Evidence map›Paper›PMID 26001373›Full record

ReviewEuropean journal of pharmacology2015

New targets to treat obesity and the metabolic syndrome.

Kathleen A Martin, Mitra V Mani, Arya Mani

Abstract readReview
In one paragraph

Review in European journal of pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 2 pooled it
5.1field-weighted citation impact, top 4% 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

51 citing papers in PubMed, 2 syntheses or guidelines pooled it, 124 citations in OpenAlex.

  1. Pooled it
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  11. Pharmacokinetics ofInternational journal of molecular sciences · 2022
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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

3 authors at 2 institutions in 1 country.

Kathleen A MartinDepartment of Internal Medicine, Yale University School of Medicine, USA.
Mitra V ManiCornell University, USA.
Arya ManiDepartment of Internal Medicine, Yale University School of Medicine, USA; Department of Genetics, Yale University School of Medicine, USA. Electronic address: arya.mani@yale.edu.
Yale University · USCornell University · US

Funding

Yale Liver CenterP30DK034989 · NIDDK · YALE UNIVERSITY · PI YASUKO IWAKIRI · 1986 to 2026
$31.1M
Novel targets of rapamycin and Akt in vascular smooth muscle cell differentiationR01HL091013 · NHLBI · YALE UNIVERSITY · PI MARTIN, KATHLEEN ANN · 2008 to 2017
$4.1M
Regulation of vascular smooth muscle cell plasticityR01HL118430 · NHLBI · YALE UNIVERSITY · PI MARTIN, KATHLEEN ANN · 2014 to 2017
$1.7M
Epigenetic control of vascular smooth muscle in cardiovascular diseaseR01HL119529 · NHLBI · YALE UNIVERSITY · PI MARTIN, KATHLEEN ANN · 2014 to 2017
$1.7M
Genetic Regulation of Arterial Wall by Canonical Wnt SignalingR01HL122830 · NHLBI · YALE UNIVERSITY · PI MANI, ARYA · 2014 to 2016
$1.6M
Hepatic Wnt/LRP6 Regulation of Plasma LipidsR01HL122822 · NHLBI · YALE UNIVERSITY · PI MANI, ARYA · 2015 to 2017
$1.3M
NHLBI NIH HHS 1R01HL122822-01NHLBI NIH HHS 1R01HL122830-01NHLBI NIH HHS R01 HL091013NHLBI NIH HHS R01 HL118430NHLBI NIH HHS R01 HL119529NHLBI NIH HHS R01 HL122822NHLBI NIH HHS R01 HL122830NIDDK NIH HHS P30 DK034989
6 · The paper itself

Abstract

Metabolic syndrome (MetS) is a cluster ofassociated metabolic traits that collectively confer unsurpassed risk for development of cardiovascular disease (CVD) and type 2 diabetes compared to any single CVD risk factor. Truncal obesity plays an exceptionally critical role among all metabolic traits of the MetS. Consequently, the prevalence of the MetS has steadily increased with the growing epidemic of obesity. Pharmacotherapy has been available for obesity for more than one decade, but with little success in improving the metabolic profiles. The serotonergic drugs and inhibitors of pancreatic lipases were among the few drugs that were initially approved to treat obesity. At the present time, only the pancreatic lipase inhibitor orlistat is approved for long-term treatment of obesity. New classes of anti-diabetic drugs, including glucagon-like peptide 1 receptor (GLP-1R) agonists and Dipeptidyl-peptidase IV (DPP-IV) inhibitors, are currently being evaluated for their effects on obesity and metabolic traits. The genetic studies of obesity and metabolic syndrome have identified novel molecules acting on the hunger and satiety peptidergic signaling of the gut-hypothalamus axis or the melanocortin system of the brain and are promising targets for future drug development. The goal is to develop drugs that not only treat obesity, but also favorably impact its associated traits.

Indexed as

AnimalsCardiovascular DiseasesHumansMetabolic SyndromeMolecular Targeted TherapyObesityRisk FactorsDiabetesDrugsHumansMetabolic syndromeObesityTargetsTherapeutics

Identifiers

PMID26001373
PMCPMC4573317
OpenAlexW1901913267

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.