Effects of Aspirin or Clopidogrel on Colorectal Cancer Chemoprevention in Patients with Type 2 Diabetes Mellitus

被引:13
|
作者
Kuan, Yi-Chun [1 ,2 ,3 ,4 ,5 ,6 ]
Huang, Kuang-Wei [7 ]
Lin, Cheng-Li [8 ,9 ]
Luo, Jiing-Chyuan [10 ]
Kao, Chia-Hung [11 ,12 ,13 ,14 ,15 ,16 ]
机构
[1] Taipei Med Univ, Taipei Neurosci Inst, Taipei 11031, Taiwan
[2] Taipei Med Univ Shuang Ho Hosp, Dept Neurol, New Taipei 23561, Taiwan
[3] Taipei Med Univ, Coll Med, Sch Med, Dept Neurol, Taipei 11031, Taiwan
[4] Natl Taiwan Univ, Coll Publ Hlth, Inst Epidemiol & Prevent Med, Taipei 10617, Taiwan
[5] Taipei Med Univ, Cochrane Taiwan, Taipei 11031, Taiwan
[6] Taipei Med Univ Shuang Ho Hosp, Ctr Evidence Based Hlth Care, New Taipei 23561, Taiwan
[7] Taipei Beitou Hlth Management Hosp, Dept Internal Med, Div Gastroenterol, Taipei 11252, Taiwan
[8] China Med Univ Hosp, Management Off Hlth Data, Taichung 40402, Taiwan
[9] China Med Univ, Coll Med, Taichung 40402, Taiwan
[10] Taipei Vet Gen Hosp, Dept Internal Med, Div Gastroenterol, Taipei 11217, Taiwan
[11] China Med Univ, Coll Med, Grad Inst Biomed Sci, Taichung 40402, Taiwan
[12] China Med Univ, Coll Med, Sch Med, Taichung 40402, Taiwan
[13] China Med Univ Hosp, Dept Nucl Med, Taichung 40402, Taiwan
[14] China Med Univ Hosp, PET Ctr, Taichung 40402, Taiwan
[15] Asia Univ, Dept Bioinformat & Med Engn, Taichung 41454, Taiwan
[16] China Med Univ Hosp, Ctr Augmented Intelligence Healthcare, Taichung 40402, Taiwan
关键词
colorectal cancer; Type 2 diabetes mellitus; aspirin; clopidogrel; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; RISK; TRIAL;
D O I
10.3390/cancers11101468
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The effect of clopidogrel, whose mechanism of action differs from that of aspirin, on CRC risk remains unknown. We investigated the effects of clopidogrel and aspirin, either as monotherapy or combined, on colorectal cancer (CRC) risk in patients with Type 2 diabetes mellitus (T2DM). Methods: We conducted a cohort study using Taiwan National Health Insurance Research Database. Four groups comprising 218,903 patients using aspirin monotherapy, 20,158 patients using clopidogrel monotherapy, 42,779 patients using dual antiplatelet therapy, and 281,840 nonuser matched controls were created using propensity score matching. Cox proportional hazards regression was used to evaluate the CRC risk during follow-up. Results: During the 13-year follow-up period, we found 9431 cases of CRC over 3,409,522 person-years. The overall incidence rates of CRC were 2.04, 3.45, 1.55, and 3.52 per 1000 person-years in the aspirin, clopidogrel, dual antiplatelet, and nonuser cohorts, respectively. The adjusted hazard ratios (aHRs) were 0.59 (95% confidence interval [CI], 0.56-0.61), 0.77 (95% CI, 0.68-0.87), and 0.37 (95% CI, 0.33-0.40) for the aspirin, clopidogrel, and dual antiplatelet cohorts, respectively. Dose- and duration-dependent chemopreventive effects were observed in the three cohorts.
引用
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页数:16
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