Division of General Internal Medicine, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.
Int J Cancer. 2021 Aug 1;149(3):535-545. doi: 10.1002/ijc.33541. Epub 2021 Mar 8.
Non-steroidal anti-inflammatory drugs (NSAIDs) and statin drugs may protect against the development of non-Hodgkin lymphoma (NHL), but data are limited, particularly for NHL subtypes. Furthermore, some in vitro, animal and epidemiologic data suggest there may be a synergistic effect of these two agents, but there has been no test of this hypothesis in NHL. We evaluated the self-reported use of NSAIDs and statins in a clinic-based study of 1703 NHL patients and 2199 frequency-matched controls. Unconditional logistic regression was used to estimate odds ratios (ORs) and 95% confidence intervals (CIs), adjusted for potential confounding variables. We observed an inverse association of regular use of low-dose aspirin with risk of NHL (OR = 0.82; 95% CI 0.70-0.96) that was stronger with longer duration of use (P < .01). There were no associations for use of regular or extra-strength aspirin, ibuprofen, other NSAIDs, statins or other cholesterol-lowering drugs with NHL risk, while an inverse association with COX-2 inhibitors was equivocal. There was also no interaction of low-dose aspirin and statins on NHL risk. Inverse associations of similar magnitude to all NHL were observed for regular use of low-dose aspirin with diffuse large B-cell, follicular, marginal zone and all other lymphomas, although not all associations were statistically significant. In conclusion, low-dose aspirin but not regular/extra strength aspirin, other NSAIDs or statin use was associated with lower risk of NHL. Beyond the potential for the primary prevention of NHL, these data also point to a role of anti-platelet or other effects of low-dose aspirin in lymphomagenesis that warrant follow-up.
非甾体抗炎药(NSAIDs)和他汀类药物可能预防非霍奇金淋巴瘤(NHL)的发展,但数据有限,特别是对于 NHL 亚型。此外,一些体外、动物和流行病学数据表明,这两种药物可能存在协同作用,但在 NHL 中尚未对此假设进行过检验。我们在一项基于诊所的 NHL 患者 1703 例和频率匹配对照 2199 例的研究中评估了 NSAIDs 和他汀类药物的自我报告使用情况。使用非条件逻辑回归估计比值比(OR)和 95%置信区间(CI),并调整了潜在混杂变量。我们观察到低剂量阿司匹林的规律使用与 NHL 风险呈负相关(OR = 0.82;95%CI 0.70-0.96),使用时间越长相关性越强(P<.01)。规律使用普通或超强剂量阿司匹林、布洛芬、其他 NSAIDs、他汀类药物或其他降胆固醇药物与 NHL 风险无关,而 COX-2 抑制剂与 NHL 风险呈负相关,但结果不确定。低剂量阿司匹林和他汀类药物之间也没有相互作用对 NHL 风险有影响。与所有 NHL 相似的负相关关系也观察到低剂量阿司匹林的规律使用与弥漫性大 B 细胞、滤泡性、边缘区和所有其他淋巴瘤,尽管并非所有相关性均具有统计学意义。总之,低剂量阿司匹林但不是普通/超强剂量阿司匹林、其他 NSAIDs 或他汀类药物的使用与 NHL 风险降低相关。除了 NHL 的一级预防的潜在可能性外,这些数据还表明低剂量阿司匹林的抗血小板或其他作用可能在淋巴瘤的发生中起作用,值得进一步研究。