Perinatal markers of estrogen exposure and risk of testicular cancer: follow-up of 1,333,873 Danish males born between 1950 and 2002

被引:18
作者
Ramlau-Hansen, Cecilia Host [1 ]
Olesen, Anne Vingaard [2 ,3 ]
Parner, Erik Thorlund [4 ]
Sorensen, Henrik Toft [5 ,6 ]
Olsen, Jorn [7 ,8 ]
机构
[1] Aarhus Univ Hosp, Dept Occupat Med, DK-8000 Aarhus, Denmark
[2] Univ Aarhus, Inst Publ Hlth, Dept Epidemiol, Aarhus, Denmark
[3] Aarhus Univ Hosp, Aalborg Psychiat Hosp, Unit Psychiat Res, DK-8000 Aarhus, Denmark
[4] Univ Aarhus, Inst Publ Hlth, Dept Biostat, Aarhus, Denmark
[5] Aarhus Univ Hosp, Dept Clin Epidemiol, DK-8000 Aarhus, Denmark
[6] Boston Univ, Dept Epidemiol, Boston, MA 02215 USA
[7] Univ Aarhus, Inst Publ Hlth, Danish Epidemiol Sci Ctr, Aarhus, Denmark
[8] Univ Calif Los Angeles, Sch Publ Hlth, Dept Epidemiol, Los Angeles, CA 90024 USA
基金
英国医学研究理事会;
关键词
Follow-up studies; Male urogenital diseases; Prenatal exposure delayed effects; Testis cancer; GERM-CELL TUMORS; UNITED-STATES; IN-UTERO; COHORT; MEN; CRYPTORCHIDISM; METAANALYSIS; NONSEMINOMA; HYPOTHESIS; DISORDERS;
D O I
10.1007/s10552-009-9403-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective To examine whether indicators of an increased prenatal estrogen exposure correlate with risk of testicular cancer. Methods This nationwide follow-up study was conducted by linking data on prenatal exposures obtained from medical and birth records for information on incident testicular cancer cases identified from the Danish Cancer Registry. The study population included all boys born between 1950 and 2002 and alive in April 1968 or later with restriction to sons of mothers born after 1935 and alive in April 1968. Results A total of 2,151 incident testicular cancer cases were identified in 29 million person-years at risk. Men born with a high birth weight ([4,150 g) had an increased risk of testicular cancer [incidence rate ratio (IRR) = 1.6 (95% CI: 1.0, 2.4)]. Having a twin sister was associated with reduced risk [IRR = 0.5 (95% CI: 0.2, 1.1)], and the IRR for sons of mothers suffering from preeclampsia indicated a low risk [IRR = 0.6 (95% CI: 0.2, 2.0)], although none of these estimates were statistically significant. Increasing sib order and preterm birth was not associated with decreased risk. Principal conclusions Results provide no strong evidence for the hypothesis.
引用
收藏
页码:1587 / 1592
页数:6
相关论文
共 34 条
[1]   Testicular nonseminoma and seminoma in relation to perinatal characteristics [J].
Akre, O ;
Ekbom, A ;
Hsieh, CC ;
Trichopoulos, D ;
Adami, HO .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (13) :883-889
[2]  
[Anonymous], 2005, Stata Statistical Software: Release 9
[3]   Risk factors for testicular cancer - differences between pure non-seminoma and mixed seminoma/non-seminoma? [J].
Aschim, E. L. ;
Haugen, T. B. ;
Tretli, S. ;
Daltveit, A. K. ;
Grotmol, T. .
INTERNATIONAL JOURNAL OF ANDROLOGY, 2006, 29 (04) :458-467
[4]  
BERNSTEIN L, 1986, JNCI-J NATL CANCER I, V76, P1035
[5]  
Bromen K, 2004, CANCER EPIDEM BIOMAR, V13, P1316
[6]  
BROWN LM, 1986, CANCER RES, V46, P4812
[7]   Perinatal factors and the risk of testicular germ cell tumors [J].
Cook, Michael B. ;
Graubard, Barry I. ;
Rubertone, Mark V. ;
Erickson, Ralph L. ;
McGlynn, Katherine A. .
INTERNATIONAL JOURNAL OF CANCER, 2008, 122 (11) :2600-2606
[8]   How valid is the prenatal estrogen excess hypothesis of testicular germ cell cancer? [J].
Dieckmann, KP ;
Endsin, G ;
Pichlmeier, U .
EUROPEAN UROLOGY, 2001, 40 (06) :677-683
[9]   Subfertility and the risk of testicular germ cell tumors (United States) [J].
Doria-Rose, VP ;
Biggs, ML ;
Weiss, NS .
CANCER CAUSES & CONTROL, 2005, 16 (06) :651-656
[10]   Growing evidence that several human cancers may originate in utero [J].
Ekbom, A .
SEMINARS IN CANCER BIOLOGY, 1998, 8 (04) :237-244