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抗生素暴露对结直肠癌风险的影响。

Impact of antibiotic exposure on the risk of colorectal cancer.

作者信息

Boursi Ben, Haynes Kevin, Mamtani Ronac, Yang Yu-Xiao

机构信息

Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA; The Integrated Cancer Prevention Center, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel; Tel-Aviv University, Tel-Aviv, Israel.

出版信息

Pharmacoepidemiol Drug Saf. 2015 May;24(5):534-42. doi: 10.1002/pds.3765. Epub 2015 Mar 23.

Abstract

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.

摘要

目的

肠道微生物群被认为是结直肠癌形成的重要促进因素,先前有报道称结直肠癌组织中存在结肠生态失调。我们的目的是评估抗生素暴露的类型和累积持续时间与结直肠癌风险之间的关联。

方法

我们使用来自英国的一个基于人群的大型数据库进行了一项巢式病例对照研究。病例定义为患有任何结直肠癌医疗编码的患者。已知患有家族性结直肠癌综合征或炎症性肠病的受试者被排除在研究之外。对于每例病例,使用发病密度抽样方法选择4名在年龄、性别、执业地点和索引日期前的随访持续时间方面相匹配的合格对照。感兴趣的暴露因素是索引日期前的抗生素治疗。使用条件逻辑回归分析估计调整后的比值比(OR)和95%置信区间(CI)。

结果

共识别出20990例病例和82054名对照。在索引日期前>10年首次暴露于青霉素的受试者中,结直肠癌的调整后OR为1.11(95%CI 1.02 - 1.20)。随着青霉素暴露次数增加至>10疗程,风险显著增加至1.20(95%CI 1.11 - 1.31)。风险也随着每年青霉素治疗的平均次数(暴露强度)增加而增加,每年每增加一次治疗的OR为1.04(95%CI 1.01 - 1.08)。暴露于抗病毒或抗真菌治疗与结直肠癌风险无关。

结论

过去多次使用青霉素与结直肠癌风险适度升高有关。

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