Evidence map›Paper›PMID 21067373›Full record

ArticleThe Journal of infectious diseases2010

Anthrax lethal and edema toxins produce different patterns of cardiovascular and renal dysfunction and synergistically decrease survival in canines.

Daniel A Sweeney, Xizhong Cui, Steven B Solomon, David A Vitberg, Thi S Migone, Dara Scher, Robert L Danner, Charles Natanson, G Mani Subramanian, Peter Q Eichacker

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

38 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. What Is Anthrax?Pathogens (Basel, Switzerland) · 2022
    Article
  3. Review
  4. American journal of physiology. Heart and circulatory physiology · 2021
    Article
  5. Article
  6. American journal of physiology. Heart and circulatory physiology · 2019
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Molecular determinants for a cardiovascular collapse in anthrax.Frontiers in bioscience (Elite edition) · 2014
    Review
  19. Article
  20. Review
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.

Daniel A SweeneyCritical Care Medicine Department, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA.
Xizhong Cui
Steven B Solomon
David A Vitberg
Thi S Migone
Dara Scher
Robert L Danner
Charles Natanson
G Mani Subramanian
Peter Q Eichacker
National Institutes of Health Clinical Center · USHuman Genome Sciences (United States) · US

Funding

Canine Model Investigating Cardiopulmonary Effects B. anthracis Edema and LethalZ01CL008090 · CLC · CLINICAL CENTER · PI EICHACKER, PETER Q · 2006 to 2008
$98k
Preclinical and Clinical Investigations of Severe Infection and Critical Illness ZIACL008060 · CLC · CLINICAL CENTER · PI DANNER, ROBERT L · 2009 to 2025
$0k
Canine Model Investigating Cardiopulmonary Effects B. anthracis Edema and LethalZIACL008090 · CLC · CLINICAL CENTER · PI EICHACKER, PETER · 2009 to 2009
$0k
Intramural NIH HHS Z01 CL008090
6 · The paper itself

Abstract

backgroundHigh mortality in the 2001 US and recent European anthrax outbreaks suggests that better understanding of the effects of the toxins produced by this bacterium is needed to improve treatment. METHODS AND

resultsHere, 24-h edema (ETx) and lethal (LeTx) toxin infusions were investigated for 96 hin sedated canines receiving mechanical ventilation. The initial study compared similarly lethal doses of ETx (n=8) or LeTx (n=15) alone. ETx was 24 times less lethal than LeTx, and the median time to death in nonsurvivors (n=6 and n=9, respectively) was shorter with ETx (42 vs 67 h; P=.04). Compared with controls(n=9), both toxins decreased arterial and central venous pressures and systemic vascular resistance and increased heart rate, cardiac index, blood urea nitrogen (BUN) level, creatinine (Cr) concentration, BUN:Cr ratio, and hepatic transaminase levels (P ≤ .05 for toxin effect or time interaction). However, ETx stimulated early diuresis,reduced serum sodium levels, and had more pronounced vasodilatory effects, compared with LeTx, as reflected by greater or earlier central venous pressures, systemic vascular resistance, and changes in the BUN:Cr ratio(P ≤ .01). LeTx progressively decreased the left ventricular ejection fraction (P ≤ .002). In a subsequent study, a lethal dose of LeTx with an equimolar nonlethal ETx dose (n=8) increased mortality, compared with LeTx alone (n=8; P= .05).

conclusionShock with ETx or LeTx may require differing supportive therapies, whereas toxin antagonists should likely target both toxins.

Indexed as

Survival AnalysisAnimalsAntigens, BacterialBacterial ToxinsBlood PressureCardiovascular SystemCreatinineDisease Models, AnimalDogsHeart RateKidneyPoisoningTransaminasesUreaVascular Resistanceanthrax toxinAntigens, BacterialBacterial ToxinsCreatinineTransaminasesUrea

Identifiers

PMID21067373
PMCPMC3061475
OpenAlexW2105205024

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.