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A proof-of-concept study of extracting patient histories for rare/intractable diseases from social media
The amount of content on social media platforms such as Twitter is expanding rapidly. Simultaneously, the lack of patient information seriously hinders the diagnosis and treatment of rare/intractable diseases. However, these patient communities are especially active on social media. Data from social...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korea Genome Organization
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7362943/ https://www.ncbi.nlm.nih.gov/pubmed/32634871 http://dx.doi.org/10.5808/GI.2020.18.2.e17 |
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author | Yamaguchi, Atsuko Queralt-Rosinach, Núria |
author_facet | Yamaguchi, Atsuko Queralt-Rosinach, Núria |
author_sort | Yamaguchi, Atsuko |
collection | PubMed |
description | The amount of content on social media platforms such as Twitter is expanding rapidly. Simultaneously, the lack of patient information seriously hinders the diagnosis and treatment of rare/intractable diseases. However, these patient communities are especially active on social media. Data from social media could serve as a source of patient-centric knowledge for these diseases complementary to the information collected in clinical settings and patient registries, and may also have potential for research use. To explore this question, we attempted to extract patient-centric knowledge from social media as a task for the 3-day Biomedical Linked Annotation Hackathon 6 (BLAH6). We selected amyotrophic lateral sclerosis and multiple sclerosis as use cases of rare and intractable diseases, respectively, and we extracted patient histories related to these health conditions from Twitter. Four diagnosed patients for each disease were selected. From the user timelines of these eight patients, we extracted tweets that might be related to health conditions. Based on our experiment, we show that our approach has considerable potential, although we identified problems that should be addressed in future attempts to mine information about rare/intractable diseases from Twitter. |
format | Online Article Text |
id | pubmed-7362943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Korea Genome Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-73629432020-07-23 A proof-of-concept study of extracting patient histories for rare/intractable diseases from social media Yamaguchi, Atsuko Queralt-Rosinach, Núria Genomics Inform Application Note The amount of content on social media platforms such as Twitter is expanding rapidly. Simultaneously, the lack of patient information seriously hinders the diagnosis and treatment of rare/intractable diseases. However, these patient communities are especially active on social media. Data from social media could serve as a source of patient-centric knowledge for these diseases complementary to the information collected in clinical settings and patient registries, and may also have potential for research use. To explore this question, we attempted to extract patient-centric knowledge from social media as a task for the 3-day Biomedical Linked Annotation Hackathon 6 (BLAH6). We selected amyotrophic lateral sclerosis and multiple sclerosis as use cases of rare and intractable diseases, respectively, and we extracted patient histories related to these health conditions from Twitter. Four diagnosed patients for each disease were selected. From the user timelines of these eight patients, we extracted tweets that might be related to health conditions. Based on our experiment, we show that our approach has considerable potential, although we identified problems that should be addressed in future attempts to mine information about rare/intractable diseases from Twitter. Korea Genome Organization 2020-06-18 /pmc/articles/PMC7362943/ /pubmed/32634871 http://dx.doi.org/10.5808/GI.2020.18.2.e17 Text en (c) 2020, Korea Genome Organization (CC) This is an open-access article distributed under the terms of the Creative Commons Attribution license(https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Application Note Yamaguchi, Atsuko Queralt-Rosinach, Núria A proof-of-concept study of extracting patient histories for rare/intractable diseases from social media |
title | A proof-of-concept study of extracting patient histories for rare/intractable diseases from social media |
title_full | A proof-of-concept study of extracting patient histories for rare/intractable diseases from social media |
title_fullStr | A proof-of-concept study of extracting patient histories for rare/intractable diseases from social media |
title_full_unstemmed | A proof-of-concept study of extracting patient histories for rare/intractable diseases from social media |
title_short | A proof-of-concept study of extracting patient histories for rare/intractable diseases from social media |
title_sort | proof-of-concept study of extracting patient histories for rare/intractable diseases from social media |
topic | Application Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7362943/ https://www.ncbi.nlm.nih.gov/pubmed/32634871 http://dx.doi.org/10.5808/GI.2020.18.2.e17 |
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