Evidence map›Paper›PMID 42619373›Full record

ReviewChinese medical journal2026

Exerkines in precision management of metabolic diseases.

Leigang Jin, Yifen Lin, Yixuan Zheng, Anli Wang, Peng Liao, Yucheng Luo, Zhongheng Sui, Xiayun Ni, Jianan Zhang, Qing Shen and 1 more

Abstract readReview
In one paragraph

Review in Chinese medical journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Leigang JinState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong 999077, China.
Yifen LinCardiology Department, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, Guangdong 510080, China.
Yixuan ZhengState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong 999077, China.
Anli WangState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong 999077, China.
Peng LiaoState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong 999077, China.
Yucheng LuoState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong 999077, China.
Zhongheng SuiState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong 999077, China.
Xiayun NiState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong 999077, China.
Jianan ZhangState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong 999077, China.
Qing ShenState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong 999077, China.
Aimin XuState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong 999077, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractRegular physical activity exerts systemic metabolic benefits that are pivotal for preventing and managing metabolic diseases. These effects are mediated in part by exerkines, which are signaling molecules released from various organs in response to exercise. Exerkines encompass polypeptides, nucleic acids, and bioactive lipids that collectively orchestrate metabolic adaptations. Recent metagenomic analyses have identified the gut microbiota as an additional source of exercise-responsive factors that modulate host metabolism and may influence individual responsiveness to training. Together, these diverse exerkines coordinate interorgan communication, enhance insulin sensitivity, maintain glucose and lipid homeostasis, and modulate inflammatory pathways. This review summarizes representative exerkines from skeletal muscle, adipose tissue, and liver, including interleukin-6, myostatin, fibroblast growth factor 21, adiponectin, and growth differentiation factor 15, which have shown promising therapeutic efficacy in preclinical studies and clinical trials for complex metabolic diseases. We also discuss microbiota-derived metabolites such as short-chain fatty acids that improve glucose and lipid metabolism, as well as host-derived metabolites including N-lactoyl-phenylalanine, betaine, and β-aminoisobutyric acid that regulate appetite, substrate utilization, and insulin action. Furthermore, we highlight recent progress in understanding how dynamic regulation of these exerkines mediates the metabolic benefits of exercise and their potential as targets for precision management of metabolic diseases. Understanding these molecular mediators of exercise provides a framework for integrating physical activity with pharmacological and nutritional strategies to improve metabolic health.

Indexed as

ExerciseMetabolic DiseasesAnimalsHumansLipid MetabolismMuscle, SkeletalMyostatinMyostatinChronic metabolic diseaseExercise-responsive factorsExerkine; Physical activityGut microbiomeMetabolitesPrecision medicine

Identifiers

PMID42619373
PMCPMC13626689

What Socratic 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 Socratic graph.