Impact of antibiotic exposure on the risk of colorectal cancer
Purpose Gut microbiota has been postulated to serve as a significant promoter of CRC formation, and colonic dysbiosis was previously reported in CRC tissue. Our aim was to evaluate the association between the type and cumulative duration of antibiotic exposure and CRC risk. Methods We conducted a ne...
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| Published in | Pharmacoepidemiology and drug safety Vol. 24; no. 5; pp. 534 - 542 |
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| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
England
Blackwell Publishing Ltd
01.05.2015
Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1053-8569 1099-1557 1099-1557 |
| DOI | 10.1002/pds.3765 |
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| Summary: | Purpose
Gut microbiota has been postulated to serve as a significant promoter of CRC formation, and colonic dysbiosis was previously reported in CRC tissue. Our aim was to evaluate the association between the type and cumulative duration of antibiotic exposure and CRC risk.
Methods
We conducted a nested case–control study using a large population‐based database from the UK. Cases were defined as those with any medical code of CRC. Subjects with known familial CRC syndromes or IBD were excluded from the study. For every case, four eligible controls matched on age, sex, practice site, and duration of follow‐up before index date were selected using incidence‐density sampling. Exposure of interest was antibiotic therapy before index date. Adjusted ORs and 95%CIs were estimated using conditional logistic regression analysis.
Results
A total of 20 990 cases and 82 054 controls were identified. The adjusted OR for CRC among subjects first exposed to penicillins >10 years prior to index date was 1.11 (95%CI 1.02–1.20). The risk increased significantly with the number of penicillin exposures up to 1.20 (95%CI 1.11–1.31) for >10 courses. The risk also increased with the average number of penicillin treatments per‐year (exposure intensity) with an OR of 1.04 (95%CI 1.01–1.08) per one additional treatment per year. Exposure to anti‐viral or anti‐fungal therapy was not associated with CRC risk.
Conclusions
Past exposure to multiple courses of penicillins is related to a modest elevation in CRC risk. Copyright © 2015 John Wiley & Sons, Ltd. |
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| Bibliography: | Supporting info item ark:/67375/WNG-N0JHGMPL-F National Center for Research Resources and the National Center for Advancing Translational Sciences, National Institutes of Health - No. UL1TR000003 ArticleID:PDS3765 istex:F94A20D89E519EA08AC469473869161524060957 This work was performed in partial fulfilment of the requirements for a Ph.D. degree of Ben Boursi, Sackler Faculty of Medicine, Tel‐Aviv University, Israel. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
| ISSN: | 1053-8569 1099-1557 1099-1557 |
| DOI: | 10.1002/pds.3765 |