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Hepatitis B Core Antibody, IgM

Code:17016|CPT:86705|LOINC:24113-3

Synonyms
Антитела класса IgM к HB-core антигену вируса гепатита В.Antibodies to hepatitis B core antigen, IgMAntibody to hepatitis B core antigen, IgMAnti-HBc, IgMHBcAb, IgMHBV core antibody (IgM)Hepatitis B core antibody, IgM
IncludesHep B Core Ab, IgM

Analysis details

Methodology

  • Immunochemiluminometric assay (ICMA)
  • Chemiluminescent immunoassay (CLIA)

Expected Turnaround Time

1 day

Special Instructions

  • Stop high-dose biotin (vitamin B7/B8, vitamin H, coenzyme R) for at least 72 hours before the blood draw
  • Do not smoke during the 30 minutes before specimen collection

How to use

The Hepatitis B Core Antibody, IgM test (anti-HBc IgM; HBV core antibody, IgM) is used with other hepatitis B virus serologic markers to characterize the clinical stage of infection. It assists in evaluating patients with suspected acute viral hepatitis, helps distinguish convalescence from evolution toward chronic infection, and, when considered alongside other HBV markers, contributes to monitoring of chronic hepatitis B for flares.

Limitations

Hepatitis B virus (HBV) is a DNA virus transmitted through blood and body fluids and remains a global cause of both acute and chronic hepatitis. The core antigen (HBcAg) is strongly immunogenic; anti-HBc IgM appears early, approximately 3–5 weeks after infection. During the late prodromal phase it may be the only specific marker, then typically declines during convalescence, whereas anti-HBc IgG can persist for years. In approximately 9% of acute HBV cases, anti-HBc IgM may be negative in the first two weeks of illness, so repeat testing is warranted in equivocal situations. Detection of HBsAg without anti-HBc IgM supports chronic infection, while emergence of anti-HBc IgM in chronic HBV indicates a flare. A reactive anti-HBc IgM result does not exclude co-infection with other hepatitis viruses, and in patients who are HBsAg positive with hepatitis symptoms but lack anti-HBc IgM, alternative etiologies (e.g., non-A, non-B hepatitis) or hepatitis D virus superinfection should be considered.

Unitqualitative
Reference interval
MinMax
01
IndicationsAssessment of suspected acute viral hepatitis when HBsAg is nonreactive or other viral hepatitis serologies have not yet become positive, Staging and longitudinal follow-up of hepatitis B infection in combination with complementary HBV serologic markers

Specimen Requirements

SpecimenSerum
ContainerGold/Tiger Top (SST, Gel Separator)
Volume1 mL (min 0.4 mL)
Storage InstructionsRoom temperature, Refrigerated, Frozen

References

Abara WE, Qaseem A, Schillie S, et al. Hepatitis B Vaccination, Screening, and Likage to Care: Best Practice Advice from American College of Physicians and the Centers for Disease Control and Prevention. Ann Intern Med. 2017 Dec 5;167(11):794-804. PubMed 29159414

Schillie S, Vellozzi C, Reingold A, et al. Prevention of Hepatitis B Virus Infection in the United States. Recommendations of the Advisory Committee on Immunization Practices. MMWR Recomm Rep. 2018 Jan 12;67(1):1-31. PubMed 29939980

Terrault NA, Lok ASF, McMahon BJ, et al. Update on Prevention, Diagnosis, and Treatment of Chronic Hepatitis B: AASLD 2018 Hepatitis B Guidance. Hepatology. 2018 Apr;67(4):1560-1599. PubMed 29405329

Workowski KA, Bolan GA, Centers for Disease Control and Prevention. Sexually Transmitted Diseases Treatment Guidelines. MMWR Recomm Rep. 2015 Jun 5;64(RR-03):1-137. PubMed 26042815

Harrison's Principles of Internal Medicine. 16th ed. New York: McGraw-Hill; 2005: 1822-1855.