Prevalence of hepatitis B virus (HBV) and latent tuberculosis co‐infection and risk of drug‐induced liver injury across two large HBV cohorts in the United States

Author:

Wong Robert J.12ORCID,Rupp Loralee3,Lu Mei4ORCID,Yang Zeyuan2,Daida Yihe G.5,Schmidt Mark6,Boscarino Joseph A.7,Gordon Stuart C.8,Chitnis Amit S.9

Affiliation:

1. Division of Gastroenterology and Hepatology Stanford University School of Medicine Stanford California USA

2. Gastroenterology Section Veterans Affairs Palo Alto Healthcare System Palo Alto California USA

3. Center for Health Policy & Health Services Research Henry Ford Health System Detroit Michigan USA

4. Department of Public Health Sciences Henry Ford Health System Detroit Michigan USA

5. Center for Integrated Health Care Research Kaiser Permanente Hawaii Portland Oregon USA

6. Center for Health Research Kaiser Permanente Northwest Portland Oregon USA

7. Biomedical Consulting Group, LLC Mahwah New Jersey USA

8. Division of Gastroenterology and Hepatology Henry Ford Health System and Wayne State University School of Medicine Detroit Michigan USA

9. Tuberculosis Section, Alameda County Public Health Department Oakland California USA

Abstract

AbstractThe epidemiology of latent tuberculosis and hepatitis B virus (HBV‐LTBI) co‐infection among U.S. populations is not well studied. We aim to evaluate LTBI testing patterns and LTBI prevalence among two large U.S. cohorts of adults with chronic HBV (CHB). Adults with CHB in the Chronic Hepatitis Cohort Study (CHeCS) and Veterans Affairs national cohort were included in the analyses. Prevalence of HBV‐LTBI co‐infection was defined as the number of HBV patients with LTBI divided by the number of HBV patients in a cohort. Multivariable logistic regression evaluated odds of HBV‐LTBI co‐infection among CHB patients who underwent TB testing. Among 6019 CHB patients in the CHeCS cohort (44% female, 47% Asian), 9.1% were tested for TB, among whom 7.7% had HBV‐LTBI co‐infection. Among HBV‐LTBI co‐infected patient, only 16.7% (n = 7) received LTBI treatment, among whom 28.6% (n = 2) developed DILI. Among 12,928 CHB patients in the VA cohort (94% male, 42% African American, 39% non‐Hispanic white), 14.7% were tested for TB, among whom 14.5% had HBV‐LTBI. Among HBV‐LTBI co‐infected patient, 18.6% (n = 51) received LTBI treatment, among whom 3.9% (n = 3) developed DILI. Presence of cirrhosis, race/ethnicity, and country of birth were observed to be associated with odds of HBV‐LTBI co‐infection among CHB patients who received TB testing. In summary, among two large distinct U.S. cohorts of adults with CHB, testing for LTBI was infrequent despite relatively high prevalence of HBV‐LTBI co‐infection. Moreover, low rates of LTBI treatment were observed among those with HBV‐LTBI co‐infection.

Funder

American College of Gastroenterology

Publisher

Wiley

Subject

Virology,Infectious Diseases,Hepatology

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