Evidence map›Paper›PMID 25978437›Full record

ArticlePloS one2015

Compensatory UTE/T2W Imaging of Inflammatory Vascular Wall in Hyperlipidemic Rabbits.

Bongjune Kim, Jaemoon Yang, Young Han Lee, Myeong-Hoon Kim, Dan Heo, Eugene Lee, Jin-Suck Suh, Seungjoo Haam, Yong-Min Huh

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 100% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 1 institution in 1 country.

Bongjune KimDepartment of Chemical and Biomolecular Engineering, Yonsei University, Seoul, Republic of Korea.
Jaemoon YangDepartment of Radiology, College of Medicine, Yonsei University, Seoul, Republic of Korea; YUHS-KRIBB Medical Convergence Research Institute, Seoul, Republic of Korea.
Young Han LeeDepartment of Radiology, College of Medicine, Yonsei University, Seoul, Republic of Korea; YUHS-KRIBB Medical Convergence Research Institute, Seoul, Republic of Korea.
Myeong-Hoon KimDepartment of Chemical and Biomolecular Engineering, Yonsei University, Seoul, Republic of Korea.
Dan HeoDepartment of Radiology, College of Medicine, Yonsei University, Seoul, Republic of Korea; Nanomedical National Core Research Center, Yonsei University, Seoul, Republic of Korea.
Eugene LeeDepartment of Radiology, College of Medicine, Yonsei University, Seoul, Republic of Korea; Nanomedical National Core Research Center, Yonsei University, Seoul, Republic of Korea.
Jin-Suck SuhDepartment of Radiology, College of Medicine, Yonsei University, Seoul, Republic of Korea; Nanomedical National Core Research Center, Yonsei University, Seoul, Republic of Korea; YUHS-KRIBB Medical Convergence Research Institute, Seoul, Republic of Korea.
Seungjoo HaamDepartment of Chemical and Biomolecular Engineering, Yonsei University, Seoul, Republic of Korea.
Yong-Min HuhDepartment of Radiology, College of Medicine, Yonsei University, Seoul, Republic of Korea.
Yonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo obtain compensatory ultra-short echo time (UTE) imaging and T2-weighted (T2W) imaging of Watanabe heritable hyperlipidemic (WHHL) rabbits following dextran-coated magnetic nanocluster (DMNC) injection for the effective in vivo detection of inflammatory vascular wall.

methodsMagnetic nanoparticle was synthesized by thermal decomposition and encapsulated with dextran to prepare DMNC. The contrast enhancement efficiency of DMNC was investigated using UTE (repetition time [TR] = 5.58 and TE = 0.07 ms) and T2W (TR = 4000 and TE = 60 ms) imaging sequences. To confirm the internalization of DMNC into macrophages, DMNC-treated macrophages were visualized by cellular transmission electron microscope (TEM) and magnetic resonance (MR) imaging. WHHL rabbits expressing macrophage-rich plaques were subjected to UTE and T2W imaging before and after intravenous DMNC (120 μmol Fe/kg) treatment. Ex vivo MR imaging of plaques and immunostaining studies were also performed.

resultsPositive and negative contrast enhancement of DMNC solutions with increasing Fe concentrations were observed in UTE and T2W imaging, respectively. The relative signal intensities of the DMNC solution containing 2.9 mM Fe were calculated as 3.53 and 0.99 in UTE and T2W imaging, respectively. DMNC uptake into the macrophage cytoplasm was visualized by electron microscopy. Cellular MR imaging of DMNC-treated macrophages revealed relative signals of 3.00 in UTE imaging and 0.98 in T2W imaging. In vivo MR images revealed significant brightening and darkening of plaque areas in the WHHL rabbit 24 h after DMNC injection in UTE and T2W imaging, respectively. Ex vivo MR imaging results agreed with these in vivo MR imaging results. Histological analysis showed that DMNCs were localized to areas of inflammatory vascular wall.

conclusionsUsing compensatory UTE and T2W imaging in conjunction with DMNC is an effective approach for the noninvasive in vivo imaging of atherosclerotic plaque.

Indexed as

AnimalsCell LineContrast MediaMacrophagesMagnetic Resonance ImagingMagnetite NanoparticlesMaleMicePlaque, AtheroscleroticRabbitsContrast MediaMagnetite Nanoparticles

Identifiers

PMID25978437
PMCPMC4433322
OpenAlexW312325486

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.