Go to:
Logótipo
Comuta visibilidade da coluna esquerda
Você está em: Start > Publications > View > Clinical model for Hereditary Transthyretin Amyloidosis age of onset prediction
Publication

Publications

Clinical model for Hereditary Transthyretin Amyloidosis age of onset prediction

Title
Clinical model for Hereditary Transthyretin Amyloidosis age of onset prediction
Type
Article in International Scientific Journal
Year
2023
Authors
Maria Pedroto
(Author)
FCUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page Without ORCID
Coelho, T
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Jorge, AM
(Author)
FCUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page Without ORCID
João Mendes-Moreira
(Author)
FEUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page Without ORCID
Journal
Vol. 14
ISSN: 1664-2295
Publisher: Frontiers Media
Indexing
Publicação em ISI Web of Knowledge ISI Web of Knowledge - 0 Citations
Publicação em Scopus Scopus - 0 Citations
Other information
Authenticus ID: P-00Y-P1Z
Abstract (EN): IntroductionHereditary transthyretin amyloidosis (ATTRv amyloidosis) is a rare neurological hereditary disease clinically characterized as severe, progressive, and life-threatening while the age of onset represents the moment in time when the first symptoms are felt. In this study, we present and discuss our results on the study, development, and evaluation of an approach that allows for time-to-event prediction of the age of onset, while focusing on genealogical feature construction. Materials and methodsThis research was triggered by the need to answer the medical problem of when will an asymptomatic ATTRv patient show symptoms of the disease. To do so, we defined and studied the impact of 77 features (ranging from demographic and genealogical to familial disease history) we studied and compared a pool of prediction algorithms, namely, linear regression (LR), elastic net (EN), lasso (LA), ridge (RI), support vector machines (SV), decision tree (DT), random forest (RF), and XGboost (XG), both in a classification as well as a regression setting; we assembled a baseline (BL) which corresponds to the current medical knowledge of the disease; we studied the problem of predicting the age of onset of ATTRv patients; we assessed the viability of predicting age of onset on short term horizons, with a classification framing, on localized sets of patients (currently symptomatic and asymptomatic carriers, with and without genealogical information); and we compared the results with an out-of-bag evaluation set and assembled in a different time-frame than the original data in order to account for data leakage. ResultsCurrently, we observe that our approach outperforms the BL model, which follows a set of clinical heuristics and represents current medical practice. Overall, our results show the supremacy of SV and XG for both the prediction tasks although impacted by data characteristics, namely, the existence of missing values, complex data, and small-sized available inputs. DiscussionWith this study, we defined a predictive model approach capable to be well-understood by medical professionals, compared with the current practice, namely, the baseline approach (BL), and successfully showed the improvement achieved to the current medical knowledge.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 11
Documents
We could not find any documents associated to the publication.
Related Publications

Of the same authors

Heterogeneity in families with ATTRV30M amyloidosis: a historical and longitudinal Portuguese case study impact for genetic counselling (2024)
Article in International Scientific Journal
Maria Pedroto; Coelho, T; Fernandes, J; Oliveira, A; Jorge, AM; João Mendes-Moreira
Predicting Age of Onset in TTR-FAP Patients with Genealogical Features (2018)
Article in International Conference Proceedings Book
Maria Pedroto; Jorge, AM; João Mendes-Moreira; Coelho, T
Improving the Prediction of Age of Onset of TTR-FAP Patients Using Graph-Embedding Features (2022)
Article in International Conference Proceedings Book
Maria Pedroto; Jorge, AM; João Mendes-Moreira; Coelho, T

Of the same journal

Editorial: Metals and cognitive decline: Pathophysiology, treatment, and prevention (2023)
Another Publication in an International Scientific Journal
Koseoglu, E; Liu, G; Agostinho Almeida
Spectral Domain-Optical Coherence Tomography As a New Diagnostic Marker for Idiopathic Normal Pressure Hydrocephalus (2017)
Article in International Scientific Journal
Afonso, JM; Manuel Falcão; Schlichtenbrede, F; Falcão-Reis F; Silva, SE; Schneider, TM
Readmissions and Mortality During the First Year After Stroke-Data From a Population-Based Incidence Study (2020)
Article in International Scientific Journal
Pedro Abreu; Magalhaes, R; Baptista, D; Elsa Azevedo; silva, mc; Correia, M
Pain in Portuguese patients with multiple sclerosis (2011)
Article in International Scientific Journal
Seixas, D; Sa, MJ; Galhardo, V; Guimaraes, J; Lima, D
Multiple Sclerosis Patient Management During the COVID-19 Pandemic: Practical Recommendations From the Portuguese Multiple Sclerosis Study Group (GEEM) (2021)
Article in International Scientific Journal
Cerqueira, JJ; Ladeira, AF; Silva, AM; Timoteo, A; Vale, J; Sousa, L; Arenga, M; Pedro Abreu; Guerreiro, R; de Sa, J

See all (17)

Recommend this page Top
Copyright 1996-2025 © Faculdade de Direito da Universidade do Porto  I Terms and Conditions  I Acessibility  I Index A-Z
Page created on: 2025-08-07 at 12:31:52 | Privacy Policy | Personal Data Protection Policy | Whistleblowing