Evidence map›Paper›PMID 26798148›Full record

ArticleDiabetes care2016

The Time Is Right for a New Classification System for Diabetes: Rationale and Implications of the β-Cell-Centric Classification Schema.

Stanley S Schwartz, Solomon Epstein, Barbara E Corkey, Struan F A Grant, James R Gavin, Richard B Aguilar

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes care, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 4 pooled it
30.0field-weighted citation impact, top 1% 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

125 citing papers in PubMed, 4 syntheses or guidelines pooled it, 318 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Type 2 Diabetes: How Much of an Autoimmune Disease?Frontiers in endocrinology · 2019
    Pooled it
  4. Pooled it
  5. Trial
  6. Article
  7. Article
  8. Review
  9. Article
  10. Adipokine in Metabolic Liver Disease: Adipo-Brain-Liver Cross talk.International journal of endocrinology · 2026
    Review
  11. Review
  12. Article
  13. Review
  14. Call for Standardization of C-Peptide Measurement.Journal of diabetes science and technology · 2025
    Review
  15. Review
  16. Journal of diabetes and metabolic disorders · 2025
    Review
  17. Review
  18. Association ofHealth science reports · 2025
    Article
  19. Review
  20. Review

65 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 1 country.

Stanley S SchwartzMain Line Health, Wynnewood, PA, and University of Pennsylvania, Philadelphia, PA stschwar@gmail.com.
Solomon EpsteinDivision of Endocrinology, Diabetes and Bone Disease, Department of Medicine, Mount Sinai Hospital, New York, NY.
Barbara E CorkeyDepartment of Medicine, Boston University School of Medicine, Boston, MA.
Struan F A GrantDivision of Human Genetics and Center for Applied Genomics, Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
James R GavinEmory University School of Medicine, Atlanta, GA.
Richard B AguilarDiabetes Nation, Sisters, OR.
Boston University · USEmory University · USMain Line Health · USMount Sinai Hospital · USUniversity of Pennsylvania · US

Funding

METABOLIC SIGNAL TRANSDUCTION IN ADIPOCYTESR01DK056690 · NIDDK · BOSTON MEDICAL CENTER · PI CORKEY, BARBARA E., SHIRIHAI, ORIAN S · 2001 to 2015
$6.3M
METABOLIC REGULATION OF INSULIN SECRETIONR01DK035914 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI CORKEY, BARBARA E., SHIRIHAI, ORIAN S · 1986 to 2013
$5.3M
Mitochondrial dynamics in beta cell function and dysfunctionR01DK074778 · NIDDK · TUFTS UNIVERSITY BOSTON · PI CORKEY, BARBARA E., SHIRIHAI, ORIAN S · 2007 to 2015
$3.5M
Genome Wide Association Study of Latent Autoimmune Diabetes in AdultsR01DK085212 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI GRANT, STRUAN F A · 2011 to 2016
$3.4M
Mitochondrial regulation of energy efficiencyR01DK099618 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CORKEY, BARBARA E., SHIRIHAI, ORIAN S · 2014 to 2018
$1.8M
Metabolic Regulation of Insulin SecretionR56DK035914 · NIDDK · BOSTON MEDICAL CENTER · PI CORKEY, BARBARA E., SHIRIHAI, ORIAN S · 2009 to 2009
$500k
METABOLIC REGULATION OF INSULIN SECRETIONR37DK035914 · NIDDK · BOSTON UNIVERSITY MEDICAL CENTER HOSP · PI CORKEY, BARBARA E. · 1991 to 1998
–
NIDDK NIH HHS DK35914NIDDK NIH HHS DK56690NIDDK NIH HHS DK74778NIDDK NIH HHS DK99618NIDDK NIH HHS R01 DK035914NIDDK NIH HHS R01 DK056690NIDDK NIH HHS R01 DK074778NIDDK NIH HHS R01 DK085212NIDDK NIH HHS R01 DK099618NIDDK NIH HHS R56 DK035914
6 · The paper itself

Abstract

The current classification system presents challenges to the diagnosis and treatment of patients with diabetes mellitus (DM), in part due to its conflicting and confounding definitions of type 1 DM, type 2 DM, and latent autoimmune diabetes of adults (LADA). The current schema also lacks a foundation that readily incorporates advances in our understanding of the disease and its treatment. For appropriate and coherent therapy, we propose an alternate classification system. The β-cell-centric classification of DM is a new approach that obviates the inherent and unintended confusions of the current system. The β-cell-centric model presupposes that all DM originates from a final common denominator-the abnormal pancreatic β-cell. It recognizes that interactions between genetically predisposed β-cells with a number of factors, including insulin resistance (IR), susceptibility to environmental influences, and immune dysregulation/inflammation, lead to the range of hyperglycemic phenotypes within the spectrum of DM. Individually or in concert, and often self-perpetuating, these factors contribute to β-cell stress, dysfunction, or loss through at least 11 distinct pathways. Available, yet underutilized, treatments provide rational choices for personalized therapies that target the individual mediating pathways of hyperglycemia at work in any given patient, without the risk of drug-related hypoglycemia or weight gain or imposing further burden on the β-cells. This article issues an urgent call for the review of the current DM classification system toward the consensus on a new, more useful system.

Indexed as

Diabetes Mellitus, Type 1Diabetes Mellitus, Type 2HumansHyperglycemiaHypoglycemic AgentsInsulin ResistanceInsulin-Secreting CellsHypoglycemic Agents

Identifiers

PMID26798148
PMCPMC5317235
OpenAlexW2269288506

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.