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

ORCID
0000-0003-4202-7810
Affiliation
Mosaiques Diagnostics GmbH, 30659 Hannover, Germany;(M.A.J.C.);(A.L.);(H.M.);(J.S.)
Jaimes Campos, Mayra Alejandra;
Affiliation
Proteomic Laboratory, Center for Genetic Engineering and Biotechnology, Havana 10600, Cuba
Andújar, Iván;
ORCID
0000-0002-8240-7255
Affiliation
Department of Internal Medicine IV (Nephrology and Hypertension), Medical University Innsbruck, 6020 Innsbruck, Austria;(F.K.);(G.M.)
Keller, Felix;
Affiliation
Department of Internal Medicine IV (Nephrology and Hypertension), Medical University Innsbruck, 6020 Innsbruck, Austria;(F.K.);(G.M.)
Mayer, Gert;
Affiliation
Steno Diabetes Center Copenhagen, 2730 Herlev, Denmark;(P.R.);(F.P.)
Rossing, Peter;
Affiliation
Non-Profit Research Institute Alliance for the Promotion of Preventive Medicine, 2800 Mechlin, Belgium;
Staessen, Jan A.;
ORCID
0000-0003-2238-2612
Affiliation
School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow G12 8TA, UK;(C.D.);(W.M.)
Delles, Christian;
Affiliation
Division of Nephrology and KfH Renal Unit, Hospital St Georg, 04129 Leipzig, Germany;
Beige, Joachim;
ORCID
0000-0002-7641-4707
Affiliation
Nephrology Section, Department of Internal Medicine, Ghent University Hospital, 9000 Ghent, Belgium;
Glorieux, Griet;
Affiliation
Hull University Teaching Hospitals NHS Trust, Castle Hill Hospital, Cottingham HU16 5JQ, UK;
Clark, Andrew L.;
ORCID
0000-0002-5685-1563
Affiliation
School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow G12 8TA, UK;(C.D.);(W.M.)
Mullen, William;
Affiliation
Institut National de la Santé et de la Recherche Médicale, Institute of Cardiovascular and Metabolic Disease, UMRS 1297, 31432 Toulouse, France;
Schanstra, Joost P.;
ORCID
0000-0003-3284-5713
Affiliation
Centre of Systems Biology, Biomedical Research Foundation of the Academy of Athens (BRFAA), 115 27 Athens, Greece;
Vlahou, Antonia;
Affiliation
Department of Clinical Medicine, University of Copenhagen, 2200 Copenhagen, Denmark;
Rossing, Kasper;
ORCID
0000-0002-8040-2258
Affiliation
Atherothrombosis and Vascular Biology Program, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC 3004, Australia;
Peter, Karlheinz;
ORCID
0000-0002-9805-9523
Affiliation
Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz UAM, 28040 Madrid, Spain;
Ortiz, Alberto;
ORCID
0000-0003-0198-5078
Affiliation
Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh EH16 4SB, UK;
Campbell, Archie;
Affiliation
Steno Diabetes Center Copenhagen, 2730 Herlev, Denmark;(P.R.);(F.P.)
Persson, Frederik;
Affiliation
Mosaiques Diagnostics GmbH, 30659 Hannover, Germany;(M.A.J.C.);(A.L.);(H.M.);(J.S.)
Latosinska, Agnieszka;
ORCID
0000-0003-0323-0306
Affiliation
Mosaiques Diagnostics GmbH, 30659 Hannover, Germany;(M.A.J.C.);(A.L.);(H.M.);(J.S.)
Mischak, Harald;
ORCID
0000-0003-1407-2534
Affiliation
Mosaiques Diagnostics GmbH, 30659 Hannover, Germany;(M.A.J.C.);(A.L.);(H.M.);(J.S.)
Siwy, Justyna;
Affiliation
Institute for Molecular Cardiovascular Research, University Hospital RWTH Aachen, 52074 Aachen, Germany
Jankowski, Joachim

(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.

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