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Chronic kidney disease in isolated core antibody positive hepatitis B patients: Risk analysis from NHANES 2017-2020
Ke Mi1, Tingdan Ye1, Calvin Q Pan2
1Center of Liver Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Insights
Isolated hepatitis B core antibody (HBcAb) positivity did not show a positive association with chronic kidney disease (CKD) risk in US adults. However, older age and elevated serum urea nitrogen were linked to higher CKD risk in this group.
Area of Science:
- Nephrology
- Hepatology
- Epidemiology
Background:
- The link between isolated hepatitis B core antibody (HBcAb) positivity and chronic kidney disease (CKD) is debated.
- Some studies suggest a connection between hepatitis B virus (HBV) infection and increased CKD risk, while others present inconclusive findings.
- This research investigates the association between isolated HBcAb positivity and CKD within the U.S. population.
Purpose of the Study:
- To evaluate the association between isolated HBcAb positivity and the prevalence of CKD in U.S. adults.
- To identify risk factors for CKD among individuals with isolated HBcAb positivity.
Main Methods:
- Analysis of data from adult participants in the NHANES 2017-2020 cycle.
- Categorization of participants into isolated HBcAb positive and non-infected groups.
- Use of logistic regression models to assess the association between isolated HBcAb positivity and CKD, with multivariate analysis to identify risk factors.
Main Results:
- CKD prevalence was higher in the isolated HBcAb positive group (7.9%) compared to the non-infected group (5.2%).
- Unadjusted analysis indicated an increased CKD risk with isolated HBcAb positivity (OR=1.25), but adjusted analyses revealed an inverse association (OR=0.76).
- Among isolated HBcAb positive individuals, older age and elevated serum urea nitrogen (BUN) were associated with higher CKD risk, while higher education was associated with reduced risk.
Conclusions:
- Despite higher CKD prevalence in the isolated HBcAb positive group, no positive association with CKD risk was found after adjustment.
- Older age and elevated BUN levels are significant risk factors for CKD in this population.
- Findings emphasize the need for individualized monitoring and management strategies for HBV-infected patients, particularly concerning antiviral therapy and post-cure follow-up.
Background:
The association between isolated hepatitis B core antibody (HBcAb) positivity and chronic kidney disease (CKD) remains debated. While some studies suggest HBV infection increases CKD risk, others report inconclusive findings. This study evaluated the association between isolated HBcAb positivityand CKD in the U.S.
Methods:
Data from adult participants in the NHANES 2017-2020 pre-pandemic cycle were analyzed based on prespecified eligibility criteria. Participants were categorized into isolated HBcAb positive and non-infected groups. Weighted means and percentages described participant characteristics, while logistic regression models evaluated the association between isolated HBcAb positive and CKD. Multivariate logistic regression identified CKD risk factors among isolated HBcAb positive individuals.
Results:
Among 7,582 participants (7072 non- infected and 510 isolated HBcAb positive), CKD prevalence was higher in isolated HBcAb positive individuals (7.9 %vs. 5.2 %, P = 0.018). Unadjusted analyses showed isolated HBcAb positivity increased CKD risk (OR = 1.25, 95 % CI: 1.04-1.50, P = 0.019). However, adjusted analyses revealed an inverse association (OR = 0.76, 95 % CI: 0.60-0.98, P = 0.034). In isolated HBcAb positive individuals, older age (OR = 1.06, P = 0.017) and serum urea nitrogen (BUN) elevation (OR = 1.20, P = 0.001) were associated with higher CKD risk, while higher education lever reduced the risk (OR = 0.28, P = 0.030).
Conclusion:
Although CKD prevalence was higher in isolated HBcAb positive patients, There was no positive association between isolated HBcAb positivity and CKD. Older age and elevated BUN levels were significantly associated with higher CKD risk, while elevated education lever reduced the risk. These findings highlight the needs for individualized monitoring and management of at-risk HBV-infected patients when offering antiviral therapy and monitoring after clinical cure of hepatitis B.
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