Bonner Matthew R, McCann Susan E, Moysich Kirsten B
Department of Social and Preventive Medicine, University at Buffalo, Buffalo, NY 14214, USA.
Nutr Cancer. 2002;44(1):35-43. doi: 10.1207/S15327914NC441_5.
The etiology of testicular cancer (TC) remains largely unknown. Few studies have investigated the role diet may play in the etiology of TC. We report on a hospital-based case-control study of TC and selected nutrients and food groups. Cases included 117 patients with primary, incident TC treated at Roswell Park Cancer Institute between 1982 and 1998. A total of 334 hospital controls were frequency matched on age to cases. Cases were categorized by histology (seminoma, nonseminoma, and mixed germ cell TC), and multinomial logistic regression and unconditional logistic regression were used to compute odds ratios (ORs) and 95% confidence intervals (CIs) comparing each histological type with the controls. For nonseminoma and mixed germ cell TC, vitamin E intake was suggestive of reduced risk (OR = 0.51, 95% CI = 0.15-1.76 and OR = 0.36, 95% CI = 0.01-1.31, respectively); for seminoma, it was suggestive of an increased risk (OR = 2.94, 95% CI = 0.99-8.78). Fat intakes were not associated with nonseminoma or mixed germ cell risk; high saturated, animal, and total fat intakes were suggestive of an increase in risk of seminoma. Overall, diet was not associated with TC. However, risk seemed to differ by histology, suggesting that seminoma, nonseminoma, and mixed germ cell TC may have different etiologies. We suggest that future investigations should continue to stratify cases by histology.
睾丸癌(TC)的病因在很大程度上仍然未知。很少有研究调查饮食在TC病因中可能起的作用。我们报告了一项基于医院的TC与选定营养素和食物组的病例对照研究。病例包括1982年至1998年期间在罗斯韦尔公园癌症研究所接受治疗的117例原发性、新发TC患者。总共334名医院对照按年龄与病例进行频率匹配。病例按组织学分类(精原细胞瘤、非精原细胞瘤和混合性生殖细胞TC),并使用多项逻辑回归和无条件逻辑回归计算比值比(OR)和95%置信区间(CI),将每种组织学类型与对照进行比较。对于非精原细胞瘤和混合性生殖细胞TC,维生素E摄入量提示风险降低(OR分别为0.51,95%CI为0.15 - 1.76和OR为0.36,95%CI为0.01 - 1.31);对于精原细胞瘤,提示风险增加(OR = 2.94,95%CI = 0.99 - 8.78)。脂肪摄入量与非精原细胞瘤或混合性生殖细胞风险无关;高饱和脂肪、动物脂肪和总脂肪摄入量提示精原细胞瘤风险增加。总体而言,饮食与TC无关。然而,风险似乎因组织学而异,这表明精原细胞瘤、非精原细胞瘤和混合性生殖细胞TC可能有不同的病因。我们建议未来的研究应继续按组织学对病例进行分层。