Guindalini Rodrigo Santa Cruz, Song Andrew, Fackenthal James D, Olopade Olufunmilayo I, Huo Dezheng
Department of Medicine, Center for Clinical Cancer Genetics and Global Health, The University of Chicago, Chicago, Illinois.
Department of Radiology and Oncology, The State of Sao Paulo Cancer Institute, University of Sao Paulo Medical School, Sao Paulo, Brazil.
Cancer. 2016 Jun 15;122(12):1913-20. doi: 10.1002/cncr.29972. Epub 2016 Mar 15.
Genetic anticipation, the earlier onset of disease in successive generations, has been reported in hereditary breast and ovarian cancer syndrome (HBOC), but little is known about its underlying mechanisms. Ascertainment bias has been suggested as a reason in previous studies. Likewise, cohort effect, which may be caused by environmental factors, can be misinterpreted as genetic anticipation.
The authors reviewed the pedigrees of 176 kindreds, segregating those with deleterious mutations in breast cancer genes 1 and 2 (BRCA1/BRCA2) who had at least 2 consecutive generations of the same cancer (breast or ovarian). By using mutation probabilities as analytical weights in weighted random-effect models, generational differences in the age at onset of breast/ovarian cancer were calculated. The analyses were further controlled for ascertainment bias by excluding probands and adjusting for birth-cohort effect in the anticipation models.
The mean age at the onset of breast cancer for the probands' generation was 41.9 years, which was 6.8 years and 9.8 years earlier than the parents' and grandparents' generations, respectively. The anticipation effect for breast cancer remained significant after excluding the probands. There was a birth-cohort effect: patients who were born in 1930s and 1940s had breast cancer 5.0 years and 7.6 years earlier than patients who were born before 1920. The difference in breast cancer age of onset across generations was no longer significant after adjusting for birth-cohort effect.
The observed anticipation effect was driven mainly by a decrease in age of onset across birth cohorts, underscoring the need for risk-reducing interventions that target changing environmental/lifestyle factors in BRCA1/BRCA2 carriers. Cancer 2016;122:1913-20. © 2016 American Cancer Society.
遗传早现现象,即疾病在连续几代人中发病年龄提前,已在遗传性乳腺癌和卵巢癌综合征(HBOC)中被报道,但对其潜在机制知之甚少。在以往研究中,有人提出确诊偏倚是一个原因。同样,可能由环境因素引起的队列效应也可能被误解为遗传早现。
作者回顾了176个家族的系谱,这些家族中携带乳腺癌1号和2号基因(BRCA1/BRCA2)有害突变,且至少有连续两代人患同一种癌症(乳腺癌或卵巢癌)。通过在加权随机效应模型中使用突变概率作为分析权重,计算乳腺癌/卵巢癌发病年龄的代际差异。通过排除先证者并在早现模型中调整出生队列效应,进一步控制分析中的确诊偏倚。
先证者一代乳腺癌的平均发病年龄为41.9岁,分别比其父母一代和祖父母一代早6.8岁和9.8岁。排除先证者后,乳腺癌的早现效应仍然显著。存在出生队列效应:20世纪30年代和40年代出生的患者患乳腺癌的年龄比1920年前出生的患者早5.0岁和7.6岁。调整出生队列效应后,各代乳腺癌发病年龄的差异不再显著。
观察到的早现效应主要是由出生队列中发病年龄的下降驱动的,这突出了针对BRCA1/BRCA2携带者改变环境/生活方式因素进行降低风险干预的必要性。《癌症》2016年;122:1913 - 20。©2016美国癌症协会。