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Intrauterine growth restriction, preterm birth and risk of end-stage renal disease during the first 50 years of life

BACKGROUND: Low birth weight (LBW) is associated with a higher risk of end-stage renal disease (ESRD). The relative impacts of absolute birth weight, birth weight in relation to gestational age and preterm birth are, however, uncertain. METHODS: The Medical Birth Registry of Norway has since 1967 re...

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Autores principales: Gjerde, Anna, Lillås, Bjørn Steinar, Marti, Hans-Peter, Reisæter, Anna Varberg, Vikse, Bjørn Egil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417009/
https://www.ncbi.nlm.nih.gov/pubmed/32040151
http://dx.doi.org/10.1093/ndt/gfaa001
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author Gjerde, Anna
Lillås, Bjørn Steinar
Marti, Hans-Peter
Reisæter, Anna Varberg
Vikse, Bjørn Egil
author_facet Gjerde, Anna
Lillås, Bjørn Steinar
Marti, Hans-Peter
Reisæter, Anna Varberg
Vikse, Bjørn Egil
author_sort Gjerde, Anna
collection PubMed
description BACKGROUND: Low birth weight (LBW) is associated with a higher risk of end-stage renal disease (ESRD). The relative impacts of absolute birth weight, birth weight in relation to gestational age and preterm birth are, however, uncertain. METHODS: The Medical Birth Registry of Norway has since 1967 recorded data on all births. All patients with ESRD since 1980 have been registered in the Norwegian Renal Registry. Data from these registries were linked. All individuals registered in the Medical Birth Registry were included and the development of ESRD was used as endpoint in Cox regression statistics. LBW and LBW for gestational age [small for gestational age (SGA)] according to the 10th percentiles were used as the main predictor variables. RESULTS: Of the 2 679 967 included subjects, 1181 developed ESRD. Compared with subjects without LBW, subjects with LBW had an adjusted hazard ratio (aHR) for ESRD of 1.61 (1.38–1.98). SGA had an aHR of 1.44 (1.22– 1.70). Further analyses showed that as compared with subjects who had none of the risk factors LBW, SGA and preterm birth, subjects with one risk factor had an aHR of 1.05 (0.84–1.31), subjects with two risk factors had an aHR of 1.67 (1.40–1.98) and subjects with three risk factors had an aHR of 2.96 (1.84–4.76). CONCLUSIONS: We conclude that LBW was associated with increased risk for ESRD during the first 50 years. Our analyses add to previous knowledge showing that only subjects with at least two of the risk factors LBW, SGA or preterm birth have increased risk.
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spelling pubmed-74170092020-08-12 Intrauterine growth restriction, preterm birth and risk of end-stage renal disease during the first 50 years of life Gjerde, Anna Lillås, Bjørn Steinar Marti, Hans-Peter Reisæter, Anna Varberg Vikse, Bjørn Egil Nephrol Dial Transplant ORIGINAL ARTICLES BACKGROUND: Low birth weight (LBW) is associated with a higher risk of end-stage renal disease (ESRD). The relative impacts of absolute birth weight, birth weight in relation to gestational age and preterm birth are, however, uncertain. METHODS: The Medical Birth Registry of Norway has since 1967 recorded data on all births. All patients with ESRD since 1980 have been registered in the Norwegian Renal Registry. Data from these registries were linked. All individuals registered in the Medical Birth Registry were included and the development of ESRD was used as endpoint in Cox regression statistics. LBW and LBW for gestational age [small for gestational age (SGA)] according to the 10th percentiles were used as the main predictor variables. RESULTS: Of the 2 679 967 included subjects, 1181 developed ESRD. Compared with subjects without LBW, subjects with LBW had an adjusted hazard ratio (aHR) for ESRD of 1.61 (1.38–1.98). SGA had an aHR of 1.44 (1.22– 1.70). Further analyses showed that as compared with subjects who had none of the risk factors LBW, SGA and preterm birth, subjects with one risk factor had an aHR of 1.05 (0.84–1.31), subjects with two risk factors had an aHR of 1.67 (1.40–1.98) and subjects with three risk factors had an aHR of 2.96 (1.84–4.76). CONCLUSIONS: We conclude that LBW was associated with increased risk for ESRD during the first 50 years. Our analyses add to previous knowledge showing that only subjects with at least two of the risk factors LBW, SGA or preterm birth have increased risk. Oxford University Press 2020-07 2020-02-10 /pmc/articles/PMC7417009/ /pubmed/32040151 http://dx.doi.org/10.1093/ndt/gfaa001 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle ORIGINAL ARTICLES
Gjerde, Anna
Lillås, Bjørn Steinar
Marti, Hans-Peter
Reisæter, Anna Varberg
Vikse, Bjørn Egil
Intrauterine growth restriction, preterm birth and risk of end-stage renal disease during the first 50 years of life
title Intrauterine growth restriction, preterm birth and risk of end-stage renal disease during the first 50 years of life
title_full Intrauterine growth restriction, preterm birth and risk of end-stage renal disease during the first 50 years of life
title_fullStr Intrauterine growth restriction, preterm birth and risk of end-stage renal disease during the first 50 years of life
title_full_unstemmed Intrauterine growth restriction, preterm birth and risk of end-stage renal disease during the first 50 years of life
title_short Intrauterine growth restriction, preterm birth and risk of end-stage renal disease during the first 50 years of life
title_sort intrauterine growth restriction, preterm birth and risk of end-stage renal disease during the first 50 years of life
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417009/
https://www.ncbi.nlm.nih.gov/pubmed/32040151
http://dx.doi.org/10.1093/ndt/gfaa001
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