Evidence map›Paper›PMID 35238006›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

Intravascular Fluorescence Molecular Imaging of Atherosclerosis.

Mohammed M Chowdhury, Zhonglie Piao, Mazen S Albaghdadi, Patrick A Coughlin, James H F Rudd, Guillermo J Tearney, Farouc A Jaffer

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
15.8field-weighted citation impact, top 1% 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

6 citing papers in PubMed, 7 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

7 authors at 3 institutions in 2 countries.

Mohammed M ChowdhuryCardiovascular Research Center, Division of Cardiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Zhonglie PiaoWellman Center for Photomedicine, Harvard Medical School and Massachusetts General Hospital, Boston, MA, USA.
Mazen S AlbaghdadiCardiovascular Research Center, Division of Cardiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Patrick A CoughlinDivision of Vascular Surgery, Department of Surgery, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK.
James H F RuddDivision of Cardiovascular Medicine, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK.
Guillermo J TearneyWellman Center for Photomedicine, Harvard Medical School and Massachusetts General Hospital, Boston, MA, USA.
Farouc A JafferCardiovascular Research Center, Division of Cardiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA. fjaffer@mgh.harvard.edu.
Massachusetts General Hospital · USHarvard University · USUniversity of Cambridge · GB

Funding

Novel PET/CT and Treatment Strategies to reduce PTS following DVTR01HL137913 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI JAFFER, FAROUC AMIN, TAWAKOL, AHMED A · 2017 to 2020
$3.3M
Intravascular NIRF-IVUS imaging of inflammation-guided arterial therapyR01HL150538 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI JAFFER, FAROUC AMIN · 2020 to 2023
$2.2M
British Heart Foundation FS/12/29/29463British Heart Foundation PG/09/083/27667NHLBI NIH HHS R01 HL137913NHLBI NIH HHS R01 HL150538
6 · The paper itself

Abstract

Optical molecular imaging using near-infrared fluorescence (NIRF) light is an emerging high-resolution imaging approach to image a wide range of molecular and cellular species in vivo. Imaging using NIR wavelengths (650-900 nm) enables deeper photon penetration into tissue and reduced tissue autofluorescence, resulting in higher sensitivity to detect exogenously administered NIR fluorophores (injectable molecular imaging agents). Greater imaging depth of several centimeters is further achievable in the NIR window as blood absorption is as an order of magnitude lower than in the visible range. Furthermore, as optical imaging is routinely performed in the cardiac catheterization laboratory (e.g., optical coherence tomography), intravascular NIRF offers a promising translational approach for clinical coronary and peripheral arterial imaging. To this point, the first human intravascular NIRF imaging study recently demonstrated the ability to detect NIR autofluorescence in patients with coronary atherosclerosis. This study provides a foundation for targeted intravascular NIRF molecular imaging studies in coronary patients. In this chapter, we detail system engineering, imaging agents and translational applications of intravascular NIRF molecular imaging.

Indexed as

AtherosclerosisCoronary Artery DiseaseHumansMolecular ImagingOptical ImagingSpectroscopy, Near-InfraredTomography, Optical CoherenceAtherosclerosisDrug-coated balloonImagingInflammationIntravascular ultrasoundNear-infrared fluorescenceOptical coherence tomographyPeripheral arterial disease

Identifiers

PMID35238006
PMCPMC9052094
OpenAlexW4214949580

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.