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  4. Risk factors of hepatitis during Anti-tuberculous treatment and implications of hepatitis virus load
 
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Risk factors of hepatitis during Anti-tuberculous treatment and implications of hepatitis virus load

Journal
Journal of Infection
Journal Volume
62
Journal Issue
6
Pages
448-455
Date Issued
2011
Author(s)
JANN-YUAN WANG  
CHEN-HUA LIU  
Hu F.-C.
Chang H.-C.
Liu J.-L.
JONG-MIN CHEN  
CHONG-JEN YU  
LI-NA LEE  
JIA-HORNG KAO  
PAN-CHYR YANG  
DOI
10.1016/j.jinf.2011.04.005
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-79958795992&doi=10.1016%2fj.jinf.2011.04.005&partnerID=40&md5=268617c90842edd2a87747630d491e3c
https://scholars.lib.ntu.edu.tw/handle/123456789/512496
Abstract
Objectives: Hepatitis during anti-tuberculous treatment (HATT) has been an obstacle in managing patients with tuberculosis (TB). We evaluate the risk factors of HATT and the clinical implications of serum viral loads in those with concomitant hepatitis B or C viruses (HBV/HCV) infection. Methods: We did a prospective study on patients with pulmonary tuberculosis in a medical center. HATT was defined as an increase in serum transaminase level of >3 times the upper limit of normal (ULN) with symptoms, or an increase in serum transaminase level of >5 times ULN without symptoms. Results: 360 TB patients were studied. The prevalence of concomitant HBV and HCV infection was 11.7% and 6.7%, respectively. HATT developed in 68 (18.9%). Cox regression analysis revealed that severe chronic kidney disease without hemodialysis, N-acetyltransferase (NAT2) slow acetylator, high initial HBV/HCV viral load, and women in those without HBV/HCV infection were significant predictors of drug-induced HATT, whereas severe chronic kidney disease without hemodialysis and men with high initial HBV/HCV viral load were significantly associated virus-induced HATT. Conclusion: HBV/HCV viral load interacts with gender and, together with severe chronic kidney disease without hemodialysis and NAT2 slow acetylator, were predictors of HATT. TB patients with these characteristics need close follow-up. ? 2011 The British Infection Association.
SDGs

[SDGs]SDG3

Other Subjects
arylamine acetyltransferase; cytochrome P450 2E1; tuberculostatic agent; abdominal discomfort; acetylator phenotype; adult; aged; alanine aminotransferase blood level; anorexia; article; aspartate aminotransferase blood level; chronic kidney disease; comorbidity; controlled study; cytochrome P450 2E1 gene; disease association; disease severity; drug fatality; drug induced disease; female; follow up; genetic susceptibility; genotype; hepatitis; hepatitis B; Hepatitis B virus; hepatitis C; Hepatitis C virus; human; hypertransaminasemia; infection risk; liver failure; lung tuberculosis; major clinical study; malaise; male; n acetyltransferase 2 gene; nausea; nonhuman; prediction; prospective study; risk factor; sex difference; side effect; virus gene; virus load; vomiting; Adolescent; Adult; Aged; Aged, 80 and over; Antitubercular Agents; Female; Hepatitis B; Hepatitis C; Humans; Male; Middle Aged; Prevalence; Prospective Studies; Risk Factors; Transaminases; Tuberculosis; Viral Load; Young Adult
Type
journal article

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