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Identifying responders to elamipretide in Barth syndrome: Hierarchical clustering for time series data
BACKGROUND: Barth syndrome (BTHS) is a rare genetic disease that is characterized by cardiomyopathy, skeletal myopathy, neutropenia, and growth abnormalities and often leads to death in childhood. Recently, elamipretide has been tested as a potential first disease-modifying drug. This study aimed to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10088720/ https://www.ncbi.nlm.nih.gov/pubmed/37041653 http://dx.doi.org/10.1186/s13023-023-02676-8 |
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author | Van den Eynde, Jef Chinni, Bhargava Vernon, Hilary Thompson, W. Reid Hornby, Brittany Kutty, Shelby Manlhiot, Cedric |
author_facet | Van den Eynde, Jef Chinni, Bhargava Vernon, Hilary Thompson, W. Reid Hornby, Brittany Kutty, Shelby Manlhiot, Cedric |
author_sort | Van den Eynde, Jef |
collection | PubMed |
description | BACKGROUND: Barth syndrome (BTHS) is a rare genetic disease that is characterized by cardiomyopathy, skeletal myopathy, neutropenia, and growth abnormalities and often leads to death in childhood. Recently, elamipretide has been tested as a potential first disease-modifying drug. This study aimed to identify patients with BTHS who may respond to elamipretide, based on continuous physiological measurements acquired through wearable devices. RESULTS: Data from a randomized, double-blind, placebo-controlled crossover trial of 12 patients with BTHS were used, including physiological time series data measured using a wearable device (heart rate, respiratory rate, activity, and posture) and functional scores. The latter included the 6-minute walk test (6MWT), Patient-Reported Outcomes Measurement Information System (PROMIS) fatigue score, SWAY Balance Mobile Application score (SWAY balance score), BTHS Symptom Assessment (BTHS-SA) Total Fatigue score, muscle strength by handheld dynamometry, 5 times sit-and-stand test (5XSST), and monolysocardiolipin to cardiolipin ratio (MLCL:CL). Groups were created through median split of the functional scores into “highest score” and “lowest score”, and “best response to elamipretide” and “worst response to elamipretide”. Agglomerative hierarchical clustering (AHC) models were implemented to assess whether physiological data could classify patients according to functional status and distinguish non-responders from responders to elamipretide. AHC models clustered patients according to their functional status with accuracies of 60–93%, with the greatest accuracies for 6MWT (93%), PROMIS (87%), and SWAY balance score (80%). Another set of AHC models clustered patients with respect to their response to treatment with elamipretide with perfect accuracy (all 100%). CONCLUSIONS: In this proof-of-concept study, we demonstrated that continuously acquired physiological measurements from wearable devices can be used to predict functional status and response to treatment among patients with BTHS. |
format | Online Article Text |
id | pubmed-10088720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100887202023-04-12 Identifying responders to elamipretide in Barth syndrome: Hierarchical clustering for time series data Van den Eynde, Jef Chinni, Bhargava Vernon, Hilary Thompson, W. Reid Hornby, Brittany Kutty, Shelby Manlhiot, Cedric Orphanet J Rare Dis Research BACKGROUND: Barth syndrome (BTHS) is a rare genetic disease that is characterized by cardiomyopathy, skeletal myopathy, neutropenia, and growth abnormalities and often leads to death in childhood. Recently, elamipretide has been tested as a potential first disease-modifying drug. This study aimed to identify patients with BTHS who may respond to elamipretide, based on continuous physiological measurements acquired through wearable devices. RESULTS: Data from a randomized, double-blind, placebo-controlled crossover trial of 12 patients with BTHS were used, including physiological time series data measured using a wearable device (heart rate, respiratory rate, activity, and posture) and functional scores. The latter included the 6-minute walk test (6MWT), Patient-Reported Outcomes Measurement Information System (PROMIS) fatigue score, SWAY Balance Mobile Application score (SWAY balance score), BTHS Symptom Assessment (BTHS-SA) Total Fatigue score, muscle strength by handheld dynamometry, 5 times sit-and-stand test (5XSST), and monolysocardiolipin to cardiolipin ratio (MLCL:CL). Groups were created through median split of the functional scores into “highest score” and “lowest score”, and “best response to elamipretide” and “worst response to elamipretide”. Agglomerative hierarchical clustering (AHC) models were implemented to assess whether physiological data could classify patients according to functional status and distinguish non-responders from responders to elamipretide. AHC models clustered patients according to their functional status with accuracies of 60–93%, with the greatest accuracies for 6MWT (93%), PROMIS (87%), and SWAY balance score (80%). Another set of AHC models clustered patients with respect to their response to treatment with elamipretide with perfect accuracy (all 100%). CONCLUSIONS: In this proof-of-concept study, we demonstrated that continuously acquired physiological measurements from wearable devices can be used to predict functional status and response to treatment among patients with BTHS. BioMed Central 2023-04-11 /pmc/articles/PMC10088720/ /pubmed/37041653 http://dx.doi.org/10.1186/s13023-023-02676-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Van den Eynde, Jef Chinni, Bhargava Vernon, Hilary Thompson, W. Reid Hornby, Brittany Kutty, Shelby Manlhiot, Cedric Identifying responders to elamipretide in Barth syndrome: Hierarchical clustering for time series data |
title | Identifying responders to elamipretide in Barth syndrome: Hierarchical clustering for time series data |
title_full | Identifying responders to elamipretide in Barth syndrome: Hierarchical clustering for time series data |
title_fullStr | Identifying responders to elamipretide in Barth syndrome: Hierarchical clustering for time series data |
title_full_unstemmed | Identifying responders to elamipretide in Barth syndrome: Hierarchical clustering for time series data |
title_short | Identifying responders to elamipretide in Barth syndrome: Hierarchical clustering for time series data |
title_sort | identifying responders to elamipretide in barth syndrome: hierarchical clustering for time series data |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10088720/ https://www.ncbi.nlm.nih.gov/pubmed/37041653 http://dx.doi.org/10.1186/s13023-023-02676-8 |
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