Rifampicin Exposure in Tuberculosis Patients with Comorbidities in Sub-Saharan Africa: Prioritising Populations for Treatment-A Systematic Review and Meta-analysis.

Publication date: Jul 03, 2025

Emerging evidence suggests that comorbidities like human immunodeficiency virus (HIV) infection, diabetes mellitus (DM), and malnutrition in tuberculosis (TB) patients can alter drug concentrations, thereby affecting the treatment outcomes. For these populations, personalised strategies such as therapeutic drug monitoring (TDM) may be essential. We investigated the variations of drug levels within comorbid populations and analysed the differences in patterns observed between sub-Saharan Africa (SSA) and non-SSA regions. We performed a systematic review and meta-analysis of rifampicin drug pharmacokinetics (PK) through searches of major databases from 1980 to December 2023. A random-effects meta-analysis model using R-studio version 4. 3.2 was conducted to estimate pooled serum rifampicin exposure (area under the concentration-time curve [AUC], and peak maximum concentration [C]) between patients with TB-HIV infection, and TB-DM. From 3300 articles screened, 24 studies met inclusion criteria, contributing 33 comorbidity subgroups for meta-analysis. In SSA, 14 subgroups assessed rifampicin PK in TB-HIV, 1 in TB-DM, and none in TB-malnutrition. The pooled mean C was below the recommended range (8-24 mg/L) for all subgroups. For TB-HIV, the pooled C was 5. 59 mg/L, 95% CI (4. 59-6. 59), I = 97% for SSA populations and 5. 59 mg/L, 95% CI (3. 65; 6. 59) for non-SSA populations. The C for TB-DM in SSA (9. 60 +/- 4. 4 mg/L) exceeded non-SSA (4. 27 mg/L, 95% CI [2. 77-5. 76]). The lowest AUC was in TB-HIV (SSA, 29. 09 mg/L h, 95% CI [21. 06; 37. 13, I = 91%]). High variability and heterogeneity (I >90%) were observed, with most studies (20/23) showing low bias. Our results emphasise the need for individualised dosing and targeted TDM implementation among TB-HIV and TB-DM populations on rifampicin in SSA. Although all populations exhibited low C levels, TB-HIV populations may be prioritised as AUC levels were lowest. In clinical settings in SSA, C-based TDM is more practical, but AUC can be used in treatment where feasible.

Concepts Keywords
Africa Analysis
December Auc
Diabetes Dm
Emergingevidence Drug
Pharmacokinetics Hiv
Meta
Mg
Pooled
Populations
Rifampicin
Ssa
Tb
Tdm
Treatment

Semantics

Type Source Name
drug DRUGBANK Rifampicin
disease MESH Tuberculosis
pathway KEGG Tuberculosis
disease IDO immunodeficiency
disease MESH infection
disease MESH diabetes mellitus
disease MESH malnutrition
disease MESH HIV infection
pathway REACTOME HIV Infection
drug DRUGBANK Methionine
disease MESH comorbidity

Original Article

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