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An unfavorable intrauterine environment may determine renal functional capacity in adulthood: a meta-analysis
Since studies show that an unfavorable environment during intrauterine development predisposes individuals to several diseases in adulthood, our objective is to assess the relation between fetal growth restriction and chronic renal disease in adults. We searched four different electronic databases t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172979/ https://www.ncbi.nlm.nih.gov/pubmed/30365822 http://dx.doi.org/10.6061/clinics/2018/e401 |
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author | Senra, Janaína Campos Carvalho, Mariana Azevedo Rodrigues, Agatha Sacramento Krebs, Vera Lúcia Jornada Gibelli, Maria Augusta Bento Cicaroni Francisco, Rossana Pulcineli Vieira Bernardes, Lisandra Stein |
author_facet | Senra, Janaína Campos Carvalho, Mariana Azevedo Rodrigues, Agatha Sacramento Krebs, Vera Lúcia Jornada Gibelli, Maria Augusta Bento Cicaroni Francisco, Rossana Pulcineli Vieira Bernardes, Lisandra Stein |
author_sort | Senra, Janaína Campos |
collection | PubMed |
description | Since studies show that an unfavorable environment during intrauterine development predisposes individuals to several diseases in adulthood, our objective is to assess the relation between fetal growth restriction and chronic renal disease in adults. We searched four different electronic databases through November 2017: CENTRAL, EMBASE, LILACS and MEDLINE. We selected studies with longitudinal or transversal designs associating kidney function in adulthood with low birth weight. Two reviewers evaluated the inclusion criteria and the risk of bias and extracted data from the included papers. Thirteen studies were selected for the systematic review and meta-analysis. We observed increased risks of presenting end-stage renal disease (risk ratio 1.31, 95% confidence interval: 1.17, 1.47), a lower glomerular filtration rate (ml/min) (mean difference 7.14; 95% confidence interval: -12.12, -2.16), microalbuminuria (risk ratio 1.40; 95% confidence interval: 1.28, 1.52) and a small increase in the albumin/creatinine ratio (mean difference 0.46; 95% confidence interval: 0.03, 0.90) in the low birth weight patients, compared with control group. These findings suggest that low birth weight is associated with renal dysfunction in adults. |
format | Online Article Text |
id | pubmed-6172979 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-61729792018-10-11 An unfavorable intrauterine environment may determine renal functional capacity in adulthood: a meta-analysis Senra, Janaína Campos Carvalho, Mariana Azevedo Rodrigues, Agatha Sacramento Krebs, Vera Lúcia Jornada Gibelli, Maria Augusta Bento Cicaroni Francisco, Rossana Pulcineli Vieira Bernardes, Lisandra Stein Clinics (Sao Paulo) Review Article Since studies show that an unfavorable environment during intrauterine development predisposes individuals to several diseases in adulthood, our objective is to assess the relation between fetal growth restriction and chronic renal disease in adults. We searched four different electronic databases through November 2017: CENTRAL, EMBASE, LILACS and MEDLINE. We selected studies with longitudinal or transversal designs associating kidney function in adulthood with low birth weight. Two reviewers evaluated the inclusion criteria and the risk of bias and extracted data from the included papers. Thirteen studies were selected for the systematic review and meta-analysis. We observed increased risks of presenting end-stage renal disease (risk ratio 1.31, 95% confidence interval: 1.17, 1.47), a lower glomerular filtration rate (ml/min) (mean difference 7.14; 95% confidence interval: -12.12, -2.16), microalbuminuria (risk ratio 1.40; 95% confidence interval: 1.28, 1.52) and a small increase in the albumin/creatinine ratio (mean difference 0.46; 95% confidence interval: 0.03, 0.90) in the low birth weight patients, compared with control group. These findings suggest that low birth weight is associated with renal dysfunction in adults. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2018-10-05 2018 /pmc/articles/PMC6172979/ /pubmed/30365822 http://dx.doi.org/10.6061/clinics/2018/e401 Text en Copyright © 2018 CLINICS http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is properly cited. |
spellingShingle | Review Article Senra, Janaína Campos Carvalho, Mariana Azevedo Rodrigues, Agatha Sacramento Krebs, Vera Lúcia Jornada Gibelli, Maria Augusta Bento Cicaroni Francisco, Rossana Pulcineli Vieira Bernardes, Lisandra Stein An unfavorable intrauterine environment may determine renal functional capacity in adulthood: a meta-analysis |
title | An unfavorable intrauterine environment may determine renal functional capacity in adulthood: a meta-analysis |
title_full | An unfavorable intrauterine environment may determine renal functional capacity in adulthood: a meta-analysis |
title_fullStr | An unfavorable intrauterine environment may determine renal functional capacity in adulthood: a meta-analysis |
title_full_unstemmed | An unfavorable intrauterine environment may determine renal functional capacity in adulthood: a meta-analysis |
title_short | An unfavorable intrauterine environment may determine renal functional capacity in adulthood: a meta-analysis |
title_sort | unfavorable intrauterine environment may determine renal functional capacity in adulthood: a meta-analysis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172979/ https://www.ncbi.nlm.nih.gov/pubmed/30365822 http://dx.doi.org/10.6061/clinics/2018/e401 |
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