Evidence map›Paper›PMID 24965561›Full record

ArticleInternational journal of rheumatic diseases2016

In vivo quantification of mouse autoimmune arthritis by PET/CT.

Smriti Kundu-Raychaudhuri, Anupam Mitra, Ananya Datta-Mitra, Abhijit J Chaudhari, Siba P Raychaudhuri

Open access · greenAbstract readComparative Study
In one paragraph

Article in International journal of rheumatic diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Development of an Ultra High Resolution PET Scanner for Imaging Rodent Paws: PawPET.IEEE transactions on radiation and plasma medical sciences · 2018
    Article
  4. 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 at 2 institutions in 1 country.

Smriti Kundu-RaychaudhuriDivision of Rheumatology, Allergy and Clinical Immunology, School of Medicine, University of California Davis, Davis, California, USA.
Anupam MitraVA Northern California Health Care System, Sacramento, California, USA.
Ananya Datta-MitraDivision of Rheumatology, Allergy and Clinical Immunology, School of Medicine, University of California Davis, Davis, California, USA.
Abhijit J ChaudhariDepartment of Radiology, School of Medicine, University of California Davis, Sacramento, California, USA.
Siba P RaychaudhuriDivision of Rheumatology, Allergy and Clinical Immunology, School of Medicine, University of California Davis, Davis, California, USA.
University of California, Davis · USVA Northern California Health Care System · US

Funding

UC DAVIS CLINICAL AND TRANSLATIONAL SCIENCE CENTER: BPCAUL1RR024146 · NCRR · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BERGLUND, LARS F · 2006 to 2011
$27.0M
Building Interdisciplinary Research Careers in Womens Health at UC Davis - Administrative SupplementK12HD051958 · NICHD · UNIVERSITY OF CALIFORNIA DAVIS · PI LANE, NANCY E · 2005 to 2023
$9.6M
NCRR NIH HHS UL1 RR024146NICHD NIH HHS K12 HD051958
6 · The paper itself

Abstract

aimTo quantify the progression and severity of mouse collagen-induced arthritis (CIA) using an in vivo imaging tool, (18) F-fluorodeoxyglucose ((18) F-FDG) PET/CT and validate it against gold standard 'histopathological' evaluation.

methodThe PET radiotracer (18) F-FDG, a marker for glucose metabolism, was injected in mice at different stages of CIA and the radiotracer distribution was imaged using a PET scanner. A sequential CT scan provided correlated anatomy. Radiotracer concentration was derived from PET/CT images for individual limb joints and on a per-limb basis at different stages of the disease. The imaging outcomes were subjected to correlation analysis with concurrently measured clinical and histological score.

resultsClinical and histological score, and hence disease severity, showed a strong linear correlation (r(2)  = 0.71, P = 0.001 and r(2)  = 0.87, P < 0.001, respectively) with radiotracer concentration measured from PET/CT during the progression of CIA.

conclusionsThe strong positive correlation of the (18) F-FDG PET/CT findings with the histopathological evaluation at different stages of the disease suggest the potential of this imaging tool for the non-invasive assessment of progression and severity in mouse autoimmune arthritis. Thus, in preclinical studies, (18) F-FDG PET/CT can be considered as a non-invasive tool to develop novel therapies of inflammatory arthritis.

Indexed as

AutoimmunityPositron Emission Tomography Computed TomographyAnimalsArthritis, ExperimentalCollagenDisease ProgressionFluorodeoxyglucose F18JointsMaleMice, Inbred DBAPredictive Value of TestsRadiopharmaceuticalsSeverity of Illness IndexTime FactorsCollagenFluorodeoxyglucose F18Radiopharmaceuticalsinflammationin vivo imagingmouse CIAPET/CTquantification

Identifiers

PMID24965561
PMCPMC4277495
OpenAlexW1970563169

What OpenQuestion holds

Textmetadata
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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.