Evidence map›Paper›PMID 42769310›Full record

ReviewMedComm2026

Brown Adipose Tissue: Molecular Mechanisms of Regulation, Physiological Functions, and Therapeutic Targets.

Xiaoli Deng, Yuanyuan Shen, Ying Sun, Lu Lu, Chongkui Sun

Abstract readReview
In one paragraph

Review in MedComm, 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

5 authors.

Xiaoli Deng *Department of Geriatrics, Institute of Geriatrics Sichuan Provincial People's Hospital University of Electronic Science and Technology Chengdu China.
Yuanyuan Shen *State Key Laboratory of Swine and Poultry Breeding Industry College of Animal Science and Technology Sichuan Agricultural University Chengdu China.
Ying SunDepartment of Geriatrics, Institute of Geriatrics Sichuan Provincial People's Hospital University of Electronic Science and Technology Chengdu China.
Lu LuState Key Laboratory of Swine and Poultry Breeding Industry College of Animal Science and Technology Sichuan Agricultural University Chengdu China.
Chongkui SunDepartment of Geriatrics, Institute of Geriatrics Sichuan Provincial People's Hospital University of Electronic Science and Technology Chengdu China.ORCID https://orcid.org/0000-0003-0362-4129

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brown adipose tissue (BAT) biology has undergone a profound evolution over the past two decades, expanding from a narrow focus on thermogenic capacity in rodents to the establishment of its pleiotropic roles in human metabolic regulation. While this transition has enabled major progress in defining underlying molecular mechanisms and strengthened the clinical rationale for targeting BAT, it has also exposed unresolved challenges and knowledge gaps. In this review, we synthesize current evidence across the field, integrating findings from molecular, physiological, and translational studies to delineate the hierarchical regulatory networks that govern BAT development and function. We focus on three themes: first, the transcriptional, epigenetic, and posttranscriptional mechanisms that establish and maintain BAT identity; second, the expanding spectrum of BAT's physiological functions beyond thermogenesis, including its crosstalk with other metabolic organs and the immune system; and third, the emerging strategies and persistent obstacles in harnessing BAT's therapeutic potential for obesity, diabetes, and related metabolic disorders. By consolidating these perspectives, we propose an integrative framework for understanding BAT as a central hub in human metabolic regulation while identifying critical knowledge gaps that warrant further investigation.

Indexed as

agingbatokinesbrown adipose tissuemetabolic diseasesthermogenesis

Identifiers

PMID42769310
PMCPMC13591113

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.