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前列腺特异性抗原水平低预示前列腺癌的长期风险:来自巴尔的摩纵向衰老研究的结果。

Low levels of prostate-specific antigen predict long-term risk of prostate cancer: results from the Baltimore Longitudinal Study of Aging.

作者信息

Fang J, Metter E J, Landis P, Chan D W, Morrell C H, Carter H B

机构信息

National Institute on Aging, Gerontology Research Center, Baltimore, Maryland, USA.

出版信息

Urology. 2001 Sep;58(3):411-6. doi: 10.1016/s0090-4295(01)01304-8.

Abstract

OBJECTIVES

To evaluate the relationship between low prostate-specific antigen (PSA) levels that are considered normal and the long-term risk of prostate cancer.

METHODS

The relative risk of, and cumulative probability of freedom from, prostate cancer by PSA level and age decade was evaluated in male participants of a longitudinal aging study, the Baltimore Longitudinal Study of Aging (National Institute on Aging). The relative risk was estimated from a Cox proportional hazards regression model for men aged 40 to 49.9 (n = 351) and 50 to 59.9 (n = 445). The disease-free probability was determined by Kaplan-Meier survival analysis.

RESULTS

The relative risk of prostate cancer for men aged 40 to 49.9 was 3.75 (range 1.6 to 8.6) when the PSA level was at or greater than the median (0.60 ng/mL) compared with men with PSA levels less than the median. This risk was similar for men aged 50 to 59.9 when comparing those with PSA levels greater than and less than the median (0.71 ng/mL). At 25 years, the cumulative probability of freedom from prostate cancer for men aged 40 to 49.9 was 89.6% (range 81% to 97%) and 71.6% (range 60% to 83%) when the PSA level was less than and greater than the median, respectively. The 25-year disease-free probability for men aged 50 to 59.9 was 83.6% (range 76% to 91%) and 58.9% (range 48% to 70%) when the PSA level was less than and greater than the median, respectively.

CONCLUSIONS

The association between the baseline serum PSA level and the subsequent risk of prostate cancer suggests that the biologic events that predispose to prostate cancer begin early in middle age. Men who have baseline PSA levels that are "normal" but reflect a higher risk of prostate cancer may be the most appropriate candidates for future prevention trials. Those men with the lowest risk of prostate cancer on the basis of the baseline PSA measurements are unlikely to benefit from frequent PSA surveillance in an effort to detect prostate cancer early.

摘要

目的

评估被视为正常的低前列腺特异性抗原(PSA)水平与前列腺癌长期风险之间的关系。

方法

在一项纵向衰老研究——巴尔的摩纵向衰老研究(美国国立衰老研究所)的男性参与者中,按PSA水平和年龄十年评估前列腺癌的相对风险以及无前列腺癌的累积概率。通过Cox比例风险回归模型估计40至49.9岁男性(n = 351)和50至59.9岁男性(n = 445)的相对风险。通过Kaplan-Meier生存分析确定无病概率。

结果

与PSA水平低于中位数的男性相比,40至49.9岁男性当PSA水平等于或高于中位数(0.60 ng/mL)时,前列腺癌的相对风险为3.75(范围1.6至8.6)。在比较PSA水平高于和低于中位数(0.71 ng/mL)的50至59.9岁男性时,该风险相似。25年后,40至49.9岁男性当PSA水平低于和高于中位数时,无前列腺癌的累积概率分别为89.6%(范围81%至97%)和71.6%(范围60%至83%)。50至59.9岁男性当PSA水平低于和高于中位数时,25年无病概率分别为83.6%(范围76%至91%)和58.9%(范围48%至70%)。

结论

基线血清PSA水平与随后前列腺癌风险之间的关联表明,易患前列腺癌的生物学事件在中年早期就开始了。基线PSA水平“正常”但反映出较高前列腺癌风险的男性可能是未来预防试验的最合适人选。基于基线PSA测量前列腺癌风险最低的那些男性不太可能从频繁的PSA监测中受益以早期检测前列腺癌。

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