TY - JOUR
T1 - Prognosis and Personalized In Silico Prediction of Treatment Efficacy in Cardiovascular and Chronic Kidney Disease
T2 - A Proof-of-Concept Study
AU - Jaimes Campos, Mayra Alejandra
AU - Andújar, Iván
AU - Keller, Felix
AU - Mayer, Gert
AU - Rossing, Peter
AU - Staessen, Jan A.
AU - Delles, Christian
AU - Beige, Joachim
AU - Glorieux, Griet
AU - Clark, Andrew L.
AU - Mullen, William
AU - Schanstra, Joost P.
AU - Vlahou, Antonia
AU - Rossing, Kasper
AU - Peter, Karlheinz
AU - Ortiz, Alberto
AU - Campbell, Archie
AU - Persson, Frederik
AU - Latosinska, Agnieszka
AU - Mischak, Harald
AU - Siwy, Justyna
AU - Jankowski, Joachim
N1 - Funding Information:
Funding for this project was provided, in part, by the German ministry for education and science (BMBF), via grant 01DN21014, to H.M., J.S. and A.L. This project was also supported by the Federal Ministry of Education and Research (BMBF) via grant number 01KU2307 (SIGNAL), under the frame of ERA PerMed to H.M. and J.S. Additional funding was provided by the European Union’s Horizon 2020 research and innovation program under grant agreement No: 848011 for the DC-ren project. M.A.J.C. was supported by the European Union’s Horizon Europe Marie Sklodowska-Curie Actions Doctoral Networks Industrial Doctorates Programme (HORIZON—MSCA—2021—DN-ID, Grant number: 101072828). A.O.’s research was supported by FIS/Fondos FEDER ERA-PerMed-JTC2022 (SPAREKID AC22/00027), Comunidad de Madrid en Biomedicina P2022/BMD-7223, CIFRA_COR-CM, Instituto de Salud Carlos III (ISCIII) RICORS program to RICORS2040 (RD21/0005/0001), funded by the European Union—NextGenerationEU, Mecanismo para la Recuperación y la Resiliencia (MRR), and SPACKDc PMP21/00109, FEDER funds, COST Action PERMEDIK CA21165, supported by COST (European Cooperation in Science and Technology), and PREVENTCKD Consortium. Project ID: 101101220, program: EU4H. DG/Agency: HADEA. J.J. was supported by grants from the German Research Foundation (DFG) (SFB/TRR 219 project ID: 322900939 and SFB 1382 project ID 403224013), as well as by the European Union’s Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement No: 764474 (CaReSyAn) and No: 860329 (Strategy-CKD).
Publisher Copyright:
© 2023 by the authors.
PY - 2023/9/1
Y1 - 2023/9/1
N2 - (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.
AB - (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.
KW - cardiovascular events
KW - chronic kidney disease
KW - coronary artery disease
KW - heart failure
KW - personalized medicine
KW - urinary biomarkers
U2 - 10.3390/ph16091298
DO - 10.3390/ph16091298
M3 - Article
SN - 1424-8247
VL - 16
JO - Pharmaceuticals
JF - Pharmaceuticals
IS - 9
M1 - 1298
ER -