Cargando…

Utilizing longitudinal microbiome taxonomic profiles to predict food allergy via Long Short-Term Memory networks

Food allergy is usually difficult to diagnose in early life, and the inability to diagnose patients with atopic diseases at an early age may lead to severe complications. Numerous studies have suggested an association between the infant gut microbiome and development of allergy. In this work, we inv...

Descripción completa

Detalles Bibliográficos
Autores principales: Metwally, Ahmed A., Yu, Philip S., Reiman, Derek, Dai, Yang, Finn, Patricia W., Perkins, David L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361419/
https://www.ncbi.nlm.nih.gov/pubmed/30716085
http://dx.doi.org/10.1371/journal.pcbi.1006693
_version_ 1783392680299986944
author Metwally, Ahmed A.
Yu, Philip S.
Reiman, Derek
Dai, Yang
Finn, Patricia W.
Perkins, David L.
author_facet Metwally, Ahmed A.
Yu, Philip S.
Reiman, Derek
Dai, Yang
Finn, Patricia W.
Perkins, David L.
author_sort Metwally, Ahmed A.
collection PubMed
description Food allergy is usually difficult to diagnose in early life, and the inability to diagnose patients with atopic diseases at an early age may lead to severe complications. Numerous studies have suggested an association between the infant gut microbiome and development of allergy. In this work, we investigated the capacity of Long Short-Term Memory (LSTM) networks to predict food allergies in early life (0-3 years) from subjects’ longitudinal gut microbiome profiles. Using the DIABIMMUNE dataset, we show an increase in predictive power using our model compared to Hidden Markov Model, Multi-Layer Perceptron Neural Network, Support Vector Machine, Random Forest, and LASSO regression. We further evaluated whether the training of LSTM networks benefits from reduced representations of microbial features. We considered sparse autoencoder for extraction of potential latent representations in addition to standard feature selection procedures based on Minimum Redundancy Maximum Relevance (mRMR) and variance prior to the training of LSTM networks. The comprehensive evaluation reveals that LSTM networks with the mRMR selected features achieve significantly better performance compared to the other tested machine learning models.
format Online
Article
Text
id pubmed-6361419
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-63614192019-02-15 Utilizing longitudinal microbiome taxonomic profiles to predict food allergy via Long Short-Term Memory networks Metwally, Ahmed A. Yu, Philip S. Reiman, Derek Dai, Yang Finn, Patricia W. Perkins, David L. PLoS Comput Biol Research Article Food allergy is usually difficult to diagnose in early life, and the inability to diagnose patients with atopic diseases at an early age may lead to severe complications. Numerous studies have suggested an association between the infant gut microbiome and development of allergy. In this work, we investigated the capacity of Long Short-Term Memory (LSTM) networks to predict food allergies in early life (0-3 years) from subjects’ longitudinal gut microbiome profiles. Using the DIABIMMUNE dataset, we show an increase in predictive power using our model compared to Hidden Markov Model, Multi-Layer Perceptron Neural Network, Support Vector Machine, Random Forest, and LASSO regression. We further evaluated whether the training of LSTM networks benefits from reduced representations of microbial features. We considered sparse autoencoder for extraction of potential latent representations in addition to standard feature selection procedures based on Minimum Redundancy Maximum Relevance (mRMR) and variance prior to the training of LSTM networks. The comprehensive evaluation reveals that LSTM networks with the mRMR selected features achieve significantly better performance compared to the other tested machine learning models. Public Library of Science 2019-02-04 /pmc/articles/PMC6361419/ /pubmed/30716085 http://dx.doi.org/10.1371/journal.pcbi.1006693 Text en © 2019 Metwally et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Metwally, Ahmed A.
Yu, Philip S.
Reiman, Derek
Dai, Yang
Finn, Patricia W.
Perkins, David L.
Utilizing longitudinal microbiome taxonomic profiles to predict food allergy via Long Short-Term Memory networks
title Utilizing longitudinal microbiome taxonomic profiles to predict food allergy via Long Short-Term Memory networks
title_full Utilizing longitudinal microbiome taxonomic profiles to predict food allergy via Long Short-Term Memory networks
title_fullStr Utilizing longitudinal microbiome taxonomic profiles to predict food allergy via Long Short-Term Memory networks
title_full_unstemmed Utilizing longitudinal microbiome taxonomic profiles to predict food allergy via Long Short-Term Memory networks
title_short Utilizing longitudinal microbiome taxonomic profiles to predict food allergy via Long Short-Term Memory networks
title_sort utilizing longitudinal microbiome taxonomic profiles to predict food allergy via long short-term memory networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361419/
https://www.ncbi.nlm.nih.gov/pubmed/30716085
http://dx.doi.org/10.1371/journal.pcbi.1006693
work_keys_str_mv AT metwallyahmeda utilizinglongitudinalmicrobiometaxonomicprofilestopredictfoodallergyvialongshorttermmemorynetworks
AT yuphilips utilizinglongitudinalmicrobiometaxonomicprofilestopredictfoodallergyvialongshorttermmemorynetworks
AT reimanderek utilizinglongitudinalmicrobiometaxonomicprofilestopredictfoodallergyvialongshorttermmemorynetworks
AT daiyang utilizinglongitudinalmicrobiometaxonomicprofilestopredictfoodallergyvialongshorttermmemorynetworks
AT finnpatriciaw utilizinglongitudinalmicrobiometaxonomicprofilestopredictfoodallergyvialongshorttermmemorynetworks
AT perkinsdavidl utilizinglongitudinalmicrobiometaxonomicprofilestopredictfoodallergyvialongshorttermmemorynetworks