Evidence map›Paper›PMID 22634342›Full record

ArticleJournal of hepatology2012

Molecular MR imaging of liver fibrosis: a feasibility study using rat and mouse models.

Miloslav Polasek, Bryan C Fuchs, Ritika Uppal, Daniel T Schühle, Jamu K Alford, Galen S Loving, Suguru Yamada, Lan Wei, Gregory Y Lauwers, Alexander R Guimaraes and 2 more

Abstract read
In one paragraph

Article in Journal of hepatology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

61 citing papers in PubMed, 113 citations in OpenAlex.

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1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Miloslav PolasekA A Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, 149 Thirteenth St., Suite 2301, Charlestown, MA 02129, United States.
Bryan C Fuchs
Ritika Uppal
Daniel T Schühle
Jamu K Alford
Galen S Loving
Suguru Yamada
Lan Wei
Gregory Y Lauwers
Alexander R Guimaraes
Kenneth K Tanabe
Peter Caravan
Harvard University · USMassachusetts General Hospital · USAthinoula A. Martinos Center for Biomedical Imaging · US

Funding

Stable, High Relaxivity MRI Contrast AgentsR01EB009062 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI CARAVAN, PETER D · 2009 to 2017
$4.9M
TARGETTING DIFFUSE LIVER METASTASES WITH HERPES VIRUSR01CA076183 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI TANABE, KENNETH K · 2000 to 2010
$3.0M
NUCLEAR MAGNETIC RESONANCE RESEARCHT32CA009502 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI MOORE, ANNA · 1985 to 2013
$2.0M
The Role of EGF in Human Hepatocellular TransformationK01CA140861 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FUCHS, BRYAN CHRISTOPHER · 2009 to 2013
$710k
500 MHz NMR Spectrometer for Molecular Imaging ApplicationsS10RR023385 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI ROSEN, BRUCE R · 2007 to 2007
$500k
NCI NIH HHS CA009502NCI NIH HHS CA076183NCI NIH HHS CA140861NCI NIH HHS K01 CA140861NCI NIH HHS R01 CA076183NCI NIH HHS T32 CA009502NCRR NIH HHS S10 RR023385NIBIB NIH HHS EB009062NIBIB NIH HHS R01 EB009062
6 · The paper itself

Abstract

BACKGROUND &

aimsLiver biopsy, the current clinical gold standard for fibrosis assessment, is invasive and has sampling errors, and is not optimal for screening, monitoring, or clinical decision-making. Fibrosis is characterized by excessive accumulation of extracellular matrix proteins including type I collagen. We hypothesize that molecular magnetic resonance imaging (MRI) with a probe targeted to type I collagen could provide a direct and non-invasive method of fibrosis assessment.

methodsLiver fibrosis was induced in rats with diethylnitrosamine and in mice with carbon tetrachloride. Animals were imaged prior to and immediately following i.v. administration of either collagen-targeted probe EP-3533 or non-targeted control Gd-DTPA. Magnetic resonance (MR) signal washout characteristics were evaluated from T1 maps and T1-weighted images. Liver tissue was subjected to pathologic scoring of fibrosis and analyzed for gadolinium and hydroxyproline.

resultsEP-3533-enhanced MR showed greater signal intensity on delayed imaging (normalized signal enhancement mice: control=0.39 ± 0.04, fibrotic=0.55 ± 0.03, p<0.01) and slower signal washout in the fibrotic liver compared to controls (liver t(1/2)=51.3 ± 3.6 vs. 42.0 ± 2.5 min, p<0.05 and 54.5 ± 1.9 vs. 44.1 ± 2.9 min, p<0.01 for fibrotic vs. controls in rat and mouse models, respectively). Gd-DTPA-enhanced MR could not distinguish fibrotic from control animals. EP-3533 gadolinium concentration in the liver showed strong positive correlations with hydroxyproline levels (r=0.74 (rats), r=0.77 (mice)) and with Ishak scoring (r=0.84 (rats), r=0.79 (mice)).

conclusionsMolecular MRI of liver fibrosis with a collagen-specific probe identifies fibrotic tissue in two rodent models of disease.

Indexed as

Magnetic Resonance ImagingMolecular ImagingAnimalsCarbon TetrachlorideCollagen Type IContrast MediaDiethylnitrosamineDisease Models, AnimalGadoliniumHalf-LifeHydroxyprolineLiverLiver CirrhosisMaleMiceMolecular ProbesCarbon TetrachlorideCollagen Type IContrast MediaDiethylnitrosamineGadoliniumHydroxyprolineMolecular Probes

Identifiers

PMID22634342
PMCPMC3423553
OpenAlexW2146967775

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.