Evidence map›Paper›PMID 30608114›Full record

ReviewBiochemistry2019

Targeting Type 1 Diabetes: Selective Approaches for New Therapies.

Daniel F Sheehy, Sean P Quinnell, Arturo J Vegas

Abstract readReview
In one paragraph

Review in Biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Frontiers in pharmacology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Diabetes type 1: Can it be treated as an autoimmune disorder?Reviews in endocrine & metabolic disorders · 2021
    Review
  11. Review
  12. Article
  13. Review
  14. Role of Phosphodiesterase in the Biology and Pathology of Diabetes.International journal of molecular sciences · 2020
    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

3 authors at 1 institution in 1 country.

Daniel F SheehyDepartment of Chemistry , Boston University , Boston , Massachusetts 02215 , United States.
Sean P QuinnellDepartment of Chemistry , Boston University , Boston , Massachusetts 02215 , United States.
Arturo J VegasDepartment of Chemistry , Boston University , Boston , Massachusetts 02215 , United States.ORCID 0000-0001-9522-8208
Boston University · US

Funding

Targeted immunomodulation of the diabetic islet microenvironmentDP2DK111913 · NIDDK · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI VEGAS, ARTURO · 2016 to 2016
$2.1M
NIDDK NIH HHS DP2 DK111913
6 · The paper itself

Abstract

The clinical onset of type 1 diabetes is characterized by the destruction of the insulin-producing β cells of the pancreas and is caused by autoantigen-induced inflammation (insulitis) of the islets of Langerhans. The current standard of care for type 1 diabetes mellitus patients allows for management of the disease with exogenous insulin, but patients eventually succumb to many chronic complications such as limb amputation, blindness, and kidney failure. New therapeutic approaches now on the horizon are looking beyond glycemic management and are evaluating new strategies from protecting and regenerating endogenous islets to treating the underlying autoimmunity through selective modulation of key immune cell populations. Currently, there are no effective treatments for the autoimmunity that causes the disease, and strategies that aim to delay or prevent the onset of the disease will play an important role in the future of diabetes research. In this review, we summarize many of the key efforts underway that utilize molecular approaches to selectively modulate this disease and look at new therapeutic paradigms that can transform clinical treatment.

Indexed as

AnimalsAntigen-Presenting CellsClinical Trials as TopicCytokinesDiabetes Mellitus, Type 1HumansHypoglycemic AgentsImmunity, InnateImmunologic FactorsImmunomodulationImmunotherapyInsulin-Secreting CellsThymus GlandT-LymphocytesCytokinesHypoglycemic AgentsImmunologic Factors

Identifiers

PMID30608114
PMCPMC6774349
OpenAlexW2906846231

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.