Evidence map›Paper›PMID 30681425›Full record

ArticleHealth physics2019

Effect of Sex on Biomarker Response in a Mouse Model of the Hematopoietic Acute Radiation Syndrome.

Jace W Jones, Jenna Alloush, Rajendran Sellamuthu, Hui Lin Chua, Thomas J MacVittie, Christie M Orschell, Maureen A Kane

Abstract read
In one paragraph

Article in Health physics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
3.8field-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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Sex differences in radiation research.International journal of radiation biology · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Establishing a Murine Model of the Hematopoietic Acute Radiation Syndrome.Methods in molecular biology (Clifton, N.J.) · 2023
    Review
  16. Review
  17. Review
  18. Article
  19. 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

7 authors at 2 institutions in 1 country.

Jace W JonesUniversity of Maryland, School of Pharmacy, Department of Pharmaceutical Sciences, Baltimore, MD.
Jenna AlloushUniversity of Maryland, School of Pharmacy, Department of Pharmaceutical Sciences, Baltimore, MD.
Rajendran SellamuthuIndiana University, School of Medicine, Indianapolis, IN.
Hui Lin ChuaIndiana University, School of Medicine, Indianapolis, IN.
Thomas J MacVittieUniversity of Maryland, School of Medicine, Department of Radiation Oncology, Baltimore, MD.
Christie M OrschellIndiana University, School of Medicine, Indianapolis, IN.
Maureen A KaneUniversity of Maryland, School of Pharmacy, Department of Pharmaceutical Sciences, Baltimore, MD.
University of Maryland, Baltimore · USIndiana University – Purdue University Indianapolis · US

Funding

Long-acting growth factors for treating the acute and long term effects of lethalU01AI107340 · NIAID · BOLDER BIOTECHNOLOGY, INC. · PI COX, GEORGE NORBERT, ORSCHELL, CHRISTIE M · 2013 to 2017
$2.9M
NIAID NIH HHS HHSN272201000046CNIAID NIH HHS U01 AI107340
6 · The paper itself

Abstract

Sex is an important confounding variable in biomarker development that must be incorporated into biomarker discovery and validation. Additionally, understanding of sex as a biological variable is essential for effective translation of biomarkers in animal models to human populations. Toward these ends, we conducted high-throughput targeted metabolomics using liquid chromatography tandem mass spectrometry and multiplexed immunoassay analyses using a Luminex-based system in both male and female mice in a model of total-body irradiation at a radiation dose consistent with the hematopoietic acute radiation syndrome. Metabolomic and immunoassay analyses identified metabolites and cytokines that were significantly different in plasma from naive and irradiated C57BL/6 mice consisting of equal numbers of female and male mice at 3 d after 8.0 or 8.72 Gy, an approximate LD60-70/30 dose of total-body irradiation. An additional number of metabolites and cytokines had sex-specific responses after radiation. Analyses of sham-irradiated mice illustrate the presence of stress-related changes in several cytokines due simply to undergoing the irradiation procedure, absent actual radiation exposure. Basal differences in metabolite levels between female and male were also identified as well as time-dependent changes in cytokines up to 9 d postexposure. These studies provide data toward defining the influence of sex on plasma-based biomarker candidates in a well-defined mouse model of acute radiation syndrome.

Indexed as

Acute Radiation SyndromeAnimalsBiomarkersChromatography, LiquidCytokinesFemaleHematopoiesisHigh-Throughput Screening AssaysMaleMiceMice, Inbred C57BLRadiation Injuries, ExperimentalSex FactorsTandem Mass SpectrometryTime FactorsWhole-Body IrradiationBiomarkersCytokines

Identifiers

PMID30681425
PMCPMC6384137
OpenAlexW2914810320

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.