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生殖风险因素对德国BRCA1基因突变携带者乳腺癌发病年龄的修饰作用。

Modifying effect of reproductive risk factors on the age at onset of breast cancer for German BRCA1 mutation carriers.

作者信息

Chang-Claude J, Becher H, Eby N, Bastert G, Wahrendorf J, Hamann U

机构信息

Division of Epidemiology 0345, Deutsches Krebsforschungszentrum, Heidelberg, Germany.

出版信息

J Cancer Res Clin Oncol. 1997;123(5):272-9. doi: 10.1007/BF01208638.

Abstract

Female carriers of mutations in the BRCA1 gene on chromosome 17q have a very high risk of developing breast and/or ovarian cancer during their lifetime. There is, however, little knowledge of to what extent non-genetic risk factors, such as age at menarche, age at first birth, and body mass index, alter the age at onset of disease. We identified individuals showing a high probability of linkage to BRCA1 and examined the effect of other known risk factors on disease risk. A total of 43 families with at least three breast or ovarian cancer cases, including two affected before 60 years of age, were studied for linkage to the susceptibility locus BRCA1. Blood samples from relevant family members were used to genotype for at least three chromosome 17q polymorphic markers. Information on reproductive history, hormone use and lifestyle factors was collected from female members using a self-administered questionnaire. Diagnoses of breast and ovarian cancer were verified through pathology reports and paraffin blocks were obtained when available. Multipoint LOD (logarithm of the odds) scores were calculated and individuals from 10 families with a posteriori probability for linkage greater than 0.90 were used for further analysis. Forty-six BRCA1 carriers were identified by the disease haplotype; 30 were affected with breast cancer and 5 with ovarian cancer. Proportional- hazards analysis of age at onset of breast cancer yielded increased relative risks of 1.74 for early age at menarche (< 14 years), 1.58 for late age at first birth (> or = 25 years) or nulliparity, and 2.78 for recent year of birth (> or = 1940); however, none of the risk estimates was statistically significant. When both breast and ovarian cancer were considered as disease endpoints, the birth cohort effect was stronger and age at first birth showed no effect. Our data provide some evidence that reproductive risk factors for breast cancer have an effect on age at onset for BRCA1 carriers. However, considering that our analyses were based on limited numbers, these results warrant further clarification.

摘要

17号染色体上BRCA1基因突变的女性携带者在其一生中患乳腺癌和/或卵巢癌的风险非常高。然而,对于初潮年龄、首次生育年龄和体重指数等非遗传风险因素在多大程度上改变疾病发病年龄,人们了解甚少。我们确定了与BRCA1高度连锁的个体,并研究了其他已知风险因素对疾病风险的影响。共研究了43个至少有3例乳腺癌或卵巢癌病例的家系,其中包括2例60岁之前发病的病例,以确定与易感基因座BRCA1的连锁关系。利用相关家庭成员的血样对至少3个17号染色体q臂多态性标记进行基因分型。通过自填问卷收集女性成员的生殖史、激素使用情况和生活方式因素等信息。乳腺癌和卵巢癌的诊断通过病理报告进行核实,如有石蜡块则予以获取。计算多点LOD(优势对数)得分,并使用10个家系中连锁后验概率大于0.90的个体进行进一步分析。通过疾病单倍型鉴定出46名BRCA1携带者;30例患有乳腺癌,5例患有卵巢癌。对乳腺癌发病年龄的比例风险分析显示,初潮年龄早(<14岁)的相对风险增加1.74,首次生育年龄晚(≥25岁)或未生育的相对风险增加1.58,出生年份晚(≥1940年)的相对风险增加2.78;然而,这些风险估计值均无统计学意义。当将乳腺癌和卵巢癌都视为疾病终点时,出生队列效应更强,首次生育年龄无影响。我们的数据提供了一些证据,表明乳腺癌的生殖风险因素对BRCA1携带者的发病年龄有影响。然而,鉴于我们的分析基于有限的样本数量,这些结果有待进一步阐明。

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