Evidence map›Paper›PMID 36634699›Full record

ArticleIslets2023

A small molecule improves diabetes in mice expressing human islet amyloid polypeptide.

Vriti Bhagat, C Bruce Verchere

Open access · goldAbstract read
In one paragraph

Article in Islets, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

2 authors at 1 institution in 1 country.

Vriti BhagatDepartment of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0001-9423-6759
C Bruce VerchereDepartment of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-9262-0586
University of British Columbia · CA

Funding

CIHR
6 · The paper itself

Abstract

In recent years, the number of studies on islet and beta cell autophagy have substantially increased due to growing interest in the role of autophagy in maintaining cellular homeostasis in diabetes. In type 2 diabetes, human islet amyloid polypeptide (hIAPP) aggregates to form higher structure oligomers and fibrils that are toxic to beta cells and induce islet inflammation. The primary mechanism of oligomer and fibril clearance in beta cells is through the autophagic pathway, a process that is impaired in type 2 diabetes. Thus, toxic oligomeric and fibrillar forms of hIAPP accumulate in type 2 diabetic islets. Recently, Kim

Indexed as

Diabetes Mellitus, Type 2Insulin-Secreting CellsAnimalsHumansIslet Amyloid PolypeptideMiceIslet Amyloid Polypeptideamylinamyloidautophagybeta cellsislet amyloid polypeptideIsletssmall molecule

Identifiers

PMID36634699
PMCPMC9839368
OpenAlexW4315752239

What Socratic 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 Socratic graph.