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Exploratory Analysis of Plasma Neurotensin as a Novel Biomarker for Early Detection of Colorectal Polyp and Cancer

Earlier detection of colorectal cancer (CRC) results in improved survival. Existing non-invasive biomarkers have suboptimal accuracy. Neurotensin (NTS) is involved in CRC carcinogenesis. This study evaluated the diagnostic potential of plasma NTS for colorectal polyps and cancers. Participants were...

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Autores principales: Qiu, Shengyang, Nikolaou, Stella, Fiorentino, Francesca, Rasheed, Shahnawaz, Darzi, Ara, Cunningham, David, Tekkis, Paris, Kontovounisios, Christos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10355703/
https://www.ncbi.nlm.nih.gov/pubmed/31093954
http://dx.doi.org/10.1007/s12672-019-00364-3
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author Qiu, Shengyang
Nikolaou, Stella
Fiorentino, Francesca
Rasheed, Shahnawaz
Darzi, Ara
Cunningham, David
Tekkis, Paris
Kontovounisios, Christos
author_facet Qiu, Shengyang
Nikolaou, Stella
Fiorentino, Francesca
Rasheed, Shahnawaz
Darzi, Ara
Cunningham, David
Tekkis, Paris
Kontovounisios, Christos
author_sort Qiu, Shengyang
collection PubMed
description Earlier detection of colorectal cancer (CRC) results in improved survival. Existing non-invasive biomarkers have suboptimal accuracy. Neurotensin (NTS) is involved in CRC carcinogenesis. This study evaluated the diagnostic potential of plasma NTS for colorectal polyps and cancers. Participants were selected based on national CRC referral guidelines. All subjects underwent colonoscopy. Average plasma concentrations were compared across different diagnostic groups. Predictors for detecting colorectal neoplasia were identified. Receiver operator characteristic (ROC) curve analysis assessed the diagnostic accuracy of NTS. An independent biobank was used as validation group. Of 165 participants, 46 had polyps or CRC. Significantly higher plasma NTS was found in the colonic neoplasia group (603.6 pg/ml vs. 407.2 pg/ml, p < 0.01). Risk factors for colonic polyps or cancers included Log(e) (plasma NTS concentration) (OR, 2.73; 95% CI, 1.33–5.59, p < 0.01), log(e) (Age) (OR, 15.49; 95% CI, 2.67–89.66, p < 0.01) and cigarette smoking (OR, 3.49; 95% CI, 1.31–9.26, p = 0.01). Plasma NTS had an optimal sensitivity of 60.4% and specificity of 71.6% for the diagnosis of colorectal polyps and cancers. Similar diagnostic accuracy was obtained in the validation group. Plasma NTS has the potential to be a non-invasive biomarker for colorectal neoplasia. It appears to be more accurate than existing blood markers and is unique in being able to detect precancerous polyps.
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spelling pubmed-103557032023-07-21 Exploratory Analysis of Plasma Neurotensin as a Novel Biomarker for Early Detection of Colorectal Polyp and Cancer Qiu, Shengyang Nikolaou, Stella Fiorentino, Francesca Rasheed, Shahnawaz Darzi, Ara Cunningham, David Tekkis, Paris Kontovounisios, Christos Horm Cancer Original Paper Earlier detection of colorectal cancer (CRC) results in improved survival. Existing non-invasive biomarkers have suboptimal accuracy. Neurotensin (NTS) is involved in CRC carcinogenesis. This study evaluated the diagnostic potential of plasma NTS for colorectal polyps and cancers. Participants were selected based on national CRC referral guidelines. All subjects underwent colonoscopy. Average plasma concentrations were compared across different diagnostic groups. Predictors for detecting colorectal neoplasia were identified. Receiver operator characteristic (ROC) curve analysis assessed the diagnostic accuracy of NTS. An independent biobank was used as validation group. Of 165 participants, 46 had polyps or CRC. Significantly higher plasma NTS was found in the colonic neoplasia group (603.6 pg/ml vs. 407.2 pg/ml, p < 0.01). Risk factors for colonic polyps or cancers included Log(e) (plasma NTS concentration) (OR, 2.73; 95% CI, 1.33–5.59, p < 0.01), log(e) (Age) (OR, 15.49; 95% CI, 2.67–89.66, p < 0.01) and cigarette smoking (OR, 3.49; 95% CI, 1.31–9.26, p = 0.01). Plasma NTS had an optimal sensitivity of 60.4% and specificity of 71.6% for the diagnosis of colorectal polyps and cancers. Similar diagnostic accuracy was obtained in the validation group. Plasma NTS has the potential to be a non-invasive biomarker for colorectal neoplasia. It appears to be more accurate than existing blood markers and is unique in being able to detect precancerous polyps. Springer US 2019-05-15 /pmc/articles/PMC10355703/ /pubmed/31093954 http://dx.doi.org/10.1007/s12672-019-00364-3 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by/4.0/Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Paper
Qiu, Shengyang
Nikolaou, Stella
Fiorentino, Francesca
Rasheed, Shahnawaz
Darzi, Ara
Cunningham, David
Tekkis, Paris
Kontovounisios, Christos
Exploratory Analysis of Plasma Neurotensin as a Novel Biomarker for Early Detection of Colorectal Polyp and Cancer
title Exploratory Analysis of Plasma Neurotensin as a Novel Biomarker for Early Detection of Colorectal Polyp and Cancer
title_full Exploratory Analysis of Plasma Neurotensin as a Novel Biomarker for Early Detection of Colorectal Polyp and Cancer
title_fullStr Exploratory Analysis of Plasma Neurotensin as a Novel Biomarker for Early Detection of Colorectal Polyp and Cancer
title_full_unstemmed Exploratory Analysis of Plasma Neurotensin as a Novel Biomarker for Early Detection of Colorectal Polyp and Cancer
title_short Exploratory Analysis of Plasma Neurotensin as a Novel Biomarker for Early Detection of Colorectal Polyp and Cancer
title_sort exploratory analysis of plasma neurotensin as a novel biomarker for early detection of colorectal polyp and cancer
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10355703/
https://www.ncbi.nlm.nih.gov/pubmed/31093954
http://dx.doi.org/10.1007/s12672-019-00364-3
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