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Updated: May 21, 2026

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Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
[LDL-cholesterol homogeneous assays versus Friedewald's equation]
Takashi Miida1, Satoshi Hirayama
1Department of Clinical Laboratory Medicine, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. tmiida@juntendo.ac.jp
Summary
Low-density lipoprotein cholesterol (LDL-C) is crucial for assessing heart disease risk. Current measurement methods, including Friedewald
Area of Science:
- Cardiovascular Medicine
- Clinical Chemistry
Background:
- Low-density lipoprotein (LDL) is a key risk factor for coronary artery disease and ischemic stroke.
- Clinical LDL-cholesterol (LDL-C) measurement relies on Friedewald's equation or homogeneous assays.
- Friedewald's equation, despite limitations, has been standard for ~40 years.
Purpose of the Study:
- To evaluate the current landscape of LDL-C measurement methods.
- To address the debate on the superiority of different LDL-C assays for clinical samples.
Main Methods:
- Review of widely used LDL-C calculation (Friedewald's equation) and homogeneous assay principles.
- Analysis of the availability and diversity of 12 homogeneous LDL-C assays in Japan.
- Consideration of undisclosed measurement principles for commercial assays.
Main Results:
- Friedewald's equation has limitations but remains prevalent.
- Multiple homogeneous LDL-C assays exist, utilizing different, undisclosed principles.
- The optimal method for clinical LDL-C measurement is debated.
Conclusions:
- The variety of LDL-C assays necessitates careful consideration for clinical application.
- Further research is needed to clarify the performance of different LDL-C assays.
- Standardization or clear guidelines may be required for accurate cardiovascular risk assessment.
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