Evidence map›Paper›PMID 25006545›Full record

ArticleEJNMMI research2014

Imaging RAGE expression in atherosclerotic plaques in hyperlipidemic pigs.

Lynne L Johnson, Yared Tekabe, Maria Kollaros, George Eng, Ketan Bhatia, Chong Li, Christian G Krueger, Dhanansayan Shanmuganayagam, Ann Marie Schmidt

Open access · goldAbstract read
In one paragraph

Article in EJNMMI research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. [Establishment of a rabbit model of small diameter vascular graft replacement].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2017
    Article
  8. 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

9 authors at 3 institutions in 1 country.

Lynne L JohnsonDepartment of Medicine, Columbia University Medical Center, 622 West 168 St, New York 10032, NY, USA.
Yared TekabeDepartment of Medicine, Columbia University Medical Center, 622 West 168 St, New York 10032, NY, USA.
Maria KollarosDepartment of Medicine, Columbia University Medical Center, 622 West 168 St, New York 10032, NY, USA.
George EngDepartment of Medicine, Columbia University Medical Center, 622 West 168 St, New York 10032, NY, USA.
Ketan BhatiaDepartment of Medicine, Columbia University Medical Center, 622 West 168 St, New York 10032, NY, USA.
Chong LiDepartment of Medicine, Columbia University Medical Center, 622 West 168 St, New York 10032, NY, USA.
Christian G KruegerDepartment of Veterinary Medicine, University of Wisconsin, Madison 53706, WI, USA.
Dhanansayan ShanmuganayagamDepartment of Veterinary Medicine, University of Wisconsin, Madison 53706, WI, USA.
Ann Marie SchmidtDepartment of Medicine, NYU Medical Center, New York 10016, NY, USA.
Columbia University Irving Medical Center · USUniversity of Wisconsin–Madison · USNew York University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundReceptor for advanced glycated end product (RAGE) expression is a prominent feature of atherosclerosis. We have previously shown in apoE null mice uptake of a radiolabeled anti-RAGE antibody in atherosclerotic plaque and now evaluate RAGE-directed imaging to identify advanced plaques in a large animal model.

methodsNine hyperlipidemic (HL) pigs were injected with 603.1 ± 129.5 MBq of (99m)Tc-anti-RAGE F(ab')2, and after 6 h (blood pool clearance), they underwent single-photon emission computed tomography/computed tomography (SPECT/CT) imaging of the neck, thorax, and hind limbs. Two HL pigs received (99m)Tc non-immune IgG F(ab')2, and three farm pigs were injected with (99m)Tc-anti-RAGE F(ab')2. After imaging, the pigs were euthanized. The aorta from the root to bifurcation was dissected, and the innominates, proximal carotids, and coronaries were dissected and counted, stained for H&E and RAGE, and AHA-classified.

resultsOn pathology, 24% of the arterial segments showed AHA class III or IV lesions, and these lesions were confined almost exclusively to coronaries and carotids with % stenosis from 15% to 65%. Scatter plots of %ID/g for class III/IV vs. I/II lesions showed almost complete separation. Focal vascular uptake of tracer visualized on SPECT scans corresponded to class III/IV lesions in the coronary and carotid vessels. In addition, uptake in the hind limbs was noted in the HL pigs and corresponded to RAGE staining of small arteries in the muscle sections. Correlations for the vascular lesions were r = 0.747, P = 0.001 for %ID vs. %ID/g and r = 0.83, P = 0.002 for %ID/g vs. % RAGE staining.

conclusionsUptake of radiolabeled anti-RAGE antibody in coronary and carotid fibroatheroma and in the small arteries of the hind limbs in a relevant large animal model of atherosclerosis supports the important role of RAGE in atherosclerosis and peripheral artery disease as a target for imaging and treatment.

Indexed as

AtherosclerosisHyperlipidemic pigsImagingRAGE

Identifiers

PMID25006545
PMCPMC4078320
OpenAlexW2128949318

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.