AN INDIRECT SANDWICH ELISA FOR LP(A) IN SERUM AND DRIED BLOOD SPOTS

被引:33
作者
WANG, XL
WILCKEN, DEL
DUDMAN, NPB
机构
[1] UNIV NEW S WALES,PRINCE HENRY HOSP,DEPT CARDIOVASC MED,SYDNEY,NSW,AUSTRALIA
[2] UNIV NEW S WALES,PRINCE WALES HOSP,SYDNEY,NSW,AUSTRALIA
关键词
ELISA; LP(A); DRIED BLOOD SPOT;
D O I
10.1016/0009-8981(92)90151-F
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
We have established a reproducible and inexpensive indirect sandwich ELISA for Lp(a) quantitation in both serum and dried blood spot samples. All reagents used in the assay are available commercially. The intra-assay CVs were 3.8 +/- 0.9% for serum and 4.5 +/- 1.7% for dried blood spots on filter paper. The inter-assay CVs were 6.3 +/- 2.3% and 4.5 +/- 0.1% for serum and dried blood spot, respectively. Lp(a) concentrations measured by the ELISA and a commercial RIA were highly correlated (r = 0.989, n = 60, P < 0.001). However concentrations measured by RIA were 34.3% +/- 9.7% higher than those by ELISA. Lp(a) concentrations in serum and in dried blood spots were also highly correlated (r = 0.966, n = 40, P < 0.001). This indirect ELISA is suitable for assaying large numbers of serum or dried blood spot samples. However, the differences between the concentrations measured by ELISA and RIA stress the need for standardization of Lp(a) measurements.
引用
收藏
页码:73 / 86
页数:14
相关论文
共 23 条
  • [1] ALBERS JJ, 1990, CLIN CHEM, V36, P2019
  • [2] THE ASSOCIATION BETWEEN SERUM LP(A) CONCENTRATIONS AND ANGIOGRAPHICALLY ASSESSED CORONARY ATHEROSCLEROSIS - DEPENDENCE ON SERUM LDL LEVELS
    ARMSTRONG, VW
    CREMER, P
    EBERLE, E
    MANKE, A
    SCHULZE, F
    WIELAND, H
    KREUZER, H
    SEIDEL, D
    [J]. ATHEROSCLEROSIS, 1986, 62 (03) : 249 - 257
  • [3] BERG K, 1963, ACTA PATHOL MIC SC, V59, P369
  • [4] BERG K, 1974, CLIN GENET, V6, P230
  • [5] VARIABLES AFFECTING APOLIPOPROTEIN B MEASUREMENTS IN 3-DAY-OLD TO 5-DAY-OLD BABIES - A STUDY OF 4491 NEONATES
    BLADES, BL
    DUDMAN, NPB
    WILCKEN, DEL
    [J]. PEDIATRIC RESEARCH, 1987, 21 (06) : 608 - 614
  • [6] GENETICS OF THE QUANTITATIVE LP(A) LIPOPROTEIN TRAIT .3. CONTRIBUTION OF LP(A) GLYCOPROTEIN PHENOTYPES TO NORMAL LIPID VARIATION
    BOERWINKLE, E
    MENZEL, HJ
    KRAFT, HG
    UTERMANN, G
    [J]. HUMAN GENETICS, 1989, 82 (01) : 73 - 78
  • [7] PLASMA-LIPOPROTEINS - TEACHING OLD DOGMAS NEW TRICKS
    BROWN, MS
    GOLDSTEIN, JL
    [J]. NATURE, 1987, 330 (6144) : 113 - 114
  • [8] RADIAL IMMUNODIFFUSION ASSAY OF APOLIPOPROTEIN-B IN BLOOD DRIED ON FILTER-PAPER - A POTENTIAL SCREENING METHOD FOR FAMILIAL TYPE-II HYPERCHOLESTEROLEMIA
    DUDMAN, NPB
    BLADES, BL
    WILCKEN, DEL
    AITKEN, JM
    [J]. CLINICA CHIMICA ACTA, 1985, 149 (2-3) : 117 - 127
  • [9] PARTIAL AMINO-ACID-SEQUENCE OF APOLIPOPROTEIN(A) SHOWS THAT IT IS HOMOLOGOUS TO PLASMINOGEN
    EATON, DL
    FLESS, GM
    KOHR, WJ
    MCLEAN, JW
    XU, QT
    MILLER, CG
    LAWN, RM
    SCANU, AM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (10) : 3224 - 3228
  • [10] FLESS GM, 1989, J LIPID RES, V30, P651