Incidence and associated risk factors of anti-tuberculosis drug induced liver injury among TB patients

Tuberculosis (TB) is a global health challenge. Use of anti-TB drugs to treat TB is associated with high prevalence of side effects that include anti-TB drug induced liver injury (ATDILI). The aim of this study was to determine the incidence and associated clinical risk factors of ATDILI among South African patients on treatment for TB disease. This was an ambispective case-control study of patients on treatment for TB disease receiving drug sensitive and drug resistant treatment regimens. The retrospective and prospective studies were done from January 2021 to June 2024, involving a total of 610 patients on treatment for TB disease from whom 13 had ATDILI. From the retrospective and prospective cohorts, we extracted 13 ATDILI cases and 276 controls. Additionally, 44 severe ATDILI cases were directly recruited from the hospital to enrich the number of cases in the study. Prospective patients were followed for up to 6 months, while retrospective participants had a single visit with follow-up durations determined by their parent studies. Logistic regression analysis was performed to identify clinical and demographic factors associated with the development of ATDILI). In the studied cohorts, the incidence of ATDILI was 2.1% (13/610). The ATDILI cases and controls consisted of 215 (64.6%) male patients; 57 patients were diagnosed with hepatotoxicity, 44 from the hospitalized cohort,12 from the retrospective cohort and 1 patient from the prospective cohort. The median time from the initiation of treatment to the onset of hepatotoxicity was approximately 30 days. Univariate logistic regression revealed significant differences (p < 0.05) in sex (p = 0.003), HIV status (p = 0.002), BMI (p = 0.038), hypertension (p = 0.047) smoking (p = 0.006), and alcohol consumption (p = 0.001) in relation to ATDILI. Multivariate analysis further revealed that female sex (p = 0.041), HIV status (0.022) and alcohol consumption (0.048) were independently associated with an increased risk of ATDILI. The incidence of ATDILI in this study was 2.1%, lower than the previously reported range of 3–36% and highlights the need for standardized definitions of phenotypes across studies. In univariable analysis, female sex, HIV status, BMI, hypertension, smoking, and alcohol consumption were identified as potential risk factors for ATDILI. Among these, multivariable analysis suggested that female sex, HIV status and alcohol consumption were associated with an increased risk of developing ATDILI.

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Publication Details

Journal
BMC Infectious Diseases
Published
2025-10-24
DOI
https://doi.org/10.1186/s12879-025-11796-4
Citations
1
Primary Topic
Drug-Induced Hepatotoxicity and Protection
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article
Field-Weighted Citation Impact
1.56

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article

Incidence and associated risk factors of anti-tuberculosis drug induced liver injury among TB patients

Ziyaad Waja, Tom Boyles, Ananyo Choudhury, Roslyn Thelingwani et al.
1 citations
BMC Infectious Diseases
Drug-Induced Hepatotoxicity and Protection
1.56
article

Incidence and associated risk factors of anti-tuberculosis drug induced liver injury among TB patients

Ziyaad Waja, Tom Boyles, Ananyo Choudhury, Roslyn Thelingwani, Vincent Nyangwara, Ziska Pretorius, Keitumetse Majoro, Collen Masimirembwa, Raadhiya Osman, Bekiwe Ncwana
article en
1 citations

Abstract

Tuberculosis (TB) is a global health challenge. Use of anti-TB drugs to treat TB is associated with high prevalence of side effects that include anti-TB drug induced liver injury (ATDILI). The aim of this study was to determine the incidence and associated clinical risk factors of ATDILI among South African patients on treatment for TB disease. This was an ambispective case-control study of patients on treatment for TB disease receiving drug sensitive and drug resistant treatment regimens. The retrospective and prospective studies were done from January 2021 to June 2024, involving a total of 610 patients on treatment for TB disease from whom 13 had ATDILI. From the retrospective and prospective cohorts, we extracted 13 ATDILI cases and 276 controls. Additionally, 44 severe ATDILI cases were directly recruited from the hospital to enrich the number of cases in the study. Prospective patients were followed for up to 6 months, while retrospective participants had a single visit with follow-up durations determined by their parent studies. Logistic regression analysis was performed to identify clinical and demographic factors associated with the development of ATDILI). In the studied cohorts, the incidence of ATDILI was 2.1% (13/610). The ATDILI cases and controls consisted of 215 (64.6%) male patients; 57 patients were diagnosed with hepatotoxicity, 44 from the hospitalized cohort,12 from the retrospective cohort and 1 patient from the prospective cohort. The median time from the initiation of treatment to the onset of hepatotoxicity was approximately 30 days. Univariate logistic regression revealed significant differences (p < 0.05) in sex (p = 0.003), HIV status (p = 0.002), BMI (p = 0.038), hypertension (p = 0.047) smoking (p = 0.006), and alcohol consumption (p = 0.001) in relation to ATDILI. Multivariate analysis further revealed that female sex (p = 0.041), HIV status (0.022) and alcohol consumption (0.048) were independently associated with an increased risk of ATDILI. The incidence of ATDILI in this study was 2.1%, lower than the previously reported range of 3–36% and highlights the need for standardized definitions of phenotypes across studies. In univariable analysis, female sex, HIV status, BMI, hypertension, smoking, and alcohol consumption were identified as potential risk factors for ATDILI. Among these, multivariable analysis suggested that female sex, HIV status and alcohol consumption were associated with an increased risk of developing ATDILI.

BMC Infectious DiseasesVol. 25(1)
Johns Hopkins University (US), University of the Witwatersrand (ZA), Johns Hopkins Medicine (US), African Institute of Biomedical Science and Technology (ZW), Perinatal HIV Research Unit (ZA)
Bill and Melinda Gates Foundation, World Health Organization, South African Medical Research Council, Medical Research Council
Openalex Percentile: Top 14%
Drug-Induced Hepatotoxicity and Protection
1.56
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