Evidence map›Paper›PMID 22935803›Full record

ReviewNature reviews. Drug discovery2012

Leptin revisited: its mechanism of action and potential for treating diabetes.

Roberto Coppari, Christian Bjørbæk

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Drug discovery, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 143 papers.

0numbers the graph read from it
0cells of the map it votes in
143citing papers in PubMed
13.2field-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.

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

143 citing papers in PubMed, 291 citations in OpenAlex.

  1. Trial
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  12. Research Progress on Leptin in Metabolic Dysfunction-associated Fatty Liver Disease.Journal of clinical and translational hepatology · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. History and future of leptin: Discovery, regulation and signaling.Metabolism: clinical and experimental · 2024
    Review
  19. Article
  20. Review

83 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 2 institutions in 1 country.

Roberto CoppariDepartment of Internal Medicine, Division of Hypothalamic Research, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA. roberto.coppari@utsouthwestern.edu
Christian Bjørbæk
Beth Israel Deaconess Medical Center · USSouthwestern Medical Center · US

Funding

Transgenic CoreP30DK046200 · NIDDK · TUFTS MEDICAL CENTER · PI GREENBERG, ANDREW S, PERISSI, VALENTINA · 1992 to 2021
$25.0M
Regulation of Hypothalamic Proopiomelanocortin by LeptinR01DK060673 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BJORBAEK, CHRISTIAN · 2002 to 2010
$2.5M
The Physiological Relevance of SIRT1 in Brain on Energy and Glucose HomeostasisR01DK080836 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI COPPARI, ROBERTO · 2009 to 2012
$1.5M
Leptin Signaling in Hypothalamic Neurons and Glutamate ReceptorsR01DK094040 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KIM, YOUNG-BUM · 2012 to 2015
$1.5M
Mechanisms of Central Leptin Resistance in ObesityR01DK065743 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BJORBAEK, CHRISTIAN · 2005 to 2008
$1.2M
NIDDK NIH HHS DK080836NIDDK NIH HHS DK46200NIDDK NIH HHS DK60673NIDDK NIH HHS DK65743NIDDK NIH HHS DK94040NIDDK NIH HHS P30 DK046200NIDDK NIH HHS R01 DK060673NIDDK NIH HHS R01 DK065743NIDDK NIH HHS R01 DK080836NIDDK NIH HHS R01 DK094040
6 · The paper itself

Abstract

Since the discovery of leptin in 1994, we now have a better understanding of the cellular and molecular mechanisms underlying its biological effects. In addition to its established anti-obesity effects, leptin exerts antidiabetic actions that are independent of its regulation of body weight and food intake. In particular, leptin can correct diabetes in animal models of type 1 and type 2 diabetes. In addition, long-term leptin replacement therapy improves glycaemic control, insulin sensitivity and plasma triglycerides in patients with severe insulin resistance due to lipodystrophy. These results have spurred enthusiasm for the use of leptin therapy to treat diabetes. Here, we review the current understanding of the glucoregulatory functions of leptin, emphasizing its central mechanisms of action and lessons learned from clinical studies, and discuss possible therapeutic applications of leptin in the treatment of type 1 and type 2 diabetes.

Indexed as

AnimalsBlood GlucoseDiabetes MellitusHumansLeptinPro-OpiomelanocortinTreatment OutcomeBlood GlucoseLeptinPro-Opiomelanocortin

Identifiers

PMID22935803
PMCPMC4019022
OpenAlexW2008768221

What OpenQuestion holds

Textmetadata
LicenceTDM
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.