Evidence map›Paper›PMID 31076502›Full record

ArticleJournal of nuclear medicine : official publication, Society of Nuclear Medicine2019

Blocking of Glucagonlike Peptide-1 Receptors in the Exocrine Pancreas Improves Specificity for β-Cells in a Mouse Model of Type 1 Diabetes.

Eshita Khera, Liang Zhang, Sheryl Roberts, Ian Nessler, Darleen Sandoval, Thomas Reiner, Greg M Thurber

Open access · bronzeAbstract read
In one paragraph

Article in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Preliminary evaluation of a novel PSMA-targeting radiopharmaceutical [European journal of nuclear medicine and molecular imaging · 2025
    Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. Optoacoustic Imaging of Glucagon-like Peptide-1 Receptor with a Near-Infrared Exendin-4 Analog.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
    Article
  7. 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
  8. Article
  9. Article
  10. Review
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Eshita KheraDepartment of Chemical Engineering, University of Michigan, Ann Arbor, Michigan.
Liang ZhangDepartment of Chemical Engineering, University of Michigan, Ann Arbor, Michigan.
Sheryl RobertsDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Ian NesslerDepartment of Chemical Engineering, University of Michigan, Ann Arbor, Michigan.
Darleen SandovalDepartment of Surgery, University of Michigan Medical School, Ann Arbor, Michigan.
Thomas ReinerDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Greg M ThurberDepartment of Chemical Engineering, University of Michigan, Ann Arbor, Michigan gthurber@umich.edu.
University of Michigan–Ann Arbor · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Michael Jason de la Cruz · 1985 to 2026
$347.4M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Maximizing Antibody Drug Conjugate Efficacy through Multiple Mechanisms of ActionR35GM128819 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Greg Thurber · 2018 to 2026
$2.8M
Whole Body Imaging of Beta Cell Mass in DiabetesK01DK093766 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THURBER, GREG · 2011 to 2014
$641k
NCI NIH HHS P30 CA008748NIDDK NIH HHS K01 DK093766NIDDK NIH HHS P30 DK020572NIGMS NIH HHS R35 GM128819
6 · The paper itself

Abstract

The diabetes community has long desired an imaging agent to quantify the number of insulin-secreting β-cells, beyond just functional equivalents (insulin secretion), to help diagnose and monitor early stages of both type 1 and type 2 diabetes mellitus. Loss in the number of β-cells can be masked by a compensatory increase in function of the remaining cells. Since β-cells form only about 1% of the pancreas and decrease as the disease progresses, only a few imaging agents, such as exendin, have demonstrated clinical potential to detect a drop in the already scarce signal. However, clinical translation of imaging with exendin has been hampered by pancreatic uptake that is higher than expected in subjects with long-term diabetes who lack β-cells. Exendin binds glucagonlike peptide-1 receptor (GLP-1R), previously thought to be expressed only on β-cells, but recent studies report low levels of GLP-1R on exocrine cells, complicating β-cell mass quantification.

Indexed as

Gene Knockout TechniquesAnimalsDiabetes Mellitus, Type 1Disease Models, AnimalGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorInsulin-Secreting CellsMiceMice, Inbred C57BLPancreas, ExocrinePositron-Emission TomographyGlucagon-Like Peptide 1Glucagon-Like Peptide-1 Receptorbeta cell massexendinexocrine GLP-1Rmouse modelstreptozotocintype 1 diabetes

Identifiers

PMID31076502
PMCPMC6836864
OpenAlexW2944056919

What Socratic holds

Textmetadata
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 Socratic graph.