Evidence map›Paper›PMID 25480301›Full record

ArticleCell2014

Leptin mediates the increase in blood pressure associated with obesity.

Stephanie E Simonds, Jack T Pryor, Eric Ravussin, Frank L Greenway, Ralph Dileone, Andrew M Allen, Jaspreet Bassi, Joel K Elmquist, Julia M Keogh, Elana Henning and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 208 papers.

0numbers the graph read from it
0cells of the map it votes in
208citing papers in PubMed
13.9field-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

208 citing papers in PubMed, 339 citations in OpenAlex.

  1. Trial
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  8. Hypothalamic regulation of energy homeostasis: Quo vadis.Reviews in endocrine & metabolic disorders · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Central leptin pathways in metabolic homeostasis.Clinical science (London, England : 1979) · 2025
    Review
  17. Article
  18. Article
  19. Review
  20. Review

148 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 12 institutions in 3 countries.

Stephanie E SimondsDepartment of Physiology, Monash Obesity and Diabetes Institute, Monash University, Clayton, VIC 3800, Australia.
Jack T PryorWarwick Medical School, University of Warwick, Coventry CV4 7AL, UK; Neurosolutions Ltd., Coventry CV4 7ZS, UK.
Eric RavussinThe Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Frank L GreenwayThe Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Ralph DileoneDepartment of Psychiatry, Yale School of Medicine, New Haven, CT 06511, USA.
Andrew M AllenDepartment of Physiology, The University of Melbourne, Victoria 3010, Australia.
Jaspreet BassiDepartment of Physiology, The University of Melbourne, Victoria 3010, Australia.
Joel K ElmquistDivision of Endocrinology & Metabolism, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Julia M KeoghUniversity of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK.
Elana HenningUniversity of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK.
Martin G MyersDivision of Metabolism, Endocrinology, and Diabetes, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Julio LicinioMind and Brain Theme, South Australian Health and Medical Research Institute and Department of Psychiatry, School of Medicine, Flinders University, Adelaide, SA 5001, Australia.
Russell D BrownDepartment of Physiology, Monash Obesity and Diabetes Institute, Monash University, Clayton, VIC 3800, Australia.
Pablo J EnrioriDepartment of Physiology, Monash Obesity and Diabetes Institute, Monash University, Clayton, VIC 3800, Australia.
Stephen O'RahillyUniversity of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK.
Scott M SternsonJanelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA.
Kevin L GroveDivision of Diabetes, Obesity & Metabolism, Oregon National Primate Research Center, Portland, OR 97239, USA.
David C SpanswickDepartment of Physiology, Monash Obesity and Diabetes Institute, Monash University, Clayton, VIC 3800, Australia; Warwick Medical School, University of Warwick, Coventry CV4 7AL, UK.
I Sadaf FarooqiUniversity of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK. Electronic address: isf20@cam.ac.uk.
Michael A CowleyDepartment of Physiology, Monash Obesity and Diabetes Institute, Monash University, Clayton, VIC 3800, Australia. Electronic address: michael.cowley@monash.edu.
Monash University · AUAddenbrooke's Hospital · GBPennington Biomedical Research Center · USUniversity of Melbourne · AUUniversity of Warwick · GBWellcome Trust · GBJanelia Research Campus · USOregon National Primate Research Center · USSouth Australian Health and Medical Research Institute · AUThe University of Texas Southwestern Medical Center · USUniversity of Michigan–Ann Arbor · USYale University · US

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2005 to 2026
$26.5M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Molecular Mechanisms of Leptin Receptor/Jak2 ActionR37DK056731 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MYERS, MARTIN G · 2008 to 2017
$3.5M
Howard Hughes Medical InstituteMedical Research Council G0600717Medical Research Council MC_UU_12012/1Medical Research Council MC_UU_12012/5NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK072476NIDDK NIH HHS P30DK072476NIDDK NIH HHS R37 DK056731Wellcome Trust 082390/Z/07/ZWellcome Trust 095515Wellcome Trust 098497
6 · The paper itself

Abstract

Obesity is associated with increased blood pressure (BP), which in turn increases the risk of cardiovascular diseases. We found that the increase in leptin levels seen in diet-induced obesity (DIO) drives an increase in BP in rodents, an effect that was not seen in animals deficient in leptin or leptin receptors (LepR). Furthermore, humans with loss-of-function mutations in leptin and the LepR have low BP despite severe obesity. Leptin's effects on BP are mediated by neuronal circuits in the dorsomedial hypothalamus (DMH), as blocking leptin with a specific antibody, antagonist, or inhibition of the activity of LepR-expressing neurons in the DMH caused a rapid reduction of BP in DIO mice, independent of changes in weight. Re-expression of LepRs in the DMH of DIO LepR-deficient mice caused an increase in BP. These studies demonstrate that leptin couples changes in weight to changes in BP in mammalian species.

Indexed as

AnimalsHypertensionLeptinMice, Inbred C57BLMutationNeuronsObesityReceptors, LeptinSignal TransductionLeptinReceptors, Leptin

Identifiers

PMID25480301
PMCPMC4259491
OpenAlexW2147984307

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.