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Association between low-grade inflammation and Breast cancer and B-cell Myeloma and Non-Hodgkin Lymphoma: findings from two prospective cohorts

机译:低度炎症和乳腺癌与B细胞骨髓瘤和非霍奇金淋巴瘤之间的关联:两个前瞻性队列研究的结果

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摘要

Chronic inflammation may be involved in cancer development and progression. Using 28 inflammatory-related proteins collected from prospective blood samples from two case-control studies nested in the Italian component of the European Prospective Investigation into Cancer and nutrition (n = 261) and in the Northern Sweden Health and Disease Study (n = 402), we tested the hypothesis that an inflammatory score is associated with breast cancer (BC) and Β-cell Non-Hodgkin Lymphoma (B-cell NHL, including 68 multiple myeloma cases) onset. We modelled the relationship between this inflammatory score and the two cancers studied: (BC and B-cell NHL) using generalised linear models, and assessed, through adjustments the role of behaviours and lifestyle factors. Analyses were performed by cancer types pooling both populations, and stratified by cohorts, and time to diagnosis. Our results suggested a lower inflammatory score in B-cell NHL cases (β = −1.28, p = 0.012), and, to lesser, extent with BC (β = −0.96, p = 0.33) compared to controls, mainly driven by cancer cases diagnosed less than 6 years after enrolment. These associations were not affected by subsequent adjustments for potential intermediate confounders, notably behaviours. Sensitivity analyses indicated that our findings were not affected by the way the inflammatory score was calculated. These observations call for further studies involving larger populations, larger variety of cancer types and repeated measures of larger panel of inflammatory markers.
机译:慢性炎症可能与癌症的发生和发展有关。使用从两项病例对照研究的预期血液样本中收集的28种炎症相关蛋白,这些研究嵌套在欧洲癌症与营养前瞻性调查的意大利部分(n = 261)和瑞典北部的健康与疾病研究(n = 402)中,我们测试了炎症评分与乳腺癌(BC)和Β细胞非霍奇金淋巴瘤(B细胞NHL,包括68例多发性骨髓瘤病例)发病有关的假设。我们使用广义线性模型对这种炎症评分与所研究的两种癌症(BC和B细胞NHL)之间的关系进行了建模,并通过调整行为和生活方式因素的作用进行了评估。通过汇总两个人群的癌症类型进行分析,并按队列和诊断时间进行分层。我们的研究结果表明,与主要由癌症驱动的对照组相比,B细胞非霍奇金淋巴瘤病例的炎症评分较低(β= -1.28,p = 0.012),而与BC相比,其程度较低(β0.9= −0.96,p = 0.33)。入院后不到6年诊断为病例。这些关联不受潜在中间混杂因素(尤其是行为)的后续调整的影响。敏感性分析表明,我们的发现不受炎症评分的计算方式的影响。这些观察结果要求进一步的研究涉及更大的人群,更多种类的癌症类型以及对更大范围的炎症标志物的重复测量。

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