Bunker Clareann H, Zmuda Joseph M, Patrick Alan L, Wheeler Victor W, Weissfeld Joel L, Kuller Lewis H, Cauley Jane A
Department of Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Cancer Causes Control. 2006 Oct;17(8):1083-9. doi: 10.1007/s10552-006-0047-1.
To test the hypothesis that bone mineral density (BMD), a possible surrogate of lifetime exposure to hormone/growth factor/vitamin D/calcium exposure, is higher in prostate cancer cases than controls.
Hip BMD was measured by dual X-ray absorptiometry in 222 Afro-Caribbean screening-detected prostate cancer cases and 1,503 screened non-cases, aged 45-79, in the population-based Tobago Prostate Survey. Because possible skeletal metastases may modulate BMD, men with prostate specific antigen >20 ng/ml or highly undifferentiated tumors (Gleason score > or = 8) were excluded. Mean BMD, adjusted for age and body mass index, was compared in cases and non-cases by analysis of variance. Risk across age group-specific BMD quartiles was compared using logistic regression.
Overall, adjusted mean hip BMD was higher in cases (1.157 g/cm2) than non-cases (1.134 g/cm2) (p = 0.02). In men aged 60-79, prostate cancer risk was two-fold higher (OR, 2.12; 95% CI: 1.21-3.71) in the highest BMD quartile compared to the lowest. There was no association in younger men (interaction, p = 0.055).
High bone density is associated with prostate cancer among older men, consistent with an etiological role for lifetime exposure to factors which modulate bone density. However, other etiologies may dominate prostate cancer risk among younger men.
检验以下假设,即骨矿物质密度(BMD)作为终生激素/生长因子/维生素D/钙暴露的一个可能替代指标,在前列腺癌病例中高于对照组。
在基于人群的多巴哥前列腺调查中,采用双能X线吸收法测量了222例非洲加勒比裔经筛查发现的前列腺癌病例和1503例经筛查的非病例(年龄在45 - 79岁)的髋部骨密度。由于可能的骨转移会调节骨密度,因此排除了前列腺特异性抗原>20 ng/ml或高度未分化肿瘤(Gleason评分>或 = 8)的男性。通过方差分析比较病例组和非病例组经年龄和体重指数调整后的平均骨密度。使用逻辑回归比较各年龄组特定骨密度四分位数的风险。
总体而言,病例组经调整后的平均髋部骨密度(1.157 g/cm²)高于非病例组(1.134 g/cm²)(p = 0.02)。在60 - 79岁的男性中,骨密度最高四分位数组的前列腺癌风险是最低四分位数组的两倍(OR,2.12;95% CI:1.21 - 3.71)。在较年轻男性中无关联(交互作用,p = 0.055)。
高骨密度与老年男性的前列腺癌相关,这与终生暴露于调节骨密度的因素的病因学作用一致。然而,其他病因可能在年轻男性的前列腺癌风险中占主导地位。