Evidence map›Paper›PMID 24100998›Full record

ReviewNature medicine2013

Brown and beige fat: development, function and therapeutic potential.

Matthew Harms, Patrick Seale

Registry-linked trialOpen access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04819321 (Study of White Adipose Tissue Remodeling by Cryolipolysis in Humans), which is not on this map. Cited by 1,263 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,263citing papers in PubMed, 2 pooled it
82.8field-weighted citation impact, top 1% of its field
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.

NCT04819321 naunknown statusnot on this mapstarted 2021, after this paper: background citation

Study of White Adipose Tissue Remodeling by Cryolipolysis in Humans

TypeinterventionalSponsorFederal University of Minas GeraisRan2021 to 2022Enrolled12ConditionsLipid Metabolism Disorders, Metabolic DiseaseArmsCoolSculpting® System
3 · Its place in the literature

Who cites it

1,263 citing papers in PubMed, 2 syntheses or guidelines pooled it, 2,280 citations in OpenAlex.

  1. Pooled it
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  8. Exosome trafficking is a key regulator of adipocyte thermogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2026
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1,203 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Matthew HarmsInstitute for Diabetes, Obesity and Metabolism, Department of Cell and Developmental Biology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Patrick Seale
University of Pennsylvania · US

Funding

Molecular Regulation of Brown Adipose Cell Fate in Somitic Stem CellsDP2OD007288 · OD · UNIVERSITY OF PENNSYLVANIA · PI SEALE, PATRICK · 2010 to 2010
$2.4M
NIH HHS DP2OD007288
6 · The paper itself

Abstract

Adipose tissue, best known for its role in fat storage, can also suppress weight gain and metabolic disease through the action of specialized, heat-producing adipocytes. Brown adipocytes are located in dedicated depots and express constitutively high levels of thermogenic genes, whereas inducible 'brown-like' adipocytes, also known as beige cells, develop in white fat in response to various activators. The activities of brown and beige fat cells reduce metabolic disease, including obesity, in mice and correlate with leanness in humans. Many genes and pathways that regulate brown and beige adipocyte biology have now been identified, providing a variety of promising therapeutic targets for metabolic disease.

Indexed as

AdipocytesAdipose Tissue, BrownAnimalsHumansMetabolic DiseasesMicePeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaSympathetic Nervous SystemTranscription FactorsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, mouseTranscription Factors

Identifiers

PMID24100998
OpenAlexW2119649463

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.