Insulin-like growth factors and risk of benign prostatic hyperplasia

被引:66
作者
Chokkalingam, AP
Gao, YT
Deng, J
Stanczyk, FZ
Sesterhenn, IA
Mostofi, FK
Fraumeni, JF
Hsing, AW
机构
[1] Natl Canc Inst, Div Canc Epidemiol & Genet, Rockville, MD 20852 USA
[2] Shanghai Canc Inst, Shanghai, Peoples R China
[3] Univ So Calif, Keck Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90089 USA
[4] Univ So Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA 90089 USA
[5] Armed Forces Inst Pathol, Washington, DC 20306 USA
关键词
IGF; growth factors; binding proteins; China; epidemiology;
D O I
10.1002/pros.10096
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. Insulin-like growth factors (IGFs) have potent mitogenic and antiapoptotic effects on prostate tissue, whereas IGF binding proteins (IGFBI's) inhibit growth of prostatic tissue. The IGF axis has been implicated in prostate cancer risk, but its role in benign prostatic hyperplasia (BPH) is unclear. METHODS. Plasma levels of IGF-I, IGF II, IGFBP-1, and IGFBP-3 were determined from the fasting bloods of 206 BPH cases admitted for treatment and 306 randomly selected population controls in Shanghai, China. RESULTS. Relative to the lowest tertile, men in the highest tertile of IGF-I levels had a significantly elevated risk of BPH (odds ratio [OR]=2.80, 95% confidence interval [95%, CI] =1.60-4.92; P-trend < 0.001). Results for IGF-I were more pronounced after adjustment for serum androgens. In contrast, men in the highest IGFBP-3 tertile had a significantly reduced risk (OR=0.40; 95% CI=0.23-0.69; P-trend < 0.001). No associations of BPH with IGF-II and IGFBP-1 were observed. CONCLUSION. As has been previously observed for prostate cancer, we found that IGF-I and IGFBP-3 are associated with BPH risk in China. Further investigation is needed to elucidate the role of the IGF axis in BPH etiology.
引用
收藏
页码:98 / 105
页数:8
相关论文
共 27 条
  • [1] THE DEVELOPMENT OF HUMAN BENIGN PROSTATIC HYPERPLASIA WITH AGE
    BERRY, SJ
    COFFEY, DS
    WALSH, PC
    EWING, LL
    [J]. JOURNAL OF UROLOGY, 1984, 132 (03) : 474 - 479
  • [2] Breslow NE, 1980, IARC SCI PUBL, V1
  • [3] Plasma insulin-like growth factor I and prostate cancer risk: A prospective study
    Chan, JM
    Stampfer, MJ
    Giovannucci, E
    Gann, PH
    Ma, J
    Wilkinson, P
    Hennekens, CH
    Pollak, M
    [J]. SCIENCE, 1998, 279 (5350) : 563 - 566
  • [4] Chokkalingam AP, 2001, CANCER EPIDEM BIOMAR, V10, P421
  • [5] Chokkalingam AP, 2001, CANCER RES, V61, P4333
  • [6] INSULIN-LIKE GROWTH-FACTOR AXIS ABNORMALITIES IN PROSTATIC STROMAL CELLS FROM PATIENTS WITH BENIGN PROSTATIC HYPERPLASIA
    COHEN, P
    PEEHL, DM
    BAKER, B
    LIU, F
    HINTZ, RL
    ROSENFELD, RG
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (05) : 1410 - 1415
  • [7] INSULIN-LIKE GROWTH-FACTORS (IGFS), IGF RECEPTORS, AND IGF-BINDING PROTEINS IN PRIMARY CULTURES OF PROSTATE EPITHELIAL-CELLS
    COHEN, P
    PEEHL, DM
    LAMSON, G
    ROSENFELD, RG
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 73 (02) : 401 - 407
  • [8] Effect of two years of growth hormone and insulin-like growth factor-I suppression on prostate diseases in acromegalic patients
    Colao, A
    Marzullo, P
    Spiezia, S
    Giaccio, A
    Ferone, D
    Cerbone, G
    Di Sarno, A
    Lombardi, G
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (10) : 3754 - 3761
  • [9] GRIGNON D, 1994, IN VIVO, V8, P415
  • [10] Grimberg A, 2000, J CELL PHYSIOL, V183, P1, DOI 10.1002/(SICI)1097-4652(200004)183:1<1::AID-JCP1>3.0.CO