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Birth characteristics and risk of Ewing sarcoma
PURPOSE: The incidence of Ewing sarcoma varies according to race and ethnicity, and genetic susceptibility is known to affect disease risk. Apart from these factors, the etiology of Ewing sarcoma is largely unknown. METHODS: We compared the birth characteristics of a population-based series of 556 E...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460323/ https://www.ncbi.nlm.nih.gov/pubmed/37335392 http://dx.doi.org/10.1007/s10552-023-01737-4 |
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author | Wiemels, Joseph L. Wang, Rong Feng, Qianxi Yee, Amy C. Morimoto, Libby M. Metayer, Catherine Ma, Xiaomei |
author_facet | Wiemels, Joseph L. Wang, Rong Feng, Qianxi Yee, Amy C. Morimoto, Libby M. Metayer, Catherine Ma, Xiaomei |
author_sort | Wiemels, Joseph L. |
collection | PubMed |
description | PURPOSE: The incidence of Ewing sarcoma varies according to race and ethnicity, and genetic susceptibility is known to affect disease risk. Apart from these factors, the etiology of Ewing sarcoma is largely unknown. METHODS: We compared the birth characteristics of a population-based series of 556 Ewing sarcoma cases born in California in 1978–2015 and diagnosed in 1988–2015 with those of 27,800 controls selected from statewide birth records and frequency-matched to cases on the year of birth, using multivariable logistic regression models. We also assessed whether Ewing sarcoma clustered within families. RESULTS: Compared to non-Hispanic White subjects, Black (odds ratio [OR] = 0.07, 95% confidence interval [CI] 0.03–0.18), Asian (OR = 0.57, 95% CI 0.41–0.80), and Hispanic (OR = 0.73, 95% CI 0.62–0.88) individuals had a significantly lower risk of Ewing sarcoma. Race and ethnicity differences were more profound for metastatic Ewing sarcoma. Birthweight was also identified as a significant risk factor (OR = 1.09, 95% CI 1.00–1.18 for each 500 g increase in birthweight). A separate family-based cancer clustering analysis did not suggest any strong role for familial predisposition alleles. CONCLUSIONS: This population-based study with minimal selection bias provides support for a role of accelerated fetal growth in the etiology of Ewing sarcoma in addition to more precise estimates of racial and ethnic variations in disease risk. This comparatively large analysis of birth characteristics and Ewing sarcoma in a multiethnic population should stimulate further investigations into genetic and environmental causes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10552-023-01737-4. |
format | Online Article Text |
id | pubmed-10460323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-104603232023-08-28 Birth characteristics and risk of Ewing sarcoma Wiemels, Joseph L. Wang, Rong Feng, Qianxi Yee, Amy C. Morimoto, Libby M. Metayer, Catherine Ma, Xiaomei Cancer Causes Control Brief Report PURPOSE: The incidence of Ewing sarcoma varies according to race and ethnicity, and genetic susceptibility is known to affect disease risk. Apart from these factors, the etiology of Ewing sarcoma is largely unknown. METHODS: We compared the birth characteristics of a population-based series of 556 Ewing sarcoma cases born in California in 1978–2015 and diagnosed in 1988–2015 with those of 27,800 controls selected from statewide birth records and frequency-matched to cases on the year of birth, using multivariable logistic regression models. We also assessed whether Ewing sarcoma clustered within families. RESULTS: Compared to non-Hispanic White subjects, Black (odds ratio [OR] = 0.07, 95% confidence interval [CI] 0.03–0.18), Asian (OR = 0.57, 95% CI 0.41–0.80), and Hispanic (OR = 0.73, 95% CI 0.62–0.88) individuals had a significantly lower risk of Ewing sarcoma. Race and ethnicity differences were more profound for metastatic Ewing sarcoma. Birthweight was also identified as a significant risk factor (OR = 1.09, 95% CI 1.00–1.18 for each 500 g increase in birthweight). A separate family-based cancer clustering analysis did not suggest any strong role for familial predisposition alleles. CONCLUSIONS: This population-based study with minimal selection bias provides support for a role of accelerated fetal growth in the etiology of Ewing sarcoma in addition to more precise estimates of racial and ethnic variations in disease risk. This comparatively large analysis of birth characteristics and Ewing sarcoma in a multiethnic population should stimulate further investigations into genetic and environmental causes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10552-023-01737-4. Springer International Publishing 2023-06-19 2023 /pmc/articles/PMC10460323/ /pubmed/37335392 http://dx.doi.org/10.1007/s10552-023-01737-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Brief Report Wiemels, Joseph L. Wang, Rong Feng, Qianxi Yee, Amy C. Morimoto, Libby M. Metayer, Catherine Ma, Xiaomei Birth characteristics and risk of Ewing sarcoma |
title | Birth characteristics and risk of Ewing sarcoma |
title_full | Birth characteristics and risk of Ewing sarcoma |
title_fullStr | Birth characteristics and risk of Ewing sarcoma |
title_full_unstemmed | Birth characteristics and risk of Ewing sarcoma |
title_short | Birth characteristics and risk of Ewing sarcoma |
title_sort | birth characteristics and risk of ewing sarcoma |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460323/ https://www.ncbi.nlm.nih.gov/pubmed/37335392 http://dx.doi.org/10.1007/s10552-023-01737-4 |
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