|
|
||||||||
Technical Briefs |
1 (Department of Clinical Laboratory, Nagoya University Hospital, Nagoya, Japan;
aaddress correspondence to this author at: Department of Endocrinology, Metabolism, and Nephrology, Kochi Medical School, Kochi University, Kohasu, Oko-cho, Nankoku 783-8505, Japan; fax 81-88-880-2344, e-mail iwasaki{at}med.kochi-u.ac.jp)
Abstract
Background: Although a homogeneous assay for serum LDL-cholesterol (LDL-C) has become a routine clinical procedure, problems remain in assay performance characteristics.
Methods: We examined the performance of a recently developed automated homogeneous assay (New-Daiichi assay) for serum LDL-C and compared the results with those obtained by the current homogeneous method (Denka-Seiken assay) or by ultracentrifugation as a control.
Results: The New-Daiichi assay showed satisfactory basic performance characteristics such as reproducibility, linearity, and stability. There was no interference in the assay by various substances examined. The LDL-C values obtained with this method correlated well with those obtained by ultracentrifugation. In samples from patients with obstructive jaundice, both methods detected cholesterol from abnormal lipoproteins (such as lipoprotein-X and -Y), but the New-Daiichi assay was less reactive and more specific for LDL-C.
Conclusion: The new method has improved performance for the accurate measurement of LDL-C in clinical practice.
The following articles in journals at HighWire Press have cited this article:
![]() |
C. Garcia-Hejl, P. Vest, C. Renard, A. Merens-Gonthier, A. Boukhira, and H. Thefenne-Astier Falsely Low LDL Cholesterol Results and Cholestasis. Clin. Chem., November 1, 2006; 52(11): 2125 - 2127. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |