Non–HDL Cholesterol Shows Improved Accuracy for Cardiovascular Risk Score Classification Compared to Direct or Calculated LDL Cholesterol in a Dyslipidemic Population

Author:

van Deventer Hendrick E1,Miller W Greg2,Myers Gary L3,Sakurabayashi Ikunosuke4,Bachmann Lorin M2,Caudill Samuel P3,Dziekonski Andrzej2,Edwards Selvin3,Kimberly Mary M3,Korzun William J2,Leary Elizabeth T5,Nakajima Katsuyuki6,Nakamura Masakazu7,Shamburek Robert D1,Vetrovec George W2,Warnick G Russell8,Remaley Alan T1

Affiliation:

1. National Institutes of Health, Bethesda, MD

2. Virginia Commonwealth University, Richmond, VA

3. Centers for Disease Control Prevention, Atlanta, GA

4. Jichi Medical University, Tochigi-ken, Japan

5. Pacific Biomarkers and Pacific Biometrics Research Foundation, Seattle, WA

6. Otsuka Pharmaceutical, Tokyo, Japan

7. Osaka Medical Center for Health Science and Promotion, Osaka, Japan

8. Health Diagnostics Laboratory, Richmond, VA

Abstract

BACKGROUNDOur objective was to evaluate the accuracy of cardiovascular disease (CVD) risk score classification by direct LDL cholesterol (dLDL-C), calculated LDL cholesterol (cLDL-C), and non–HDL cholesterol (non–HDL-C) compared to classification by reference measurement procedures (RMPs) performed at the CDC.METHODSWe examined 175 individuals, including 138 with CVD or conditions that may affect LDL-C measurement. dLDL-C measurements were performed using Denka, Kyowa, Sekisui, Serotec, Sysmex, UMA, and Wako reagents. cLDL-C was calculated by the Friedewald equation, using each manufacturer's direct HDL-C assay measurements, and total cholesterol and triglyceride measurements by Roche and Siemens (Advia) assays, respectively.RESULTSFor participants with triglycerides <2.26 mmol/L (<200 mg/dL), the overall misclassification rate for the CVD risk score ranged from 5% to 17% for cLDL-C methods and 8% to 26% for dLDL-C methods when compared to the RMP. Only Wako dLDL-C had fewer misclassifications than its corresponding cLDL-C method (8% vs 17%; P < 0.05). Non–HDL-C assays misclassified fewer patients than dLDL-C for 4 of 8 methods (P < 0.05). For participants with triglycerides ≥2.26 mmol/L (≥200 mg/dL) and <4.52 mmol/L (<400 mg/dL), dLDL-C methods, in general, performed better than cLDL-C methods, and non–HDL-C methods showed better correspondence to the RMP for CVD risk score than either dLDL-C or cLDL-C methods.CONCLUSIONSExcept for hypertriglyceridemic individuals, 7 of 8 dLDL-C methods failed to show improved CVD risk score classification over the corresponding cLDL-C methods. Non–HDL-C showed overall the best concordance with the RMP for CVD risk score classification of both normal and hypertriglyceridemic individuals.

Funder

Genzyme

Pointe Scientific

Pacific Biometrics Research Foundation provided

Virginia Commonwealth University

National Institutes of Health

Warren Grant Magnuson Clinical Center

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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