KEY BIOMARKER: HBeAg testing

HBeAg indicates immune activity, helps define disease phase, and differentiates between active* and inactive chronic hepatitis B (CHB)1-3

Who to Test

 

BEFORE TREATMENT

All newly diagnosed CHB patients:

To determine immune-tolerant vs immune-active phase of infection2

 

Pregnant women who are HBsAg+:

To assess risk of vertical transmission2,4

HBeAg testing before treatment table

Who to Test

 

DURING TREATMENT

All patients: To monitor HBeAg seroconversion2

 

AFTER TREATMENT

Patients with suspected reactivation or liver flares2

HBeAg testing during and after treatment table

HBeAg and its association with long-term outcomes4-6

 

HBeAg/ANTI-HBe SEROCONVERSION HAS BEEN ASSOCIATED WITH:
Favorable
prognosis
Lower incidence
of cirrhosis
Lower incidence
of HCC

Earlier HBeAg seroconversion may also be associated with improved long-term outcomes.7

 

In a long-term follow-up study (N=770), patients who experienced HBeAg seroconversion after age 40 had a higher risk of cirrhosis and HCC compared with those who seroconverted before age 30 (HR=17.6 [95% CI: 7.15–43.5; P<0.0001] and HR=5.22 [95% CI: 1.17–23.3; P=0.030], respectively).7

* Per AASLD guidelines, immune-active CHB is defined by ALT ≥2X ULN or significant histologic disease with HBV DNA >2,000 IU/mL (HBeAg-negative) or >20,000 IU/mL (HBeAg-positive).2

 

AASLD=American Association for the Study of Liver Diseases; ALT=alanine aminotransferase; anti-HBe=anti–hepatitis B e-antigen; CI=confidence interval; DNA=deoxyribonucleic acid; HBeAg+=hepatitis B e-antigen–positive; HBeAg-=hepatitis B e-antigen–negative; HBsAg+=hepatitis B surface antigen–positive; HBV=hepatitis B virus; HCC=hepatocellular carcinoma; HR=hazard ratio; ULN=upper limit of normal.

Learn about HBV DNA as a biomarker

References

  1. Understanding your test results. Hepatitis B Foundation. Accessed April 5, 2026. https://www.hepb.org/prevention-and-diagnosis/diagnosis/understanding-your-test-results/#:~:text=Understanding

  2. Terrault NA, et al. Hepatology. 2018;67(4):1560-1599.

  3. Wong GLH, Lemoine M. J Hepatol. 2025;82(5):918-925.

  4. European Association for the Study of the Liver. J Hepatol. 2025;83(2):502-583.

  5. Niederau C, et al. N Engl J Med. 1996;334(22):1422-1427.

  6. Lin CL, Kao JH. Clin Mol Hepatol. 2016;22(4):423-431.

  7. Chen YC, et al. Hepatology. 2010;51(2):435-444.