3 GENERATIONS OF HIGH-DENSITY-LIPOPROTEIN CHOLESTEROL ASSAYS COMPAREDWITH ULTRACENTRIFUGATION DEXTRAN SULFATE-MG2+ METHOD/
Citation
N. Harris et al., 3 GENERATIONS OF HIGH-DENSITY-LIPOPROTEIN CHOLESTEROL ASSAYS COMPAREDWITH ULTRACENTRIFUGATION DEXTRAN SULFATE-MG2+ METHOD/, Clinical chemistry, 43(5), 1997, pp. 816-823
Categorie Soggetti
Medical Laboratory Technology
SICI code
0009-9147(1997)43:5<816:3GOHCA>2.0.ZU;2-O
Abstract
We report on the analytical performance of three generations of HDL-ch
olesterol assays: phosphotungstic acid/Mg2+, Spinpro(R), and a homogen
eous method, N-geneous(TM). The run-to-run imprecision (CV) of all ass
ays was less than or equal to 4.9%, and all results correlated highly
with those of a modified reference procedure (r greater than or equal
to 0.96). At triglycerides concentrations <4000 mg/L, these field meth
ods showed an acceptable systematic error (y = 1.12x - 47, 1.05x - 23,
and 0.96x + 8 for the phosphotungstate, Spinpro, and N-geneous assays
, respectively), and the total error of the field methods met the curr
ent National Cholesterol Education Program (NCEP) performance goal of
less than or equal to 22%. Regression analyses of results for samples
with triglycerides >4000 mg/L produced the following results for the a
bove respective assays: y = 1.08x - 4.2, 1.02x + 3.6, and 0.85x + 108.
In this hypertriglyceridemic group, only the N-geneous assay (at an H
DL-cholesterol content of 240 mg/L) had a total error (35%) that excee
ded the NCEP limit. Bilirubin and ascorbate produced a negative interf
erence with the phosphotungstate and Spinpro assays but had little eff
ect on the N-geneous assay.