Evidence mapPaperPMID 37765106Full record

ArticlePharmaceuticals (Basel, Switzerland)2023

Prognosis and Personalized In Silico Prediction of Treatment Efficacy in Cardiovascular and Chronic Kidney Disease: A Proof-of-Concept Study.

Mayra Alejandra Jaimes Campos, Iván Andújar, Felix Keller, Gert Mayer, Peter Rossing, Jan A Staessen, Christian Delles, Joachim Beige, Griet Glorieux, Andrew L Clark and 12 more

Abstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  4. Review
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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

22 authors.

Mayra Alejandra Jaimes CamposMosaiques Diagnostics GmbH, 30659 Hannover, Germany.ORCID 0000-0003-4202-7810
Iván AndújarProteomic Laboratory, Center for Genetic Engineering and Biotechnology, Havana 10600, Cuba.
Felix KellerDepartment of Internal Medicine IV (Nephrology and Hypertension), Medical University Innsbruck, 6020 Innsbruck, Austria.ORCID 0000-0002-8240-7255
Gert MayerDepartment of Internal Medicine IV (Nephrology and Hypertension), Medical University Innsbruck, 6020 Innsbruck, Austria.
Peter RossingSteno Diabetes Center Copenhagen, 2730 Herlev, Denmark.
Jan A StaessenNon-Profit Research Institute Alliance for the Promotion of Preventive Medicine, 2800 Mechlin, Belgium.
Christian DellesSchool of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow G12 8TA, UK.ORCID 0000-0003-2238-2612
Joachim BeigeDivision of Nephrology and KfH Renal Unit, Hospital St Georg, 04129 Leipzig, Germany.
Griet GlorieuxNephrology Section, Department of Internal Medicine, Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0002-7641-4707
Andrew L ClarkHull University Teaching Hospitals NHS Trust, Castle Hill Hospital, Cottingham HU16 5JQ, UK.
William MullenSchool of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow G12 8TA, UK.ORCID 0000-0002-5685-1563
Joost P SchanstraInstitut National de la Santé et de la Recherche Médicale, Institute of Cardiovascular and Metabolic Disease, UMRS 1297, 31432 Toulouse, France.
Antonia VlahouCentre of Systems Biology, Biomedical Research Foundation of the Academy of Athens (BRFAA), 115 27 Athens, Greece.ORCID 0000-0003-3284-5713
Kasper RossingDepartment of Clinical Medicine, University of Copenhagen, 2200 Copenhagen, Denmark.
Karlheinz PeterAtherothrombosis and Vascular Biology Program, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC 3004, Australia.ORCID 0000-0002-8040-2258
Alberto OrtizInstituto de Investigación Sanitaria de la Fundación Jiménez Díaz UAM, 28040 Madrid, Spain.ORCID 0000-0002-9805-9523
Archie CampbellCentre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh EH16 4SB, UK.ORCID 0000-0003-0198-5078
Frederik PerssonSteno Diabetes Center Copenhagen, 2730 Herlev, Denmark.
Agnieszka LatosinskaMosaiques Diagnostics GmbH, 30659 Hannover, Germany.
Harald MischakMosaiques Diagnostics GmbH, 30659 Hannover, Germany.ORCID 0000-0003-0323-0306
Justyna SiwyMosaiques Diagnostics GmbH, 30659 Hannover, Germany.ORCID 0000-0003-1407-2534
Joachim JankowskiInstitute for Molecular Cardiovascular Research, University Hospital RWTH Aachen, 52074 Aachen, Germany.

Funding

RECEPTORS MEDIATING DRUG DEPENDENCER01DA007223 · UNIVERSITY OF TORONTO · 1991 to 2005
$903k
Bundesministerium für Bildung und Forschung 01DN21014Comunidad de Madrid en Biomedicina P2022/BMD-7223EU4Health 101101220European Cooperation in Science and Technology CA21165European Union - NextGenerationEU. Mecanismo para la Recuperación y la Resiliencia (MRR) and SPACKDc PMP21/00109European Union's Horizon 2020 848011European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie 764474, 860329European Union's Horizon Europe Marie Skłodowska-Curie Actions Doctoral Networks - Industrial Doctorates Programme 101072828FIS/Fondos FEDER ERA-PerMed-JTC2022 AC22/00027German Research Foundation (DFG) 322900939, 403224013
6 · The paper itself

Abstract

(1) Background: Kidney and cardiovascular diseases are responsible for a large fraction of population morbidity and mortality. Early, targeted, personalized intervention represents the ideal approach to cope with this challenge. Proteomic/peptidomic changes are largely responsible for the onset and progression of these diseases and should hold information about the optimal means of treatment and prevention. (2) Methods: We investigated the prediction of renal or cardiovascular events using previously defined urinary peptidomic classifiers CKD273, HF2, and CAD160 in a cohort of 5585 subjects, in a retrospective study. (3) Results: We have demonstrated a highly significant prediction of events, with an HR of 2.59, 1.71, and 4.12 for HF, CAD, and CKD, respectively. We applied in silico treatment, implementing on each patient's urinary profile changes to the classifiers corresponding to exactly defined peptide abundance changes, following commonly used interventions (MRA, SGLT2i, DPP4i, ARB, GLP1RA, olive oil, and exercise), as defined in previous studies. Applying the proteomic classifiers after the in silico treatment indicated the individual benefits of specific interventions on a personalized level. (4) Conclusions: The in silico evaluation may provide information on the future impact of specific drugs and interventions on endpoints, opening the door to a precision-based medicine approach. An investigation into the extent of the benefit of this approach in a prospective clinical trial is warranted.

Indexed as

cardiovascular eventschronic kidney diseasecoronary artery diseaseheart failurepersonalized medicineurinary biomarkers

Identifiers

PMID37765106
PMCPMC10537115

What Socratic 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 Socratic graph.