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Low birth weight, later renal function, and the roles of adulthood blood pressure, diabetes, and obesity in a British birth cohort

Low birth weight has been shown to be associated with later renal function, but it is unclear to what extent this is explained by other established kidney disease risk factors. Here we investigate the roles of diabetes, hypertension, and obesity using data from the Medical Research Council National...

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Autores principales: Silverwood, Richard J, Pierce, Mary, Hardy, Rebecca, Sattar, Naveed, Whincup, Peter, Ferro, Charles, Savage, Caroline, Kuh, Diana, Nitsch, Dorothea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898099/
https://www.ncbi.nlm.nih.gov/pubmed/23760284
http://dx.doi.org/10.1038/ki.2013.223
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author Silverwood, Richard J
Pierce, Mary
Hardy, Rebecca
Sattar, Naveed
Whincup, Peter
Ferro, Charles
Savage, Caroline
Kuh, Diana
Nitsch, Dorothea
author_facet Silverwood, Richard J
Pierce, Mary
Hardy, Rebecca
Sattar, Naveed
Whincup, Peter
Ferro, Charles
Savage, Caroline
Kuh, Diana
Nitsch, Dorothea
author_sort Silverwood, Richard J
collection PubMed
description Low birth weight has been shown to be associated with later renal function, but it is unclear to what extent this is explained by other established kidney disease risk factors. Here we investigate the roles of diabetes, hypertension, and obesity using data from the Medical Research Council National Survey of Health and Development, a socially stratified sample of 5362 children born in March 1946 in England, Scotland, and Wales, and followed since. The birth weight of 2192 study members with complete data was related to three markers of renal function at age 60–64 (estimated glomerular filtration rate (eGFR) calculated using cystatin C (eGFRcys), eGFR calculated using creatinine and cystatin C (eGFRcr-cys), and the urine albumin–creatinine ratio) using linear regression. Each 1 kg lower birth weight was associated with a 2.25 ml/min per 1.73 m(2) (95% confidence interval 0.80–3.71) lower eGFRcys and a 2.13 ml/min per 1.73 m(2) (0.69–3.58) lower eGFRcr-cys. There was no evidence of an association with urine albumin–creatinine ratio. These associations with eGFR were not confounded by socioeconomic position and were not explained by diabetes or hypertension, but there was some evidence that they were stronger in study members who were overweight in adulthood. Thus, our findings highlight the role of lower birth weight in renal disease and suggest that in those born with lower birth weight particular emphasis should be placed on avoiding becoming overweight.
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spelling pubmed-38980992014-01-24 Low birth weight, later renal function, and the roles of adulthood blood pressure, diabetes, and obesity in a British birth cohort Silverwood, Richard J Pierce, Mary Hardy, Rebecca Sattar, Naveed Whincup, Peter Ferro, Charles Savage, Caroline Kuh, Diana Nitsch, Dorothea Kidney Int Clinical Investigation Low birth weight has been shown to be associated with later renal function, but it is unclear to what extent this is explained by other established kidney disease risk factors. Here we investigate the roles of diabetes, hypertension, and obesity using data from the Medical Research Council National Survey of Health and Development, a socially stratified sample of 5362 children born in March 1946 in England, Scotland, and Wales, and followed since. The birth weight of 2192 study members with complete data was related to three markers of renal function at age 60–64 (estimated glomerular filtration rate (eGFR) calculated using cystatin C (eGFRcys), eGFR calculated using creatinine and cystatin C (eGFRcr-cys), and the urine albumin–creatinine ratio) using linear regression. Each 1 kg lower birth weight was associated with a 2.25 ml/min per 1.73 m(2) (95% confidence interval 0.80–3.71) lower eGFRcys and a 2.13 ml/min per 1.73 m(2) (0.69–3.58) lower eGFRcr-cys. There was no evidence of an association with urine albumin–creatinine ratio. These associations with eGFR were not confounded by socioeconomic position and were not explained by diabetes or hypertension, but there was some evidence that they were stronger in study members who were overweight in adulthood. Thus, our findings highlight the role of lower birth weight in renal disease and suggest that in those born with lower birth weight particular emphasis should be placed on avoiding becoming overweight. Nature Publishing Group 2013-12 2013-06-12 /pmc/articles/PMC3898099/ /pubmed/23760284 http://dx.doi.org/10.1038/ki.2013.223 Text en Copyright © 2013 International Society of Nephrology http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Clinical Investigation
Silverwood, Richard J
Pierce, Mary
Hardy, Rebecca
Sattar, Naveed
Whincup, Peter
Ferro, Charles
Savage, Caroline
Kuh, Diana
Nitsch, Dorothea
Low birth weight, later renal function, and the roles of adulthood blood pressure, diabetes, and obesity in a British birth cohort
title Low birth weight, later renal function, and the roles of adulthood blood pressure, diabetes, and obesity in a British birth cohort
title_full Low birth weight, later renal function, and the roles of adulthood blood pressure, diabetes, and obesity in a British birth cohort
title_fullStr Low birth weight, later renal function, and the roles of adulthood blood pressure, diabetes, and obesity in a British birth cohort
title_full_unstemmed Low birth weight, later renal function, and the roles of adulthood blood pressure, diabetes, and obesity in a British birth cohort
title_short Low birth weight, later renal function, and the roles of adulthood blood pressure, diabetes, and obesity in a British birth cohort
title_sort low birth weight, later renal function, and the roles of adulthood blood pressure, diabetes, and obesity in a british birth cohort
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898099/
https://www.ncbi.nlm.nih.gov/pubmed/23760284
http://dx.doi.org/10.1038/ki.2013.223
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