Evidence map›Paper›PMID 25803075›Full record

ReviewBiological chemistry2015

Molecular mechanisms of erythrocyte aging.

Richard S Hoehn, Peter L Jernigan, Alex L Chang, Michael J Edwards, Timothy A Pritts

Abstract readReview
In one paragraph

Review in Biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
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  5. Article
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  7. Açaì (Cells · 2022
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
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  15. Article
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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

5 authors.

Richard S Hoehn
Peter L Jernigan
Alex L Chang
Michael J Edwards
Timothy A Pritts

Funding

Red blood cell microparticles and lung inflammation after hemorrhage and resuscitationR01GM107625 · NIGMS · UNIVERSITY OF CINCINNATI · PI PRITTS, TIMOTHY A · 2014 to 2022
$3.0M
NIGMS NIH HHS R01 GM107625
6 · The paper itself

Abstract

Anemia and hemorrhagic shock are leading causes of morbidity and mortality worldwide, and transfusion of human blood products is the ideal treatment for these conditions. As human erythrocytes age during storage in blood banks they undergo many biochemical and structural changes, termed the red blood cell 'storage lesion'. Specifically, ATP and pH levels decrease as metabolic end products, oxidative stress, cytokines, and cell-free hemoglobin increase. Also, membrane proteins and lipids undergo conformational and organizational changes that result in membrane loss, viscoelastic changes and microparticle formation. As a result, transfusion of aged blood is associated with a host of adverse consequences such as decreased tissue perfusion, increased risk of infection, and increased mortality. This review summarizes current research detailing the known parts of the erythrocyte storage lesion and their physiologic consequences.

Indexed as

Blood BanksCytokinesErythrocyte AgingErythrocytesHemoglobinsHumansOxidative StressCytokinesHemoglobins

Identifiers

PMID25803075
PMCPMC5673117

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.