Evidence map›Paper›PMID 25088223›Full record

ReviewExpert review of clinical immunology2014

Epigenetic coordination of acute systemic inflammation: potential therapeutic targets.

Vidula Vachharajani, Tiefu Liu, Charles E McCall

Open access · greenAbstract readReview
In one paragraph

Review in Expert review of clinical immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. NADAntioxidants (Basel, Switzerland) · 2023
    Review
  5. The Role of Histone Deacetylases in Acute Lung Injury-Friend or Foe.International journal of molecular sciences · 2023
    Review
  6. Review
  7. Review
  8. Induced Ketosis as a Treatment for Neuroprogressive Disorders: Food for Thought?The international journal of neuropsychopharmacology · 2020
    Review
  9. Review
  10. Clinical significance of sirtuin 1 level in sepsis: correlation with disease risk, severity, and mortality risk.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Sirtuins and Immuno-Metabolism of Sepsis.International journal of molecular sciences · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Vidula VachharajaniDepartment of Anesthesiology, Section on Critical Care, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC 27157, USA.
Tiefu Liu
Charles E McCall
Wake Forest University · US

Funding

NF-kB and Chromatin Changes in Human SepsisR01AI065791 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MCCALL, CHARLES EMORY · 2006 to 2015
$4.3M
Bioenergetic and Epigenetic Reprogramming by Obesity in SepsisR01GM099807 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI VACHHARAJANI, VIDULA · 2012 to 2020
$3.1M
Epigenetics of Severe Systemic InflammationR01AI079144 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MCCALL, CHARLES EMORY · 2010 to 2014
$2.0M
Mitochondrial Biogenesis is Regulated by RelB During InflammationR01GM102497 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MCCALL, CHARLES EMORY · 2014 to 2017
$1.2M
NIAID NIH HHS R01 AI065791NIAID NIH HHS R01AI065791NIAID NIH HHS R01 AI079144NIAID NIH HHS R01AI079144NIGMS NIH HHS R01 GM099807NIGMS NIH HHS R01GM099807NIGMS NIH HHS R01 GM102497
6 · The paper itself

Abstract

Epigenetic reprogramming of thousands of genes directs the course of acute systemic inflammation, which is highly lethal when dysregulated during sepsis. No molecular-based treatments for sepsis are available. A new concept supports that sepsis is an immunometabolic disease and that loss of control of nuclear epigenetic regulator sirtuin 1 (SIRT-1), a NAD(+) sensor directs immune and metabolic pathways during sepsis. SIRT-1, acting as homeostasis checkpoint, controls hyper- and hypo-inflammatory responses of sepsis at the microvascular interface, which disseminates inflammatory injury to cause multiple organ failure. Modifying SIRT-1 activity, which can prevent or treat established sepsis in mice, may provide a new way to treat sepsis by epigenetically restoring immunometabolic homeostasis.

Indexed as

Molecular Targeted TherapyAnimalsCapillary PermeabilityDisease Models, AnimalEpigenesis, GeneticHomeostasisHumansImmunomodulationInflammationMetabolomeMiceSepsisSirtuin 1SIRT1 protein, humanSirtuin 1acute inflammationepigeneticsimmunometabolismleukocyte adhesionmicrovascular dysfunctionsepsisSIRT-1

Identifiers

PMID25088223
PMCPMC4634938
OpenAlexW2127658943

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.