The Martin/Hopkins method of low-density lipoprotein (LDL) cholesterol assessment is more accurate that the usual calculation method, according to an analysis of the FOURIER trial.
Among FOURIER participants with stable cardiovascular disease, the median Martin/Hopkins LDL cholesterol level was 2 mg/dL below the reference standard of preparative ultracentrifugation -- a statistically similar result, whereas the Friedewald method underestimated LDL cholesterol by 4 mg/dL (P<0.001).
The Martin/Hopkins method correlated significantly better with preparative ultracentrifugation than did the Friedewald, according to a group led by Seth Martin, MD, MHS, of Johns Hopkins University School of Medicine in Baltimore, reporting online in .
While 22.9% of Martin/Hopkins LDL cholesterol values were at least 5 mg/dL different from reference and 2.6% were off by more than 10 mg/dL, these proportions were 40.1% and 13.3% with Friedewald estimation, respectively (P<0.001 for each).
The Martin/Hopkins method "uses the same standard lipid measurements of total and HDL [high-density lipoprotein] cholesterol and triglycerides as the Friedewald equation does, but it uses a personalized rather than fixed conversion factor in calculating LDL cholesterol levels," Martin and colleagues noted.
The Friedewald formula has been used to calculate LDL cholesterol for more than 40 years, Neil Stone, MD, of Northwestern University Feinberg School of Medicine in Chicago, pointed out in an invited commentary.
Now, "just as it's timely to consider nonfasting lipid measurements in routine clinical assessment, it may also be timely to consider the clinical advantages of the Martin/Hopkins method for LDL-C determination compared with that derived from the Friedewald equation," he said.
"With doubts about LDL cholesterol accuracy, the clinician-patient discussion about the potential for net benefit by adding a nonstatin treatment is hampered," Stone added.
The difference between methods was more pronounced when triglyceride levels exceeded 150 mg/dL.
For this analysis, Martin's group relied on FOURIER patients who had multiple LDL cholesterol values from Martin/Hopkins, Friedewald, and ultracentrifugation assessment (n=12,742).
"But not everything that matters depends on measurement," Stone concluded. "Clinical judgment and shared decision making as suggested in recent guidelines are still required to put treatment decisions based on LDL cholesterol measurements in the appropriate perspective for the individual patient."
Disclosures
Martin reported receiving personal fees for serving on scientific advisory boards for Amgen, Sanofi/ Regeneron, Quest Diagnostics, and Akcea Therapeutics, as well as grants and research support from the PJ Schafer Cardiovascular Research Fund, the David and June Trone Family Foundation, American Heart Association, Aetna Foundation, Maryland Innovation Initiative, Nokia, Google, and Apple outside the submitted work; in addition, he declared having patent applications pending.
Stone disclosed no relevant conflicts of interest.
Primary Source
JAMA Cardiology
Martin SS, et al "Comparison of low-density lipoprotein cholesterol assessment by Martin/Hopkins estimation, Friedewald estimation, and preparative ultracentrifugation: insights from the FOURIER trial" JAMA Cardiol 2018; DOI: 10.1001/jamacardio.2018.1533.
Secondary Source
JAMA Cardiology
Stone NJ "Measuring low-density lipoprotein cholesterol: when is more accurate better?" JAMA Cardiol 2018; DOI: 10.1001/jamacardio.2018.1575.