Evidence map›Paper›PMID 32999398›Full record

ArticleScientific reports2020

Pre-clinical dose-ranging efficacy, pharmacokinetics, tissue biodistribution, and toxicity of a targeted contrast agent for MRI of amyloid deposition in Alzheimer's disease.

Andrew A Badachhape, Peter K Working, Mayank Srivastava, Prajwal Bhandari, Igor V Stupin, Laxman Devkota, Eric A Tanifum, Ananth V Annapragada, Ketan B Ghaghada

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
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  13. Advances in nanoprobes for molecular MRI of Alzheimer's disease.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    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.

Andrew A BadachhapeDepartment of Radiology, Baylor College of Medicine, Houston, TX, 77030, USA.
Peter K WorkingAlzeca Biosciences Inc., Houston, TX, 77057, USA.
Mayank SrivastavaThe Singleton Department of Pediatric Radiology, Texas Children's Hospital, Houston, TX, 77030, USA.
Prajwal BhandariDepartment of Radiology, Baylor College of Medicine, 1102 Bates Street, Suite 850, Houston, TX, 77030, USA.
Igor V StupinThe Singleton Department of Pediatric Radiology, Texas Children's Hospital, Houston, TX, 77030, USA.
Laxman DevkotaDepartment of Pediatrics-Oncology, Baylor College of Medicine, Houston, TX, 77030, USA.
Eric A TanifumThe Singleton Department of Pediatric Radiology, Texas Children's Hospital, Houston, TX, 77030, USA.
Ananth V AnnapragadaThe Singleton Department of Pediatric Radiology, Texas Children's Hospital, Houston, TX, 77030, USA.
Ketan B GhaghadaThe Singleton Department of Pediatric Radiology, Texas Children's Hospital, Houston, TX, 77030, USA. kbghagha@texaschildrens.org.

Funding

Targeting the immunosuppressive tumor microenvironment to enhance efficacy of radiotherapy and immuno-radiotherapy for oral cancerU01DE028233 · NIDCR · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ANNAPRAGADA, ANANTH V, SIKORA, ANDREW · 2018 to 2022
$3.9M
Molecular and Vascular MRI of Placenta AccretaR01HD094347 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI ANNAPRAGADA, ANANTH V, FOX, KARIN ANNELIESE · 2018 to 2022
$2.2M
Novel MRI Contrast Agent for Detection of Beta AmyloidR44AG051292 · NIA · ALZECA BIOSCIENCES, INC. · PI WORKING, PETER · 2017 to 2018
$1.6M
NIA NIH HHS R44 AG051292NICHD NIH HHS R01 HD094347NIDCR NIH HHS U01 DE028233NIH HHS R44AG051292
6 · The paper itself

Abstract

In these preclinical studies, we describe ADx-001, an Aβ-targeted liposomal macrocyclic gadolinium (Gd) imaging agent, for MRI of amyloid plaques. The targeting moiety is a novel lipid-PEG conjugated styryl-pyrimidine. An MRI-based contrast agent such as ADx-001 is attractive because of the lack of radioactivity, ease of distribution, long shelf life, and the prevalence of MRI scanners. Dose-ranging efficacy studies were performed on a 1 T MRI scanner using a transgenic APP/PSEN1 mouse model of Alzheimer's disease. ADx-001 was tested at 0.10, 0.15, and 0.20 mmol Gd/kg. Gold standard post-mortem amyloid immunostaining was used for the determination of sensitivity and specificity. ADx-001 toxicity was evaluated in rats and monkeys at doses up to 0.30 mmol Gd/kg. ADx-001 pharmacokinetics were determined in monkeys and its tissue distribution was evaluated in rats. ADx-001-enhanced MRI demonstrated significantly higher (p < 0.05) brain signal enhancement in transgenic mice relative to wild type mice at all dose levels. ADx-001 demonstrated high sensitivity at 0.20 and 0.15 mmol Gd/kg and excellent specificity at all dose levels for in vivo imaging of β amyloid plaques. ADx-001 was well tolerated in rats and monkeys and exhibited the slow clearance from circulation and tissue biodistribution typical of PEGylated nanoparticles.

Indexed as

Alzheimer DiseaseAmyloidAmyloid beta-Protein PrecursorAnimalsContrast MediaDisease Models, AnimalDose-Response Relationship, DrugHumansMacaca fascicularisMagnetic Resonance ImagingMaleMiceMice, TransgenicPeptide FragmentsPlaque, AmyloidPresenilin-1AmyloidAmyloid beta-Protein PrecursorContrast MediaPeptide FragmentsPresenilin-1

Identifiers

PMID32999398
PMCPMC7527957

What OpenQuestion holds

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LicenceCC BY
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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.