Evidence map›Paper›PMID 41802585›Full record

ReviewInternational journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases2026

The role of medical imaging in translational research into early pulmonary tuberculosis.

Yingda L Xie, Iman Raza, Stephanus T Malherbe, Emily A Kendall, Hanif Esmail

Abstract readReview
In one paragraph

Review in International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yingda L XieDepartment of Medicine and Public Health Research Institute, Rutgers New Jersey Medical School, Newark, United States.
Iman RazaUCL Centre for Global Tuberculosis Research and WHO Collaborating Centre for Tuberculosis Research and Innovation, Institute for Global Health, University College London, London, UK; MRC Clinical Trials Unit at University College London, London, UK.
Stephanus T MalherbeSouth African Medical Research Council Centre for Tuberculosis Research, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Emily A KendallDivision of Infectious Diseases, Department of Medicine, Johns Hopkins University, Baltimore, USA.
Hanif EsmailUCL Centre for Global Tuberculosis Research and WHO Collaborating Centre for Tuberculosis Research and Innovation, Institute for Global Health, University College London, London, UK; MRC Clinical Trials Unit at University College London, London, UK. Electronic address: h.esmail@ucl.ac.uk.

Funding

Who are the Ultra-positive, culture-negative? Understanding the trajectories of individuals in Uganda with trace M. tuberculosis nucleic acid in sputumR01HL153611 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI KENDALL, EMILY A · 2020 to 2024
$3.2M
Imaging signatures of early tuberculosisR01AI175555 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Yingda Linda Xie · 2024 to 2026
$2.0M
NHLBI NIH HHS R01 HL153611NIAID NIH HHS R01 AI175555Wellcome Trust
6 · The paper itself

Abstract

Early detection of tuberculosis (TB) is central to global efforts for TB care and prevention. Conventional symptom-based screening and sputum microbiology fail to identify a substantial proportion of cases, particularly those that are asymptomatic or have low bacillary burden. Non-invasive medical imaging offers a critical solution for visualizing pulmonary pathology before individuals with TB develop characteristic symptoms. Chest X-ray has long been central to community screening, and recent advances in computer-aided detection systems endorsed by the World Health Organization have improved scalability and reduced reliance on expert interpretation. However, limitations in sensitivity for the earliest stages of disease and reduced specificity in individuals with prior lung pathology persist, underscoring the need for further research to improve performance for early TB detection. High-resolution modalities, such as computed tomography, magnetic resonance imaging, and functional imaging approaches, such as positron emission tomography and single-photon emission computed tomography, provide unparalleled insights into lesion dynamics, disease activity, and treatment response. They can be utilized to benchmark the development of novel diagnostic tests for bacteriologically unconfirmed TB and define imaging correlates of early disease progression and resolution. Furthermore, emerging innovations in pathogen-specific radiotracers may enable localization of viable bacilli in vivo. As a result, these new high-resolution imaging technologies offer transformative potential to address key knowledge gaps in the natural history, pathogenesis, dissemination, and therapeutic approaches to early pulmonary TB. Together, clinical imaging provides a framework for the development and validation of clinically relevant biomarkers and quantitative readouts that capture early, asymptomatic TB pathology and disease activity before conventional microbiologic confirmation. Future work should focus on integrating advanced imaging with microbiology, host-response biomarkers, and artificial intelligence to define actionable imaging phenotypes that inform early diagnosis, risk stratification, and treatment decision-making across diverse settings.

Indexed as

Diagnostic ImagingTranslational Research, BiomedicalTuberculosis, PulmonaryEarly DiagnosisHumansLungMagnetic Resonance ImagingMycobacterium tuberculosisTomography, X-Ray ComputedAsymptomaticChest X-rayComputed tomographyComputer-aided diagnosticsPositron emission tomographySubclinical

Identifiers

PMID41802585
PMCPMC13629039

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.