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1
Department of Laboratory Medicine, Municipal Ho-Pin Hospital, 33 Sec 2, Chung-Hwa Rd., Taipei, Taiwan, R.O.C.
2
School of Medical Technology, College of Medicine,
National Taiwan University, 7 Chung-Shan South Rd., 10016 Taipei,
Taiwan, R.O.C.
3
Department of Laboratory Medicine, College of Medicine,
National Taiwan University Hospital, National Taiwan University, 7
Chung-Shan South Rd., 10016 Taipei, Taiwan, R.O.C.
a Author for correspondence. Fax 886-2-3224263;
We evaluated the performance of two homogeneous assays for quantifying
HDL cholesterol (HDL-C) and compared them with the phosphotungstic acid
(PTA)/MgCl2 assay. Both homogeneous HDL-C assays were
precise, having a within-run CV of <1.20% and a between-run CV of
<4.07%. The HDL-C values (y) measured by the two
homogeneous methods correlated well with those by the
PTA/MgCl2 method (x): y =
1.00x + 64.98 mg/L, r = 0.987,
Sy|x = 27.99 mg/L (n = 152)
for the polyethylene glycol-modified enzymes/
-cyclodextrin sulfate
(PEGME) assay (Kyowa), and y = 0.84x +
106.51 mg/L, r = 0.984,
Sy|x = 26.10 mg/L (n = 152)
for the polyanionpolymer/detergent (PPD) assay (Daiichi). The
specificity of the PEGME method seemed better than that of the PPD
method, as the PPD method was markedly interfered with by supplemental
LDL-C. Addition of 20 g/L triglycerides produced a negative error of
~18% in both homogeneous assays. Bilirubin and hemoglobin had little
influence on the PEGME method; hemoglobin had little effect on the PPD
method. Bilirubin, however, markedly decreased the readings by the PPD
method. We found the PEGME assay superior to the PPD assay for routine
HDL-C testing, because the PPD assay is relatively inaccurate and not
specific.
Key Words: indexing terms: methods comparison triglycerides atherosclerosis
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