Cargando…
A novel faecal Lachnoclostridium marker for the non-invasive diagnosis of colorectal adenoma and cancer
OBJECTIVE: There is a need for early detection of colorectal cancer (CRC) at precancerous-stage adenoma. Here, we identified novel faecal bacterial markers for diagnosing adenoma. DESIGN: This study included 1012 subjects (274 CRC, 353 adenoma and 385 controls) from two independent Asian groups. Can...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306980/ https://www.ncbi.nlm.nih.gov/pubmed/31776231 http://dx.doi.org/10.1136/gutjnl-2019-318532 |
_version_ | 1783548754244141056 |
---|---|
author | Liang, Jessie Qiaoyi Li, Tong Nakatsu, Geicho Chen, Ying-Xuan Yau, Tung On Chu, Eagle Wong, Sunny Szeto, Chun Ho Ng, Siew C Chan, Francis K L Fang, Jing-Yuan Sung, Joseph J Y Yu, Jun |
author_facet | Liang, Jessie Qiaoyi Li, Tong Nakatsu, Geicho Chen, Ying-Xuan Yau, Tung On Chu, Eagle Wong, Sunny Szeto, Chun Ho Ng, Siew C Chan, Francis K L Fang, Jing-Yuan Sung, Joseph J Y Yu, Jun |
author_sort | Liang, Jessie Qiaoyi |
collection | PubMed |
description | OBJECTIVE: There is a need for early detection of colorectal cancer (CRC) at precancerous-stage adenoma. Here, we identified novel faecal bacterial markers for diagnosing adenoma. DESIGN: This study included 1012 subjects (274 CRC, 353 adenoma and 385 controls) from two independent Asian groups. Candidate markers were identified by metagenomics and validated by targeted quantitative PCR. RESULTS: Metagenomic analysis identified ‘m3’ from a Lachnoclostridium sp., Fusobacterium nucleatum (Fn) and Clostridium hathewayi (Ch) to be significantly enriched in adenoma. Faecal m3 and Fn were significantly increased from normal to adenoma to CRC (p<0.0001, linear trend by one-way ANOVA) in group I (n=698), which was further confirmed in group II (n=313; p<0.0001). Faecal m3 may perform better than Fn in distinguishing adenoma from controls (areas under the receiver operating characteristic curve (AUROCs) m3=0.675 vs Fn=0.620, p=0.09), while Fn performed better in diagnosing CRC (AUROCs Fn=0.862 vs m3=0.741, p<0.0001). At 78.5% specificity, m3 and Fn showed sensitivities of 48.3% and 33.8% for adenoma, and 62.1% and 77.8% for CRC, respectively. In a subgroup tested with faecal immunochemical test (FIT; n=642), m3 performed better than FIT in detecting adenoma (sensitivities for non-advanced and advanced adenomas of 44.2% and 50.8% by m3 (specificity=79.6%) vs 0% and 16.1% by FIT (specificity=98.5%)). Combining with FIT improved sensitivity of m3 for advanced adenoma to 56.8%. The combination of m3 with Fn, Ch, Bacteroides clarus and FIT performed best for diagnosing CRC (specificity=81.2% and sensitivity=93.8%). CONCLUSION: This study identifies a novel bacterial marker m3 for the non-invasive diagnosis of colorectal adenoma. |
format | Online Article Text |
id | pubmed-7306980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-73069802020-06-23 A novel faecal Lachnoclostridium marker for the non-invasive diagnosis of colorectal adenoma and cancer Liang, Jessie Qiaoyi Li, Tong Nakatsu, Geicho Chen, Ying-Xuan Yau, Tung On Chu, Eagle Wong, Sunny Szeto, Chun Ho Ng, Siew C Chan, Francis K L Fang, Jing-Yuan Sung, Joseph J Y Yu, Jun Gut Gut Microbiota OBJECTIVE: There is a need for early detection of colorectal cancer (CRC) at precancerous-stage adenoma. Here, we identified novel faecal bacterial markers for diagnosing adenoma. DESIGN: This study included 1012 subjects (274 CRC, 353 adenoma and 385 controls) from two independent Asian groups. Candidate markers were identified by metagenomics and validated by targeted quantitative PCR. RESULTS: Metagenomic analysis identified ‘m3’ from a Lachnoclostridium sp., Fusobacterium nucleatum (Fn) and Clostridium hathewayi (Ch) to be significantly enriched in adenoma. Faecal m3 and Fn were significantly increased from normal to adenoma to CRC (p<0.0001, linear trend by one-way ANOVA) in group I (n=698), which was further confirmed in group II (n=313; p<0.0001). Faecal m3 may perform better than Fn in distinguishing adenoma from controls (areas under the receiver operating characteristic curve (AUROCs) m3=0.675 vs Fn=0.620, p=0.09), while Fn performed better in diagnosing CRC (AUROCs Fn=0.862 vs m3=0.741, p<0.0001). At 78.5% specificity, m3 and Fn showed sensitivities of 48.3% and 33.8% for adenoma, and 62.1% and 77.8% for CRC, respectively. In a subgroup tested with faecal immunochemical test (FIT; n=642), m3 performed better than FIT in detecting adenoma (sensitivities for non-advanced and advanced adenomas of 44.2% and 50.8% by m3 (specificity=79.6%) vs 0% and 16.1% by FIT (specificity=98.5%)). Combining with FIT improved sensitivity of m3 for advanced adenoma to 56.8%. The combination of m3 with Fn, Ch, Bacteroides clarus and FIT performed best for diagnosing CRC (specificity=81.2% and sensitivity=93.8%). CONCLUSION: This study identifies a novel bacterial marker m3 for the non-invasive diagnosis of colorectal adenoma. BMJ Publishing Group 2020-07 2019-11-27 /pmc/articles/PMC7306980/ /pubmed/31776231 http://dx.doi.org/10.1136/gutjnl-2019-318532 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Gut Microbiota Liang, Jessie Qiaoyi Li, Tong Nakatsu, Geicho Chen, Ying-Xuan Yau, Tung On Chu, Eagle Wong, Sunny Szeto, Chun Ho Ng, Siew C Chan, Francis K L Fang, Jing-Yuan Sung, Joseph J Y Yu, Jun A novel faecal Lachnoclostridium marker for the non-invasive diagnosis of colorectal adenoma and cancer |
title | A novel faecal Lachnoclostridium marker for the non-invasive diagnosis of colorectal adenoma and cancer |
title_full | A novel faecal Lachnoclostridium marker for the non-invasive diagnosis of colorectal adenoma and cancer |
title_fullStr | A novel faecal Lachnoclostridium marker for the non-invasive diagnosis of colorectal adenoma and cancer |
title_full_unstemmed | A novel faecal Lachnoclostridium marker for the non-invasive diagnosis of colorectal adenoma and cancer |
title_short | A novel faecal Lachnoclostridium marker for the non-invasive diagnosis of colorectal adenoma and cancer |
title_sort | novel faecal lachnoclostridium marker for the non-invasive diagnosis of colorectal adenoma and cancer |
topic | Gut Microbiota |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306980/ https://www.ncbi.nlm.nih.gov/pubmed/31776231 http://dx.doi.org/10.1136/gutjnl-2019-318532 |
work_keys_str_mv | AT liangjessieqiaoyi anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT litong anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT nakatsugeicho anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT chenyingxuan anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT yautungon anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT chueagle anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT wongsunny anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT szetochunho anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT ngsiewc anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT chanfranciskl anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT fangjingyuan anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT sungjosephjy anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT yujun anovelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT liangjessieqiaoyi novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT litong novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT nakatsugeicho novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT chenyingxuan novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT yautungon novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT chueagle novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT wongsunny novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT szetochunho novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT ngsiewc novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT chanfranciskl novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT fangjingyuan novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT sungjosephjy novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer AT yujun novelfaecallachnoclostridiummarkerforthenoninvasivediagnosisofcolorectaladenomaandcancer |