Bruun Laila, Becker Charlotte, Hugosson Jonas, Lilja Hans, Christensson Anders
Department of Nephrology and Transplantation, Lund University, University Hospital (UMAS), Malmö, Sweden.
Prostate. 2005 Nov 1;65(3):216-21. doi: 10.1002/pros.20286.
The degree of variability in prostate-specific antigen (PSA) measurements is important for interpreting test results in screening programs, and particularly for interpreting the significance of changes between repeated tests. This study aimed to determine the long-term intra-individual variation for PSA in healthy men.
A randomly selected cohort of men in a biennial prostate cancer screening program (ERSPC) conducted in Sweden from 1995-1996 to 2001-2002. We studied men who had total PSA (tPSA) levels < 2.0 ng/ml in 2001-2002. This included 791 men with tPSA < or = 0.61 ng/ml (group A), 1,542 men with tPSA < or = 0.99 ng/ml (group B), and 1,029 men with tPSA 1.00-1.99 ng/ml (group C). The intra-individual variability of free PSA (fPSA) and tPSA was assessed by calculating coefficients of variation (CV) for each individual's PSA measurements from the first and second round of screening (1995-1996 and 1997-1998).
Intra-individual CV (geometric means) for tPSA were 13.7%, 12.7%, and 11.5% in groups A, B, and C, respectively. Corresponding CVs for fPSA were significantly lower, ranging from 12.1% to 10.4%. The estimated biological variation of tPSA and fPSA in groups A to C were 12.5%, 11.4%, 10.0% and 9.7%, 7.8%, 7.5%, respectively.
In healthy men with PSA levels less than 2 ng/ml, the natural long-term variability for tPSA was less than 14%, and with 95% probability, a change in tPSA greater than 30% indicates a change beyond normal random variation.
前列腺特异性抗原(PSA)测量值的变异程度对于解读筛查项目中的检测结果很重要,尤其对于解读重复检测之间变化的意义。本研究旨在确定健康男性PSA的长期个体内变异。
在瑞典于1995 - 1996年至2001 - 2002年开展的一项两年一次的前列腺癌筛查项目(ERSPC)中随机选取一组男性。我们研究了在2001 - 2002年总PSA(tPSA)水平<2.0 ng/ml的男性。这包括791名tPSA≤0.61 ng/ml的男性(A组)、1542名tPSA≤0.99 ng/ml的男性(B组)以及1029名tPSA为1.00 - 1.99 ng/ml的男性(C组)。通过计算每位男性在第一轮和第二轮筛查(1995 - 1996年和1997 - 1998年)中PSA测量值的变异系数(CV)来评估游离PSA(fPSA)和tPSA的个体内变异性。
A组、B组和C组中tPSA的个体内CV(几何均值)分别为13.7%、12.7%和11.5%。fPSA的相应CV显著更低,范围为12.1%至10.4%。A组至C组中tPSA和fPSA的估计生物学变异分别为12.5%、11.4%、10.0%和9.7%、7.8%、7.5%。
在PSA水平低于2 ng/ml的健康男性中,tPSA的自然长期变异小于14%,并且有95%的概率,tPSA变化大于30%表明变化超出正常随机变异范围。