Evidence map›Paper›PMID 21859730›Full record

Trial reportHaematologica2011

Alterations of red blood cell metabolome in overhydrated hereditary stomatocytosis.

Dhouha Darghouth, Bérengère Koehl, Jean François Heilier, Geoffrey Madalinski, Petra Bovee, Giel Bosman, Jean Delaunay, Christophe Junot, Paul-Henri Roméo

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Haematologica, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
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  7. Review
  8. Article
  9. Ion Transport in Eryptosis, the Suicidal Death of Erythrocytes.Frontiers in cell and developmental biology · 2020
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Drug-loaded erythrocytes: on the road toward marketing approval.Drug design, development and therapy · 2016
    Review
  17. Article
  18. Article
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

9 authors at 1 institution in 1 country.

Dhouha DarghouthInstitut de Radiobiologie Cellulaire et Moléculaire, Laboratoire de Recherche sur la Réparation et la Transcription dans les Cellules, Gif-sur-Yvette cedex, France.
Bérengère Koehl
Jean François Heilier
Geoffrey Madalinski
Petra Bovee
Giel Bosman
Jean Delaunay
Christophe Junot
Paul-Henri Roméo
Institut de Radiobiologie Cellulaire et Moléculaire · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overhydrated hereditary stomatocytosis, clinically characterized by hemolytic anemia, is a rare disorder of the erythrocyte membrane permeability to monovalent cations, associated with mutations in the Rh-associated glycoprotein gene. We assessed the red blood cell metabolome of 4 patients with this disorder and showed recurrent metabolic abnormalities associated with this disease but not due to the diminished half-life of their erythrocytes. Glycolysis is exhausted with accumulation of ADP, pyruvate, lactate, and malate. Ascorbate metabolic pathway is altered probably due to a limited entry of dehydroascorbate. Although no major oxydative stress has been reported in patients with overhydrated hereditary stomatocytosis, we found decreased amounts of oxydized glutathione, creatine and ergothioneine, suggesting transporter abnormalities and/or uncharacterized oxydative stress. These results pinpoint major metabolic defects of overhydrated hereditary stomatocytosis erythrocytes and emphasize the relevance of red blood cell metabolomics for a better understanding of the pathophysiological bases of hemolytic anemia associated with erythrocyte abnormalities.

Indexed as

GlycolysisMetabolomeOxidative StressAdultAnemia, Hemolytic, CongenitalBlood ProteinsErythrocytesFemaleGlutathione DisulfideHumansMaleMembrane GlycoproteinsMutationBlood ProteinsGlutathione DisulfideMembrane GlycoproteinsRHAG protein, human

Identifiers

PMID21859730
PMCPMC3232270
OpenAlexW2161600832

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.