Evidence map›Paper›PMID 29326366›Full record

ArticleDiabetes2018

Highly Proliferative α-Cell-Related Islet Endocrine Cells in Human Pancreata.

Carol J Lam, Aaron R Cox, Daniel R Jacobson, Matthew M Rankin, Jake A Kushner

Abstract read
In one paragraph

Article in Diabetes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Evolving Characteristics of Type 2 Diabetes Mellitus in East Asia.Endocrinology and metabolism (Seoul, Korea) · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Scaling Insulin-Producing Cells by Multiple Strategies.Endocrinology and metabolism (Seoul, Korea) · 2024
    Review
  10. Article
  11. β-Cell Heterogeneity and Plasticity.Advances in anatomy, embryology, and cell biology · 2024
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

Carol J LamMcNair Medical Institute, Baylor College of Medicine, Houston, TX.
Aaron R CoxMcNair Medical Institute, Baylor College of Medicine, Houston, TX jake.kushner@mac.com racox@bcm.edu.
Daniel R JacobsonDivision of Endocrinology and Diabetes, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, PA.
Matthew M RankinDivision of Endocrinology and Diabetes, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, PA.
Jake A KushnerMcNair Medical Institute, Baylor College of Medicine, Houston, TX jake.kushner@mac.com racox@bcm.edu.ORCID 0000-0002-3646-1744
Baylor College of Medicine · USChildren's Hospital of Philadelphia · US

Funding

Diabetes Endocrinology Research CenterP30DK079638 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI CHAN, LAWRENCE · 2008 to 2012
$6.4M
Cell Lineage and Homeostasis of Pancreatic Beta Cells in the AgedR01AG040110 · NIA · BAYLOR COLLEGE OF MEDICINE · PI KUSHNER, JAKE ALDEN · 2011 to 2015
$1.7M
NIA NIH HHS R01 AG040110NIDDK NIH HHS P30 DK079638
6 · The paper itself

Abstract

The proliferative response of non-β islet endocrine cells in response to type 1 diabetes (T1D) remains undefined. We quantified islet endocrine cell proliferation in a large collection of nondiabetic control and T1D human pancreata across a wide range of ages. Surprisingly, islet endocrine cells with abundant proliferation were present in many adolescent and young-adult T1D pancreata. But the proliferative islet endocrine cells were also present in similar abundance within control samples. We queried the proliferating islet cells with antisera against various islet hormones. Although pancreatic polypeptide, somatostatin, and ghrelin cells did not exhibit frequent proliferation, glucagon-expressing α-cells were highly proliferative in many adolescent and young-adult samples. Notably, α-cells only comprised a fraction (∼1/3) of the proliferative islet cells within those samples; most proliferative cells did not express islet hormones. The proliferative hormone-negative cells uniformly contained immunoreactivity for ARX (indicating α-cell fate) and cytoplasmic Sox9 (Sox9

Indexed as

Cell ProliferationDiabetes Mellitus, Type 1AdolescentAdultCase-Control StudiesCell LineageCell PlasticityChildChild, PreschoolFemaleGhrelinGlucagonGlucagon-Secreting CellsHomeodomain ProteinsHumansInfantARX protein, humanGhrelinGlucagonHomeodomain ProteinsKi-67 AntigenPancreatic PolypeptideSomatostatinSOX9 protein, humanSOX9 Transcription FactorTranscription Factors

Identifiers

PMID29326366
PMCPMC5860854
OpenAlexW2784061946

What OpenQuestion 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 OpenQuestion graph.