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[采用新开发的乳胶比浊免疫分析法测定血清PSA和PAP的价值]

[Value of serum PSA and PAP measurement with newly developed latex turbidimetric immunoassay].

作者信息

Akino H, Tsuka H, Okada K, Tsuchiya Y, Matsubara M, Arimura K

机构信息

Department of Urology, Fukui Medical School.

出版信息

Hinyokika Kiyo. 1995 Jun;41(6):439-45.

PMID:7544063
Abstract

Serum prostate specific antigen (PSA) and prostatic acid-phosphatase (PAP) levels in normal controls, and patients with prostate cancer, benign prostate hypertrophy (BPH) and other urological diseases were examined with a newly developed latex turbidimetric immunoassay (LPIA ACE PSA, LPIA ACE PAP, IATRON LABORATORIES, INC., Tokyo, Japan). The advantageous characteristics of this method are small amount (10 microliters) of serum required and short time (about 20 min.) for performing this assay. There was a high linear correlation between LPIA ACE PSA and MARKIT-F PA (r2 = 0.953), between LPIA ACE PSA and TANDEM-E PSA (r2 = 0.881) and between LPIA ACE PAP and ABBOTT-PAP EIA (r2 = 0.946). When the BPH patients (n = 110) were used as negative controls, the cut-off value of PSA was determined to be 4.3 ng/ml. Using this level as the cut-off value, the sensitivity was 78% (42 positive/54 untreated prostate cancer patients), specificity (negative rate in BPH patients) was 95% and efficiency was 89%. In a follow-up study of prostate cancer, the PSA value was elevated above the cut-off value in 68% at the time of clinical progression. These findings suggest that LPIA ACE PSA is a useful tool for serum PSA measurement. The cut-off value of PAP measured with LPIA ACE PAP was 9.0 ng/ml, which was determined by the same method as PSA. The sensitivity, specificity and efficiency ware 39%, 96% and 77%, respectively. These findings indicate that PAP is less useful than PSA in the diagnosis of prostate cancer.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用新开发的乳胶比浊免疫分析法(LPIA ACE PSA、LPIA ACE PAP,日本东京医创株式会社)检测正常对照者以及前列腺癌、良性前列腺增生(BPH)和其他泌尿系统疾病患者的血清前列腺特异性抗原(PSA)和前列腺酸性磷酸酶(PAP)水平。该方法的优势在于所需血清量少(10微升)且检测时间短(约20分钟)。LPIA ACE PSA与MARKIT - F PA之间(r2 = 0.953)、LPIA ACE PSA与TANDEM - E PSA之间(r2 = 0.881)以及LPIA ACE PAP与ABBOTT - PAP EIA之间(r2 = 0.946)存在高度线性相关性。以BPH患者(n = 110)作为阴性对照时,PSA的临界值确定为4.3纳克/毫升。以此水平作为临界值,敏感性为78%(42例阳性/54例未经治疗的前列腺癌患者),特异性(BPH患者中的阴性率)为95%,效率为89%。在前列腺癌的随访研究中,临床进展时68%的患者PSA值高于临界值。这些结果表明LPIA ACE PSA是血清PSA检测的有用工具。用LPIA ACE PAP检测的PAP临界值为9.0纳克/毫升,其确定方法与PSA相同。敏感性、特异性和效率分别为39%、96%和77%。这些结果表明,在前列腺癌诊断中PAP不如PSA有用。(摘要截短至250字)

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