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Positive Predictive Value for Multitarget Stool DNA After Bariatric and Metabolic Surgery
BACKGROUND AND AIMS: Bariatric and metabolic surgery (BMS) may adversely affect noninvasive stool tests for colorectal cancer (CRC) screening through several mechanisms. Multitarget stool DNA (mt-sDNA) is approved for CRC screening; however, performance in post-BMS patients is unknown. As the rates...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10597571/ https://www.ncbi.nlm.nih.gov/pubmed/37876832 http://dx.doi.org/10.1016/j.gastha.2023.06.005 |
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author | Ebner, Derek W. Burger, Kelli N. Broderick, Brendan Mahoney, Douglas W. Kellogg, Todd A. Acosta, Andres Kisiel, John B. |
author_facet | Ebner, Derek W. Burger, Kelli N. Broderick, Brendan Mahoney, Douglas W. Kellogg, Todd A. Acosta, Andres Kisiel, John B. |
author_sort | Ebner, Derek W. |
collection | PubMed |
description | BACKGROUND AND AIMS: Bariatric and metabolic surgery (BMS) may adversely affect noninvasive stool tests for colorectal cancer (CRC) screening through several mechanisms. Multitarget stool DNA (mt-sDNA) is approved for CRC screening; however, performance in post-BMS patients is unknown. As the rates of BMS are anticipated to increase with rising incidence of obesity, it is important to evaluate mt-sDNA test performance among these patients. METHODS: In a multisite academic and community-based practice, we obtained mt-sDNA results from 10/2014 to 12/2019 through electronic records and an institutional BMS registry. Average CRC risk patients with BMS prior to a positive mt-sDNA underwent a detailed chart review. Follow-up colonoscopy findings were compared to those among BMS patients screened with colonoscopy alone and a historical cohort of patients without BMS, screened by mt-sDNA. The primary study endpoint was the positive predictive value (PPV) for advanced colorectal neoplasia. RESULTS: Among 336 average-risk patients who had mt-sDNA after BMS, mt-sDNA was positive in 49 (14.6%), 47/49 (96%) underwent follow-up colonoscopy, and the PPV for advanced neoplasia was 12/47 (25.5%). This is similar to the PPV for advanced colorectal neoplasia (425/1542, 28%) in a historical cohort of persons without prior BMS, screened by mt-sDNA at our center (P = .86). Among those who had prior BMS, the rate of advanced neoplasia was higher after mt-sDNA compared to screening colonoscopy alone. CONCLUSION: Despite anatomic and physiologic mechanisms that could alter blood or DNA content in stool, BMS does not appear to adversely affect the PPV of mt-sDNA. |
format | Online Article Text |
id | pubmed-10597571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-105975712023-10-24 Positive Predictive Value for Multitarget Stool DNA After Bariatric and Metabolic Surgery Ebner, Derek W. Burger, Kelli N. Broderick, Brendan Mahoney, Douglas W. Kellogg, Todd A. Acosta, Andres Kisiel, John B. Gastro Hep Adv Article BACKGROUND AND AIMS: Bariatric and metabolic surgery (BMS) may adversely affect noninvasive stool tests for colorectal cancer (CRC) screening through several mechanisms. Multitarget stool DNA (mt-sDNA) is approved for CRC screening; however, performance in post-BMS patients is unknown. As the rates of BMS are anticipated to increase with rising incidence of obesity, it is important to evaluate mt-sDNA test performance among these patients. METHODS: In a multisite academic and community-based practice, we obtained mt-sDNA results from 10/2014 to 12/2019 through electronic records and an institutional BMS registry. Average CRC risk patients with BMS prior to a positive mt-sDNA underwent a detailed chart review. Follow-up colonoscopy findings were compared to those among BMS patients screened with colonoscopy alone and a historical cohort of patients without BMS, screened by mt-sDNA. The primary study endpoint was the positive predictive value (PPV) for advanced colorectal neoplasia. RESULTS: Among 336 average-risk patients who had mt-sDNA after BMS, mt-sDNA was positive in 49 (14.6%), 47/49 (96%) underwent follow-up colonoscopy, and the PPV for advanced neoplasia was 12/47 (25.5%). This is similar to the PPV for advanced colorectal neoplasia (425/1542, 28%) in a historical cohort of persons without prior BMS, screened by mt-sDNA at our center (P = .86). Among those who had prior BMS, the rate of advanced neoplasia was higher after mt-sDNA compared to screening colonoscopy alone. CONCLUSION: Despite anatomic and physiologic mechanisms that could alter blood or DNA content in stool, BMS does not appear to adversely affect the PPV of mt-sDNA. 2023 2023-07-01 /pmc/articles/PMC10597571/ /pubmed/37876832 http://dx.doi.org/10.1016/j.gastha.2023.06.005 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Ebner, Derek W. Burger, Kelli N. Broderick, Brendan Mahoney, Douglas W. Kellogg, Todd A. Acosta, Andres Kisiel, John B. Positive Predictive Value for Multitarget Stool DNA After Bariatric and Metabolic Surgery |
title | Positive Predictive Value for Multitarget Stool DNA After Bariatric and Metabolic Surgery |
title_full | Positive Predictive Value for Multitarget Stool DNA After Bariatric and Metabolic Surgery |
title_fullStr | Positive Predictive Value for Multitarget Stool DNA After Bariatric and Metabolic Surgery |
title_full_unstemmed | Positive Predictive Value for Multitarget Stool DNA After Bariatric and Metabolic Surgery |
title_short | Positive Predictive Value for Multitarget Stool DNA After Bariatric and Metabolic Surgery |
title_sort | positive predictive value for multitarget stool dna after bariatric and metabolic surgery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10597571/ https://www.ncbi.nlm.nih.gov/pubmed/37876832 http://dx.doi.org/10.1016/j.gastha.2023.06.005 |
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