Alpha-fetoprotein in plasma and serum of healthy adults: Preanalytical, analytical and biological sources of variation and construction of age-dependent reference intervals

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Standard

Alpha-fetoprotein in plasma and serum of healthy adults : Preanalytical, analytical and biological sources of variation and construction of age-dependent reference intervals. / Christiansen, Michael; Høgdall, Claus Kim; Andersen, Jens Rikardt; Nørgaard-Pedersen, B.

In: Scandinavian Journal of Clinical and Laboratory Investigation, Vol. 61, No. 3, 2001, p. 205-215.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Christiansen, M, Høgdall, CK, Andersen, JR & Nørgaard-Pedersen, B 2001, 'Alpha-fetoprotein in plasma and serum of healthy adults: Preanalytical, analytical and biological sources of variation and construction of age-dependent reference intervals', Scandinavian Journal of Clinical and Laboratory Investigation, vol. 61, no. 3, pp. 205-215. https://doi.org/10.1080/003655101300133649

APA

Christiansen, M., Høgdall, C. K., Andersen, J. R., & Nørgaard-Pedersen, B. (2001). Alpha-fetoprotein in plasma and serum of healthy adults: Preanalytical, analytical and biological sources of variation and construction of age-dependent reference intervals. Scandinavian Journal of Clinical and Laboratory Investigation, 61(3), 205-215. https://doi.org/10.1080/003655101300133649

Vancouver

Christiansen M, Høgdall CK, Andersen JR, Nørgaard-Pedersen B. Alpha-fetoprotein in plasma and serum of healthy adults: Preanalytical, analytical and biological sources of variation and construction of age-dependent reference intervals. Scandinavian Journal of Clinical and Laboratory Investigation. 2001;61(3):205-215. https://doi.org/10.1080/003655101300133649

Author

Christiansen, Michael ; Høgdall, Claus Kim ; Andersen, Jens Rikardt ; Nørgaard-Pedersen, B. / Alpha-fetoprotein in plasma and serum of healthy adults : Preanalytical, analytical and biological sources of variation and construction of age-dependent reference intervals. In: Scandinavian Journal of Clinical and Laboratory Investigation. 2001 ; Vol. 61, No. 3. pp. 205-215.

Bibtex

@article{4b09c897991a49e38a75aa21916b12ad,
title = "Alpha-fetoprotein in plasma and serum of healthy adults: Preanalytical, analytical and biological sources of variation and construction of age-dependent reference intervals",
abstract = "Alpha-fetoprotein (AFP) is a tumor marker for hepatomas and germ cell tumors, and the serum concentration has prognostic significance in other diseases. We examined the normal serum concentration of AFP in adults and sources of variation in the immunochemical variation of AFP. The serum concentration of the tumor marker alpha-fetoprotein (S-AFP) was log-normally distributed in 284 adult blood donors. S-AFP increased with age (p < 10-7), whereas no gender-related difference was found. Reference intervals (95-interpercentile) were constructed for persons ≤40 years (0.60-9.30kIU/L) and >40 years (1.40-12.60 kIU/L). The concentration of AFP was significantly, albeit slightly, higher in serum than in plasma, whereas hemolysis, pretreatment with KCl and food intake did not influence S-AFP. S-AFP only changed 6% when measured twice 2 months apart (p = 0.04). Three enzyme immunoassays, using three different anti-AFP monoclonal antibodies for detection, were compared and two assays gave S-AFP values significantly higher, 2.8% (p = 0.03) and 19.0% (p < 10-4), than the other assay. Thus, the choice of antibody may influence the result of immunochemical concentration determination. This can be explained by the existence of conformational variants of AFP with different antibody reactivities, and calls for careful standardization of monoclonal antibodies used in assays for AFP. With broad population reference ranges and slight intra-personal variation, the most effective reference range for S-AFP is previous values obtained in the same person.",
keywords = "Age dependence, Alpha-fetoprotein, Blood donors, Malignancy, Monoclonal antibodies, Sex variation, Tumor marker",
author = "Michael Christiansen and H{\o}gdall, {Claus Kim} and Andersen, {Jens Rikardt} and B N{\o}rgaard-Pedersen",
note = "(Ekstern)",
year = "2001",
doi = "10.1080/003655101300133649",
language = "English",
volume = "61",
pages = "205--215",
journal = "Scandinavian Journal of Clinical and Laboratory Investigation. Supplement",
issn = "0085-591X",
publisher = "Taylor & Francis",
number = "3",

}

RIS

TY - JOUR

T1 - Alpha-fetoprotein in plasma and serum of healthy adults

T2 - Preanalytical, analytical and biological sources of variation and construction of age-dependent reference intervals

AU - Christiansen, Michael

AU - Høgdall, Claus Kim

AU - Andersen, Jens Rikardt

AU - Nørgaard-Pedersen, B

N1 - (Ekstern)

PY - 2001

Y1 - 2001

N2 - Alpha-fetoprotein (AFP) is a tumor marker for hepatomas and germ cell tumors, and the serum concentration has prognostic significance in other diseases. We examined the normal serum concentration of AFP in adults and sources of variation in the immunochemical variation of AFP. The serum concentration of the tumor marker alpha-fetoprotein (S-AFP) was log-normally distributed in 284 adult blood donors. S-AFP increased with age (p < 10-7), whereas no gender-related difference was found. Reference intervals (95-interpercentile) were constructed for persons ≤40 years (0.60-9.30kIU/L) and >40 years (1.40-12.60 kIU/L). The concentration of AFP was significantly, albeit slightly, higher in serum than in plasma, whereas hemolysis, pretreatment with KCl and food intake did not influence S-AFP. S-AFP only changed 6% when measured twice 2 months apart (p = 0.04). Three enzyme immunoassays, using three different anti-AFP monoclonal antibodies for detection, were compared and two assays gave S-AFP values significantly higher, 2.8% (p = 0.03) and 19.0% (p < 10-4), than the other assay. Thus, the choice of antibody may influence the result of immunochemical concentration determination. This can be explained by the existence of conformational variants of AFP with different antibody reactivities, and calls for careful standardization of monoclonal antibodies used in assays for AFP. With broad population reference ranges and slight intra-personal variation, the most effective reference range for S-AFP is previous values obtained in the same person.

AB - Alpha-fetoprotein (AFP) is a tumor marker for hepatomas and germ cell tumors, and the serum concentration has prognostic significance in other diseases. We examined the normal serum concentration of AFP in adults and sources of variation in the immunochemical variation of AFP. The serum concentration of the tumor marker alpha-fetoprotein (S-AFP) was log-normally distributed in 284 adult blood donors. S-AFP increased with age (p < 10-7), whereas no gender-related difference was found. Reference intervals (95-interpercentile) were constructed for persons ≤40 years (0.60-9.30kIU/L) and >40 years (1.40-12.60 kIU/L). The concentration of AFP was significantly, albeit slightly, higher in serum than in plasma, whereas hemolysis, pretreatment with KCl and food intake did not influence S-AFP. S-AFP only changed 6% when measured twice 2 months apart (p = 0.04). Three enzyme immunoassays, using three different anti-AFP monoclonal antibodies for detection, were compared and two assays gave S-AFP values significantly higher, 2.8% (p = 0.03) and 19.0% (p < 10-4), than the other assay. Thus, the choice of antibody may influence the result of immunochemical concentration determination. This can be explained by the existence of conformational variants of AFP with different antibody reactivities, and calls for careful standardization of monoclonal antibodies used in assays for AFP. With broad population reference ranges and slight intra-personal variation, the most effective reference range for S-AFP is previous values obtained in the same person.

KW - Age dependence

KW - Alpha-fetoprotein

KW - Blood donors

KW - Malignancy

KW - Monoclonal antibodies

KW - Sex variation

KW - Tumor marker

UR - http://www.scopus.com/inward/record.url?scp=17744381949&partnerID=8YFLogxK

U2 - 10.1080/003655101300133649

DO - 10.1080/003655101300133649

M3 - Journal article

C2 - 11386607

AN - SCOPUS:17744381949

VL - 61

SP - 205

EP - 215

JO - Scandinavian Journal of Clinical and Laboratory Investigation. Supplement

JF - Scandinavian Journal of Clinical and Laboratory Investigation. Supplement

SN - 0085-591X

IS - 3

ER -

ID: 251989293