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Association between gallstones and the risk of biliary tract cancer: a systematic review and meta-analysis

OBJECTIVES: Biliary tract cancers (BTCs) are rare but highly fatal. Although the etiology of BTC is poorly understood, gallstones are proposed to be a major risk factor. We conducted a systematic review and meta-analysis to examine the associations between gallstone characteristics and BTC risk. MET...

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Autores principales: Huang, Dan, Joo, Hyundeok, Song, Nan, Cho, Sooyoung, Kim, Woosung, Shin, Aesun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Epidemiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060519/
https://www.ncbi.nlm.nih.gov/pubmed/33541011
http://dx.doi.org/10.4178/epih.e2021011
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author Huang, Dan
Joo, Hyundeok
Song, Nan
Cho, Sooyoung
Kim, Woosung
Shin, Aesun
author_facet Huang, Dan
Joo, Hyundeok
Song, Nan
Cho, Sooyoung
Kim, Woosung
Shin, Aesun
author_sort Huang, Dan
collection PubMed
description OBJECTIVES: Biliary tract cancers (BTCs) are rare but highly fatal. Although the etiology of BTC is poorly understood, gallstones are proposed to be a major risk factor. We conducted a systematic review and meta-analysis to examine the associations between gallstone characteristics and BTC risk. METHODS: We searched the MEDLINE, Embase, and Cochrane Central databases and systematically reviewed cohort and case-control studies published before April 9, 2018. All the included studies reported appropriate risk estimates and confidence intervals (CIs) for associations between the presence, size, number, or duration of gallstones and the risk of BTC, including gallbladder cancer (GBC), extrahepatic bile duct cancer (EBDC), and ampulla of Vater cancer (AOVC). Summary odds ratios (ORs) and their 95% CIs were calculated using a random-effects model in the meta-analysis. Subgroup analyses were conducted to inspect sources of potential heterogeneity, and the Egger test was performed to assess publication bias. RESULTS: Seven cohort studies and 23 case-control studies in Asian, European, and American populations were included. The presence of gallstones was associated with an increased risk of BTC (OR, 4.38; 95% CI, 3.23 to 5.93; I(2)=91.2%), GBC (OR, 7.26; 95% CI, 4.33 to 12.18), EBDC (OR, 3.17; 95% CI, 2.24 to 4.50), and AOVC (OR, 3.28; 95% CI, 1.33 to 8.11). Gallstone size (>1 vs. <1 cm; OR, 1.88; 95% CI, 1.10 to 3.22) was significantly associated with the risk of GBC. CONCLUSIONS: Gallstone characteristics, such as presence, size, and number, are associated with an increased risk of BTC. However, significantly high heterogeneity in the meta-analyses is a limitation of this study.
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spelling pubmed-80605192021-05-04 Association between gallstones and the risk of biliary tract cancer: a systematic review and meta-analysis Huang, Dan Joo, Hyundeok Song, Nan Cho, Sooyoung Kim, Woosung Shin, Aesun Epidemiol Health Systematic Review OBJECTIVES: Biliary tract cancers (BTCs) are rare but highly fatal. Although the etiology of BTC is poorly understood, gallstones are proposed to be a major risk factor. We conducted a systematic review and meta-analysis to examine the associations between gallstone characteristics and BTC risk. METHODS: We searched the MEDLINE, Embase, and Cochrane Central databases and systematically reviewed cohort and case-control studies published before April 9, 2018. All the included studies reported appropriate risk estimates and confidence intervals (CIs) for associations between the presence, size, number, or duration of gallstones and the risk of BTC, including gallbladder cancer (GBC), extrahepatic bile duct cancer (EBDC), and ampulla of Vater cancer (AOVC). Summary odds ratios (ORs) and their 95% CIs were calculated using a random-effects model in the meta-analysis. Subgroup analyses were conducted to inspect sources of potential heterogeneity, and the Egger test was performed to assess publication bias. RESULTS: Seven cohort studies and 23 case-control studies in Asian, European, and American populations were included. The presence of gallstones was associated with an increased risk of BTC (OR, 4.38; 95% CI, 3.23 to 5.93; I(2)=91.2%), GBC (OR, 7.26; 95% CI, 4.33 to 12.18), EBDC (OR, 3.17; 95% CI, 2.24 to 4.50), and AOVC (OR, 3.28; 95% CI, 1.33 to 8.11). Gallstone size (>1 vs. <1 cm; OR, 1.88; 95% CI, 1.10 to 3.22) was significantly associated with the risk of GBC. CONCLUSIONS: Gallstone characteristics, such as presence, size, and number, are associated with an increased risk of BTC. However, significantly high heterogeneity in the meta-analyses is a limitation of this study. Korean Society of Epidemiology 2021-02-03 /pmc/articles/PMC8060519/ /pubmed/33541011 http://dx.doi.org/10.4178/epih.e2021011 Text en ©2021, Korean Society of Epidemiology https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 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 the original work is properly cited.
spellingShingle Systematic Review
Huang, Dan
Joo, Hyundeok
Song, Nan
Cho, Sooyoung
Kim, Woosung
Shin, Aesun
Association between gallstones and the risk of biliary tract cancer: a systematic review and meta-analysis
title Association between gallstones and the risk of biliary tract cancer: a systematic review and meta-analysis
title_full Association between gallstones and the risk of biliary tract cancer: a systematic review and meta-analysis
title_fullStr Association between gallstones and the risk of biliary tract cancer: a systematic review and meta-analysis
title_full_unstemmed Association between gallstones and the risk of biliary tract cancer: a systematic review and meta-analysis
title_short Association between gallstones and the risk of biliary tract cancer: a systematic review and meta-analysis
title_sort association between gallstones and the risk of biliary tract cancer: a systematic review and meta-analysis
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060519/
https://www.ncbi.nlm.nih.gov/pubmed/33541011
http://dx.doi.org/10.4178/epih.e2021011
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