Evidence map›Paper›PMID 38537079›Full record

ArticleBlood advances2024

Amino acid supplementation confers protection to red blood cells before Plasmodium falciparum bystander stress.

Heather Colvin Binns, Elmira Alipour, Cameron E Sherlock, Dinah S Nahid, John F Whitesides, Anderson O'Brien Cox, Cristina M Furdui, Glen S Marrs, Daniel B Kim-Shapiro, Regina Joice Cordy

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Heather Colvin BinnsDepartment of Biology, Wake Forest University, Winston-Salem, NC.ORCID 0000-0003-4979-879X
Elmira AlipourDepartment of Physics, Wake Forest University, Winston-Salem, NC.
Cameron E SherlockDepartment of Biology, Wake Forest University, Winston-Salem, NC.ORCID 0009-0007-0603-5799
Dinah S NahidDepartment of Biology, Wake Forest University, Winston-Salem, NC.
John F WhitesidesDepartment of Microbiology and Immunology, Wake Forest University School of Medicine, Winston-Salem, NC.
Anderson O'Brien CoxProteomics and Metabolomics Shared Resource, Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC.ORCID 0000-0001-5491-1019
Cristina M FurduiProteomics and Metabolomics Shared Resource, Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC.ORCID 0000-0003-3771-7999
Glen S MarrsDepartment of Biology, Wake Forest University, Winston-Salem, NC.ORCID 0000-0003-3006-3152
Daniel B Kim-ShapiroDepartment of Physics, Wake Forest University, Winston-Salem, NC.
Regina Joice CordyDepartment of Biology, Wake Forest University, Winston-Salem, NC.
Wake Forest University · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
PRIDE: Functional and Translational Genomics of Blood DisordersR25HL106365 · NHLBI · AUGUSTA UNIVERSITY · PI PACE, BETTY SUE · 2010 to 2024
$5.2M
Redox Biology and Medicine Training ProgramT32GM127261 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FURDUI, CRISTINA MARIA, POOLE, LESLIE B · 2018 to 2022
$975k
Redox Biology and Medicine Training ProgramT32GM149818 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Cristina Maria Furdui, LESLIE B POOLE · 2023 to 2026
$861k
A systems biology investigation of the interplay between gut microbes and blood metabolites in the development of malarial anemiaK01HL143112 · NHLBI · WAKE FOREST UNIVERSITY · PI CORDY, REGINA J · 2018 to 2022
$745k
Live Cell Fluorescent Imaging SystemS10OD032281 · OD · WAKE FOREST UNIVERSITY · PI MARRS, GLEN · 2022 to 2022
$250k
NCI NIH HHS P30 CA012197NHLBI NIH HHS K01 HL143112NHLBI NIH HHS R25 HL106365NIGMS NIH HHS T32 GM127261NIGMS NIH HHS T32 GM149818NIH HHS S10 OD032281
6 · The paper itself

Abstract

abstractMalaria is a highly oxidative parasitic disease in which anemia is the most common clinical symptom. A major contributor to the malarial anemia pathogenesis is the destruction of bystander, uninfected red blood cells (RBCs). Metabolic fluctuations are known to occur in the plasma of individuals with acute malaria, emphasizing the role of metabolic changes in disease progression and severity. Here, we report conditioned medium from Plasmodium falciparum culture induces oxidative stress in uninfected, catalase-depleted RBCs. As cell-permeable precursors to glutathione, we demonstrate the benefit of pre-exposure to exogenous glutamine, cysteine, and glycine amino acids for RBCs. Importantly, this pretreatment intrinsically prepares RBCs to mitigate oxidative stress.

Indexed as

Amino AcidsErythrocytesOxidative StressPlasmodium falciparumHumansMalaria, FalciparumAmino Acids

Identifiers

PMID38537079
PMCPMC11131086
OpenAlexW4393217546

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.