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Does one size fit all? The case for ethnic-specific standards of fetal growth
BACKGROUND: Birth weight for gestational age is a widely-used proxy for fetal growth. Although the need for different standards for males and females is generally acknowledged, the physiologic vs pathologic nature of ethnic differences in fetal growth is hotly debated and remains unresolved. METHODS...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266898/ https://www.ncbi.nlm.nih.gov/pubmed/18179721 http://dx.doi.org/10.1186/1471-2393-8-1 |
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author | Kierans, William J Joseph, KS Luo, Zhong-Cheng Platt, Robert Wilkins, Russell Kramer, Michael S |
author_facet | Kierans, William J Joseph, KS Luo, Zhong-Cheng Platt, Robert Wilkins, Russell Kramer, Michael S |
author_sort | Kierans, William J |
collection | PubMed |
description | BACKGROUND: Birth weight for gestational age is a widely-used proxy for fetal growth. Although the need for different standards for males and females is generally acknowledged, the physiologic vs pathologic nature of ethnic differences in fetal growth is hotly debated and remains unresolved. METHODS: We used all stillbirth, live birth, and deterministically linked infant deaths in British Columbia from 1981 to 2000 to examine fetal growth and perinatal mortality in Chinese (n = 40,092), South Asian (n = 38,670), First Nations, i.e., North American Indian (n = 56,097), and other (n = 731,109) births. We used a new analytic approach based on total fetuses at risk to compare the four ethnic groups in perinatal mortality, mean birth weight, and "revealed" (< 10(th )percentile) small-for-gestational age (SGA) among live births based on both a single standard and four ethnic-specific standards. RESULTS: Despite their lower mean birth weights and higher SGA rates (when based on a single standard), Chinese and South Asian infants had lower perinatal mortality risks throughout gestation. The opposite pattern was observed for First Nations births: higher mean birth weights, lower revealed SGA rates, and higher perinatal mortality risks. When SGA was based on ethnic-specific standards, however, the pattern was concordant with that observed for perinatal mortality. CONCLUSION: The concordance of perinatal mortality and SGA rates when based on ethnic-specific standards, and their discordance when based on a single standard, strongly suggests that the observed ethnic differences in fetal growth are physiologic, rather than pathologic, and make a strong case for ethnic-specific standards. |
format | Text |
id | pubmed-2266898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22668982008-03-12 Does one size fit all? The case for ethnic-specific standards of fetal growth Kierans, William J Joseph, KS Luo, Zhong-Cheng Platt, Robert Wilkins, Russell Kramer, Michael S BMC Pregnancy Childbirth Research Article BACKGROUND: Birth weight for gestational age is a widely-used proxy for fetal growth. Although the need for different standards for males and females is generally acknowledged, the physiologic vs pathologic nature of ethnic differences in fetal growth is hotly debated and remains unresolved. METHODS: We used all stillbirth, live birth, and deterministically linked infant deaths in British Columbia from 1981 to 2000 to examine fetal growth and perinatal mortality in Chinese (n = 40,092), South Asian (n = 38,670), First Nations, i.e., North American Indian (n = 56,097), and other (n = 731,109) births. We used a new analytic approach based on total fetuses at risk to compare the four ethnic groups in perinatal mortality, mean birth weight, and "revealed" (< 10(th )percentile) small-for-gestational age (SGA) among live births based on both a single standard and four ethnic-specific standards. RESULTS: Despite their lower mean birth weights and higher SGA rates (when based on a single standard), Chinese and South Asian infants had lower perinatal mortality risks throughout gestation. The opposite pattern was observed for First Nations births: higher mean birth weights, lower revealed SGA rates, and higher perinatal mortality risks. When SGA was based on ethnic-specific standards, however, the pattern was concordant with that observed for perinatal mortality. CONCLUSION: The concordance of perinatal mortality and SGA rates when based on ethnic-specific standards, and their discordance when based on a single standard, strongly suggests that the observed ethnic differences in fetal growth are physiologic, rather than pathologic, and make a strong case for ethnic-specific standards. BioMed Central 2008-01-08 /pmc/articles/PMC2266898/ /pubmed/18179721 http://dx.doi.org/10.1186/1471-2393-8-1 Text en Copyright © 2008 Kierans et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kierans, William J Joseph, KS Luo, Zhong-Cheng Platt, Robert Wilkins, Russell Kramer, Michael S Does one size fit all? The case for ethnic-specific standards of fetal growth |
title | Does one size fit all? The case for ethnic-specific standards of fetal growth |
title_full | Does one size fit all? The case for ethnic-specific standards of fetal growth |
title_fullStr | Does one size fit all? The case for ethnic-specific standards of fetal growth |
title_full_unstemmed | Does one size fit all? The case for ethnic-specific standards of fetal growth |
title_short | Does one size fit all? The case for ethnic-specific standards of fetal growth |
title_sort | does one size fit all? the case for ethnic-specific standards of fetal growth |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266898/ https://www.ncbi.nlm.nih.gov/pubmed/18179721 http://dx.doi.org/10.1186/1471-2393-8-1 |
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