Evidence map›Paper›PMID 25195017›Full record

ReviewNuclear medicine and biology

Nuclear imaging: a powerful novel approach for tuberculosis.

Daniel H Johnson, Laura E Via, Peter Kim, Dominick Laddy, Chuen-Yen Lau, Edward A Weinstein, Sanjay Jain

Abstract readReview
In one paragraph

Review in Nuclear medicine and biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 11% of its field
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

16 citing papers in PubMed, 30 citations in OpenAlex.

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  11. Tailoring Trehalose for Biomedical and Biotechnological Applications.Pure and applied chemistry. Chimie pure et appliquee · 2017
    Article
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  16. PET/CT imaging ofClinical and translational imaging
    Review
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

7 authors at 3 institutions in 1 country.

Daniel H JohnsonNIAID/NIH, Bethesda, MD. Electronic address: daniel.johnson@nih.gov.
Laura E ViaNIAID/NIH, Bethesda, MD.
Peter KimNIAID/NIH, Bethesda, MD.
Dominick LaddyAeras, Rockville MD.
Chuen-Yen LauNIAID/NIH, Bethesda, MD.
Edward A WeinsteinFDA/CDER, Silver Spring, MD.
Sanjay JainCenter for Infection and Inflammation Imaging Research, Center for Tuberculosis Research and Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD.
National Institutes of Health · USAeras · USJohns Hopkins University · US

Funding

Novel imaging biomarkers to address fundamental controversies in TB pathogenesisDP2OD006492 · OD · JOHNS HOPKINS UNIVERSITY · PI JAIN, SANJAY · 2009 to 2014
$2.9M
CAP: Development of a Tuberculosis-Specific PET Imaging AgentZIAAI001164 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BARRY, CLIFTON · 2012 to 2017
$1.3M
Molecular Imaging for Macrophage-Associated Pulmonary InflammationR01HL116316 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI JAIN, SANJAY · 2012 to 2014
$1.2M
Intramural NIH HHSNHLBI NIH HHS R01 HL116316NHLBI NIH HHS R01-HL116316NIH HHS DP2 OD006492NIH HHS DP2-OD006492
6 · The paper itself

Abstract

Nearly 20 years after the World Health Organization declared tuberculosis (TB) a global public health emergency, TB still remains a major global threat with 8.6 million new cases and 1.3 million deaths annually. Mycobacterium tuberculosis adapts to a quiescent physiological state, and is notable for complex interaction with the host, producing poorly-understood disease states ranging from latent infection to fully active disease. Of the approximately 2.5 billion people latently infected with M. tuberculosis, many will develop reactivation disease (relapse), years after the initial infection. While progress has been made on some fronts, the alarming spread of multidrug-resistant, extensively drug-resistant, and more recently totally-drug resistant strains is of grave concern. New tools are urgently needed for rapidly diagnosing TB, monitoring TB treatments and to allow unique insights into disease pathogenesis. Nuclear bioimaging is a powerful, noninvasive tool that can rapidly provide three-dimensional views of disease processes deep within the body and conduct noninvasive longitudinal assessments of the same patient. In this review, we discuss the application of nuclear bioimaging to TB, including the current state of the field, considerations for radioprobe development, study of TB drug pharmacokinetics in infected tissues, and areas of research and clinical needs that could be addressed by nuclear bioimaging. These technologies are an emerging field of research, overcome several fundamental limitations of current tools, and will have a broad impact on both basic research and patient care. Beyond diagnosis and monitoring disease, these technologies will also allow unique insights into understanding disease pathogenesis; and expedite bench-to-bedside translation of new therapeutics. Finally, since molecular imaging is readily available for humans, validated tracers will become valuable tools for clinical applications.

Indexed as

Nuclear MedicineDiagnostic ImagingHumansMycobacterium tuberculosisTuberculosisDrug-resistancePETPharmacokineticsProbe-designSPECT

Identifiers

PMID25195017
PMCPMC4192067
OpenAlexW2096913570

What OpenQuestion holds

Textmetadata
LicenceTDM
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.