Evidence map›Paper›PMID 39245434›Full record

ReviewMetabolism: clinical and experimental2024

History and future of leptin: Discovery, regulation and signaling.

Heike Münzberg, Steven B Heymsfield, Hans-Rudolf Berthoud, Christopher D Morrison

Abstract readReviewHistorical Article
In one paragraph

Review in Metabolism: clinical and experimental, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  6. The role of tanycytes in the regulation of energy balance.Reviews in endocrine & metabolic disorders · 2026
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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

4 authors.

Heike MünzbergPennington Biomedical Research Center, LSU System, Baton Rouge, LA, United States of America. Electronic address: Heike.Munzberg@pbrc.edu.
Steven B HeymsfieldPennington Biomedical Research Center, LSU System, Baton Rouge, LA, United States of America.
Hans-Rudolf BerthoudPennington Biomedical Research Center, LSU System, Baton Rouge, LA, United States of America.
Christopher D MorrisonPennington Biomedical Research Center, LSU System, Baton Rouge, LA, United States of America.

Funding

Leptin and Central Control of ThermoregulationR01DK092587 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MUENZBERG-GRUENING, HEIKE · 2012 to 2024
$3.5M
Metabolic Changes: Connecting temperature sensing neurons to sympathetic adipose tissue stimulationR01AT011683 · NCCIH · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MUENZBERG-GRUENING, HEIKE · 2021 to 2025
$2.5M
Neural circuits coordinating protein intake: Role of FGF21R01DK123083 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MORRISON, CHRISTOPHER D · 2020 to 2024
$1.6M
FGF21-dependent mechanisms driving changes in energy expenditure during dietary protein restrictionR01DK121370 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MORRISON, CHRISTOPHER D · 2020 to 2023
$1.5M
NCCIH NIH HHS R01 AT011683NIDDK NIH HHS R01 DK092587NIDDK NIH HHS R01 DK121370NIDDK NIH HHS R01 DK123083
6 · The paper itself

Abstract

The cloning of leptin 30 years ago in 1994 was an important milestone in obesity research. Prior to the discovery of leptin, obesity was stigmatized as a condition caused by lack of character and self-control. Mutations in either leptin or its receptor were the first single gene mutations found to cause severe obesity, and it is now recognized that obesity is caused mostly by a dysregulation of central neuronal circuits. Since the discovery of the leptin-deficient obese mouse (ob/ob) the cloning of leptin (ob aka lep) and leptin receptor (db aka lepr) genes, we have learned much about leptin and its action in the central nervous system. The first hope that leptin would cure obesity was quickly dampened because humans with obesity have increased leptin levels and develop leptin resistance. Nevertheless, leptin target sites in the brain represent an excellent blueprint to understand how neuronal circuits control energy homeostasis. Our expanding understanding of leptin function, interconnection of leptin signaling with other systems and impact on distinct physiological functions continues to guide and improve the development of safe and effective interventions to treat metabolic illnesses. This review highlights past concepts and current emerging concepts of the hormone leptin, leptin receptor signaling pathways and central targets to mediate distinct physiological functions.

Indexed as

LeptinObesityReceptors, LeptinSignal TransductionAnimalsHistory, 20th CenturyHistory, 21st CenturyHumansLeptinReceptors, LeptinEnergy expenditureFeedingGlucose homeostasisLeptin receptorLeptin transportNeuronal circuitsReward

Identifiers

PMID39245434
PMCPMC11570342

What OpenQuestion holds

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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.