Division of Cancer Etiology, Department of Population Sciences, Beckman Research Institute, City of Hope, 1500 East Duarte Road, Duarte, CA 91010, USA.
Am J Epidemiol. 2010 Jun 15;171(12):1262-9. doi: 10.1093/aje/kwq090. Epub 2010 May 27.
Although advanced parental age at one's birth has been associated with increased risk of breast and prostate cancers, few studies have examined its effect on adult-onset sporadic hematologic malignancies. The authors examined the association of parents' ages at women's births with risk of hematologic malignancies among 110,999 eligible women aged 22-84 years recruited into the prospective California Teachers Study. Between 1995 and 2007, 819 women without a family history of hematologic malignancies were diagnosed with incident lymphoma, leukemia (primarily acute myeloid leukemia), or multiple myeloma. Multivariable-adjusted Cox proportional hazards models provided estimates of relative risks and 95% confidence intervals. Paternal age was positively associated with non-Hodgkin lymphoma after adjustment for race and birth order (relative risk for age > or =40 vs. <25 years = 1.51, 95% confidence interval: 1.08, 2.13; P-trend = 0.01). Further adjustment for maternal age did not materially alter the association. By contrast, the elevated non-Hodgkin lymphoma risk associated with advanced maternal age (> or =40 years) became null when paternal age was included in the statistical model. No association was observed for acute myeloid leukemia or multiple myeloma. Advanced paternal age may play a role in non-Hodgkin lymphoma etiology. Potential etiologic mechanisms include de novo gene mutations, aberrant paternal gene imprinting, or telomere/telomerase biology.
尽管出生时父母年龄较大与乳腺癌和前列腺癌风险增加有关,但很少有研究探讨其对成人发病的散发性血液系统恶性肿瘤的影响。作者研究了女性出生时父母年龄与 110999 名年龄在 22-84 岁之间符合条件的、无血液系统恶性肿瘤家族史的女性罹患血液系统恶性肿瘤的风险之间的关系。在 1995 年至 2007 年间,819 名女性被诊断患有非霍奇金淋巴瘤、白血病(主要是急性髓系白血病)或多发性骨髓瘤。多变量调整后的 Cox 比例风险模型提供了相对风险和 95%置信区间的估计值。在调整了种族和出生顺序后,父亲年龄与非霍奇金淋巴瘤呈正相关(年龄>或=40 岁与<25 岁的相对风险为 1.51,95%置信区间:1.08,2.13;P 趋势=0.01)。进一步调整母亲年龄并没有改变这种关联。相比之下,当将父亲年龄纳入统计模型时,与母亲年龄较大(>或=40 岁)相关的非霍奇金淋巴瘤风险变得没有统计学意义。急性髓系白血病或多发性骨髓瘤与父亲年龄无关。父亲年龄较大可能在非霍奇金淋巴瘤的病因中起作用。潜在的病因机制包括新发生的基因突变、父源基因印记异常或端粒/端粒酶生物学。