首页> 外文期刊>Journal of innate immunity >Serum Acute Phase Protein and Inflammatory Cytokine Network Correlations: Comparison of a Pre-Rheumatoid Arthritis and Non-Rheumatoid Arthritis Community Cohort
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Serum Acute Phase Protein and Inflammatory Cytokine Network Correlations: Comparison of a Pre-Rheumatoid Arthritis and Non-Rheumatoid Arthritis Community Cohort

机译:血清急性期蛋白和炎性细胞因子网络的相关性:类风湿关节炎和非类风湿关节炎社区队列的比较。

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Serum concentrations of acute phase proteins, inflammatory cytokines, and other immunological components were individually assayed using high-sensitivity ELISA in a com-munity-based cohort of preclinical rheumatoid arthritis (pre-RA) and matched non-RA control (CN) subjects. Bivariate correlations of the biomarker panel concentrations were compared in pre-RA versus CN and female versus male subjects. Clinically elevated CRP levels (8+ mg/l) occurred in a higher (p = 0.010) frequency in 46 pre-RA (n = 8, 17.4%) subjects than in 179 CN (n = 9, 5.0%), and were independent of age, gender, smoking behaviors, and serum rheumatoid factor. Selected age and gender differences were found in levels of the immunological network factors. In each study group, the ratio of sTNF-RI to IL-2sRα mean concentrations was 2-fold higher in men than in women. Aging correlated positively with CRP, ASAA, and TNF-α levels, but negatively with IL-1β. Bivariate correlations were similar in pre-RA subjects versus CN and by gender, with few exceptions. Factor loadings in principal component analysis of the total subjects indicated that age- and gender-related variables constituted the two main components. Using multiple regression analyses, an integrative working model of all variable interrelations was generated. The tentative, directional model supports a concept of gender dimorphism of the ratio of sTNF-RI to IL-2sRα serum concentrations and displays differing effects of age on TNF-α versus IL-1β levels. These findings indicate complex age, gender, and cytokine interrelations in control of the immune systems network. Future research in testing such inflammatory pathways promises a better understanding of predisposition to diseases, like RA.
机译:急性期蛋白,炎性细胞因子和其他免疫学成分的血清浓度是在社区基于临床前类风湿性关节炎(pre-RA)和匹配的非RA对照(CN)受试者的队列中使用高灵敏度ELISA进行单独测定的。在RA之前,CN和女性与男性受试者中比较了生物标志物组浓度的双变量相关性。临床上升高的CRP水平(8+ mg / l)发生在RA之前的46位患者(n = 8,17.4%)高于(179 = CN,n = 9,5.0%),发生频率较高(p = 0.010),并且与年龄,性别,吸烟行为和血清类风湿因子无关。在免疫网络因素水平上发现了选定的年龄和性别差异。在每个研究组中,男性的sTNF-RI与IL-2sRα平均浓度之比比女性高2倍。衰老与CRP,ASAA和TNF-α水平呈正相关,但与IL-1β呈负相关。 RA之前的受试者与CN和按性别划分的双变量相关性相似,只有少数例外。总受试者主成分分析中的因素负荷表明,与年龄和性别相关的变量是两个主要成分。使用多元回归分析,生成了所有变量相关性的综合工作模型。初步的定向模型支持sTNF-RI与IL-2sRα血清浓度之比的性别双态性概念,并显示年龄对TNF-α和IL-1β水平的不同影响。这些发现表明,在控制免疫系统网络方面,年龄,性别和细胞因子之间存在复杂的关系。测试此类炎症途径的未来研究有望更好地了解诸如RA等疾病的易感性。

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