Abstract

BackgroundThe country of Georgia has a high prevalence of tuberculosis (TB) and hepatitis C virus (HCV) infection. PurposeTo determine whether HCV co-infection increases the risk of incident drug-induced hepatitis among patients on first-line anti-TB drug therapy.MethodsProspective cohort study; HCV serology was obtained on all study subjects at the time of TB diagnosis; hepatic enzyme tests (serum alanine aminotransferase [ALT] activity) were obtained at baseline and monthly during treatment. ResultsAmong 326 study patients with culture-confirmed TB, 68 (21%) were HCV co-infected, 14 (4.3%) had chronic hepatitis B virus (HBV) infection (hepatitis B virus surface antigen positive [HBsAg+]), and 6 (1.8%) were HIV co-infected. Overall, 19% of TB patients developed mild to moderate incident hepatotoxicity. In multi-variable analysis, HCV co-infection (adjusted Hazards Ratio [aHR]=3.2, 95% CI=1.6-6.5) was found to be an independent risk factor for incident anti-TB drug-induced hepatotoxicity. Survival analysis showed that HCV co-infected patients developed hepatitis more quickly compared to HCV seronegative patients with TB.ConclusionA high prevalence of HCV co-infection was found among patients with TB in Georgia. Drug-induced hepatotoxicity was significantly associated with HCV co-infection but severe drug-induced hepatotoxicity (WHO grade III or IV) was rare.

Highlights

  • The World Health Organization (WHO) estimates there were 8.6 million new cases of tuberculosis (TB) globally in 2012 and 1.3 million deaths due to TB[1]

  • TB is widespread in Georgia and other countries of the former Soviet Union and it has emerged as a major public health problem, including a high prevalence of multi-drug resistant TB (MDR-TB) [2,3,4,5]

  • Patients with active TB disease and hepatitis C virus (HCV) co-infection in our study had a similar HCV genotype distribution to that previously reported in Georgia [19]; we found no differences in incident hepatotoxicity by HCV genotype

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Summary

Introduction

The World Health Organization (WHO) estimates there were 8.6 million new cases of tuberculosis (TB) globally in 2012 and 1.3 million deaths due to TB[1]. TB is widespread in Georgia and other countries of the former Soviet Union and it has emerged as a major public health problem, including a high prevalence of multi-drug resistant TB (MDR-TB) [2,3,4,5]. The country of Georgia has a high prevalence of tuberculosis (TB) and hepatitis C virus (HCV) infection. Purpose: To determine whether HCV co-infection increases the risk of incident drug-induced hepatitis among patients on first-line anti-TB drug therapy. In multi-variable analysis, HCV co-infection (adjusted Hazards Ratio [aHR]=3.2, 95% CI=1.6-6.5) was found to be an independent risk factor for incident anti-TB drug-induced hepatotoxicity. Conclusion: A high prevalence of HCV co-infection was found among patients with TB in Georgia. Drug-induced hepatotoxicity was significantly associated with HCV co-infection but severe drug-induced hepatotoxicity (WHO grade III or IV) was rare

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