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睾丸癌风险与母亲生育胎次:一项基于人群的队列研究。

Testicular cancer risk and maternal parity: a population-based cohort study.

作者信息

Westergaard T, Andersen P K, Pedersen J B, Frisch M, Olsen J H, Melbye M

机构信息

Department of Epidemiology Research, Danish Epidemiology Science Centre, Statens Serum Institut, Copenhagen.

出版信息

Br J Cancer. 1998 Apr;77(7):1180-5. doi: 10.1038/bjc.1998.196.

Abstract

The aim was to study, in a population-based cohort design, whether first-born sons run a higher risk of testicular cancer than later born sons; to investigate whether this difference in risk was affected by birth cohort, age of the son, maternal age, interval to previous delivery and other reproductive factors; and, finally, to evaluate to what extent changes in women's parity over time might explain the increasing incidence of testicular cancer. By using data from the Civil Registration System, a database was established of all women born in Denmark since 1935 and all their children alive in 1968 or born later. Sons with testicular cancer were identified in the Danish Cancer Registry. Among 1015994 sons followed for 15981 967 person-years, 626 developed testicular cancer (443 non-seminomas, 183 seminomas). Later born sons had a decreased risk of testicular cancer (RR = 0.80, 95% CI = 0.67-0.95) compared with first-born sons. The RR was 0.79 (95% CI = 0.64-0.98) for non-seminomas and 0.81 (95% CI = 0.58-1.13) for seminomas. There was no association between testicular cancer risk and overall parity of the mother, maternal or paternal age at the birth of the son, or maternal age at first birth. The decreased risk of testicular cancer among later born sons was not modified by age, birth cohort, interval to the previous birth, sex of the first-born child, or maternal age at birth of the son or at first birth. The increased proportion of first-borns from birth cohort 1946 to birth cohort 1969 only explained around 3% of an approximated two-fold increase in incidence between the cohorts. Our data document a distinctly higher risk of testicular cancer in first-born compared with later born sons and suggest that the most likely explanation should be sought among exposures in utero. The increase in the proportion of first-borns in the population has only contributed marginally to the increase in testicular cancer incidence.

摘要

本研究采用基于人群的队列设计,旨在探讨长子患睾丸癌的风险是否高于晚育子;调查这种风险差异是否受出生队列、儿子年龄、母亲年龄、上次分娩间隔及其他生殖因素的影响;最后,评估女性生育胎次随时间的变化在多大程度上可解释睾丸癌发病率的上升。通过使用民事登记系统的数据,建立了一个数据库,纳入了自1935年以来出生在丹麦的所有女性及其在1968年或之后存活的所有子女。在丹麦癌症登记处识别出患睾丸癌的儿子。在随访15981967人年的1015994名儿子中,626人患睾丸癌(443例非精原细胞瘤,183例精原细胞瘤)。与长子相比,晚育子患睾丸癌的风险降低(RR = 0.80,95%CI = 0.67 - 0.95)。非精原细胞瘤的RR为0.79(95%CI = 0.64 - 0.98),精原细胞瘤的RR为0.81(95%CI = 0.58 - 1.13)。睾丸癌风险与母亲的总生育胎次、儿子出生时母亲或父亲的年龄,或母亲首次生育时的年龄之间无关联。晚育子患睾丸癌风险的降低不受年龄、出生队列、上次生育间隔、头胎孩子的性别,或儿子出生时或母亲首次生育时母亲年龄的影响。从出生队列1946年到出生队列1969年,头胎出生比例的增加仅解释了两个队列间发病率约两倍增加中的3%左右。我们的数据表明,与晚育子相比,长子患睾丸癌的风险明显更高,并提示最有可能的解释应从子宫内暴露中寻找。人群中头胎出生比例的增加对睾丸癌发病率上升的贡献微乎其微。

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