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Melanosis coli: A factor not associated with histological progression of colorectal polyps

OBJECTIVE: In this study we aimed to investigate the association of melanosis coli (MC) and the colorectal polyp detection rate (PDR). METHODS: In all, 1104 MC patients and 62 181 non‐MC participants were enrolled. And 2208 controls were matched by participants' age and gender, and quality of b...

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Autores principales: Zhang, Yan, Zhan, Ting Ting, Dong, Zhi Yu, Sun, Hui Hui, Wang, Jun Wen, Chen, Ying, Xu, Shu Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541455/
https://www.ncbi.nlm.nih.gov/pubmed/35661415
http://dx.doi.org/10.1111/1751-2980.13100
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author Zhang, Yan
Zhan, Ting Ting
Dong, Zhi Yu
Sun, Hui Hui
Wang, Jun Wen
Chen, Ying
Xu, Shu Chang
author_facet Zhang, Yan
Zhan, Ting Ting
Dong, Zhi Yu
Sun, Hui Hui
Wang, Jun Wen
Chen, Ying
Xu, Shu Chang
author_sort Zhang, Yan
collection PubMed
description OBJECTIVE: In this study we aimed to investigate the association of melanosis coli (MC) and the colorectal polyp detection rate (PDR). METHODS: In all, 1104 MC patients and 62 181 non‐MC participants were enrolled. And 2208 controls were matched by participants' age and gender, and quality of bowel preparation using the propensity score matching (PSM) method. Additionally, 490 polyps in MC and 980 in controls matched by age and gender, and size and location of polyps were analyzed. The association of PDR and pathological features of polyps with MC were also analyzed. RESULTS: MC patients showed a higher PDR (44.3% vs 39.3%, P = 0.006) and detection rate of low‐grade adenoma (45.4% vs 36.7%, P = 0.002) but fewer large polyps (≥10 mm) (18.8% vs 26.9%, P = 0.001), fewer polyps in the left colon (33.5% vs 40.0%, P = 0.018), and a lower detection rate of advanced adenoma/adenocarcinoma (17.4% vs 24.3%, P = 0.003) than the matched controls. On multivariate logistic regression analysis, MC was independently associated with an increased PDR (odds ratio 1.184, 95% confidence interval 1.045–1.343, P = 0.008). Analysis targeting polyps showed that there were significant differences in age, gender, location, and pathology (P < 0.001) between polyps with and without MC. However, after adjusting for participants' age and gender, size and location of polyps, there was no difference between the two groups in pathology (P = 0.635). CONCLUSION: MC is independently associated with increased colorectal PDR, but not with histological progression of polyps.
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spelling pubmed-95414552022-10-14 Melanosis coli: A factor not associated with histological progression of colorectal polyps Zhang, Yan Zhan, Ting Ting Dong, Zhi Yu Sun, Hui Hui Wang, Jun Wen Chen, Ying Xu, Shu Chang J Dig Dis ORIGINAL ARTICLES OBJECTIVE: In this study we aimed to investigate the association of melanosis coli (MC) and the colorectal polyp detection rate (PDR). METHODS: In all, 1104 MC patients and 62 181 non‐MC participants were enrolled. And 2208 controls were matched by participants' age and gender, and quality of bowel preparation using the propensity score matching (PSM) method. Additionally, 490 polyps in MC and 980 in controls matched by age and gender, and size and location of polyps were analyzed. The association of PDR and pathological features of polyps with MC were also analyzed. RESULTS: MC patients showed a higher PDR (44.3% vs 39.3%, P = 0.006) and detection rate of low‐grade adenoma (45.4% vs 36.7%, P = 0.002) but fewer large polyps (≥10 mm) (18.8% vs 26.9%, P = 0.001), fewer polyps in the left colon (33.5% vs 40.0%, P = 0.018), and a lower detection rate of advanced adenoma/adenocarcinoma (17.4% vs 24.3%, P = 0.003) than the matched controls. On multivariate logistic regression analysis, MC was independently associated with an increased PDR (odds ratio 1.184, 95% confidence interval 1.045–1.343, P = 0.008). Analysis targeting polyps showed that there were significant differences in age, gender, location, and pathology (P < 0.001) between polyps with and without MC. However, after adjusting for participants' age and gender, size and location of polyps, there was no difference between the two groups in pathology (P = 0.635). CONCLUSION: MC is independently associated with increased colorectal PDR, but not with histological progression of polyps. Wiley Publishing Asia Pty Ltd 2022-06-29 2022 /pmc/articles/PMC9541455/ /pubmed/35661415 http://dx.doi.org/10.1111/1751-2980.13100 Text en © 2022 The Authors. Journal of Digestive Diseases published by Chinese Medical Association Shanghai Branch, Chinese Society of Gastroenterology, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle ORIGINAL ARTICLES
Zhang, Yan
Zhan, Ting Ting
Dong, Zhi Yu
Sun, Hui Hui
Wang, Jun Wen
Chen, Ying
Xu, Shu Chang
Melanosis coli: A factor not associated with histological progression of colorectal polyps
title Melanosis coli: A factor not associated with histological progression of colorectal polyps
title_full Melanosis coli: A factor not associated with histological progression of colorectal polyps
title_fullStr Melanosis coli: A factor not associated with histological progression of colorectal polyps
title_full_unstemmed Melanosis coli: A factor not associated with histological progression of colorectal polyps
title_short Melanosis coli: A factor not associated with histological progression of colorectal polyps
title_sort melanosis coli: a factor not associated with histological progression of colorectal polyps
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541455/
https://www.ncbi.nlm.nih.gov/pubmed/35661415
http://dx.doi.org/10.1111/1751-2980.13100
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