Richiardi L, Akre O, Bellocco R, Ekbom A
Department of Medical Epidemiology, Karolinska Institute, Berzelius väg 15C, SE-17177 Stockholm, Sweden.
Br J Cancer. 2002 Aug 27;87(5):545-50. doi: 10.1038/sj.bjc.6600470.
We aimed to investigate the role of perinatal determinants on the risk for germ-cell testicular cancer, with respect to the aetiological heterogeneity between seminomas and non-seminomas. A case-control study of 628 case patients with testicular cancer (308 seminomas and 320 non-seminomas) and 2309 individually matched controls was nested within a cohort of boys born from 1920 to 1980 in two Swedish regions (Uppsala-Orebro Health Care Region and Stockholm). Cases were diagnosed from 1958 to 1998 and were identified through the Swedish National Cancer Registry. Perinatal information on cases and controls was collected through charts available at maternity wards. Gestational duration, categorised in three categories (<37, 37-41, >41 weeks), was negatively associated with the risk for testicular cancer (P value for linear trend=0.008). A protective effect of long gestational duration and an increased risk for high birth weight were found for seminomas. Non-seminomas were associated with short gestational duration, particularly among those with low birth order (odds ratio: 3.02, 95% confidence intervals: 1.53-5.97) and high maternal age (odds ratio: 2.33, 95% confidence intervals: 1.19-4.55). No significant differences were found in tests for heterogeneity between the two histological groups. Our data support the hypothesis that intrauterine environment affects the risk for germ-cell testicular cancer. Seminomas and non-seminomas seemed to have similar risk patterns, although they are not entirely congruent.
我们旨在研究围产期决定因素在睾丸生殖细胞癌风险中的作用,同时考虑精原细胞瘤和非精原细胞瘤之间的病因异质性。一项病例对照研究纳入了628例睾丸癌患者(308例精原细胞瘤和320例非精原细胞瘤)以及2309例个体匹配的对照,该研究嵌套于1920年至1980年在瑞典两个地区(乌普萨拉 - 厄勒布鲁医疗保健地区和斯德哥尔摩)出生的男孩队列中。病例于1958年至1998年被诊断出来,并通过瑞典国家癌症登记处识别。病例和对照的围产期信息通过产科病房的病历收集。孕期持续时间分为三类(<37周、37 - 41周、>41周),与睾丸癌风险呈负相关(线性趋势P值 = 0.008)。发现孕期持续时间长对精原细胞瘤有保护作用,而出生体重高会增加精原细胞瘤风险。非精原细胞瘤与孕期持续时间短有关,特别是在出生顺序低的人群中(比值比:3.02,95%置信区间:1.53 - 5.97)以及母亲年龄大的人群中(比值比:2.33,95%置信区间:1.19 - 4.55)。在两个组织学组之间的异质性检验中未发现显著差异。我们的数据支持子宫内环境影响睾丸生殖细胞癌风险的假设。精原细胞瘤和非精原细胞瘤似乎具有相似的风险模式,尽管它们并不完全一致。