Evidence map›Paper›PMID 33647027›Full record

ArticlePloS one2021

Maltohexaose-indocyanine green (MH-ICG) for near infrared imaging of endocarditis.

Kiyoko Takemiya, Joachim J Røise, Maomao He, Chung Taing, Alexander G Rodriguez, Niren Murthy, Mark M Goodman, W Robert Taylor

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Kiyoko TakemiyaDivision of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, United states of America.ORCID 0000-0003-0968-5125
Joachim J RøiseDepartment of Bioengineering, University of California at Berkeley, Berkeley, California, United States of America.ORCID 0000-0002-1794-7570
Maomao HeDepartment of Bioengineering, University of California at Berkeley, Berkeley, California, United States of America.
Chung TaingDepartment of Chemistry, University of California at Berkeley, Berkeley, California, United States of America.ORCID 0000-0002-3124-7167
Alexander G RodriguezDivision of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, United states of America.
Niren MurthyDepartment of Bioengineering, University of California at Berkeley, Berkeley, California, United States of America.
Mark M GoodmanDepartment of Radiology and Imaging Sciences, Emory Center for Systems Imaging, Emory University School of Medicine, Atlanta, Georgia, United states of America.
W Robert TaylorDivision of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, United states of America.
University of California, Berkeley · USEmory University · USGeorgia Institute of Technology · US

Funding

Imaging bacterial infections with 2nd generation maltodextrinsR01EB029320 · NIBIB · EMORY UNIVERSITY · PI GOODMAN, MARK MYRON, MURTHY, NIREN · 2020 to 2023
$2.7M
18F Conjugated Maltodextrins for the Detection of Medical Device InfectionsR01EB020008 · NIBIB · EMORY UNIVERSITY · PI GOODMAN, MARK MYRON, MURTHY, NIREN · 2015 to 2018
$2.4M
NIBIB NIH HHS R01 EB020008NIBIB NIH HHS R01 EB029320
6 · The paper itself

Abstract

Infectious endocarditis is a life-threatening disease, and diagnostics are urgently needed to accurately diagnose this disease especially in the case of prosthetic valve endocarditis. We show here that maltohexaose conjugated to indocyanine green (MH-ICG) can detect Staphylococcus aureus (S. aureus) infection in a rat model of infective endocarditis. The affinity of MH-ICG to S. aureus was determined and had a Km and Vmax of 5.4 μM and 3.0 X 10-6 μmol/minutes/108 CFU, respectively. MH-ICG had no detectable toxicity to mammalian cells at concentrations as high as 100 μM. The in vivo efficiency of MH-ICG in rats was evaluated using a right heart endocarditis model, and the accumulation of MH-ICG in the bacterial vegetations was 2.5 ± 0.2 times higher than that in the control left ventricular wall. The biological half-life of MH-ICG in healthy rats was 14.0 ± 1.3 minutes, and approximately 50% of injected MH-ICG was excreted into the feces after 24 hours. These data demonstrate that MH-ICG was internalized by bacteria with high specificity and that MH-ICG specifically accumulated in bacterial vegetations in a rat model of endocarditis. These results demonstrate the potential efficacy of this agent in the detection of infective endocarditis.

Indexed as

AnimalsCardiac Imaging TechniquesCell SurvivalCHO CellsColoring AgentsCricetulusDisease Models, AnimalEndocarditis, BacterialGlycoconjugatesHeart VentriclesHumansIndocyanine GreenInfrared RaysMaleOligosaccharidesRatsColoring AgentsGlycoconjugatesIndocyanine GreenmaltohexaoseOligosaccharides

Identifiers

PMID33647027
PMCPMC7920357
OpenAlexW3134607293

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.