Evidence map›Paper›PMID 38981607›Full record

ReviewAmerican journal of physiology. Cell physiology2024

Exercise as a tool to mitigate metabolic disease.

Joao Victor Esteves, Kristin I Stanford

Abstract readReview
In one paragraph

Review in American journal of physiology. Cell physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
–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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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.

Joao Victor EstevesDorothy M. Davis Heart and Lung Research Institute, The Ohio State University Wexner Medical Center, Columbus, Ohio, United States.ORCID 0000-0001-8274-000X
Kristin I StanfordDorothy M. Davis Heart and Lung Research Institute, The Ohio State University Wexner Medical Center, Columbus, Ohio, United States.ORCID 0000-0002-0681-7746

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Engineering the release of oxylipins through the skinR01DK133859 · NIDDK · OHIO STATE UNIVERSITY · PI GALLEGO-PEREZ, DANIEL, STANFORD, KRISTIN I · 2023 to 2025
$1.9M
American Heart Association (AHA) AHA 23SFRNPCS1067042American Heart Association-American Stroke Association 23SFRNPCS1067042HHS | National Institutes of Health (NIH) R01DK133859-01A1NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK133859
6 · The paper itself

Abstract

Metabolic diseases, notably obesity and type 2 diabetes (T2D), have reached alarming proportions and constitute a significant global health challenge, emphasizing the urgent need for effective preventive and therapeutic strategies. In contrast, exercise training emerges as a potent intervention, exerting numerous positive effects on metabolic health through adaptations to the metabolic tissues. Here, we reviewed the major features of our current understanding with respect to the intricate interplay between metabolic diseases and key metabolic tissues, including adipose tissue, skeletal muscle, and liver, describing some of the main underlying mechanisms driving pathogenesis, as well as the role of exercise to combat and treat obesity and metabolic disease.

Indexed as

Adipose TissueDiabetes Mellitus, Type 2ExerciseMetabolic DiseasesMuscle, SkeletalAnimalsEnergy MetabolismExercise TherapyHumansLiverObesityadipose tissueinsulin resistancelivermetabolismskeletal muscle

Identifiers

PMID38981607
PMCPMC11427015

What OpenQuestion holds

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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 OpenQuestion graph.