首页> 外文OA文献 >Assessing interactions between the associationsudof common genetic susceptibility variants,udreproductive history and body mass index withudbreast cancer risk in the breast cancer associationudconsortium: a combined case-control study
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Assessing interactions between the associationsudof common genetic susceptibility variants,udreproductive history and body mass index withudbreast cancer risk in the breast cancer associationudconsortium: a combined case-control study

机译:评估协会之间的互动 ud常见的遗传易感性变体, ud生殖史和体重指数与 ud乳腺癌协会的乳腺癌风险 ud联合体:一项综合病例对照研究

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摘要

Introduction: Several common breast cancer genetic susceptibility variants have recently been identified. Weudaimed to determine how these variants combine with a subset of other known risk factors to influence breastudcancer risk in white women of European ancestry using case-control studies participating in the Breast CancerudAssociation Consortium.udMethods: We evaluated two-way interactions between each of age at menarche, ever having had a live birth,udnumber of live births, age at first birth and body mass index (BMI) and each of 12 single nucleotideudpolymorphisms (SNPs) (10q26-rs2981582 (FGFR2), 8q24-rs13281615, 11p15-rs3817198 (LSP1), 5q11-rs889312ud(MAP3K1), 16q12-rs3803662 (TOX3), 2q35-rs13387042, 5p12-rs10941679 (MRPS30), 17q23-rs6504950 (COX11), 3p24-rs4973768 (SLC4A7), CASP8-rs17468277, TGFB1-rs1982073 and ESR1-rs3020314). Interactions were tested for byudfitting logistic regression models including per-allele and linear trend main effects for SNPs and risk factors,udrespectively, and single-parameter interaction terms for linear departure from independent multiplicative effects.udResults: These analyses were applied to data for up to 26,349 invasive breast cancer cases and up to 32,208udcontrols from 21 case-control studies. No statistical evidence of interaction was observed beyond that expected byudchance. Analyses were repeated using data from 11 population-based studies, and results were very similar.udConclusions: The relative risks for breast cancer associated with the common susceptibility variants identified touddate do not appear to vary across women with different reproductive histories or body mass index (BMI). Theudassumption of multiplicative combined effects for these established genetic and other risk factors in risk predictionudmodels appears justified.
机译:简介:最近发现了几种常见的乳腺癌遗传易感性变异。我们试图通过参加乳腺癌 udAssociation联合会的病例对照研究来确定这些变异体如何与其他已知风险因素的子集结合,以影响欧洲裔白人女性的乳腺癌癌症风险。 udMethods:我们评估了两个月经初潮的各个年龄,活产的人数,活产的数量,初生的年龄和体重指数(BMI)与12个单核苷酸的多核苷酸(SNP)之间的相互作用(10q26-rs2981582(FGFR2 ),8q24-rs13281615、11p15-rs3817198(LSP1),5q11-rs889312 ud(MAP3K1),16q12-rs3803662(TOX3),2q35-rs13387042、5p12-rs10941679(MRPS30),17q23-rs6504950(COX11),3p24- (SLC4A7),CASP8-rs17468277,TGFB1-rs1982073和ESR1-rs3020314)。通过逻辑拟合模型检验交互作用,包括分别针对SNP和风险因素的等位基因和线性趋势主效应,以及用于单变量交互项与独立乘性效应线性偏离的单参数交互项。 ud结果:将这些分析应用于来自21个病例对照研究的多达26,349例浸润性乳腺癌病例和多达32,208 udcontrol的数据。没有观察到交互作用的统计证据,超出了预期。使用来自11项基于人群的研究的数据重复进行分析,结果非常相似。 ud结论:与具有不同生殖史或身体的女性相比,与确定为 uddate的常见易感性变量相关的乳腺癌的相对风险似乎没有差异质量指数(BMI)。在风险预测 udmodel中对于这些已确定的遗传和其他风险因素的乘积联合效应的假设似乎是有道理的。

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