Evidence map›Paper›PMID 36804714›Full record

ReviewEpilepsy & behavior : E&B2023

2DG and glycolysis as therapeutic targets for status epilepticus.

Thomas P Sutula, Nathan B Fountain

Open access · greenAbstract readReview
In one paragraph

Review in Epilepsy & behavior : E&B, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

2 authors at 2 institutions in 1 country.

Thomas P SutulaDepartment of Neurology, University of Wisconsin, Madison, WI, USA; Hexokine Therapeutics, Inc., Madison, WI, USA. Electronic address: sutula@neurology.wisc.edu.
Nathan B FountainDepartment of Neurology, F.E. Dreifuss Comprehensive Epilepsy Program, University of Virginia, Charlottesville, VA, USA; Hexokine Therapeutics, Inc., Madison, WI, USA.
University of Virginia · USUniversity of Wisconsin–Madison · US

Funding

NINDS NIH HHS X01 NS066866
6 · The paper itself

Abstract

2-deoxy-D-glucose (2DG) is a glucose analog differing from glucose only by removal of an oxygen atom at the 2 position, which prevents the isomerization of glucose-6-phosphate to fructose-6-phosphate, and thereby reversibly inhibits glycolysis. PET studies of regional brain glucose utilization positron-emitting 18F-2DG demonstrate that brain regions generating seizures have diminished glucose utilization during interictal conditions, but rapidly transition to markedly increased glucose delivery and utilization during seizures, particularly in status epilepticus (SE). 2-deoxy-D-glucose has acute antiseizure actions in multiple in vivo and in vitro seizure models, including models of SE induced by the chemo convulsants pilocarpine and kainic acid, suggesting that focal enhanced delivery of 2DG to ictal brain circuits is a potential novel anticonvulsant intervention for the treatment of SE.

Indexed as

DeoxyglucoseStatus EpilepticusGlucoseGlycolysisHumansPilocarpineSeizuresDeoxyglucoseGlucosePilocarpine2-deoxy-D-glucoseEpilepsyGlycolytic inhibitionMetabolismSeizures

Identifiers

PMID36804714
PMCPMC10032166
OpenAlexW4321011925

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.