Evidence map›Paper›PMID 40585886›Full record

ReviewJournal of the Endocrine Society2025

Ketones and Insulin: A Paradoxical Interplay With Implications for Glucose Metabolism.

Kaja Falkenhain

Abstract readReview
In one paragraph

Review in Journal of the Endocrine Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Triglyceride Accumulation in Adipocytes Modulated by Insulin Dynamics.International journal of molecular sciences · 2025
    Article
  4. 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

1 author.

Kaja FalkenhainPennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA.ORCID https://orcid.org/0000-0002-3240-964X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ketone bodies have emerged as critical metabolic regulators with apparent hormone-like signaling properties. Exogenous ketone supplements allow for immediate induction of ketosis, providing a valuable tool to investigate ketone signaling. Particularly the glucose-lowering effect of exogenously administered β-hydroxybutyrate has attracted attention; yet the mechanisms underlying this effect remain elusive. This review synthesizes historical and contemporary studies investigating the interplay between ketone bodies and insulin, which appears to at least partly mediate the hypoglycemic effect of ketones. Early studies suggested that chronic exposure to ketones led to initial stimulation of insulin secretion but ultimately resulted in exhaustion of β cells and subsequent hyperglycemia. More recent investigations confirm an insulin stimulatory effect of ketones in isolated islets, rodent models, and human participants-though the effect appears dependent on the metabolic context including availability of glucose and duration of exposure. These insulinogenic properties of ketone bodies themselves are particularly intriguing given a state of ketosis-when induced endogenously, either via fasting or a diet very low in carbohydrates-is commonly associated with very low concentrations of insulin and holds promise for clinical utility of diabetes reversal or treatment. Similarly, exogenous ketones are now suggested to hold therapeutic potential in the context of dysregulated glucose metabolism. Collectively, these findings underscore the nuanced and complex metabolic role of ketones that warrant further studies aimed at disentangling the effect of ketones both as alternative fuel source and signaling metabolite.

Indexed as

diabeteshyperglycemiainsulinketosismetabolismβ-hydroxybutyrate

Identifiers

PMID40585886
PMCPMC12204319

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.