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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Etiologic heterogeneity among non-Hodgkin lymphoma subtypes
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Etiologic heterogeneity among non-Hodgkin lymphoma subtypes

机译:非霍奇金淋巴瘤亚型之间的病因异质性

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Understanding patterns of etiologic commonality and heterogeneity for non-Hodgkin lymphomas may illuminate lym-phomagenesis. We present the first systematic comparison of risks by lymphoma subtype for a broad range of putative risk factors in a population-based case-control study, including diffuse large B-cell (DLBCL; N = 416), follicular (N = 318), and marginal zone lymphomas (N = 106), and chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/ SLL; N = 133). We required at least 2 of 3 analyses to support differences in risk:(1) polytomous logistic regression,(2) homogeneity tests, or (3) dichoto-mous logistic regression, analyzing all 7 possible pairwise comparisons among the subtypes, corresponding to various groupings by clinical behavior, genetic features, and differentiation. Late birth order and high body mass index (> 35) kg/m2) increased risk for DLBCL alone. Autoimmune conditions increased risk for marginal zone lymphoma alone. The tumor necrosis factor G-308A polymorphism (rs1800629) increased risks for both DLBCL and marginal zone lym-phoma. Exposure to certain dietary het-erocyclic amines from meat consumption increased risk for CLL/SLL alone. We observed no significant risk factors for follicular lymphoma alone. These data clearly support both etiologic commonality and heterogeneity for lymphoma subtypes, suggesting that immune dysfunction is of greater etiologic importance for DLBCL and marginal zone lymphoma than for CLL/SLL and follicular lymphoma.
机译:了解非霍奇金淋巴瘤的病因学共性和异质性可能会阐明淋巴瘤的发生。我们在一项基于人群的病例对照研究中,首次提出了针对淋巴瘤亚型的广泛推定风险因素的系统风险比较,包括弥漫性大B细胞(DLBCL; N = 416),滤泡性(N = 318),和边缘区淋巴瘤(N = 106),以及慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL / SLL; N = 133)。我们需要进行至少3个分析中的2个以支持风险差异:(1)多态逻辑回归,(2)同质性检验,或(3)二项逻辑回归,分析亚型之间的所有7种可能的成对比较,对应于各种按临床行为,遗传特征和分化分组。早产顺序和高体重指数(> 35)kg / m2)会增加DLBCL的风险。自身免疫性疾病增加了仅边缘区淋巴瘤的风险。肿瘤坏死因子G-308A多态性(rs1800629)增加了DLBCL和边缘区淋巴瘤的风险。食用肉类引起的某些饮食中的杂环胺会增加单独CLL / SLL的风险。我们没有观察到单独的滤泡性淋巴瘤的重要危险因素。这些数据清楚地支持了淋巴瘤亚型的病因学共性和异质性,表明对于DLBCL和边缘区淋巴瘤,免疫功能障碍的病因学重要性比对CLL / SLL和滤泡性淋巴瘤更大。

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