Evidence map›Paper›PMID 33467677›Full record

ReviewCells2021

The Metabolic Role of GRK2 in Insulin Resistance and Associated Conditions.

Daniela Sorriento, Maria Rosaria Rusciano, Valeria Visco, Antonella Fiordelisi, Federica Andrea Cerasuolo, Paolo Poggio, Michele Ciccarelli, Guido Iaccarino

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Artificial Intelligence in Hypertension Management: An Ace up Your Sleeve.Journal of cardiovascular development and disease · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Heart failure in diabetes.Metabolism: clinical and experimental · 2021
    Review
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

8 authors at 2 institutions in 1 country.

Daniela SorrientoDipartimento di Scienze Biomediche Avanzate, Università Federico II di Napoli, 80131 Napoli, Italy.ORCID 0000-0002-1599-4509
Maria Rosaria RuscianoDipartimento di Medicina, Chirurgia ed Odontoiatria, Università degli Studi di Salerno, 84081 Baronissi, Italy.ORCID 0000-0002-7112-6503
Valeria ViscoDipartimento di Medicina, Chirurgia ed Odontoiatria, Università degli Studi di Salerno, 84081 Baronissi, Italy.
Antonella FiordelisiDipartimento di Scienze Biomediche Avanzate, Università Federico II di Napoli, 80131 Napoli, Italy.
Federica Andrea CerasuoloDipartimento di Scienze Biomediche Avanzate, Università Federico II di Napoli, 80131 Napoli, Italy.
Paolo PoggioUnità per lo Studio delle Patologie Aortiche, Valvolari e Coronariche, Centro Cardiologico Monzino IRCCS, 20138 Milan, Italy.
Michele CiccarelliDipartimento di Medicina, Chirurgia ed Odontoiatria, Università degli Studi di Salerno, 84081 Baronissi, Italy.ORCID 0000-0003-2379-1960
Guido IaccarinoDipartimento di Scienze Biomediche Avanzate, Università Federico II di Napoli, 80131 Napoli, Italy.ORCID 0000-0002-8997-835X
University of Salerno · ITCentro Cardiologico Monzino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insulin resistance (IRES) is a pathophysiological condition characterized by the reduced response to insulin of several tissues, including myocardial and skeletal muscle. IRES is associated with obesity, glucose intolerance, dyslipidemia, and hypertension, evolves toward type 2 diabetes, and increases the risk of developing cardiovascular diseases. Several studies designed to explore the mechanisms involved in IRES allowed the identification of a multitude of potential molecular targets. Among the most promising, G Protein Coupled Receptor Kinase type 2 (GRK2) appears to be a suitable one given its functional implications in many cellular processes. In this review, we will discuss the metabolic role of GRK2 in those conditions that are characterized by insulin resistance (diabetes, hypertension, heart failure), and the potentiality of its inhibition as a therapeutic strategy to revert both insulin resistance and its associated phenotypes.

Indexed as

Insulin ResistanceAnimalsDiabetes MellitusDiabetes Mellitus, Type 2G-Protein-Coupled Receptor Kinase 2Heart FailureHumansHypertensionInflammationInsulinInsulin-Secreting CellsMiceMuscle, SkeletalMyocardiumPeptidesPhenotypeG-Protein-Coupled Receptor Kinase 2GRK2 protein, humanGRK2 protein, mouseInsulinPeptidesdiabetesGRK2heart failurehypertensioninsulin resistance

Identifiers

PMID33467677
PMCPMC7830135
OpenAlexW3120132272

What Socratic 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 Socratic graph.