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Immunoglobulin E and cancer: a meta-analysis and a large Swedish cohort study.

机译:免疫球蛋白E和癌症:荟萃分析和大型瑞典队列研究。

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We quantified associations between IgE and cancer in a meta-analysis and cohort study. Pubmed and Embase were searched to extract information using predefined inclusion criteria. In the Apolipoprotein MOrtality RISk (AMORIS) database, 24,820 persons had IgE measurements. Multivariate Cox proportional hazard models were used to analyze associations between IgE and cancer. Twenty-seven studies were reviewed from which seven case-control studies were included for analysis. The pooled relative risk (random effects model) was 0.97 (95% CI 0.86-1.09). Cell types of tumor origin (mesenchymal tissue or cells of the nervous system, lymphatic or hematopoietic tissue, and epithelium) modified the effect. In the AMORIS cohort, 862 persons developed cancer. Hazard ratios comparing quartiles of IgE were similar to the findings in the meta-analysis (HR 0.87 (95% CI 0.72-1.06); 0.94 (0.78-1.14); 0.90 (0.74-1.10) for the 2nd, 3rd, and 4th quartile compared to the 1st quartile), but there was no pattern by tumor origin. Both studies showed a weak inverse association between IgE and cancer, but a pattern by cancer type was only seen in the meta-analysis. Our findings suggest the need for prospective studies studying IgE and cancer. Measurements of IgE should be combined with other information, e.g., bio-banked samples containing other key immunological discriminators.
机译:我们在荟萃分析和队列研究中量化IgE和癌症之间的关联。搜索PubMed和Embase以使用预定义的包含标准提取信息。在载脂蛋白死亡率风险(Amoris)数据库中,24,820人具有IgE测量。多变量Cox比例危险模型用于分析IgE和癌症之间的关联。从中审查了二十七项研究,其中七项病例对照研究进行了分析。汇集的相对风险(随机效果模型)为0.97(95%CI 0.86-1.09)。肿瘤源细胞类型(神经系统的间充质组织或细胞,淋巴或造血组织,上皮)修饰了效果。在Amoris Cohort中,862人发育癌症。比较IgE四分位数的危险比与META分析中的结果相似(HR 0.87(95%CI 0.72-1.06); 0.94(0.78-1.14); 2nd,第3和第4四分位数0.90(0.74-1.10)与第一个四分位数相比,但肿瘤起源没有模式。这两项研究表明IgE和癌症之间的逆转关系较弱,但在Meta分析中仅观察到癌症类型的模式。我们的研究结果表明需要研究IgE和癌症的前瞻性研究。 IgE的测量应与其他信息相结合,例如含有其他关键免疫鉴别器的生物银行样本。

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