Evidence map›Paper›PMID 26886298›Full record

ArticleMolecular imaging and biology2016

Strain Differences Determine the Suitability of Animal Models for Noninvasive In Vivo Beta Cell Mass Determination with Radiolabeled Exendin.

Stefanie M A Willekens, Lieke Joosten, Otto C Boerman, Alexander Balhuizen, Decio L Eizirik, Martin Gotthardt, Maarten Brom

Open access · hybridAbstract read
In one paragraph

Article in Molecular imaging and biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Reply: From Mice to Humans: The Exocrine Pancreas Does Not Matter in Human GLP-1 Receptor Imaging.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Molecular imaging of β-cells: diabetes and beyond.Advanced drug delivery reviews · 2019
    Review
  9. Article
  10. 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

7 authors at 3 institutions in 2 countries.

Stefanie M A WillekensDepartment of Radiology and Nuclear Medicine, Radboud University Medical Center, PO BOX 9101, 6500 HB, Nijmegen, The Netherlands. Stefanie.willekens@radboudumc.nl.
Lieke JoostenDepartment of Radiology and Nuclear Medicine, Radboud University Medical Center, PO BOX 9101, 6500 HB, Nijmegen, The Netherlands.
Otto C BoermanDepartment of Radiology and Nuclear Medicine, Radboud University Medical Center, PO BOX 9101, 6500 HB, Nijmegen, The Netherlands.
Alexander BalhuizenULB Center for Diabetes Research, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Decio L EizirikULB Center for Diabetes Research, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Martin GotthardtDepartment of Radiology and Nuclear Medicine, Radboud University Medical Center, PO BOX 9101, 6500 HB, Nijmegen, The Netherlands.
Maarten BromDepartment of Radiology and Nuclear Medicine, Radboud University Medical Center, PO BOX 9101, 6500 HB, Nijmegen, The Netherlands.
Radboud University Medical Center · NLUniversité Libre de Bruxelles · BERadboud University Nijmegen · NL

Funding

Non-invasive beta-cell imaging using a Ga-68-labeled glucagone-like peptide-1 anaR01AG030328 · NIA · RADBOUD UNIVERSITY NIJMEGEN MED CTR · PI GOTTHARDT, MARTIN · 2006 to 2008
$438k
NIA NIH HHS R01 AG030328
6 · The paper itself

Abstract

purposeNoninvasive beta cell mass (BCM) quantification is a crucial tool to understand diabetes development and progression. [(111)In]exendin is a promising agent for in vivo beta cell imaging, but tracer testing has been hampered by the lack of well-defined rodent models. PROCEDURES: Biodistribution and pancreatic uptake of [(111)In]exendin were compared in rats and mice. In selected models, the amount of [(111)In]exendin accumulation in the pancreas and other organs was determined using a model of alloxan-induced beta cell loss. GLP-1R expression levels were analyzed by RT-PCR and immunohistochemistry.

resultsNamely Brown Norway rats showed beta-cell-specific tracer accumulation and favorable pancreas-to-background ratios for noninvasive BCM determination. Mice displayed receptor-mediated [(111)In]exendin uptake in endocrine and exocrine pancreas, in spite of very low GLP-1R expression in exocrine tissue.

conclusionsRats display better characteristics for in vivo BCM determination than mice and are suggested as a more adequate model for humans.

Indexed as

AlloxanAnimalsExenatideImmunohistochemistryIndium RadioisotopesInsulin-Secreting CellsMice, Inbred StrainsModels, AnimalPeptidesRadiopharmaceuticalsRatsReal-Time Polymerase Chain ReactionSpecies SpecificityTissue DistributionVenomsAlloxanExenatideIndium RadioisotopesPeptidesRadiopharmaceuticalsVenomsBeta cell massDiabetesExendinGLP-1RReceptor targeting

Identifiers

PMID26886298
PMCPMC5010585
OpenAlexW2469693912

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.