In-silico simulated prototype-patients using TPMS technology to study a potential adverse effect of sacubitril and valsartan.

Unveiling the mechanism of action of a drug is key to understand the benefits and adverse reactions of a medication in an organism. However, in complex diseases such as heart diseases there is not a unique mechanism of action but a wide range of different responses depending on the patient. Explorin...

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Main Authors: Guillem Jorba, Joaquim Aguirre-Plans, Valentin Junet, Cristina Segú-Vergés, José Luis Ruiz, Albert Pujol, Narcís Fernández-Fuentes, José Manuel Mas, Baldo Oliva
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0228926
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spelling doaj-b6a9cf8a9bc0471c821aed9b45a5eda82021-05-21T04:31:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01152e022892610.1371/journal.pone.0228926In-silico simulated prototype-patients using TPMS technology to study a potential adverse effect of sacubitril and valsartan.Guillem JorbaJoaquim Aguirre-PlansValentin JunetCristina Segú-VergésJosé Luis RuizAlbert PujolNarcís Fernández-FuentesJosé Manuel MasBaldo OlivaUnveiling the mechanism of action of a drug is key to understand the benefits and adverse reactions of a medication in an organism. However, in complex diseases such as heart diseases there is not a unique mechanism of action but a wide range of different responses depending on the patient. Exploring this collection of mechanisms is one of the clues for a future personalized medicine. The Therapeutic Performance Mapping System (TPMS) is a Systems Biology approach that generates multiple models of the mechanism of action of a drug. Each molecular mechanism generated could be associated to particular individuals, here defined as prototype-patients, hence the generation of models using TPMS technology may be used for detecting adverse effects to specific patients. TPMS operates by (1) modelling the responses in humans with an accurate description of a protein network and (2) applying a Multilayer Perceptron-like and sampling strategy to find all plausible solutions. In the present study, TPMS is applied to explore the diversity of mechanisms of action of the drug combination sacubitril/valsartan. We use TPMS to generate a wide range of models explaining the relationship between sacubitril/valsartan and heart failure (the indication), as well as evaluating their association with macular degeneration (a potential adverse effect). Among the models generated, we identify a set of mechanisms of action associated to a better response in terms of heart failure treatment, which could also be associated to macular degeneration development. Finally, a set of 30 potential biomarkers are proposed to identify mechanisms (or prototype-patients) more prone of suffering macular degeneration when presenting good heart failure response. All prototype-patients models generated are completely theoretical and therefore they do not necessarily involve clinical effects in real patients. Data and accession to software are available at http://sbi.upf.edu/data/tpms/.https://doi.org/10.1371/journal.pone.0228926
collection DOAJ
language English
format Article
sources DOAJ
author Guillem Jorba
Joaquim Aguirre-Plans
Valentin Junet
Cristina Segú-Vergés
José Luis Ruiz
Albert Pujol
Narcís Fernández-Fuentes
José Manuel Mas
Baldo Oliva
spellingShingle Guillem Jorba
Joaquim Aguirre-Plans
Valentin Junet
Cristina Segú-Vergés
José Luis Ruiz
Albert Pujol
Narcís Fernández-Fuentes
José Manuel Mas
Baldo Oliva
In-silico simulated prototype-patients using TPMS technology to study a potential adverse effect of sacubitril and valsartan.
PLoS ONE
author_facet Guillem Jorba
Joaquim Aguirre-Plans
Valentin Junet
Cristina Segú-Vergés
José Luis Ruiz
Albert Pujol
Narcís Fernández-Fuentes
José Manuel Mas
Baldo Oliva
author_sort Guillem Jorba
title In-silico simulated prototype-patients using TPMS technology to study a potential adverse effect of sacubitril and valsartan.
title_short In-silico simulated prototype-patients using TPMS technology to study a potential adverse effect of sacubitril and valsartan.
title_full In-silico simulated prototype-patients using TPMS technology to study a potential adverse effect of sacubitril and valsartan.
title_fullStr In-silico simulated prototype-patients using TPMS technology to study a potential adverse effect of sacubitril and valsartan.
title_full_unstemmed In-silico simulated prototype-patients using TPMS technology to study a potential adverse effect of sacubitril and valsartan.
title_sort in-silico simulated prototype-patients using tpms technology to study a potential adverse effect of sacubitril and valsartan.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2020-01-01
description Unveiling the mechanism of action of a drug is key to understand the benefits and adverse reactions of a medication in an organism. However, in complex diseases such as heart diseases there is not a unique mechanism of action but a wide range of different responses depending on the patient. Exploring this collection of mechanisms is one of the clues for a future personalized medicine. The Therapeutic Performance Mapping System (TPMS) is a Systems Biology approach that generates multiple models of the mechanism of action of a drug. Each molecular mechanism generated could be associated to particular individuals, here defined as prototype-patients, hence the generation of models using TPMS technology may be used for detecting adverse effects to specific patients. TPMS operates by (1) modelling the responses in humans with an accurate description of a protein network and (2) applying a Multilayer Perceptron-like and sampling strategy to find all plausible solutions. In the present study, TPMS is applied to explore the diversity of mechanisms of action of the drug combination sacubitril/valsartan. We use TPMS to generate a wide range of models explaining the relationship between sacubitril/valsartan and heart failure (the indication), as well as evaluating their association with macular degeneration (a potential adverse effect). Among the models generated, we identify a set of mechanisms of action associated to a better response in terms of heart failure treatment, which could also be associated to macular degeneration development. Finally, a set of 30 potential biomarkers are proposed to identify mechanisms (or prototype-patients) more prone of suffering macular degeneration when presenting good heart failure response. All prototype-patients models generated are completely theoretical and therefore they do not necessarily involve clinical effects in real patients. Data and accession to software are available at http://sbi.upf.edu/data/tpms/.
url https://doi.org/10.1371/journal.pone.0228926
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