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LKM-1 Antibody Test -
Detects LKM-1 antibodies to diagnose autoimmune hepatitis, causing jaundice or fatigue
Synonym LKM-1 Test
Test Code IMMT26040123
Test Type Immunology
Pre-Test Condition No special
Report Availability 1–2 D(s)
# Test(s) 1
Test details Sample Report
LKM-1 Antibody Test Sample Report Cowin-PathLab
Synonym LKM-1 Test
Test Code IMMT26040123
Test Category Autoimmune Hepatitis
Pre-Test Condition No special
Medical History Share & see Updates
Report Availability 1–2 D(s)
Specimen/Sample Refer Updates
Stability @21-26 deg. C 8 H(s)
Stability @ 2-8 deg. C 7 D(s)
Stability @ Frozen 6 M(s)
# Test(s) 1
Processing Method Immunoassay
Overview: LKM-1 Antibody Test
Introduction: The LKM-1 Antibody Test detects LKM-1 antibodies to diagnose autoimmune hepatitis, causing jaundice or fatigue. Aligned with 2023 AASLD guidelines, it uses immunoassay for high specificity, supporting liver screening. This test is critical for guiding diagnosis, treatment planning, and improving outcomes in immunology for patients with suspected type 2 autoimmune hepatitis.
Other Names: LKM-1 Assay, Type 2 Autoimmune Hepatitis Test.
FDA Status: Laboratory-developed test (LDT), meeting immunology standards for diagnostic accuracy.
Historical Milestone: LKM-1 antibody testing emerged in the 1980s with autoimmune hepatitis research. Immunoassay methods improved in the 2000s, enhancing diagnostic precision.
Purpose: Detects LKM-1 antibodies to diagnose autoimmune hepatitis, guides treatment, and evaluates patients with jaundice or fatigue.
Test Parameters: 1. LKM-1 Antibodies
Pretest Condition: No fasting required. Collect serum or saliva. Report history of jaundice, fatigue, or liver dysfunction.
Specimen: Serum (SST, 2-5 mL), Saliva (sterile container, 1-2 mL). Transport in a biohazard container.
Sample Stability at Room Temperature: 8 hours
Sample Stability at Refrigeration: 7 days
Sample Stability at Frozen: 6 months
Medical History: Document jaundice, fatigue, abdominal pain, or family history of autoimmune diseases. Include current medications, especially immunosuppressants.
Consent: Written consent required, detailing the tests purpose, autoimmune hepatitis implications, and risks of blood or saliva collection.
Procedural Considerations: Uses immunoassay to detect LKM-1 antibodies in serum or saliva. Results are available in 1-2 days, supporting rapid clinical decisions. Performed in laboratories, often for type 2 autoimmune hepatitis diagnosis.
Factors Affecting Result Accuracy: Hemolysis, lipemia, or improper sample storage can affect results. Insufficient sample volume may reduce accuracy.
Clinical Significance: Positive LKM-1 antibodies confirm type 2 autoimmune hepatitis, guiding immunosuppressive therapy. Negative results may require further autoimmune testing.
Specialist Consultation: Consult a hepatologist for result interpretation and treatment planning.
Additional Supporting Tests: ANA, SMA, or liver biopsy to confirm autoimmune hepatitis diagnosis.
Test Limitations: Specific to type 2 autoimmune hepatitis; other liver diseases may require additional testing. Clinical correlation is needed.
References: AASLD Hepatitis Guidelines, 2023; Hepatology, Manns MP, 2022.

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