NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Measurement of circulating forms of prostate-specific antigen in whole blood immediately after venipuncture: implications for point-of-care testing.

Author(s): Piironen T, Nurmi M, Irjala K, Heinonen O, Lilja H, Lövgren T, Pettersson K

Publication: Clin Chem, 2001, Vol. 47, Page 703-11

PubMed ID: 11274021 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of delayed analysis, exercise prior to specimen collection, and the use of EDTA or heparin anticoagulated whole blood or plasma versus serum to measure total prostate specific antigen (PSA-T), free PSA (PSA-F), and PSA-alpha1-antichymotrypsin complex (PSA-ACT).

Conclusion of Paper

Delayed analysis for up to 48 hours, exercise prior to specimen collection, and the use of anticoagulated whole blood rather than serum had no effects on the measurement of PSA-T, PSA-F, or PSA-ACT in specimens from males.

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of delayed analysis, exercise prior to specimen collection, and the use of EDTA or heparin anticoagulated whole blood or plasma versus serum to measure PSA-T, PSA-F, and PSA-ACT. The effects of delayed analysis were observed by either measuring the recovery of purified PSA, from spiked blood and serum from females, at defined time points during storage at room temperature, or by measuring endogenous PSA at defined time points after venipuncture. Exercise consisted of 15 minutes on a stationary bike.

    Summary of Findings:

    Riding a stationary bike for 15 minutes prior to specimen collection did not affect the amount of PSA-T, PSA-F, or PSA-ACT measured in EDTA whole blood compared with levels measured in specimens collected before the exercise, even when analysis of the blood was delayed for up to 100 minutes. When purified PSA was used to spike serum from a female, the majority of enzymatic reactivity was gone after a 15 minute delay before analysis. The authors state that the elimination curves of purified PSA-F were similar between serum, EDTA whole blood, heparin whole blood, EDTA plasma, and heparin plasma. For both healthy males and those with prostate cancer or benign prostatic hyperplasia, room temperature storage of heparin whole blood, EDTA whole blood, or serum prior to analysis, for up to 48 h (healthy) or 4 h (patients), did not affect PSA-T, PSA-F, or PSA-ACT (measured for patients only). Very strong correlations in PSA-T and PSA-F values were observed between whole blood and serum specimens.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Normal
    • Neoplastic - Benign
    • Neoplastic - Carcinoma
    Platform:
    AnalyteTechnology Platform
    Glycoprotein Immunoassay
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Acquisition Time of biospecimen collection Prior to exercise
    After exercise
    Storage Time at room temperature 1 min
    15 min
    30 min
    60 min
    100 min
    2 h
    4 h
    12 h
    48 h
    Biospecimen Aliquots and Components Blood and blood products Plasma
    Serum
    Whole blood
    Biospecimen Acquisition Anticoagulant EDTA
    Heparin

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