Evidence map›Paper›PMID 39080381›Full record

ArticleScientific reports2024

Computer-aided prognosis of tuberculous meningitis combining imaging and non-imaging data.

Liane S Canas, Trinh H K Dong, Daniel Beasley, Joseph Donovan, Jon O Cleary, Richard Brown, Nguyen Thuy Thuong Thuong, Phu Hoan Nguyen, Ha Thi Nguyen, Reza Razavi and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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  5. 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

14 authors.

Liane S CanasSchool of Biomedical Engineering & Imaging Sciences, King's College London, London, UK. liane.dos_santos_canas@kcl.ac.uk.
Trinh H K DongSchool of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
Daniel BeasleySchool of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
Joseph DonovanOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Jon O ClearySchool of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
Richard BrownSchool of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
Nguyen Thuy Thuong ThuongNuffield Department of Medicine, University of Oxford, Oxford, UK.
Phu Hoan NguyenNuffield Department of Medicine, University of Oxford, Oxford, UK.
Ha Thi NguyenNuffield Department of Medicine, University of Oxford, Oxford, UK.
Reza RazaviSchool of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
Sebastien OurselinSchool of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
Guy E ThwaitesNuffield Department of Medicine, University of Oxford, Oxford, UK.
Marc ModatSchool of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
Vietnam ICU Translational Applications Laboratory (VITAL) Investigators

Funding

EPSRC EP/T022205/1Wellcome EPSRC Centre for Medical Engineering 203148/Z/16/ZWellcome TrustWellcome Trust 215010/Z/18/Z
6 · The paper itself

Abstract

Tuberculous meningitis (TBM) is the most lethal form of tuberculosis. Clinical features, such as coma, can predict death, but they are insufficient for the accurate prognosis of other outcomes, especially when impacted by co-morbidities such as HIV infection. Brain magnetic resonance imaging (MRI) characterises the extent and severity of disease and may enable more accurate prediction of complications and poor outcomes. We analysed clinical and brain MRI data from a prospective longitudinal study of 216 adults with TBM; 73 (34%) were HIV-positive, a factor highly correlated with mortality. We implemented an end-to-end framework to model clinical and imaging features to predict disease progression. Our model used state-of-the-art machine learning models for automatic imaging feature encoding, and time-series models for forecasting, to predict TBM progression. The proposed approach is designed to be robust to missing data via a novel tailored model optimisation framework. Our model achieved a 60% balanced accuracy in predicting the prognosis of TBM patients over the six different classes. HIV status did not alter the performance of the models. Furthermore, our approach identified brain morphological lesions caused by TBM in both HIV and non-HIV-infected, associating lesions to the disease staging with an overall accuracy of 96%. These results suggest that the lesions caused by TBM are analogous in both populations, regardless of the severity of the disease. Lastly, our models correctly identified changes in disease symptomatology and severity in 80% of the cases. Our approach is the first attempt at predicting the prognosis of TBM by combining imaging and clinical data, via a machine learning model. The approach has the potential to accurately predict disease progression and enable timely clinical intervention.

Indexed as

BrainMachine LearningMagnetic Resonance ImagingTuberculosis, MeningealAdultDisease ProgressionFemaleHIV InfectionsHumansLongitudinal StudiesMaleMiddle AgedPrognosisProspective StudiesDenseNetLong short-term memory networkMachine learningMRI imagingPrognosisTuberculous meningitis

Identifiers

PMID39080381
PMCPMC11289120

What Socratic holds

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Registered trials

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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 Socratic graph.