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[使用特异性和灵敏的酶联免疫吸附测定法“E-plate EIKEN PSA”检测游离前列腺特异性抗原(PSA)、α1-抗糜蛋白酶复合PSA及游离/总PSA比值的临床应用]

[Clinical utility of the free prostate specific antigen (PSA), alpha 1-antichymotrypsin-complexed PSA, and free/total PSA ratio using the specific and sensitive enzyme-linked immunosorbent assay "E-plate EIKEN PSA"].

作者信息

Imai K, Yamanaka H, Kubota Y, Miki M, Ito T, Akaza H, Uchida K, Egawa S, Kuriyama M, Watanabe H, Okihara K, Kotake T, Usami M, Arai Y, Maeda H, Sagiyama K, Saito Y, Sakai H, Shida K

机构信息

Atagawa Onsen Hospital.

出版信息

Hinyokika Kiyo. 1998 Oct;44(10):755-63.

PMID:9850846
Abstract

We studied the clinical significance of serum prostate specific antigen (PSA) ratio: free-PSA/total-PSA and free-PSA/complex-PSA to discriminate between prostate cancer (PC) and prostate benign disease (non-PCa) by using total-PSA, alpha 1-antichymotrypsin complexed (complex)-PSA and free-PSA enzyme-linked immunosorbent assay (ELISA) kits newly developed at EIKEN Chemical Co, Ltd. Fre-PSA and complex-PSA ELISA kits demonstrated high sensitivity and specificity. Total-PSA ELISA kit also demonstrated equimolarity for free-PSA and complex-PSA. On the total-PSA range of 4-10 ng/ml, free-PSA/total-PSA% (f/t%) and free-PSA/complex-PSA% (f/c%) were very useful to discriminate between PCa and non-PCa by receiver operating characteristic curve analysis as well as PSA density (PSA-D) but not free-PSA level. F/t% and f/c% were even useful to discriminate early stage PCa (i.e. A1 or B0) from non-PCa by the Mann-Whitney U-test.

摘要

我们使用由荣研化学株式会社新开发的总前列腺特异性抗原(PSA)、α1-抗糜蛋白酶复合(复合)PSA和游离PSA酶联免疫吸附测定(ELISA)试剂盒,研究了血清PSA比值:游离PSA/总PSA和游离PSA/复合PSA在鉴别前列腺癌(PC)和前列腺良性疾病(非PCa)方面的临床意义。游离PSA和复合PSA ELISA试剂盒显示出高灵敏度和特异性。总PSA ELISA试剂盒对游离PSA和复合PSA也显示出等摩尔性。在总PSA范围为4 - 10 ng/ml时,通过受试者工作特征曲线分析以及PSA密度(PSA-D),游离PSA/总PSA%(f/t%)和游离PSA/复合PSA%(f/c%)在鉴别PCa和非PCa方面非常有用,但游离PSA水平则不然。通过曼-惠特尼U检验,f/t%和f/c%在鉴别早期PCa(即A1或B0)和非PCa方面甚至也很有用。

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