Rosa Lorena, Cook Paz, Pfeiffer Ruth M, Kemp Troy J, Hildesheim Allan, Pehlivanoglu Burcin, Adsay Volkan, Bellolio Enrique, Araya Juan Carlos, Pinto Ligia, Ferreccio Catterina, Aguayo Gloria, Viñuela Eduardo, Koshiol Jill
Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Advanced Center for Chronic Diseases, Universidad de Chile and Pontificia Universidad Católica de Chile, Santiago, Chile.
Int J Cancer. 2025 Apr 1;156(7):1380-1392. doi: 10.1002/ijc.35238. Epub 2024 Oct 31.
Inflammation has been associated with the development of gallbladder cancer (GBC). However, little is known about the associations of both, inflammation and the use of non-steroidal anti-inflammatory drugs (NSAIDs), with preneoplastic lesions. We analyzed the association of NSAIDs and gallbladder dysplasia in 82 patients with dysplasia and 1843 patients with gallstones among symptomatic patients from a high-risk population. We also analyzed associations for 33 circulating immune-related proteins in a subsample of all 68 dysplasia cases diagnosed at the time of sample selection and 136 gallstone controls. We calculated age- and sex-adjusted odds ratios (ORs) and 95% confidence intervals (95% CIs). Biliary colic was reported among most cases (97.6%) and controls (83.9%). NSAID use was inversely associated with gallbladder dysplasia (OR: 0.48, 95%CI: 0.26-0.83). Comparing the highest versus lowest category of each immune-related protein, eight proteins were inversely associated with dysplasia with sex- and age-adjusted ORs ranging from 0.30 (95%CI: 0.12-0.77) for IL-33 to 0.76 (95%CI: 0.59-0.99) for MIP-1B. Of those, GRO remained associated with dysplasia (OR: 0.64, 95%CI: 0.45-0.91) and BCA-1 was borderline associated (OR: 0.74, 95%CI: 0.54-1.01) after adjusting the logistic regression model for sex, age, and NSAIDs. In conclusion, NSAID users were less likely to have gallbladder dysplasia, suggesting that NSAIDs might be beneficial for symptomatic gallstones patients. The inverse association between immune-related markers and dysplasia requires additional research, ideally in prospective studies with asymptomatic participants, to understand the role of the inflammatory response in the natural history of GBC and to address the biological effect of NSAIDs.
炎症与胆囊癌(GBC)的发生有关。然而,关于炎症和非甾体抗炎药(NSAIDs)的使用与癌前病变之间的关联,人们知之甚少。我们分析了来自高危人群的有症状患者中,82例发育异常患者和1843例胆结石患者使用NSAIDs与胆囊发育异常之间的关联。我们还在样本选择时诊断出的所有68例发育异常病例和136例胆结石对照的子样本中,分析了33种循环免疫相关蛋白之间的关联。我们计算了年龄和性别调整后的优势比(OR)和95%置信区间(95%CI)。大多数病例(97.6%)和对照(83.9%)都报告有胆绞痛。NSAIDs的使用与胆囊发育异常呈负相关(OR:0.48,95%CI:0.26-0.83)。比较每种免疫相关蛋白的最高类别与最低类别,8种蛋白与发育异常呈负相关,年龄和性别调整后的OR范围从IL-33的0.30(95%CI:0.12-0.77)到MIP-1B的0.76(95%CI:0.59-0.99)。其中,在对逻辑回归模型进行性别、年龄和NSAIDs调整后,GRO仍与发育异常相关(OR:0.64,95%CI:0.45-0.91),BCA-1具有临界相关性(OR:0.74,95%CI:0.54-1.01)。总之,使用NSAIDs的患者发生胆囊发育异常的可能性较小,这表明NSAIDs可能对有症状的胆结石患者有益。免疫相关标志物与发育异常之间的负相关需要进一步研究,理想情况下是对无症状参与者进行前瞻性研究,以了解炎症反应在GBC自然史中的作用,并探讨NSAIDs的生物学效应。