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Antibiotic use and risk of colorectal cancer: a systematic review and dose-response meta-analysis.
Simin, Johanna; Fornes, Romina; Liu, Qing; Olsen, Renate Slind; Callens, Steven; Engstrand, Lars; Brusselaers, Nele.
Affiliation
  • Simin J; Centre for Translational Microbiome Research (CTMR), Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Biomedicum kvarter 8A. Solnavägen 9, SE-171 65, Stockholm, Sweden. Johanna.simin@ki.se.
  • Fornes R; Science for Life Laboratory (SciLifeLab), SE-171 21, Stockholm, Sweden. Johanna.simin@ki.se.
  • Liu Q; Centre for Translational Microbiome Research (CTMR), Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Biomedicum kvarter 8A. Solnavägen 9, SE-171 65, Stockholm, Sweden.
  • Olsen RS; Science for Life Laboratory (SciLifeLab), SE-171 21, Stockholm, Sweden.
  • Callens S; Centre for Translational Microbiome Research (CTMR), Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Biomedicum kvarter 8A. Solnavägen 9, SE-171 65, Stockholm, Sweden.
  • Engstrand L; Science for Life Laboratory (SciLifeLab), SE-171 21, Stockholm, Sweden.
  • Brusselaers N; Centre for Translational Microbiome Research (CTMR), Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Biomedicum kvarter 8A. Solnavägen 9, SE-171 65, Stockholm, Sweden.
Br J Cancer ; 123(12): 1825-1832, 2020 12.
Article in En | MEDLINE | ID: mdl-32968205
ABSTRACT

BACKGROUND:

It is understudied whether the posed association of oral antibiotics with colorectal cancer (CRC) varies between antibiotic spectrums, colorectal continuum, and if a non-linear dose-dependent relationship is present.

DESIGN:

Three electronic databases and a trial platform were searched for all relevant studies, from inception until February 2020, without restrictions. Random-effects meta-analyses provided pooled effect-sizes (ES) with 95% confidence intervals (CI). Dose-response analyses modelling the relationship between number of days exposed to antibiotics and CRC risk were extended to non-linear multivariable random-effects models.

RESULTS:

Of 6483 identified publications ten were eligible, including 4.1 million individuals and over 73,550 CRC cases. The pooled CRC risk was increased among individuals who ever-used antibiotics (ES = 1.17, 95%CI 1.05-1.30), particularly for broad-spectrum antibiotics (ES = 1.70, 95%CI 1.26-2.30), but not for narrow-spectrum antibiotic (ES = 1.11, 95% 0.93-1.32). The dose-response analysis did not provide strong evidence of any particular dose-response association, and the risk patterns were rather similar for colon and rectal cancer.

DISCUSSION:

The antibiotic use associated CRC risk seemingly differs between broad- and narrow-spectrum antibiotics, and possibly within the colorectal continuum. It remains unclear whether this association is causal, requiring more mechanistic studies and further clarification of drug-microbiome interactions.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Rectal Neoplasms / Colonic Neoplasms / Anti-Bacterial Agents Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Main subject: Rectal Neoplasms / Colonic Neoplasms / Anti-Bacterial Agents Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Year: 2020 Type: Article