Clinical Chemistry
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Clinical Chemistry 46: 1830-1832, 2000;
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(Clinical Chemistry. 2000;46:1830-1832.)
© 2000 American Association for Clinical Chemistry, Inc.


Articles

Inaccuracy of Calculated LDL-Cholesterol in Type 2 Diabetes: Consequences for Patient Risk Classification and Therapeutic Decisions

Ana Maria Wägner1, José Luis Sánchez-Quesada2, Antonio Pérez1, Mercedes Rigla1, Mariano Cortés2, Francisco Blanco-Vaca2,3 and Jordi Ordóñez-Llanos2,4,a

Departments of
1 Endocrinology and Nutrition and
2 Biochemistry, and
3 Research Institute, Hospital de Sant Pau, 08025 Barcelona, Spain
4 Department of Biochemistry and Molecular Biology, Universitat Autònoma, 08025 Barcelona, Spain
a Department of Biochemistry, Hospital de Sant Pau, Avgda Sant Antoni Ma Claret 167, 08025 Barcelona, Spain; Address correspondence to this author at: fax 34-93-2919196, e-mail 2038@hsp.santpau.es


   Introduction
 
LDL-cholesterol (LDLc) is the main lipid marker in cardiovascular risk estimation and the principal therapeutic target in both diabetic and nondiabetic subjects (1)(2). The designated comparison method for the determination of LDLc, using ultracentrifugation and precipitation, known as "ß-quantification" (3), is cumbersome and time-consuming and requires expensive instrumentation and trained personnel. The Friedewald equation (4) {LDLc = total cholesterol - HDLc - [triglycerides (in mmol/L)/2.17 or triglycerides (in mg/dL)/5]}, the most frequently used method for the calculation of LDLc, assumes that VLDL particles maintain a nearly constant cholesterol:triglyceride ratio. However, this assumption is invalid in the presence of chylomicronemia and increased VLDL or intermediate-density lipoprotein particles (4)(5)(6)(7).

Because diabetic dyslipidemia includes quantitative and qualitative abnormalities in lipoprotein particles, including VLDL and their remnants (8)(9)(10), the use of the Friedewald equation in diabetic patients has been questioned (11)(12)(13). HDL-cholesterol (HDLc), often determined after chemical precipitation of apolipoprotein B (apoB)-containing lipoproteins, has technical drawbacks that could interfere with the accuracy of LDLc calculation (14). New homogeneous, direct methods have improved HDLc determination (15). However, the consequences on patient classification and therapy of using direct, more precise methods for HDLc in the estimation of LDLc by the Friedewald equation have, to our knowledge, not been assessed.

We previously proposed an equation that included total triglycerides and cholesterol, and apoB that was more accurate than the Friedewald equation in estimating LDLc (16). Because diabetic dyslipidemia includes hyperapoB (17), an equation that includes apoB in the estimation of LDLc could be of special interest in these patients. Thus, our aims were to ascertain whether a direct HDLc method increases . . . [Full Text of this Article]


   References
 



The following articles in journals at HighWire Press have cited this article:


Home page
Diabetes CareHome page
A. M. Wagner, A. Perez, E. Zapico, and J. Ordonez-Llanos
Non-HDL Cholesterol and Apolipoprotein B in the Dyslipidemic Classification of Type 2 Diabetic Patients
Diabetes Care, July 1, 2003; 26(7): 2048 - 2051.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
G. R. Warnick, M. Nauck, and N. Rifai
Evolution of Methods for Measurement of HDL-Cholesterol: From Ultracentrifugation to Homogeneous Assays
Clin. Chem., September 1, 2001; 47(9): 1579 - 1596.
[Abstract] [Full Text] [PDF]




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