Evidence map›Paper›PMID 36552107›Full record

ReviewBrain sciences2022

Brain-to-BAT - and Back?: Crosstalk between the Central Nervous System and Thermogenic Adipose Tissue in Development and Therapy of Obesity.

Andreas Till, Charlotte Fries, Wiebke K Fenske

Open access · goldAbstract readReview
In one paragraph

Review in Brain sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 21% 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.

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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Improving incretin-mediated body weight loss via energy expenditure.Trends in endocrinology and metabolism: TEM · 2026
    Review
  2. Review
  3. Organ crosstalk and dysfunction in sepsis.Annals of intensive care · 2024
    Review
  4. Review
  5. Article
  6. Article
  7. 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

3 authors.

Andreas TillDepartment of Internal Medicine I, Division of Endocrinology, Diabetes and Metabolism, University Medical Center Bonn, D-53127 Bonn, Germany.ORCID 0000-0002-0139-9143
Charlotte FriesDepartment of Internal Medicine I, Division of Endocrinology, Diabetes and Metabolism, University Medical Center Bonn, D-53127 Bonn, Germany.
Wiebke K FenskeDepartment of Internal Medicine I, Division of Endocrinology, Diabetes and Metabolism, University Medical Center Bonn, D-53127 Bonn, Germany.

Funding

Deutsche Forschungsgemeinschaft AOBJ: 624808Deutsche Forschungsgemeinschaft AOBJ: 667675Deutsche Forschungsgemeinschaft AOBJ: 676866Deutsche Forschungsgemeinschaft AOBJ: TRR 333/1 - 450149205Else Kroener Fresenius Foundation FenskeFederal Ministry of Education and Research 01EO1501Federal Ministry of Education and Research IFB Adiposity Disease
6 · The paper itself

Abstract

The body of mammals harbors two distinct types of adipose tissue: while cells within the white adipose tissue (WAT) store surplus energy as lipids, brown adipose tissue (BAT) is nowadays recognized as the main tissue for transforming chemical energy into heat. This process, referred to as 'non-shivering thermogenesis', is facilitated by the uncoupling of the electron transport across mitochondrial membranes from ATP production. BAT-dependent thermogenesis acts as a safeguarding mechanism under reduced ambient temperature but also plays a critical role in metabolic and energy homeostasis in health and disease. In this review, we summarize the evolutionary structure, function and regulation of the BAT organ under neuronal and hormonal control and discuss its mutual interaction with the central nervous system. We conclude by conceptualizing how better understanding the multifaceted communicative links between the brain and BAT opens avenues for novel therapeutic approaches to treat obesity and related metabolic disorders.

Indexed as

adipocytesbariatric surgerybatokinesdiabetesghrelinGIPGLP-1glucagongut microbiomehypothalamusinsulinleptinobesityRYGBsecretinSNSUCP1

Identifiers

PMID36552107
PMCPMC9775239
OpenAlexW4311050024

What OpenQuestion holds

Textmetadata
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.