Evidence map›Paper›PMID 37710290›Full record

ArticleJournal of nanobiotechnology2023

Magnetic separation and concentration of Aβ 1-42 molecules dispersed at the threshold concentration for Alzheimer's disease diagnosis in clinically-relevant volumes of sample.

Alessandro Surpi, Mauro Murgia, Sonia López-Amoedo, Manuel A González-Gómez, Yolanda Piñeiro, José Rivas, Valeria Perugini, Matteo Santin, Tomás Sobrino, Pierpaolo Greco and 2 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

12 authors.

Alessandro SurpiIstituto per lo Studio dei Materiali Nanostrutturati (CNR-ISMN), Bologna, 40129, Italy. surpi@bo.imm.cnr.it.
Mauro MurgiaIstituto per lo Studio dei Materiali Nanostrutturati (CNR-ISMN), Bologna, 40129, Italy.
Sonia López-AmoedoTranslational Stroke Laboratory (TREAT), Clinical Neurosciences Research Laboratory (LINC) , Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, 15782, Spain.
Manuel A González-GómezNANOMAG Laboratory, Applied Physics Department, iMATUS Materials Institute, Universidade de Santiago de Compostela, Santiago de Compostela, 15782, Spain.
Yolanda PiñeiroNANOMAG Laboratory, Applied Physics Department, iMATUS Materials Institute, Universidade de Santiago de Compostela, Santiago de Compostela, 15782, Spain.
José RivasNANOMAG Laboratory, Applied Physics Department, iMATUS Materials Institute, Universidade de Santiago de Compostela, Santiago de Compostela, 15782, Spain.
Valeria PeruginiCentre for Regenerative Medicine and Devices, School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton, UK.
Matteo SantinCentre for Regenerative Medicine and Devices, School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton, UK.
Tomás SobrinoCentro de Investigación Biomédica en Red en Enfermedades Neurodegenerativas (CIBERNED), Instituto de Salud Carlos III, Madrid, 28029, Spain.
Pierpaolo GrecoCenter for Translational Neurophysiology (IIT), Italian Institute of Technology, Ferrara, 44121, Italy.
Francisco CamposTranslational Stroke Laboratory (TREAT), Clinical Neurosciences Research Laboratory (LINC) , Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, 15782, Spain. francisco.campos.perez@sergas.es.
Valentin Alek DediuIstituto per lo Studio dei Materiali Nanostrutturati (CNR-ISMN), Bologna, 40129, Italy. valentin.dediu@cnr.it.

Funding

Horizon 2020 Framework Programme 732678
6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is the leading cause of dementia and loss of autonomy in the elderly, implying a progressive cognitive decline and limitation of social activities. The progressive aging of the population is expected to exacerbate this problem in the next decades. Therefore, there is an urgent need to develop quantitative diagnostic methodologies to assess the onset the disease and its progression especially in the initial phases.

resultsHere we describe a novel technology to extract one of the most important molecular biomarkers of AD (Aβ

conclusionsThis easy to automate technology allows an efficient separation of AD molecular biomarkers from volumes of biological solutions complying with the current clinical protocols and, ultimately, leads to accurate measurements of biomarkers. The technology paves a new way for a quantitative AD diagnosis at the earliest stage and it is also adaptable for the biomarker analysis of other pathologies.

Indexed as

Alzheimer DiseaseCognitive DysfunctionAgedAgingHumansMagnetic FieldsMicrofluidicsAlzheimer’s diseaseDiagnosisMagnetic nanoparticlesMolecular recognition

Identifiers

PMID37710290
PMCPMC10503095

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.