Perinatal factors and the risk of testicular germ cell tumors

被引:45
作者
Cook, Michael B. [1 ]
Graubard, Barry I. [1 ]
Rubertone, Mark V. [2 ]
Erickson, Ralph L. [3 ]
McGlynn, Katherine A. [1 ]
机构
[1] NCI, NIH, Hormonal & Reprod Epidemiol Branch, Div Canc Epidemiol & Genet,Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[2] USA, Ctr Hlth Promot & Prevent Med, Silver Spring, MD USA
[3] Walter Reed Army Inst Res, Silver Spring, MD USA
关键词
nonseminoma; perinatal risk factors; seminoma; testicular cancer;
D O I
10.1002/ijc.23424
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Testicular germ cell tumors (TGCT) are the most common cancer among young men in the United States and Western Europe. Prior evidence suggests that TGCT may arise in perinatal life, although few risk factors have yet been identified. To study the etiology of TGCT, the US Servicemen's Testicular Tumor Environmental and Endocrine Determinants (STEED) case-control study enrolled participants and their mothers between 2002 and 2005. Five hundred twenty-seven mothers of cases and 561 mothers of controls provided information on perinatal variables. Logistic regression was used to calculate odds ratios (OR) and 95% confidence intervals (95%Cl) associated with the candidate risk factors. Analyses were conducted for all TGCT together and for each histologic subgroup (seminoma and nonseminoma) separately. Young maternal age (<20 vs. 20-29 years, OR = 1.51, 95%Cl: 1.09-2.10), young paternal age (<25 vs. 25-29 years, OR = 1.45, 95%Cl: 1.08-1.94), maternal parity (3 vs. 1, OR = 0.63, 95%Cl: 0.44-0.90) and breech birth (OR = 1.92, 95%Cl: 1.03-3.56) were associated with risk of TGCT. For seminoma, young maternal age (<20 vs. 20-29 years, OR = 1.67, 95%Cl: 1.10-2.54), young paternal age (<25 vs. 25-29 years, OR = 1.53, 95 % Cl: 1.03-2.27), maternal parity (3 vs. 1, OR = 0.58, 95%Cl: 0.35-0.96) and low birth weight (<2,500 g vs. 2,500-4,000 g, OR = 1.82, 95%Cl: 1.00-3.30) were risk factors. Nonseminoma was associated with breech birth (OR = 2.44, 95%Cl: 1.25-4.78) and Cesarean section (OR = 2.10, 95%Cl: 1.25-3.54). These results support the hypothesis that TGCT may originate in very early life. (c) 2008 Wiley-Liss, Inc.
引用
收藏
页码:2600 / 2606
页数:7
相关论文
共 48 条
  • [31] Birth order, sibship size, and risk for germ-cell testicular cancer
    Richiardi, L
    Akre, O
    Lambe, M
    Granath, F
    Montgomery, SM
    Ekbom, A
    [J]. EPIDEMIOLOGY, 2004, 15 (03) : 323 - 329
  • [32] Genetic and environmental risk factors for testicular cancer
    Richiardi, Lorenzo
    Pettersson, Andreas
    Akre, Olof
    [J]. INTERNATIONAL JOURNAL OF ANDROLOGY, 2007, 30 (04): : 230 - 240
  • [33] The Defense Medical Surveillance System and the Department of Defense serum repository: Glimpses of the future of public health surveillance
    Rubertone, MV
    Brundage, JF
    [J]. AMERICAN JOURNAL OF PUBLIC HEALTH, 2002, 92 (12) : 1900 - 1904
  • [34] Sabroe S, 1998, INT J CANCER, V78, P140, DOI 10.1002/(SICI)1097-0215(19981005)78:2<140::AID-IJC2>3.0.CO
  • [35] 2-Z
  • [36] Sanderson M, 1998, AM J EPIDEMIOL, V147, P136
  • [37] The 'oestrogen hypothesis' - where do we stand now?
    Sharpe, RM
    [J]. INTERNATIONAL JOURNAL OF ANDROLOGY, 2003, 26 (01): : 2 - 15
  • [38] ARE ESTROGENS INVOLVED IN FALLING SPERM COUNTS AND DISORDERS OF THE MALE REPRODUCTIVE-TRACT
    SHARPE, RM
    SKAKKEBAEK, NE
    [J]. LANCET, 1993, 341 (8857) : 1392 - 1395
  • [39] SKAKKEBAEK NE, 1972, LANCET, V2, P516
  • [40] Sonke GS, 2007, ONCOL RES, V16, P383