Test ID LMPP Lipoprotein Metabolism Profile, Serum
Reporting Name
Lipoprotein Metabolism ProfileUseful For
Diagnosing dyslipoproteinemia
Quantitation of cholesterol and triglycerides in very-low-density lipoprotein (VLDL), LDL, HDL, and chylomicrons
Identification of LpX
Classifying hyperlipoproteinemias (lipoprotein phenotyping)
Evaluating patients with abnormal lipid values (cholesterol, triglyceride, HDL, LDL)
Quantifying lipoprotein a (Lp[a]) cholesterol
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
TCS | Cholesterol, Total, CDC, S | No | Yes |
TRIGC | Triglycerides, CDC, S | No | Yes |
APLBS | Apolipoprotein B, S | No | Yes |
HDLS | HDL Cholesterol, CDC, S | No | Yes |
LMPP1 | Lipoprotein Metabolism Profile 1 | No | Yes |
Specimen Type
SerumNecessary Information
Patient's age and sex are required.
Specimen Required
Patient Preparation:
1. Fasting-overnight (12-14 hours)
2. Patient must not consume any alcohol for 24 hours before the specimen is drawn.
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 5 mL
Specimen Minimum Volume
2 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 7 days | |
Frozen | 60 days |
Special Instructions
Reference Values
Age |
2-9 years |
10-17 years |
>18 years |
Total Cholesterol (mg/dL) |
* Acceptable: <170 Borderline high: 170-199 High: ≥200 |
** Desirable: <200 Borderline high: 200-239 High: ≥ 240 |
|
Triglycerides (mg/dL) |
* Acceptable: <75 Borderline high: 75-99 High: ≥100 |
* Acceptable: <90 Borderline high: 90-129 High: ≥130 |
** Normal: <150 Borderline high: 150-199 High: 200-499 Very high: ≥500 |
LDL Cholesterol (mg/dL) |
* Acceptable: <110 Borderline high: 110-129 High: ≥130 |
*** Desirable: <100 Above Desirable: 100-129 Borderline high: 130-159 High: 160-189 Very high: ≥190 |
|
LDL Triglycerides (mg/dL) |
≤ 50 |
≤ 50 |
|
Apolipoprotein B (mg/dL) |
* Acceptable: <90 Borderline high: 90-109 High: ≥110 |
*** Desirable: <90 Above Desirable: 90-99 Borderline high: 100-119 High: 120-139 Very high: ≥140 |
|
HDL Cholesterol (mg/dL) |
* Low: <40 Borderline low: 40-45 Acceptable: > 45 |
*** Males: ≥40 Females: ≥50
|
|
VLDL Cholesterol (mg/dL) |
<30 |
<30 |
|
VLDLTriglycerides (mg/dL) |
<90 |
<120 |
|
Beta VLDL Cholesterol (mg/dL) |
<15 |
<15 |
|
Beta VLDL Triglycerides (mg/dL) |
<15 |
<15 |
|
Chylomicron Cholesterol |
Undetectable |
Undetectable |
|
Chylomicron Triglycerides |
Undetectable |
Undetectable |
|
Lp(a) cholesterol |
<5 |
<5 |
|
LpX |
Undetectable |
Undetectable |
Reference values have not been established for patients that are <2 years of age.
* Expert Panel on Integrated Guidelines for Cardiovascular Health and Risk Reduction in Children and Adolescents
** National Cholesterol Education Program (NCEP)
***National Lipid Association
Day(s) and Time(s) Performed
Monday through Saturday; 4 p.m.
CPT Code Information
80061-Lipid panel (includes: HDL [CPT Code 83718], total cholesterol [CPT Code 82465], and triglycerides [CPT Code 84478])
82172-Apolipoprotein B
83700-Lp(a) cholesterol electrophoresis
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
LMPP | Lipoprotein Metabolism Profile | In Process |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
TCS | Cholesterol, Total, CDC, S | 2093-3 |
HDLS | HDL Cholesterol, CDC, S | 2085-9 |
TRIGC | Triglycerides, CDC, S | 2571-8 |
APLBS | Apolipoprotein B, S | 1884-6 |
2839 | LDL Cholesterol | 2089-1 |
2840 | LDL Triglycerides | 3046-0 |
2844 | VLDL cholesterol | 2091-7 |
2847 | VLDL triglycerides | 3047-8 |
2842 | Beta VLDL Cholesterol | 66499-5 |
2843 | Beta VLDL triglycerides | 3045-2 |
2855 | Chylomicron cholesterol | 34467-1 |
2856 | Chylomicron triglycerides | 35363-1 |
2849 | Lp(a) Cholesterol | 35388-8 |
23924 | LpX | 42178-4 |
23937 | Interpretation | 59462-2 |
Clinical Information
Lipoprotein metabolism profile analysis adds practical information about the etiology of cholesterol and/or triglyceride elevation. In some patients, increased serum lipids reflect elevated levels of intermediate-density lipoprotein (IDL), very-low-density lipoprotein (VLDL), lipoprotein a (Lp[a]), or even the abnormal lipoprotein complex-LpX. These elevations can be indicative of a genetic deficiency in lipid metabolism or transport, nephrotic syndrome, endocrine dysfunction or even cholestasis. Identification of the lipoprotein associated with lipid elevation is achieved using the gold-standard methods, which include ultracentrifugation, selective precipitation, electrophoresis, and direct measurement of cholesterol and triglycerides in isolated lipoprotein fractions. Proper characterization of a patient's dyslipidemic phenotype aids clinical decisions and guides appropriate therapy.
Classifying the hyperlipoproteinemias into phenotypes places disorders that affect plasma lipid and lipoprotein concentrations into convenient groups for evaluation and treatment. A clear distinction must be made between primary (inherited) and secondary (liver disease, alcoholism, metabolic diseases) causes of dyslipoproteinemia. Lipoprotein profiling will identify the presence of Lp(a) and LpX and distinguish between the following dyslipidemias:
-Exogenous hyperlipemia (Type I)
-Familial hypercholesterolemia (Type IIa)
-Familial combined hyperlipidemia (Type IIb)
-Familial dysbetalipoproteinemia (Type III)
-Endogenous hyperlipemia (Type IV)
-Mixed hyperlipemia (Type V)
Interpretation
For discussion of primary disorders associated with dyslipidemias see Lipids and Lipoproteins in Blood Plasma (Serum) in Special Instructions.
Patients with increased Lp(a) cholesterol values have been associated with increased risk for the development of atherothrombotic disease. Aggressive LDL reduction is the recommended treatment approach in most patients with increased Lp(a).
Lipoprotein-X (LpX) is an abnormal lipoprotein that appears in the sera of patients with obstructive jaundice, and is an indicator of cholestasis. The presence of LpX will be reported if noted during Lp(a) cholesterol analysis.
Clinical Reference
1. Grundy SM, Stone NJ, Bailey AL, et al: 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation 2019 Jun 18;139(25):e1082-e1143
2. Expert panel on integrated guidelines for cardiovascular health and risk reduction in children and adolescents: summary report. Pediatrics. 2011 Dec;128 Suppl 5:S213-S256
3. Rosenson RS, Najera SD, Hegele RA: Heterozygous familial hypercholesterolemia presenting as chylomicronemia syndrome. J Clin Lipidol. 2017 Jan - Feb;11(1):294-296. doi: 10.1016/j.jacl.2016.12.005
4. Hopkins PN, Brinton EA, Nanjee MN: Hyperlipoproteinemia type 3: the forgotten phenotype. Curr Atheroscler Rep. 2014 Sep;16(9):440. doi: 10.1007/s11883-014-0440-2
5. Gotoda T, Shirai K, Ohta T, Kobayashi J, Yokoyama S, Oikawa S, et al: Diagnosis and management of type I and type V hyperlipoproteinemia. J Atheroscler J Atheroscler Thromb. 2012;19(1):1-12
Analytic Time
3 days (not reported on Saturday or Sunday)Method Name
Ultracentrifugation/Electrophoresis/Automated Enzymatic/Colorimetric Analysis
Forms
If not ordering electronically, complete, print, and send a Cardiovascular Test Request (T724) with the specimen.