Evidence map›Paper›PMID 31420521›Full record

ReviewThe Journal of biological chemistry2019

Cutting fuel offers new clues in diabetic mystery.

P Darrell Neufer

Abstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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.

P Darrell NeuferEast Carolina Diabetes and Obesity Institute and Department of Physiology, Brody School of Medicine, East Carolina University, Greenville, North Carolina 27834. Electronic address: neuferp@ecu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Competing theories have held opposite views on the role of flux through β-oxidation in causing insulin resistance. New transcriptomics, proteomics, and metabolomics data of skeletal muscle from mice in which lipid oxidation is limited by restricting entry of fat into mitochondria reveal extensive remodeling of metabolic pathways, consistent with an overall reduction in metabolic efficiency and improved metabolic health. These findings point to a potential new therapeutic approach for treating insulin resistance and type 2 diabetes.

Indexed as

Insulin ResistanceLipid MetabolismAnimalsDiabetes Mellitus, Type 2HumansMetabolomicsMiceMitochondria, MuscleMuscle, SkeletalOxidation-ReductionProteomics

Identifiers

PMID31420521
PMCPMC6699854

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.