Evidence map›Paper›PMID 16075047›Full record

ArticleThe Journal of clinical investigation2005

Akt1 in the cardiovascular system: friend or foe?

Brian T O'Neill, E Dale Abel

Open access · bronzeAbstract readComment
In one paragraph

Article in The Journal of clinical investigation, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 136 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Benefits of SGLT2 inhibitors in arrhythmias.Frontiers in cardiovascular medicine · 2022
    Review
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  14. Cardiac adaptation to exercise training in health and disease.Pflugers Archiv : European journal of physiology · 2020
    Review
  15. Sustained Stimulation of βDiabetes, metabolic syndrome and obesity : targets and therapy · 2020
    Article
  16. Article
  17. Article
  18. Metabolic Effects of Metformin in the Failing Heart.International journal of molecular sciences · 2018
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Brian T O'NeillDivision of Endocrinology, Metabolism and Diabetes and Program in Human Molecular Biology and Genetics, University of Utah School of Medicine, Salt Lake City, Utah 84112, USA.
E Dale Abel
University of Utah · US

Funding

ANIMAL MODELS OF DIABETIC CARDIOVASCULAR COMPLICATIONSU01HL070525 · NHLBI · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A · 2001 to 2005
$3.7M
Insulin resistance and cardiac dysfunction in obesityR01HL073167 · NHLBI · UNIVERSITY OF UTAH · PI ABEL, EVAN DALE · 2003 to 2007
$2.0M
Insulin Signaling and the Heart in DiabetesR01HL070070 · NHLBI · UNIVERSITY OF UTAH · PI ABEL, EVAN DALE · 2004 to 2007
$1.5M
NHLBI NIH HHS HL 70070NHLBI NIH HHS HL 70525NHLBI NIH HHS HL 73167NHLBI NIH HHS R01 HL070070NHLBI NIH HHS R01 HL073167NHLBI NIH HHS U01 HL070525
6 · The paper itself

Abstract

Akt is an important signaling molecule that modulates many cellular processes such as cell growth, survival, and metabolism. Akt activation has been proposed as a potential strategy for increasing cardiomyocyte survival following ischemia. In mammalian cells, 3 distinct isoforms of Akt exist, but their precise roles in cardiovascular biology were previously unknown. Three separate studies published in this issue of the JCI now provide important new insight into the central role of Akt1 in the regulation of angiogenesis and the maladaptive or deleterious consequences of chronic unregulated Akt activation in the heart (see the related articles beginning on pages 2108, 2119, and 2128). Here we discuss the implications of these exciting new studies.

Indexed as

Enzyme ActivationAnimalsCell SurvivalHeartHumansIsoenzymesMyocardial IschemiaMyocardiumMyocytes, CardiacNeovascularization, PathologicProtein Serine-Threonine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-aktAKT1 protein, humanIsoenzymesProtein Serine-Threonine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-akt

Identifiers

PMID16075047
PMCPMC1180557
OpenAlexW2165009569

What OpenQuestion holds

Textmetadata
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.