Grasso Chiara, Zugna Daniela, Fiano Valentina, Robles Rodriguez Nena, Maule Milena, Gillio-Tos Anna, Ciuffreda Libero, Lista Patrizia, Segnan Nereo, Merletti Franco, Richiardi Lorenzo
Cancer Epidemiology Unit-CeRMS, Department of Medical Sciences, University of Turin and CPO Piedmont, Turin, Italy.
Medical Oncology Division 1, University Hospital "Città della Salute e della Scienza", Turin, Italy.
PLoS One. 2016 Dec 30;11(12):e0169174. doi: 10.1371/journal.pone.0169174. eCollection 2016.
BACKGROUND/OBJECTIVES: It has been suggested that subfertility and testicular cancer share genetic and environmental risk factors. We studied both subfertility and the strongest known testicular cancer susceptibility gene, the c-KIT ligand (KITLG), whose pathway is involved in spermatogenesis.
The EPSAM case-control study is comprised of testicular cancer patients from the Province of Turin, Italy, diagnosed between 1997 and 2008. The present analysis included 245 cases and 436 controls from EPSAM, who were aged 20 years or older at diagnosis/recruitment. The EPSAM questionnaire collected information on factors such as number of children, age at first attempt to conceive, duration of attempt to conceive, use of assisted reproduction techniques, physician-assigned diagnosis of infertility, number of siblings, and self-reported cryptorchidism. Genotyping of the KITLG single nucleotide polymorphism (SNP) rs995030 was performed on the saliva samples of 202 cases and 329 controls.
Testicular cancer was associated with the number of children fathered 5 years before diagnosis (odds ratio (OR) per additional child: 0.78, 95% confidence interval (CI): 0.58-1.04) and sibship size (OR per additional sibling: 0.76, 95% CI: 0.66-0.88). When considering the reproductive history until 1 year before diagnosis, attempting to conceive for at least 12 months or fathering a child using assisted reproduction techniques was not associated with the risk of testicular cancer, nor was age at first attempt to conceive or physician-assigned diagnosis of infertility. The SNP rs995030 was strongly associated with risk of testicular cancer (per allele OR: 1.83; 95%CI: 1.26-2.64), but it did not modify the association between number of children and the risk of testicular cancer.
This study supports the repeatedly reported inverse association between number of children and risk of testicular cancer, but it does not find evidence of an association for other indicators of subfertility.
背景/目的:有人提出,生育力低下和睾丸癌存在共同的遗传和环境风险因素。我们对生育力低下以及已知最强的睾丸癌易感基因——c-KIT配体(KITLG)进行了研究,其通路参与精子发生过程。
EPSAM病例对照研究纳入了1997年至2008年间在意大利都灵省确诊的睾丸癌患者。本分析包括来自EPSAM的245例病例和436例对照,他们在诊断/招募时年龄在20岁及以上。EPSAM问卷收集了以下因素的信息:子女数量、首次尝试受孕年龄、尝试受孕持续时间、辅助生殖技术的使用、医生诊断的不育症、兄弟姐妹数量以及自我报告的隐睾症。对202例病例和329例对照的唾液样本进行了KITLG单核苷酸多态性(SNP)rs995030的基因分型。
睾丸癌与诊断前5年生育的子女数量相关(每增加一个孩子的比值比(OR):0.78,95%置信区间(CI):0.58 - 1.04)以及同胞数量相关(每增加一个兄弟姐妹的OR:0.76,95%CI:0.66 - 0.88)。当考虑诊断前1年的生殖史时,尝试受孕至少12个月或使用辅助生殖技术生育孩子与睾丸癌风险无关,首次尝试受孕年龄或医生诊断的不育症也与睾丸癌风险无关。SNP rs995030与睾丸癌风险密切相关(每个等位基因的OR:1.83;95%CI:1.26 - 2.64),但它并未改变子女数量与睾丸癌风险之间的关联。
本研究支持了多次报道的子女数量与睾丸癌风险之间的负相关关系,但未发现其他生育力低下指标存在关联的证据。