Evidence map›Paper›PMID 30789496›Full record

ArticleHealth physics2019

Lifelong Residual bone Marrow Damage in Murine Survivors of the Hematopoietic Acute Radiation Syndrome (H-ARS): A Compilation of Studies Comprising the Indiana University Experience.

Hui Lin Chua, P Artur Plett, Alexa Fisher, Carol H Sampson, Sasidhar Vemula, Hailin Feng, Rajendran Sellamuthu, Tong Wu, Thomas J MacVittie, Christie M Orschell

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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
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

27 citing papers in PubMed, 45 citations in OpenAlex.

  1. Radiomitigators: Breakthroughs in Post-Radiation Recovery.Antioxidants (Basel, Switzerland) · 2026
    Review
  2. Article
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  5. Cell Therapies for Acute Radiation Syndrome.International journal of molecular sciences · 2024
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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

10 authors at 2 institutions in 1 country.

Hui Lin ChuaIndiana University, School of Medicine, Indianapolis, IN.
P Artur PlettIndiana University, School of Medicine, Indianapolis, IN.
Alexa FisherIndiana University, School of Medicine, Indianapolis, IN.
Carol H SampsonIndiana University, School of Medicine, Indianapolis, IN.
Sasidhar VemulaIndiana University, School of Medicine, Indianapolis, IN.
Hailin FengIndiana University, School of Medicine, Indianapolis, IN.
Rajendran SellamuthuIndiana University, School of Medicine, Indianapolis, IN.
Tong WuIndiana University, School of Medicine, Indianapolis, IN.
Thomas J MacVittieUniversity of Maryland, School of Medicine, Baltimore, MD.
Christie M OrschellIndiana University, School of Medicine, Indianapolis, IN.
Indiana University – Purdue University Indianapolis · USUniversity of Maryland, Baltimore · 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
A megakaryocyte/PGE2/osteoblast triad in the normal and aged nicheR01AG046246 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI KACENA, MELISSA A, PELUS, LOUIS M · 2013 to 2017
$1.1M
NIAID NIH HHS HHSN272201000046CNIAID NIH HHS U01 AI107340NIA NIH HHS R01 AG046246
6 · The paper itself

Abstract

Accurate analyses of the delayed effects of acute radiation exposure in survivors of the hematopoietic acute radiation syndrome are hampered by low numbers of mice for examination due to high lethality from the acute syndrome, increased morbidity and mortality in survivors, high cost of husbandry for long-term studies, biological variability, and inconsistencies of models from different laboratories complicating meta-analyses. To address this, a compilation of 38 similar hematopoietic acute radiation syndrome studies conducted over a 7-y period in the authors' laboratory, comprising more than 1,500 irradiated young adult C57BL/6 mice and almost 600 day-30 survivors, was assessed for hematopoietic delayed effects of acute radiation exposure at various times up to 30 mo of age. Significant loss of long-term repopulating potential of phenotypically defined primitive hematopoietic stem cells was documented in hematopoietic acute radiation syndrome survivors, as well as significant decreases in all hematopoietic lineages in peripheral blood, prominent myeloid skew, significantly decreased bone marrow cellularity, and numbers of lineage-negative Sca-1+ cKit+ CD150+ cells (KSL CD150+; the phenotype known to be enriched for hematopoietic stem cells), and increased cycling of KSL CD150+ cells. Studies interrogating the phenotype of bone marrow cells capable of initiation of suspension cultures and engraftment in competitive transplantation assays documented the phenotype of hematopoietic stem cells in hematopoietic acute radiation syndrome survivors to be the same as that in nonirradiated age-matched controls. This compilation study adds rigor and validity to our initial findings of persistent hematopoietic dysfunction in hematopoietic acute radiation syndrome survivors that arises at the level of the hematopoietic stem cell and which affects all classes of hematopoietic cells for the life of the survivor.

Indexed as

Acute Radiation SyndromeAnimalsBone MarrowCell CycleFemaleHematopoiesisMaleMiceMice, Inbred C57BLRadiation Injuries, Experimental

Identifiers

PMID30789496
PMCPMC6388630
OpenAlexW2917531193

What OpenQuestion holds

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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.