Evidence map›Paper›PMID 37762058›Full record

ArticleInternational journal of molecular sciences2023

A Multiplexed Urinary Biomarker Panel Has Potential for Alzheimer's Disease Diagnosis Using Targeted Proteomics and Machine Learning.

Jenny Hällqvist, Rui C Pinto, Wendy E Heywood, Jonjo Cordey, Alexander J M Foulkes, Catherine F Slattery, Claire A Leckey, Eimear C Murphy, Henrik Zetterberg, Jonathan M Schott and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

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  5. 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 at 5 institutions in 2 countries.

Jenny HällqvistTranslational Mass Spectrometry Research Group, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.ORCID 0000-0001-6709-3211
Rui C PintoFaculty of Medicine, School of Public Health, Imperial College London, London SW7 2BX, UK.ORCID 0000-0002-8527-4873
Wendy E HeywoodTranslational Mass Spectrometry Research Group, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.
Jonjo CordeyTranslational Mass Spectrometry Research Group, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.
Alexander J M FoulkesNational Hospital for Neurology and Neurosurgery, Queen Square London, London WC1N 3BG, UK.
Catherine F SlatteryDarent Valley Hospital, Dartford DA2 8DA, UK.
Claire A LeckeyTranslational Mass Spectrometry Research Group, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.
Eimear C MurphyDementia Research Centre, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.
Henrik ZetterbergDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at the University of Gothenburg, S-431 80 Mölndal, Sweden.
Jonathan M SchottNational Hospital for Neurology and Neurosurgery, Queen Square London, London WC1N 3BG, UK.
Kevin MillsTranslational Mass Spectrometry Research Group, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.ORCID 0000-0003-0763-8288
Ross W PatersonNational Hospital for Neurology and Neurosurgery, Queen Square London, London WC1N 3BG, UK.
Great Ormond Street Hospital · GBUK Dementia Research Institute · GBDarent Valley Hospital · GBImperial College London · GBNational Hospital for Neurology and Neurosurgery · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As disease-modifying therapies are now available for Alzheimer's disease (AD), accessible, accurate and affordable biomarkers to support diagnosis are urgently needed. We sought to develop a mass spectrometry-based urine test as a high-throughput screening tool for diagnosing AD. We collected urine from a discovery cohort (n = 11) of well-characterised individuals with AD (n = 6) and their asymptomatic, CSF biomarker-negative study partners (n = 5) and used untargeted proteomics for biomarker discovery. Protein biomarkers identified were taken forward to develop a high-throughput, multiplexed and targeted proteomic assay which was tested on an independent cohort (n = 21). The panel of proteins identified are known to be involved in AD pathogenesis. In comparing AD and controls, a panel of proteins including MIEN1, TNFB, VCAM1, REG1B and ABCA7 had a classification accuracy of 86%. These proteins have been previously implicated in AD pathogenesis. This suggests that urine-targeted mass spectrometry has potential utility as a diagnostic screening tool in AD.

Indexed as

Alzheimer DiseaseUrinary TractBiomarkersHumansIntracellular Signaling Peptides and ProteinsMachine LearningNeoplasm ProteinsProteomicsBiomarkersIntracellular Signaling Peptides and ProteinsMIEN1 protein, humanNeoplasm ProteinsAlzheimer’sbiomarkersdiagnosismachine learningmass spectrometryproteomicsurine

Identifiers

PMID37762058
PMCPMC10531486
OpenAlexW4386483704

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.