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Association of serum bilirubin levels with risk of cancer development and total death
Serum levels of bilirubin, a strong antioxidant, may influence cancer risk. We aimed to assess the association between serum bilirubin levels and cancer risk. Data were retrieved from 10-year electronic medical records at Kyushu University Hospital (Japan) for patients aged 20 to 69 years old. The a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225648/ https://www.ncbi.nlm.nih.gov/pubmed/34168201 http://dx.doi.org/10.1038/s41598-021-92442-2 |
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author | Inoguchi, Toyoshi Nohara, Yasunobu Nojiri, Chinatsu Nakashima, Naoki |
author_facet | Inoguchi, Toyoshi Nohara, Yasunobu Nojiri, Chinatsu Nakashima, Naoki |
author_sort | Inoguchi, Toyoshi |
collection | PubMed |
description | Serum levels of bilirubin, a strong antioxidant, may influence cancer risk. We aimed to assess the association between serum bilirubin levels and cancer risk. Data were retrieved from 10-year electronic medical records at Kyushu University Hospital (Japan) for patients aged 20 to 69 years old. The associations of baseline bilirubin levels with cancer risk (lung, colon, breast, prostate, and cervical) were evaluated using a gradient boosting decision tree (GBDT) model, a machine learning algorithm, and Cox proportional hazard regression model, adjusted for age, smoking, body mass index, and diabetes. The number of study subjects was 29,080. Median follow-up time was 4.7 years. GBDT models illustrated that baseline bilirubin levels were negatively and non-linearly associated with the risk of lung (men), colon, and cervical cancer. In contrast, a U-shaped association was observed for breast and prostate cancer. Cox hazard regression analyses confirmed that baseline bilirubin levels (< 1.2 mg/dL) were negatively associated with lung cancer risk in men (HR = 0.474, 95% CI 0.271–0.828, P = 0.009) and cervical cancer risk (HR = 0.365, 95% CI 0.136–0.977, P = 0.045). Additionally, low bilirubin levels (< 0.6 mg/dL) were associated with total death (HR = 1.744, 95% CI 1.369–2.222, P < 0.001). Serum bilirubin may have a beneficial effect on the risk of some types of cancers. |
format | Online Article Text |
id | pubmed-8225648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82256482021-07-02 Association of serum bilirubin levels with risk of cancer development and total death Inoguchi, Toyoshi Nohara, Yasunobu Nojiri, Chinatsu Nakashima, Naoki Sci Rep Article Serum levels of bilirubin, a strong antioxidant, may influence cancer risk. We aimed to assess the association between serum bilirubin levels and cancer risk. Data were retrieved from 10-year electronic medical records at Kyushu University Hospital (Japan) for patients aged 20 to 69 years old. The associations of baseline bilirubin levels with cancer risk (lung, colon, breast, prostate, and cervical) were evaluated using a gradient boosting decision tree (GBDT) model, a machine learning algorithm, and Cox proportional hazard regression model, adjusted for age, smoking, body mass index, and diabetes. The number of study subjects was 29,080. Median follow-up time was 4.7 years. GBDT models illustrated that baseline bilirubin levels were negatively and non-linearly associated with the risk of lung (men), colon, and cervical cancer. In contrast, a U-shaped association was observed for breast and prostate cancer. Cox hazard regression analyses confirmed that baseline bilirubin levels (< 1.2 mg/dL) were negatively associated with lung cancer risk in men (HR = 0.474, 95% CI 0.271–0.828, P = 0.009) and cervical cancer risk (HR = 0.365, 95% CI 0.136–0.977, P = 0.045). Additionally, low bilirubin levels (< 0.6 mg/dL) were associated with total death (HR = 1.744, 95% CI 1.369–2.222, P < 0.001). Serum bilirubin may have a beneficial effect on the risk of some types of cancers. Nature Publishing Group UK 2021-06-24 /pmc/articles/PMC8225648/ /pubmed/34168201 http://dx.doi.org/10.1038/s41598-021-92442-2 Text en © The Author(s) 2021 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 | Article Inoguchi, Toyoshi Nohara, Yasunobu Nojiri, Chinatsu Nakashima, Naoki Association of serum bilirubin levels with risk of cancer development and total death |
title | Association of serum bilirubin levels with risk of cancer development and total death |
title_full | Association of serum bilirubin levels with risk of cancer development and total death |
title_fullStr | Association of serum bilirubin levels with risk of cancer development and total death |
title_full_unstemmed | Association of serum bilirubin levels with risk of cancer development and total death |
title_short | Association of serum bilirubin levels with risk of cancer development and total death |
title_sort | association of serum bilirubin levels with risk of cancer development and total death |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225648/ https://www.ncbi.nlm.nih.gov/pubmed/34168201 http://dx.doi.org/10.1038/s41598-021-92442-2 |
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