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诊断前与过敏相关的血清细胞因子与胶质瘤之间的关联。

Association between Prediagnostic Allergy-Related Serum Cytokines and Glioma.

作者信息

Schwartzbaum Judith, Seweryn Michal, Holloman Christopher, Harris Randall, Handelman Samuel K, Rempala Grzegorz A, Huang Ruo-Pan, Burkholder Brett, Brandemihl Adam, Kallberg Henrik, Johannesen Tom Borge, Ahlbom Anders, Feychting Maria, Grimsrud Tom K

机构信息

Division of Epidemiology, College of Public Health, Ohio State University, Columbus, Ohio, United States of America; Comprehensive Cancer Center, Ohio State University, Columbus, Ohio, United States of America.

Division of Biostatistics, College of Public Health, Ohio State University, Columbus, Ohio, United States of America; Mathematical Biosciences Institute, Columbus, Ohio, United States of America; Department of Mathematics, University of Lodz, Lodz, Poland.

出版信息

PLoS One. 2015 Sep 9;10(9):e0137503. doi: 10.1371/journal.pone.0137503. eCollection 2015.

Abstract

Allergy is inversely related to glioma risk. To determine whether prediagnostic allergy-related serum proteins are associated with glioma, we conducted a nested case-control study of seven cytokines (IL4, IL13, IL5, IL6, IL10, IFNG, TGFB2), two soluble cytokine receptors (sIL4RA, sIL13RA2) and three allergy-related transcription factors (FOXP3, STAT3, STAT6) using serum specimens from the Janus Serum Bank Cohort in Oslo, Norway. Blood donors subsequently diagnosed with glioma (n = 487) were matched to controls (n = 487) on age and date of blood draw and sex. We first estimated individual effects of the 12 serum proteins and then interactions between IL4 and IL13 and their receptors using conditional logistic regression. We next tested equality of case-control inter-correlations among the 12 serum proteins. We found that TGFB2 is inversely related to glioblastoma (Odds Ratio (OR) = 0.87, 95% Confidence Interval (CI)) = 0.76, 0.98). In addition, ≤ 5 years before diagnosis, we observed associations between IL4 (OR = 0.82, 95% CI = 0.66, 1.01), sIL4RA (OR = 0.80, 95% CI = 0.65, 1.00), their interaction (OR = 1.06, 95% CI = 1.01, 1.12) and glioblastoma. This interaction was apparent > 20 years before diagnosis (IL4-sIL4RA OR = 1.20, 95% CI = 1.05, 1.37). Findings for glioma were similar. Case correlations were different from control correlations stratified on time before diagnosis. Five years or less before diagnosis, correlations among case serum proteins were weaker than were those among controls. Our findings suggest that IL4 and sIL4RA reduce glioma risk long before diagnosis and early gliomagenesis affects circulating immune function proteins.

摘要

过敏与胶质瘤风险呈负相关。为了确定诊断前与过敏相关的血清蛋白是否与胶质瘤有关,我们利用挪威奥斯陆贾纳斯血清库队列的血清样本,对7种细胞因子(IL4、IL13、IL5、IL6、IL10、IFNG、TGFB2)、2种可溶性细胞因子受体(sIL4RA、sIL13RA2)和3种与过敏相关的转录因子(FOXP3、STAT3、STAT6)进行了一项巢式病例对照研究。随后被诊断为胶质瘤的献血者(n = 487)在年龄、采血日期和性别方面与对照组(n = 487)进行匹配。我们首先估计了12种血清蛋白的个体效应,然后使用条件逻辑回归分析了IL4和IL13及其受体之间的相互作用。接下来,我们检验了12种血清蛋白病例对照间相关性的相等性。我们发现TGFB2与胶质母细胞瘤呈负相关(比值比(OR)= 0.87,95%置信区间(CI)= 0.76,0.98)。此外,在诊断前≤5年,我们观察到IL4(OR = 0.82,95% CI = 0.66,1.01)、sIL4RA(OR = 0.80,95% CI = 0.65,1.00)、它们的相互作用(OR = 1.06,95% CI = 1.01,1.12)与胶质母细胞瘤之间存在关联。这种相互作用在诊断前>20年时很明显(IL4 - sIL4RA OR = 1.20,95% CI = 1.05,1.37)。胶质瘤的研究结果相似。病例相关性与诊断前时间分层的对照相关性不同。在诊断前5年或更短时间,病例血清蛋白之间的相关性比对照组之间的相关性弱。我们的研究结果表明,IL4和sIL4RA在诊断前很久就降低了胶质瘤风险,并且早期胶质瘤发生影响循环免疫功能蛋白。

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