Lipid Profile With Non-HDL Cholesterol
Also known as: LP, Non-HDL Cholesterol
Use
The Third Report of the National Cholesterol Education Program (NCEP) Expert Panel's revised guidelines1 for the treatment of cholesterol in adults called for increased attention to the metabolic syndrome and diabetes. These guidelines highlighted the increased inaccuracy of the LDL-C measurement in these patients because of elevated triglycerides. To overcome the inaccuracy of the calculated LDL-C method when triglycerides are elevated, measurement of nonhigh-density lipoprotein (non-HDL) was recommended as a better means to follow these patients toward their treatment goals. Non-HDL-C is a calculation (total cholesterol minus HDL-C), ie, the sum of the VLDL-C, LDL-C, and IDL-C. While LDL-C has long been the primary focus of cholesterol reduction efforts, researchers have identified several other lipoproteins that also affect cardiovascular health. The advantage of non-HDL-C measurement is that it accounts for cholesterol in the other potentially atherogenic lipoprotein particles, which include VLDL-C, IDL-C, LDL-C, and lipoprotein(a). Studies2,3 have shown that the measurement of non-HDL-C, rather than LDL-C, would be a better target for therapy, especially in persons with a triglyceride level >200 mg/dL. Cut-points for non-HDL-C are 30 mg/dL higher than the LCL-C cut-points (eg, if the patient's LDL-C goal is <160 mg/dL, the non-HDL-C goal should be <190 mg/dL).
Special Instructions
State patient's age and sex on the request form. Patient should ideally follow a stable diet for two to three weeks prior to blood collection. Fasting is not necessary, but recommended for patients requiring precise triglyceride measurements for conditions like hypertriglyceridemia.
Limitations
LDL cholesterol cannot be accurately calculated if the triglyceride level exceeds 800 mg/dL. Lipid panels should be avoided for up to three months following an acute myocardial infarction, except that cholesterol can be measured within the first 24 hours post-event. Greatly elevated triglycerides (>400 mg/dL) or improper specimen labeling are grounds for rejection.
Methodology
Other
Biomarkers
LOINC Codes
- 43396-1
- 2093-3
- 2571-8
- 2085-9
- 13458-5
- 13457-7
- 8251-1
Result Turnaround Time
1 day
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
2 mL
Minimum Volume
0.7 mL
Container
Red-top tube, gel-barrier tube, or green-top (lithium heparin) tube. Do not use oxalate, EDTA, or citrate plasma.
Collection Instructions
Separate serum from cells within 45 minutes of collection.
Patient Preparation
Patient should be on a stable diet, ideally for two to three weeks prior to collection. Fasting for 12 to 14 hours is recommended where triglyceride levels are critical for diagnosis.
Storage Instructions
Maintain specimen at room temperature.
Causes for Rejection
Specimen with greatly elevated triglycerides (>400 mg/dL); improper specimen labeling
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 3 days |
| Refrigerated | 14 days |
| Frozen | 14 days |
