Evidence map›Paper›PMID 34389161›Full record

ReviewTrends in pharmacological sciences2021

Treatment strategies for glucose-6-phosphate dehydrogenase deficiency: past and future perspectives.

Adriana A Garcia, Ana Koperniku, Julio C B Ferreira, Daria Mochly-Rosen

Open access · greenAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
12.3field-weighted citation impact, top 1% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 49 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

4 authors at 2 institutions in 2 countries.

Adriana A GarciaDepartment of Chemical and Systems Biology, School of Medicine, Stanford University, Stanford, CA, USA.
Ana KopernikuDepartment of Chemical and Systems Biology, School of Medicine, Stanford University, Stanford, CA, USA.
Julio C B FerreiraDepartment of Chemical and Systems Biology, School of Medicine, Stanford University, Stanford, CA, USA; Department of Anatomy, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
Daria Mochly-RosenDepartment of Chemical and Systems Biology, School of Medicine, Stanford University, Stanford, CA, USA. Electronic address: mochly@stanford.edu.
Stanford University · USUniversidade de São Paulo · BR

Funding

Development of a novel treatment for hyperbilirubinemia-induced kernicterusR01HD084422 · NICHD · STANFORD UNIVERSITY · PI MOCHLY-ROSEN, DARIA, STEVENSON, DAVID K · 2016 to 2020
$1.6M
Molecular Pharmacology Training GrantT32GM113854 · NIGMS · STANFORD UNIVERSITY · PI MOCHLY-ROSEN, DARIA · 2015 to 2019
$1.1M
PSYCHOSTIMULANT EFFECTS: QEEG MEASURES IN ADHD CHILDRENF32HD008442 · NICHD · UNIVERSITY OF COLORADO DENVER · PI LOO, SANDRA K · 1998 to 1999
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NICHD NIH HHS F32 HD008442NICHD NIH HHS R01 HD084422NIGMS NIH HHS T32 GM113854
6 · The paper itself

Abstract

Glucose-6-phosphate dehydrogenase (G6PD) maintains redox balance in a variety of cell types and is essential for erythrocyte resistance to oxidative stress. G6PD deficiency, caused by mutations in the G6PD gene, is present in ~400 million people worldwide, and can cause acute hemolytic anemia. Currently, there are no therapeutics for G6PD deficiency. We discuss the role of G6PD in hemolytic and nonhemolytic disorders, treatment strategies attempted over the years, and potential reasons for their failure. We also discuss potential pharmacological pathways, including glutathione (GSH) metabolism, compensatory NADPH production routes, transcriptional upregulation of the G6PD gene, highlighting potential drug targets. The needs and opportunities described here may motivate the development of a therapeutic for hematological and other chronic diseases associated with G6PD deficiency.

Indexed as

Glucosephosphate Dehydrogenase DeficiencyGlutathioneHumansMutationOxidation-ReductionOxidative StressGlutathioneenzyme activatorsG6PD deficiencyN-acetyl-cysteinetherapeutic strategytranscriptional regulators

Identifiers

PMID34389161
PMCPMC8448981
OpenAlexW3191754580

What Socratic 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 Socratic graph.