Chondroitin Sulphate and Glucosamine Use Depend on Nonsteroidal Anti-inflammatory Drug Use to Modify the Risk for Colorectal Cancer

被引:6
|
作者
Ibanez-Sanz, Gemma [1 ,2 ,3 ,4 ]
Guino, Elisabet [1 ,3 ,4 ]
Morros, Rosa [5 ,6 ,7 ]
Angeles Quijada-Manuitt, Maria [8 ,9 ]
Carmen de la Pena-Negro, Luisa [1 ,2 ,10 ]
Moreno, Victor [1 ,3 ,4 ,11 ]
机构
[1] Inst Catala Oncol, Oncol Data Analyt Program, Av Gran Via 199-203, Barcelona 08908, Spain
[2] Hosp Univ Bellvitge, Serv Aparell Digestiu, Barcelona, Spain
[3] Inst Invest Biomed Bellvitge IDIBELL, Programa ONCOBELL, Colorectal Canc Grp, Barcelona, Spain
[4] Consorcio Invest Biomed Red Epiderniol & Salud Pu, Madrid, Spain
[5] Univ Autonoma Barcelona, Dept Farmacol Terapeut & Toxicol, Barcelona, Spain
[6] Inst Catala Salut ICS, Girona, Spain
[7] Fundacio Inst Univ Recerca Atencio Primaria Salut, Barcelona, Spain
[8] Hosp Santa Creu i St Pau, Serv Farmacol Clin, Barcelona, Spain
[9] Univ Barcelona, Dept Patol & Terapeut Expt, Unitat Docent Campus Bellvitge, Barcelona, Spain
[10] Hosp Viladecans, Serv Aparell Digestiu, Viladecans, Spain
[11] Univ Barcelona, Fac Med & Ciencies Salut, Dept Ciencies Clin, Barcelona, Spain
关键词
SUPPLEMENT USE; PRIMARY-CARE; ASPIRIN; PREVENTION; CHEMOPREVENTION; ASSOCIATIONS; INFORMATION; HEALTH; SAFETY;
D O I
10.1158/1055-9965.EPI-19-1051
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A safe and effective colorectal cancer chemoprevention agent remains to be discovered. There is little evidence regarding the protective effect of chondroitin sulphate and glucosamine on colorectal cancer. We aimed to assess the association between colorectal cancer risk and the use of chondroitin sulphate and glucosamine using a large cohort with dispensed data. Methods: We performed a population-based case-control study in Catalonia using primary care reimbursed medication records (SIDIAP database). The study included 25,811 cases with an incident diagnosis of colorectal cancer and 129,117 matched controls between 2010 and 2015. Results: The prevalence of ever use was 9.0% (n = 13,878) for chondroitin sulphate, 7.3% (n = 11,374) for glucosamine, and 35% for regular use of nonsteroidal anti-inflammatory drugs (NSAID; n = 45,774). A decreased risk of colorectal cancer was observed among chondroitin sulphate use [OR: 0.96; 95% confidence interval (CI), 0.91-1.01], glucosamine use (OR: 0.92; 95% CI, 0.87-0.97), and concurrent use of chondroitin sulphate and glucosamine (OR: 0.83; 95% CI, 0.70-0.98). Especially for glucosamine, there was a dose-response association regarding duration and cumulative dose. The analysis stratified by simultaneous use with other NSAIDs showed that these drugs used without other NSAIDs do not reduce risk (OR: 1.06; 95% CI, 0.74-1.51). However, they may have a synergistic protective effect when used with other NSAIDs (OR: 0.80; 95% CI, 0.72-0.88). Conclusions: This study does not provide strong support for an independent protective association of chondroitin sulphate or glucosamine on colorectal cancer risk in our population. However, these drugs may have a synergistic beneficial effect among NSAID users. Impact: Chondroitin sulphate or glucosamine may contribute to the protective effect of NSAID use in colorectal cancer.
引用
收藏
页码:1809 / 1816
页数:8
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