Nutritional Deficiencies and Management in Tuberculosis: Pharmacotherapeutic and Clinical Implications.

Publication date: May 30, 2025

Tuberculosis is an infectious condition caused by Mycobacterium tuberculosis, primarily targeting the pulmonary system, with the potential to disseminate to various other organs via the haematogenous pathway, ranking among the top ten causes of global mortality. Tuberculosis remains a serious public health problem worldwide. This narrative review aims to emphasise the clinical importance of the inter-relationships between nutrition, pharmacotherapy, and the most common drug-nutrient interactions in the context of tuberculosis and multi-drug-resistant tuberculosis management. Nowadays, pharmacologic approaches utilise polytherapeutic regimens that, although showing increased efficacy, prominently affect the nutritional status of patients and modify multiple metabolic pathways, thus influencing both the effectiveness of therapy and the patient outcomes. There is much evidence that antituberculosis drugs are associated with deficiencies in essential vitamins and various micronutrients, leading to serious adverse consequences. Moreover, poor nutrition exacerbates TB outcomes, and TB further exacerbates nutritional status, a vicious cycle that is particularly prevalent in low-resource environments. Nutritional support is necessary, and clinicians ought to evaluate it on a patient-by-patient basis, as empirical evidence has shown that it can improve immune recovery, decrease tuberculosis-associated morbidity, and increase adherence to therapy. However, drug-food interactions are increasingly prevalent, and patients with tuberculosis require personalised dietary and pharmacological regimens. In this context, antituberculosis treatment requires a holistic approach, based on the collaboration of the prescribing physician, pharmacist, and nutritionist, to assess the patient’s needs from a nutritional and pharmacological perspective, with the ultimate goal of decreasing mortality and improving the prognosis of patients through personalised therapies.

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Concepts Keywords
Mycobacterium Antitubercular Agents
Nutritional Antitubercular Agents
Therapy antituberculosis therapy
Tuberculosis clinical nutrition
Vicious drug–food interactions
Food-Drug Interactions
Humans
Malnutrition
Micronutrients
Micronutrients
Nutritional Status
Nutritional Support
nutritional support
Tuberculosis
tuberculosis deficiencies
tuberculosis management
Tuberculosis, Multidrug-Resistant

Semantics

Type Source Name
disease MESH Nutritional Deficiencies
disease MESH Tuberculosis
pathway KEGG Tuberculosis
drug DRUGBANK Pentaerythritol tetranitrate
disease MESH causes
disease MESH clinical importance
disease MESH drug-resistant tuberculosis
disease MESH nutritional status
pathway KEGG Metabolic pathways
pathway REACTOME Vitamins
disease MESH morbidity
disease MESH drug-food interactions
disease MESH co infection
disease IDO susceptibility
disease MESH treatment failure
disease IDO pathogen
disease IDO drug susceptibility
disease MESH aids
pathway REACTOME Immune System
disease IDO host
disease IDO bacteria
disease IDO replication
disease MESH infection
disease MESH parasite infections
disease IDO cell
disease IDO bactericidal
drug DRUGBANK Isoniazid
drug DRUGBANK Rifampicin
drug DRUGBANK Ethambutol
drug DRUGBANK Pyrazinamide
drug DRUGBANK Levofloxacin
drug DRUGBANK Streptomycin
disease MESH colic
disease IDO process
disease IDO bacteriostatic
disease IDO production
drug DRUGBANK Ethanol
disease MESH recurrence
drug DRUGBANK Bedaquiline
drug DRUGBANK Pretomanid
drug DRUGBANK Linezolid
drug DRUGBANK Moxifloxacin
drug DRUGBANK Delamanid
drug DRUGBANK Clofazimine
drug DRUGBANK Cycloserine
drug DRUGBANK Rifapentine
disease MESH HIV infections
disease MESH immune reconstitution inflammatory syndrome
disease IDO organism
disease MESH syndrome
disease MESH infectious diseases
pathway REACTOME Digestion
disease MESH oxidative stress
drug DRUGBANK Trestolone
drug DRUGBANK Coenzyme M
disease MESH abnormalities
pathway REACTOME Intestinal absorption
drug DRUGBANK Leptin
disease MESH protein energy malnutrition
disease MESH obesity
pathway REACTOME Metabolism
pathway REACTOME Glucose metabolism
disease MESH starvation
disease IDO protein
disease MESH iron deficiency
drug DRUGBANK Zinc
drug DRUGBANK Vitamin D
disease MESH inflammation
pathway REACTOME Complement cascade
disease MESH atrophy
disease MESH leukopenia
disease MESH hypersensitivity
disease MESH vitamin deficiency
disease MESH scurvy
drug DRUGBANK Iron
drug DRUGBANK Copper
drug DRUGBANK Selenium
drug DRUGBANK Folic Acid
disease MESH physical barriers
disease MESH anxiety
drug DRUGBANK Tretinoin
drug DRUGBANK Indoleacetic acid
disease MESH death
disease MESH overweight
disease IDO history

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