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雷尼替丁和尼扎替丁对胃肠道癌风险的影响。

Effects of ranitidine and nizatidine on the risk of gastrointestinal cancer.

作者信息

Kang Hyejung, Nam Chung Mo, Choi Dong-Woo, Park Sohee

机构信息

Department of Health Informatics and Biostatistics, Graduate School of Public Health, Yonsei University, Seoul, Republic of Korea.

Department of Preventive Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.

出版信息

Front Oncol. 2023 Jul 27;13:1182174. doi: 10.3389/fonc.2023.1182174. eCollection 2023.

Abstract

PURPOSE

Gastrointestinal (GI) cancer occurs in digestive organs such as the stomach, colon, liver, esophagus, and pancreas. About 83,034 cases occurred in Korea alone in 2020. Dietary factors, alcohol consumption, (), and lifestyle factors increase the incidence of diseases such as gastritis, peptic ulcer, pancreatitis, and gastroesophageal reflux disease (GERD), which can develop into GI cancer. However, in 2019, the US Food and Drug Administration announced that the drugs ranitidine and nizatidine, which are used for digestive disorders, contain carcinogens. In this study, we investigated the effects of ranitidine and nizatidine on the development of GI cancer.

MATERIALS AND METHODS

In this study, using National Health Insurance Service-National Sample Cohort (NHIS-NSC) version 2.5 (updated from 2002 to 2019), subjects who developed GI cancer were enrolled in the case group, and those who were at risk of, but did not develop, cancer were enrolled in the control group. Thereafter, risk-set matching was performed (1:3 ratio) by sex and age at the time of diagnosis of cancer in the case group. Through this procedure, 22,931 cases and 68,793 controls were identified. The associations of ranitidine and/or nizatidine with GI cancer were confirmed by adjusted odds ratios (aORs) and 95% confidence intervals (CIs) calculated through conditional logistic regression analysis.

RESULTS

The aORs of ranitidine and/or nizatidine users were lower than those of nonusers in all average prescription days groups (< 30 days/year: aOR [95% CI] = 0.79 [0.75-0.82]; 30-59 days/year: aOR [95% CI] = 0.66 [0.59-0.73]; 60-89 days/year: aOR [95% CI] = 0.69 [0.59-0.81]; ≥ 90 days/year: aOR [95% CI] = 0.69 [0.59-0.79]). Sensitivity analyses were conducted with different lag periods for the onset of GI cancer after drug administration, and these analyses yielded consistent results. Additional analyses were also performed by dividing subjects into groups based on cancer types and CCI scores, and these analyses produced the same results.

CONCLUSION

Our study, using nationwide retrospective cohort data, did not find evidence suggesting that ranitidine and nizatidine increase the risk of GI cancer. In fact, we observed that the incidence of GI cancer was lower in individuals who used the drugs compared to nonusers. These findings suggest a potential beneficial effect of these drugs on cancer risk, likely attributed to their ability to improve digestive function.

摘要

目的

胃肠道(GI)癌发生于胃、结肠、肝脏、食管和胰腺等消化器官。2020年仅在韩国就发生了约83034例病例。饮食因素、酒精摄入、()和生活方式因素会增加胃炎、消化性溃疡、胰腺炎和胃食管反流病(GERD)等疾病的发病率,而这些疾病可能发展为胃肠道癌。然而,2019年美国食品药品监督管理局宣布,用于治疗消化系统疾病的药物雷尼替丁和尼扎替丁含有致癌物。在本研究中,我们调查了雷尼替丁和尼扎替丁对胃肠道癌发生发展的影响。

材料与方法

在本研究中,使用2.5版国家健康保险服务-国家样本队列(NHIS-NSC,更新时间为2002年至2019年),将发生胃肠道癌的受试者纳入病例组,将有患癌风险但未患癌的受试者纳入对照组。此后,在病例组癌症诊断时,按性别和年龄进行风险集匹配(1:3比例)。通过该程序,确定了22931例病例和68793例对照。通过条件逻辑回归分析计算调整后的优势比(aORs)和95%置信区间(CIs),以确认雷尼替丁和/或尼扎替丁与胃肠道癌的关联。

结果

在所有平均处方天数组中,雷尼替丁和/或尼扎替丁使用者的aORs均低于非使用者(每年<30天:aOR[95%CI]=0.79[(0.75-0.82)];每年30-59天:aOR[95%CI]=0.66[(0.59-0.73)];每年60-89天:aOR[95%CI]=0.69[(0.59-0.81)];每年≥90天:aOR[95%CI]=0.69[(0.59-0.79)])。对药物给药后胃肠道癌发病的不同滞后时间进行了敏感性分析,这些分析得出了一致的结果。还根据癌症类型和CCI评分将受试者分组进行了额外分析,这些分析也得出了相同的结果。

结论

我们使用全国性回顾性队列数据的研究未发现证据表明雷尼替丁和尼扎替丁会增加胃肠道癌的风险。事实上,我们观察到使用这些药物的个体中胃肠道癌的发病率低于未使用者。这些发现表明这些药物对癌症风险可能具有有益作用,这可能归因于它们改善消化功能的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25d7/10415903/be67593384a7/fonc-13-1182174-g001.jpg

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