Article Text |
id | pubmed-3257045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-32570452012-01-12 Intrauterine growth restriction is associated with persistent aortic wall thickening and glomerular proteinuria during infancy Zanardo, Vincenzo Fanelli, Tiziana Weiner, Gary Fanos, Vassilios Zaninotto, Martina Visentin, Silvia Cavallin, Francesco Trevisanuto, Daniele Cosmi, Erich Kidney Int Original Article Low birth weight, caused either by preterm birth or by intrauterine growth restriction, has recently been associated with increased rates of adult renal and cardiovascular disease. Since aortic intima–media thickening is a noninvasive marker of preclinical vascular disease, we compared abdominal aortic intima–media thickness among intrauterine growth restricted and equivalent gestational age fetuses in utero and at 18 months of age. The relationship between intrauterine growth restriction, fetal aortic thickening, and glomerular function during infancy was measured by enrolling 44 mothers with single-fetus pregnancies at 32 weeks gestation: 23 growth restricted and 21 of appropriate gestational age as controls. Abdominal aortic intima–media thickness was measured by ultrasound at enrollment and again at 18 months of age. Fetuses with intrauterine growth restriction had significantly higher abdominal aortic intima–media thickness compared with age controls when measured both in utero and at 18 months. At 18 months, the median urinary microalbumin and median albumin–creatinine ratio were significantly higher in those infants who experienced intrauterine growth restriction compared to the controls. Our results show that intrauterine growth restriction is associated with persistent aortic wall thickening and significantly higher microalbuminuria during infancy. Nature Publishing Group 2011-07 2011-04-13 /pmc/articles/PMC3257045/ /pubmed/21490588 http://dx.doi.org/10.1038/ki.2011.99 Text en Copyright © 2011 International Society of Nephrology http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Zanardo, Vincenzo Fanelli, Tiziana Weiner, Gary Fanos, Vassilios Zaninotto, Martina Visentin, Silvia Cavallin, Francesco Trevisanuto, Daniele Cosmi, Erich Intrauterine growth restriction is associated with persistent aortic wall thickening and glomerular proteinuria during infancy |
title | Intrauterine growth restriction is associated with persistent aortic wall thickening and glomerular proteinuria during infancy |
title_full | Intrauterine growth restriction is associated with persistent aortic wall thickening and glomerular proteinuria during infancy |
title_fullStr | Intrauterine growth restriction is associated with persistent aortic wall thickening and glomerular proteinuria during infancy |
title_full_unstemmed | Intrauterine growth restriction is associated with persistent aortic wall thickening and glomerular proteinuria during infancy |
title_short | Intrauterine growth restriction is associated with persistent aortic wall thickening and glomerular proteinuria during infancy |
title_sort | intrauterine growth restriction is associated with persistent aortic wall thickening and glomerular proteinuria during infancy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257045/ https://www.ncbi.nlm.nih.gov/pubmed/21490588 http://dx.doi.org/10.1038/ki.2011.99 |
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