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A novel scoring system to analyze combined effect of lifestyle factors on pancreatic cancer risk: a retrospective case-control study

Although several risk factors for the onset of pancreatic ductal adenocarcinoma (PDAC) have been identified, currently, no scoring system to systemically evaluate the risk of PDAC has been established. In this study, we aimed to use a population of over 1200 patients to build a novel scoring system,...

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Autores principales: Pang, Tianshu, Ding, Guoping, Wu, Zhengrong, Jiang, Guixing, Yang, Yifei, Zhang, Xiaofei, Cao, Liping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651911/
https://www.ncbi.nlm.nih.gov/pubmed/29057932
http://dx.doi.org/10.1038/s41598-017-13182-w
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author Pang, Tianshu
Ding, Guoping
Wu, Zhengrong
Jiang, Guixing
Yang, Yifei
Zhang, Xiaofei
Cao, Liping
author_facet Pang, Tianshu
Ding, Guoping
Wu, Zhengrong
Jiang, Guixing
Yang, Yifei
Zhang, Xiaofei
Cao, Liping
author_sort Pang, Tianshu
collection PubMed
description Although several risk factors for the onset of pancreatic ductal adenocarcinoma (PDAC) have been identified, currently, no scoring system to systemically evaluate the risk of PDAC has been established. In this study, we aimed to use a population of over 1200 patients to build a novel scoring system, and evaluated combined effects of risk factors for PDAC patients.A set of 4904 participants including 1274 PDAC patients and 3630 non-cancer individuals were recruited for the single-center study over 17-year period (1997~2013). Systematic logical analysis were presented for case and control groups, and a risk rating system was constructed to assess combined risk factors. Seven independent risk factors were identified with the increased risk of PDAC, were selected into the risk score. A merged risk assessment model was established, demonstrating significantly increased PDAC risk in following a number of rising scores. Individuals with scores from 1 to more than 4, the responding OR (95% CI) were 3.06 (2.57~3.65), 7.08 (5.63~8.91), 22.4 (14.2~35.4), and 31.4 (12.7~77.5), respectively. The integer-based risk score in the study can be used for risk stratification to accurately evaluate PDAC occurrence at an early stage. This scoring system provides an accurate risk assessment of PDAC risk.
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spelling pubmed-56519112017-10-26 A novel scoring system to analyze combined effect of lifestyle factors on pancreatic cancer risk: a retrospective case-control study Pang, Tianshu Ding, Guoping Wu, Zhengrong Jiang, Guixing Yang, Yifei Zhang, Xiaofei Cao, Liping Sci Rep Article Although several risk factors for the onset of pancreatic ductal adenocarcinoma (PDAC) have been identified, currently, no scoring system to systemically evaluate the risk of PDAC has been established. In this study, we aimed to use a population of over 1200 patients to build a novel scoring system, and evaluated combined effects of risk factors for PDAC patients.A set of 4904 participants including 1274 PDAC patients and 3630 non-cancer individuals were recruited for the single-center study over 17-year period (1997~2013). Systematic logical analysis were presented for case and control groups, and a risk rating system was constructed to assess combined risk factors. Seven independent risk factors were identified with the increased risk of PDAC, were selected into the risk score. A merged risk assessment model was established, demonstrating significantly increased PDAC risk in following a number of rising scores. Individuals with scores from 1 to more than 4, the responding OR (95% CI) were 3.06 (2.57~3.65), 7.08 (5.63~8.91), 22.4 (14.2~35.4), and 31.4 (12.7~77.5), respectively. The integer-based risk score in the study can be used for risk stratification to accurately evaluate PDAC occurrence at an early stage. This scoring system provides an accurate risk assessment of PDAC risk. Nature Publishing Group UK 2017-10-20 /pmc/articles/PMC5651911/ /pubmed/29057932 http://dx.doi.org/10.1038/s41598-017-13182-w Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pang, Tianshu
Ding, Guoping
Wu, Zhengrong
Jiang, Guixing
Yang, Yifei
Zhang, Xiaofei
Cao, Liping
A novel scoring system to analyze combined effect of lifestyle factors on pancreatic cancer risk: a retrospective case-control study
title A novel scoring system to analyze combined effect of lifestyle factors on pancreatic cancer risk: a retrospective case-control study
title_full A novel scoring system to analyze combined effect of lifestyle factors on pancreatic cancer risk: a retrospective case-control study
title_fullStr A novel scoring system to analyze combined effect of lifestyle factors on pancreatic cancer risk: a retrospective case-control study
title_full_unstemmed A novel scoring system to analyze combined effect of lifestyle factors on pancreatic cancer risk: a retrospective case-control study
title_short A novel scoring system to analyze combined effect of lifestyle factors on pancreatic cancer risk: a retrospective case-control study
title_sort novel scoring system to analyze combined effect of lifestyle factors on pancreatic cancer risk: a retrospective case-control study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651911/
https://www.ncbi.nlm.nih.gov/pubmed/29057932
http://dx.doi.org/10.1038/s41598-017-13182-w
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