Enhanced Liver Fibrosis (ELF) Score

Enhanced Liver Fibrosis (ELF) Score

Test Code

10350
81517
10350
81517
Not offered in Quest Diagnostics Nichols Institute (IFD) – San Juan Capistrano. Please provide SERVICE AREA INFORMATION to find available tests you can order.
In-home collection may be available in your area for purchase through Quest Mobile.

Clinical Significance

Enhanced Liver Fibrosis (ELF) Score - The Enhanced Liver Fibrosis (ELF) score predicts progression to cirrhosis and liver-related events in patients with advanced fibrosis due to NASH.

The ELF score is not for use in the diagnosis of NASH, the staging of fibrosis, the serial monitoring of disease progression, or the monitoring of effects of therapeutic products.

The ELF score is derived from an algorithm that combines measurements of PIIINP, TIMP-1, and HA. PIIINP is a marker of early fibrogenesis and inflammation, TIMP-1 is the circulating inhibitor of MMP enzymes that can enhance fibrogenesis, and HA ...

Test Details

Methodology

Chemiluminescent Immunoassay

Reference Range(s)

<9.80

ELF score ranges and associated risk of disease progression (development of cirrhosis or liver-related events):

<9.80 Lower
≥9.80 - <11.30 Mid
≥11.30 Higher

Alternative Name(s)

hyaluronic, P3NP, procollagen, metalloproteinase, hepatic, PIIINP, propeptide, NASH, NAFLD, Nonalcoholic, Fatty, Steatosis, Hepatitis, Steatohepatitis, TIMP

LOINC® Codes, Performing Laboratory

Methodology

Chemiluminescent Immunoassay

Reference Range(s)

<9.80

ELF score ranges and associated risk of disease progression (development of cirrhosis or liver-related events):
<9.80 Lower
≥9.80 - <11.30 Mid
≥11.30 Higher

Alternative Name(s)

hyaluronic, P3NP, procollagen, metalloproteinase, hepatic, PIIINP, propeptide, NASH, NAFLD, Nonalcoholic, Fatty, Steatosis, Hepatitis, Steatohepatitis, TIMP

Preferred Specimen(s)

1 mL serum

Minimum Volume

0.5 mL

Collection Instructions

Spin sample within two hours after collection.

Dietary supplements containing biotin may interfere in assays and may skew analyte results to be either falsely high or falsely low. For patients receiving the recommended daily doses of biotin, draw samples at least 8 hours following the last biotin supplementation. For patients on mega-doses of biotin supplements, draw samples at least 72 hours following the last biotin supplementation.

Samples with fluorescein may cause falsely depressed results. Evidence suggests that patients undergoing retinal fluorescein angiography can retain amounts of fluorescein in the body for up to 72 hours post-treatment.

Transport Container

Transport tube

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

  • Room temperature: 48 hours
  • Refrigerated: 7 days
  • Frozen: 30 days

Reject Criteria

Gross hemolysis

Setup Schedule

1 mL serum
0.5 mL
Spin sample within two hours after collection.

Dietary supplements containing biotin may interfere in assays and may skew analyte results to be either falsely high or falsely low. For patients receiving the recommended daily doses of biotin, draw samples at least 8 hours following the last biotin supplementation. For patients on mega-doses of biotin supplements, draw samples at least 72 hours following the last biotin supplementation.

Samples with fluorescein may cause falsely depressed results. Evidence suggests that patients undergoing retinal fluorescein angiography can retain amounts of fluorescein in the body for up to 72 hours post-treatment.
Transport tube
Refrigerated (cold packs)
Room temperature: 48 hours
Refrigerated: 7 days
Frozen: 30 days
Gross hemolysis
Not offered in Quest Diagnostics Nichols Institute (IFD) – San Juan Capistrano. Please provide SERVICE AREA INFORMATION to find available tests you can order.
In-home collection may be available in your area for purchase through Quest Mobile.
Test Details

Clinical Significance

Test Resources

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.

The tests listed by specialty and category are a select group of tests offered. For a complete list of Quest Diagnostics tests, please adjust the filter options chosen, or refer to our Directory of Services.