Evidence map›Paper›PMID 37423992›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Synthesis and Expression of a Targeted, Ferritin-Based Tracer for PET Imaging of Kidney Glomeruli.

Edwin J Baldelomar, Kasey C Emoto, Maria Veronica Clavijo Jordan, Jennifer R Charlton, David E Reichert, Neda Parvin, Courtnie Yokono, Bradley D Hann, Kevin M Bennett

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
4.6field-weighted citation impact, top 7% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Are noninvasive measurements of nephron number achievable in humans?Current opinion in nephrology and hypertension · 2026
    Review
  2. Development and Use of Human RecombinantACS applied bio materials · 2024
    Article
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 4 institutions in 1 country.

Edwin J BaldelomarMallinckrodt Institute of Radiology, Washington University in St. Louis, St. Louis, MO, USA.
Kasey C EmotoDepartment of Biology, University of Hawaii at Manoa, Honolulu, HI, USA.
Maria Veronica Clavijo JordanAthinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital/Harvard Medical School, Charlestown, MA, USA.
Jennifer R CharltonDepartment of Pediatrics, Division of Nephrology, University of Virginia, Charlottesville, VA, USA.
David E ReichertMallinckrodt Institute of Radiology, Washington University in St. Louis, St. Louis, MO, USA.
Neda ParvinMallinckrodt Institute of Radiology, Washington University in St. Louis, St. Louis, MO, USA.
Courtnie YokonoDepartment of Biology, University of Hawaii at Manoa, Honolulu, HI, USA.
Bradley D HannDepartment of Biology, University of Hawaii at Manoa, Honolulu, HI, USA.
Kevin M BennettMallinckrodt Institute of Radiology, Washington University in St. Louis, St. Louis, MO, USA. kmbennett@wustl.edu.
Washington University in St. Louis · USUniversity of Hawaiʻi at Mānoa · USHarvard University · USUniversity of Virginia · US

Funding

Washington University Institute of Clinical and Translational Sciences (TL1)TL1TR002344 · NCATS · WASHINGTON UNIVERSITY · PI Jay F. Piccirillo · 2017 to 2026
$8.5M
Comprehensive MRI-based evaluation of human renal microstructureR01DK111861 · NIDDK · UNIVERSITY OF VIRGINIA · PI BENNETT, KEVIN M, CHARLTON, JENNIFER R · 2017 to 2020
$1.8M
Noninvasive MRI techniques to detect pathology in murine models of renal diseaseR01DK110622 · NIDDK · WASHINGTON UNIVERSITY · PI BENNETT, KEVIN M, CHARLTON, JENNIFER R · 2017 to 2019
$1.0M
Translational imaging tools to nondestructively measure nephron massR41DK129138 · NIDDK · XN BIOTECHNOLOGIES, LLC · PI BENNETT, KEVIN M · 2021 to 2021
$300k
NCATS NIH HHS TL1 TR002344NIDDK NIH HHS R01 DK110622NIDDK NIH HHS R01 DK111861NIDDK NIH HHS R41 DK129138
6 · The paper itself

Abstract

Cationic ferritin (CF) has been developed as a multimodal, targeted imaging tracer to directly detect and map nephrons in the kidney in vivo. Direct detection of functional nephrons provides a unique, sensitive biomarker to predict or monitor kidney disease progression. CF has been developed to map functional nephron number from magnetic resonance imaging (MRI) or positron emission tomography (PET). Previous preclinical imaging studies have used non-human-derived ferritin and commercial formulations that must still be developed for translation to clinical use. Here we describe the reproducible formulation of CF (either derived from horse or from human recombinant ferritin) optimized for intravenous injection and radiolabeling by PET. The human recombinant heteropolymer ferritin is spontaneously assembled in liquid culture (Escherichia coli, E. coli) and modified to form human recombinant cationic ferritin (HrCF) to mitigate potential immunologic reactions for use in humans.

Indexed as

Escherichia coliFerritinsAnimalsHorsesKidneyKidney GlomerulusMagnetic Resonance ImagingPositron-Emission TomographyFerritinsCationic ferritinHuman recombinant ferritinMagnetic resonance imagingNephron massPositron emission tomography

Identifiers

PMID37423992
OpenAlexW4383711442

What OpenQuestion holds

Textmetadata
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.