Also Known As
LDL Subclasses
NMR Particle Test
LDL Subfractions
LDL Particle Size or Number
Formal Name
Low-Density Lipoprotein Subfraction Profile
This article was last reviewed on
This article waslast modified on
January 15, 2018.
At a Glance
Why Get Tested?

To help evaluate your risk of developing cardiovascular disease (CVD)

When To Get Tested?

When you have a personal and/or family history of CVD at an early age; when the result of your low-density lipoprotein cholesterol (LDL-C) test is within a healthy range, but your healthcare provider thinks that you may have an increased risk of developing heart disease; sometimes to help monitor the effectiveness of lipid-lowering treatment and/or lifestyle changes

Sample Required?

A blood sample drawn from a vein in your arm

Test Preparation Needed?

You may need to fast for 9-12 hours before this test; only water is permitted. Follow any instructions you are given.

You may be able to find your test results on your laboratory's website or patient portal. However, you are currently at Lab Tests Online. You may have been directed here by your lab's website in order to provide you with background information about the test(s) you had performed. You will need to return to your lab's website or portal, or contact your healthcare practitioner in order to obtain your test results.

Lab Tests Online is an award-winning patient education website offering information on laboratory tests. The content on the site, which has been reviewed by laboratory scientists and other medical professionals, provides general explanations of what results might mean for each test listed on the site, such as what a high or low value might suggest to your healthcare practitioner about your health or medical condition.

The reference ranges for your tests can be found on your laboratory report. They are typically found to the right of your results.

If you do not have your lab report, consult your healthcare provider or the laboratory that performed the test(s) to obtain the reference range.

Laboratory test results are not meaningful by themselves. Their meaning comes from comparison to reference ranges. Reference ranges are the values expected for a healthy person. They are sometimes called "normal" values. By comparing your test results with reference values, you and your healthcare provider can see if any of your test results fall outside the range of expected values. Values that are outside expected ranges can provide clues to help identify possible conditions or diseases.

While accuracy of laboratory testing has significantly evolved over the past few decades, some lab-to-lab variability can occur due to differences in testing equipment, chemical reagents, and techniques. This is a reason why so few reference ranges are provided on this site. It is important to know that you must use the range supplied by the laboratory that performed your test to evaluate whether your results are "within normal limits."

For more information, please read the article Reference Ranges and What They Mean.

What is being tested?

Low-density lipoproteins (LDL) are particles that transport lipids throughout the body. Each particle contains a combination of protein, cholesterol, triglyceride, and phospholipid molecules. Their composition changes as they circulate in the blood. Some molecules are removed and others are added, resulting in lipoprotein particles whose properties vary from large and fluffy to small and dense. LDL particle testing determines the relative amounts of particles of differing properties in the blood. This is often called subfraction testing.

Traditional lipid testing measures the amount of LDL cholesterol (LDL-C) present in the blood, but it does not evaluate the number of particles of LDL (LDL-P). Some studies have shown that increased numbers of small, dense LDL particles (sdLDL) are associated with inflammation and are more likely to cause atherosclerosis than fewer light, fluffy LDL particles. Researchers think that the presence of an increased number of sdLDL could be one of the reasons that some people have heart attacks even though their total cholesterol and LDL cholesterol concentrations are not particularly high.

Data are not clear on whether routine testing for LDL subfractions provides additional information about cardiac risk or whether results from such testing could impact decisions about treatment. The 2015 report from the National Lipid Association Annual Summary of Clinical Lipidology does refer to potential use of subfraction testing for a select population of patients; however, more clinical research is needed to determine the ultimate value in testing for LDL subfractions and how the results should be used. Recommendations on the use of LDL subfraction testing and LDL-P continue to evolve as a result of ongoing studies and include:

  • The results of a clinical study named JUPITER, studying therapies for cardiovascular disease (CVD) and finding an association between disease and LDL subfractions
  • A review of multiple studies on exercise, verifying the relationship between exercise and a reduction in both the level of small LDL particles and risk for CVD
  • A study illustrating a relationship between disease progression and increases in small LDL particles using multiple methods for measuring the particles, including ultracentrifugation (separation of particles by density), polyacrylamide gradient gel electrophoresis (separation by charge and size) and NMR (nuclear magnetic resonance) spectroscopy, which measures particles according to differences in composition
  • A 2013 Assessment by the AACC Lipoprotein and Vascular Diseases Division Working Group on Best Practices, which compared the use of apolipoprotein B (Apo B) with LDL-P as indicators of atherogenic particle numbers; the group concluded that both tests were nearly equivalent in their ability to assess CVD risk and that both were stronger than LDL-C. The group supported the adoption of either Apo B or LDL-P into CVD risk screening and treatment guidelines but expressed a current preference for Apo B because of its availability and several other factors. (See Sources) Note: Apo B is considered a potential substitute for LDL-P because a molecule of Apo B is present in each particle of LDL and very low-density lipoprotein (VLDL).
  • An analysis of genetics of LDL subfractions and related therapy in European subjects, illustrating that genetic controls for LDL subfractions differ from genetic controls for total LDL

The number of sdLDL particles a person has is partially genetically determined, partially due to sex (males tend to have more sdLDL than females), and partially due to lifestyle and a person's general state of health. Certain diseases and conditions, such as diabetes and hypertension, are associated with increased levels of sdLDL.

As mentioned above, a variety of methods are used to determine lipoprotein subfractions, including ultracentrifugation, polyacrylamide gradient gel electrophoresis, and NMR spectroscopy.

It is also usually possible to predict whether a person has a high number of sdLDL particles by looking at the person's triglyceride and high-density lipoprotein cholesterol (HDL-C) levels. These tests are typically performed as part of a lipid profile. People who have high triglyceride and low HDL-C tend to have more sdLDL. Specifically, having a triglyceride level above 120 mg/dL and an HDL-C level lower than 40 mg/dL in men and lower than 50 mg/dL in women is associated with having more sdLDL.

Subfraction testing is also available for other lipoprotein particles, such as HDL and VLDL, but these tests are mostly used in research settings and are not addressed in this article.

How is the sample collected for testing?

A blood sample is obtained by inserting a needle into a vein in the arm.

Is any test preparation needed to ensure the quality of the sample?

Current standards recommend that lipid testing be done while fasting. For 9 to 12 hours before the test, only water is permitted. Follow any instructions provided by the healthcare practitioner or lab.

Accordion Title
Common Questions
  • How is it used?

    Low-density lipoprotein particle (LDL particle or LDL-P) testing evaluates LDL particles according to their number, size, density, and/or electrical charge. It may provide useful information for assessing cardiac risk in people who have a personal or family history of heart disease at a young age, especially if their total cholesterol and LDL cholesterol (LDL-C) values are not significantly elevated. LDL subfraction testing is typically done along with or following a lipid profile.

    While for many people, the LDL-C test is a good indicator of risk of cardiovascular disease (CVD), research has found that some people with healthy levels of LDL-C still have increased risk of CVD. Similarly, individuals with some chronic conditions such as diabetes may have increased risk even though their LDL-C is at a healthy level. For these populations, it has been suggested that the number of LDL particles and/or their size might be an additional factor to consider when determining their CVD risk. In these cases, lipoprotein subfraction testing may be used to further evaluate an individual's CVD risk.

    LDL-P may also be occasionally ordered to monitor the effectiveness of treatment in decreasing the number of small, dense LDL particles (sdLDL).

    LDL subfraction testing has been used in clinical settings, while VLDL or HDL subfraction testing is currently used mostly for research purposes. This is because LDL cholesterol has been identified as the primary risk factor for heart disease and more research and development has focused on LDL measurement.

  • When is it ordered?

    This testing may be ordered as part of an overall evaluation of cardiac risk when someone has a personal or family history of early cardiovascular disease (CVD), especially when the person doesn't have typical cardiac risk factors, such as high cholesterol, high LDL cholesterol, high triglyceride, low HDL cholesterol, smoking, obesity, inactivity, diabetes, and/or hypertension.

    When a person with an increased LDL-P and/or a large proportion of small, dense LDL particles has undergone lipid-lowering treatment or lifestyle changes, the healthcare practitioner may order LDL lipoprotein subfraction testing, along with other lipid tests, to monitor the effectiveness of treatment.

    Although it is not generally recommended as a screening test, a few healthcare providers are ordering LDL-P along with a battery of other cardiac risk tests when they are attempting to determine someone's overall risk of developing CVD.

  • What does the test result mean?

    Results of an LDL-P test reflect the method and reporting format used as well as the person's total cholesterol, LDL-C, VLDL, and/or HDL cholesterol. Since different methods separate the subclasses based on different physical properties (particle number, size, density, and/or electrical charge), results may not be directly comparable method to method or laboratory to laboratory.

    In general, the result is interpreted within the framework of a lipid profile and its associated risk:

    • If a person has a large number of primarily small, dense LDL (sdLDL) and an increased LDL-P, this finding will add to the individual's risk of developing cardiovascular disease above and beyond the risk associated with the total LDL.
    • If a person has exclusively large, fluffy LDL and a lower LDL-P, this finding will add no additional risk.
  • Is there anything else I should know?

    It is important to remember that lipoprotein subfraction and LDL subfraction testing (as well as other lipid and cardiac risk factor testing) is not diagnostic. It attempts to evaluate a person's statistical risk of developing CVD, but it cannot predict the development or severity of disease in a particular person.

  • How can I change my LDL subfractions and decrease my LDL-P?

    Although there is a genetic component, lipoprotein subfractions and LDL-P can be altered by adopting a diet low in saturated fats, losing excess weight, and exercising regularly. The use of lipid-lowering drugs may also affect the subfraction distribution and LDL-P.

  • How long will it take for my results?

    It depends on the laboratory performing the test. Not every lab performs LDL-P testing as it requires specialized instruments. Your sample may be sent to a reference laboratory for testing, so it may take several days before results are available.

View Sources

Sources Used in Most Recent Review

2016 review performed by Rose Romeo, PhD, DABCC, FACB.

Yan Zhang, Sha Li, Rui-Xia Xu, Cheng-Gang Zhu, Yuan-Lin Guo, Na-Quiong Wu, Jing Sun and Jian-Jun Li. System Inflammatory Markers Are Closely Associated with Atherogenic Lipoprotein Subfractions in Patients Undergoing Coronary Angiography. Mediators of Inflammation (2015):2015 Article ID 235742 (9 pages). Available online at Accessed February 7, 2016.

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Samia Mora, Michael P. Caulfield, Jay Wohlgemuth, Zhizong Chen, Robert Superko, Charles M. Rowland, Robert J. Glynn, Paul M. Ridker, Ronald M. Kraus. Atherogenic Lipoprotein Subfractions Determined by Ion Mobility and First Cardiovascular Events After Random Allocation to High Intensity Statin or Placebo. The Justification for the Use of Statins in Prevention: An Intervention Trial Evaluating Rosuvastatin (JUPITER) Trial. Circulation (2015); 132:2220-2229. Abstract available online at Accessed February 7, 2016.

Mark A. Sarzynshi, Jeffrey Burton, Tuomo Rankinen, Steven N. Blair, Timothy S. Church, Jean-Pierre Despres, James M. Hapberg, Rian Landers-Ramos, Arthur S. Leon, Catherine R. Mikus, D.C. Rao, Richard L. Selp, James S. Skinner, Cris A. Sientz, Paul D. Thompson, Kenneth R. Wilund, William E. Kraus, Claude Bouchard. The effects of exercise of the lipoprotein subclass profile: A meta-analysis of 10 interventions. Atherosclerosis (2015) 243: 364-372. Abstract available online at Accessed February 7, 2016.

Paul T. Williams, Xue-Qiao Zhao, Santica M. Marcovina, James D. Otvos, B. Greg Brown, Ronald M. Krauss. Comparison of four methods of analysis of lipoprotein particle subfractions for their association with angiographic progression of coronary artery disease. Atherosclerosis (2015) 233: 713-720. Abstract available online at Accessed February 7, 2016.

Heejung Shim, Daniel I. Chasman, Joshua D. Smith, Samia Mora, Paul M. Ridker, Deborah A. Nickerson, Ronald M. Krauss, Matthew Stephens.. A Multivariate Genome-Wide Association Analysis of 10 LDL Subfractions, and Their Response to Statin Treatment, in 1868 Caucasians. PLOS ONE 10(4):1-20. Available online at Accessed February 7, 2016.

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