Age at menarche and age at menopause in relation to hepatocellular carcinoma in women

被引:13
作者
Mucci, LA
Kuper, HE
Tamimi, R
Lagiou, P
Spanos, E
Trichopoulos, D
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[2] Univ Athens, Sch Med, Dept Hyg & Epidemiol, GR-11527 Athens, Greece
来源
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY | 2001年 / 108卷 / 03期
关键词
D O I
暂无
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objectives To assess whether age at menarche, age at menopause, parity. and selected blood hormones are associated with risk of hepatocellular carcinoma among women. Design Case-control. Sample and setting Data collected from 50 cases of hepatocellular carcinoma among women and 62 female controls with minor trauma or surgical conditions who attended one of three hospitals in Athens, Greece between 1995 and 1998. Methods Researchers collected information on Reproductive variables and assayed sera samples for blood hormone levels and for chronic infection with Hepatitis B and C viruses. Results Individuals with hepatocellular carcinoma had a lower mean age at menarche and a significantly higher mean age at menopause. After adjusting for potential confounding, age at menopause remained an important and significant predictor, increasing the risk of hepatocellular carcinoma 24% for each later year of menopause (P < 0.001). For each year that menarche was delayed, risk of hepatocellular carcinoma declined 21% (P = 0.100). Mean levels of insulin-like growth factor-1 and its binding protein were significantly reduced in cases compared with controls, while levels of oestradiol, testosterone and sex hormone binding globulin were somewhat higher among the cases, Conclusions This study provides indirect, but converging evidence that steroid hormones in general, and oestrogens in particular, play an important role in the aetiology of hepatocellular carcinoma among women.
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页码:291 / 294
页数:4
相关论文
共 33 条
[1]  
Breslow N.E., 1980, STAT METHODS CANC RE, P192
[2]   p53 mutations in hepatocellular carcinoma related to oral contraceptive use [J].
DeBenedetti, VMG ;
Welsh, JA ;
Yu, MC ;
Bennett, WP .
CARCINOGENESIS, 1996, 17 (01) :145-149
[3]   CANCER OF THE LIVER AND THE USE OF ORAL-CONTRACEPTIVES [J].
FORMAN, D ;
VINCENT, TJ ;
DOLL, R .
BRITISH MEDICAL JOURNAL, 1986, 292 (6532) :1357-1361
[4]   Oral contraceptives and liver cancer - Results of the multicentre international liver tumor study (MILTS) [J].
Heinemann, LAJ ;
DoMinh, T ;
Guggenmoos-Holzmann, I ;
Thiel, C ;
Garbe, E ;
Feinstein, AR ;
Thomas, D ;
Brechot, C ;
Spitzer, WO ;
Watanabe, S ;
Beral, V ;
Meirik, O .
CONTRACEPTION, 1997, 56 (05) :275-284
[5]   HEPATOCELLULAR-CARCINOMA AND ORAL-CONTRACEPTIVES [J].
HENDERSON, BE ;
PRESTONMARTIN, S ;
EDMONDSON, HA ;
PETERS, RL ;
PIKE, MC .
BRITISH JOURNAL OF CANCER, 1983, 48 (03) :437-440
[6]   ORAL-CONTRACEPTIVES AND PRIMARY LIVER-CANCER AMONG YOUNG-WOMEN [J].
HSING, AW ;
HOOVER, RN ;
MCLAUGHLIN, JK ;
COCHIEN, HT ;
WACHOLDER, S ;
BLOT, WJ ;
FRAUMENI, JF .
CANCER CAUSES & CONTROL, 1992, 3 (01) :43-48
[7]   CONTRACEPTIVE STEROIDS AS A RISK FACTOR FOR HEPATOCELLULAR-CARCINOMA - A CASE CONTROL STUDY IN SOUTH-AFRICAN BLACK-WOMEN [J].
KEW, MC ;
SONG, E ;
MOHAMMED, A ;
HODKINSON, J .
HEPATOLOGY, 1990, 11 (02) :298-302
[8]  
Kuper H, 2000, INT J CANCER, V85, P498, DOI 10.1002/(SICI)1097-0215(20000215)85:4&lt
[9]  
498::AID-IJC9&gt
[10]  
3.0.CO