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Prospective Study Using Plasma Apolipoprotein A2-Isoforms to Screen for High-Risk Status of Pancreatic Cancer
SIMPLE SUMMARY: Apolipoprotein A2 isoforms (apoA2-i) have been identified as minimally invasive biomarkers for detecting pancreatic cancer (PC) and high-risk individuals for PC. We investigated the efficiency of an enrichment strategy for high-risk individuals using a combination of blood testing fo...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564617/ https://www.ncbi.nlm.nih.gov/pubmed/32937962 http://dx.doi.org/10.3390/cancers12092625 |
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author | Sato, Yu Kobayashi, Takashi Nishiumi, Shin Okada, Akihiko Fujita, Tsuyoshi Sanuki, Tsuyoshi Kobayashi, Masao Asahara, Masakyo Adachi, Masayasu Sakai, Arata Shiomi, Hideyuki Masuda, Atsuhiro Yoshida, Masaru Takeuchi, Keiko Kodama, Yuzo Kutsumi, Hiromu Nagashima, Kengo Honda, Kazufumi |
author_facet | Sato, Yu Kobayashi, Takashi Nishiumi, Shin Okada, Akihiko Fujita, Tsuyoshi Sanuki, Tsuyoshi Kobayashi, Masao Asahara, Masakyo Adachi, Masayasu Sakai, Arata Shiomi, Hideyuki Masuda, Atsuhiro Yoshida, Masaru Takeuchi, Keiko Kodama, Yuzo Kutsumi, Hiromu Nagashima, Kengo Honda, Kazufumi |
author_sort | Sato, Yu |
collection | PubMed |
description | SIMPLE SUMMARY: Apolipoprotein A2 isoforms (apoA2-i) have been identified as minimally invasive biomarkers for detecting pancreatic cancer (PC) and high-risk individuals for PC. We investigated the efficiency of an enrichment strategy for high-risk individuals using a combination of blood testing for apoA2-i with imaging examinations in the general population. We enrolled 5120 subjects in experimental pancreatic cancer screening, with 84 subjects (1.3%) showing abnormal results for apoA2-i. Pancreatic diseases were recognized in about 30% of subjects with an apoA2-ATQ/AT level of ≤35 μg/mL. Among them, 1 pancreatic cancer and 15 high-risk individuals with intraductal papillary mucinous neoplasm were detected. ApoA2-i has the potential to enrich PC and high-risk status by increasing the diagnostic probability before imaging examinations. ABSTRACT: Apolipoprotein A2-ATQ/AT (apoA2-ATQ/AT) has been identified as a minimally invasive biomarker for detecting pancreatic cancer (PC) and high-risk (HR) individuals for PC. To establish an efficient enrichment strategy for HR, we carried out a plasma apoA2-ATQ/AT level-based prospective screening study among the general population. The subjects for the screening study were recruited at six medical check-up facilities in Japan between October 2015 and January 2017. We evaluated the positive predictive value (PPV) of the plasma apoA2-ATQ/AT level of ≤35 μg/mL for detecting PC and HR. Furthermore, we prospectively confirmed its diagnostic accuracy with another post-diagnosis population in a cross-sectional study. We enrolled 5120 subjects in experimental screening, with 84 subjects (1.3%) showing positive results for apoA2-ATQ/AT. Pancreatic abnormalities were recognized in 26 of the 84 subjects from imaging examinations. Pancreatic abnormalities detected included 1 PC and 15 HR abnormalities, such as cystic lesions including intraductal papillary mucinous neoplasm. The PPV of apoA2-ATQ/AT for detecting PC and HR was 33.3%. Moreover, a combination study with another cross-sectional study revealed that the area under the curve for apoA2-ATQ/AT to distinguish PC from healthy controls was 0.903. ApoA2-ATQ/AT has the potential to enrich PC and HR by increasing the diagnostic probability before imaging examinations. |
format | Online Article Text |
id | pubmed-7564617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75646172020-10-29 Prospective Study Using Plasma Apolipoprotein A2-Isoforms to Screen for High-Risk Status of Pancreatic Cancer Sato, Yu Kobayashi, Takashi Nishiumi, Shin Okada, Akihiko Fujita, Tsuyoshi Sanuki, Tsuyoshi Kobayashi, Masao Asahara, Masakyo Adachi, Masayasu Sakai, Arata Shiomi, Hideyuki Masuda, Atsuhiro Yoshida, Masaru Takeuchi, Keiko Kodama, Yuzo Kutsumi, Hiromu Nagashima, Kengo Honda, Kazufumi Cancers (Basel) Article SIMPLE SUMMARY: Apolipoprotein A2 isoforms (apoA2-i) have been identified as minimally invasive biomarkers for detecting pancreatic cancer (PC) and high-risk individuals for PC. We investigated the efficiency of an enrichment strategy for high-risk individuals using a combination of blood testing for apoA2-i with imaging examinations in the general population. We enrolled 5120 subjects in experimental pancreatic cancer screening, with 84 subjects (1.3%) showing abnormal results for apoA2-i. Pancreatic diseases were recognized in about 30% of subjects with an apoA2-ATQ/AT level of ≤35 μg/mL. Among them, 1 pancreatic cancer and 15 high-risk individuals with intraductal papillary mucinous neoplasm were detected. ApoA2-i has the potential to enrich PC and high-risk status by increasing the diagnostic probability before imaging examinations. ABSTRACT: Apolipoprotein A2-ATQ/AT (apoA2-ATQ/AT) has been identified as a minimally invasive biomarker for detecting pancreatic cancer (PC) and high-risk (HR) individuals for PC. To establish an efficient enrichment strategy for HR, we carried out a plasma apoA2-ATQ/AT level-based prospective screening study among the general population. The subjects for the screening study were recruited at six medical check-up facilities in Japan between October 2015 and January 2017. We evaluated the positive predictive value (PPV) of the plasma apoA2-ATQ/AT level of ≤35 μg/mL for detecting PC and HR. Furthermore, we prospectively confirmed its diagnostic accuracy with another post-diagnosis population in a cross-sectional study. We enrolled 5120 subjects in experimental screening, with 84 subjects (1.3%) showing positive results for apoA2-ATQ/AT. Pancreatic abnormalities were recognized in 26 of the 84 subjects from imaging examinations. Pancreatic abnormalities detected included 1 PC and 15 HR abnormalities, such as cystic lesions including intraductal papillary mucinous neoplasm. The PPV of apoA2-ATQ/AT for detecting PC and HR was 33.3%. Moreover, a combination study with another cross-sectional study revealed that the area under the curve for apoA2-ATQ/AT to distinguish PC from healthy controls was 0.903. ApoA2-ATQ/AT has the potential to enrich PC and HR by increasing the diagnostic probability before imaging examinations. MDPI 2020-09-14 /pmc/articles/PMC7564617/ /pubmed/32937962 http://dx.doi.org/10.3390/cancers12092625 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sato, Yu Kobayashi, Takashi Nishiumi, Shin Okada, Akihiko Fujita, Tsuyoshi Sanuki, Tsuyoshi Kobayashi, Masao Asahara, Masakyo Adachi, Masayasu Sakai, Arata Shiomi, Hideyuki Masuda, Atsuhiro Yoshida, Masaru Takeuchi, Keiko Kodama, Yuzo Kutsumi, Hiromu Nagashima, Kengo Honda, Kazufumi Prospective Study Using Plasma Apolipoprotein A2-Isoforms to Screen for High-Risk Status of Pancreatic Cancer |
title | Prospective Study Using Plasma Apolipoprotein A2-Isoforms to Screen for High-Risk Status of Pancreatic Cancer |
title_full | Prospective Study Using Plasma Apolipoprotein A2-Isoforms to Screen for High-Risk Status of Pancreatic Cancer |
title_fullStr | Prospective Study Using Plasma Apolipoprotein A2-Isoforms to Screen for High-Risk Status of Pancreatic Cancer |
title_full_unstemmed | Prospective Study Using Plasma Apolipoprotein A2-Isoforms to Screen for High-Risk Status of Pancreatic Cancer |
title_short | Prospective Study Using Plasma Apolipoprotein A2-Isoforms to Screen for High-Risk Status of Pancreatic Cancer |
title_sort | prospective study using plasma apolipoprotein a2-isoforms to screen for high-risk status of pancreatic cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564617/ https://www.ncbi.nlm.nih.gov/pubmed/32937962 http://dx.doi.org/10.3390/cancers12092625 |
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