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Developing a Blood Cell‐Based Diagnostic Test for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Using Peripheral Blood Mononuclear Cells

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is characterized by debilitating fatigue that profoundly impacts patients' lives. Diagnosis of ME/CFS remains challenging, with most patients relying on self‐report, questionnaires, and subjective measures to receive a diagnosis, and m...

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Autores principales: Xu, Jiabao, Lodge, Tiffany, Kingdon, Caroline, Strong, James W. L., Maclennan, John, Lacerda, Eliana, Kujawski, Slawomir, Zalewski, Pawel, Huang, Wei E., Morten, Karl J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602530/
https://www.ncbi.nlm.nih.gov/pubmed/37653608
http://dx.doi.org/10.1002/advs.202302146
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author Xu, Jiabao
Lodge, Tiffany
Kingdon, Caroline
Strong, James W. L.
Maclennan, John
Lacerda, Eliana
Kujawski, Slawomir
Zalewski, Pawel
Huang, Wei E.
Morten, Karl J.
author_facet Xu, Jiabao
Lodge, Tiffany
Kingdon, Caroline
Strong, James W. L.
Maclennan, John
Lacerda, Eliana
Kujawski, Slawomir
Zalewski, Pawel
Huang, Wei E.
Morten, Karl J.
author_sort Xu, Jiabao
collection PubMed
description Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is characterized by debilitating fatigue that profoundly impacts patients' lives. Diagnosis of ME/CFS remains challenging, with most patients relying on self‐report, questionnaires, and subjective measures to receive a diagnosis, and many never receiving a clear diagnosis at all. In this study, a single‐cell Raman platform and artificial intelligence are utilized to analyze blood cells from 98 human subjects, including 61 ME/CFS patients of varying disease severity and 37 healthy and disease controls. These results demonstrate that Raman profiles of blood cells can distinguish between healthy individuals, disease controls, and ME/CFS patients with high accuracy (91%), and can further differentiate between mild, moderate, and severe ME/CFS patients (84%). Additionally, specific Raman peaks that correlate with ME/CFS phenotypes and have the potential to provide insights into biological changes and support the development of new therapeutics are identified. This study presents a promising approach for aiding in the diagnosis and management of ME/CFS and can be extended to other unexplained chronic diseases such as long COVID and post‐treatment Lyme disease syndrome, which share many of the same symptoms as ME/CFS.
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spelling pubmed-106025302023-10-27 Developing a Blood Cell‐Based Diagnostic Test for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Using Peripheral Blood Mononuclear Cells Xu, Jiabao Lodge, Tiffany Kingdon, Caroline Strong, James W. L. Maclennan, John Lacerda, Eliana Kujawski, Slawomir Zalewski, Pawel Huang, Wei E. Morten, Karl J. Adv Sci (Weinh) Research Articles Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is characterized by debilitating fatigue that profoundly impacts patients' lives. Diagnosis of ME/CFS remains challenging, with most patients relying on self‐report, questionnaires, and subjective measures to receive a diagnosis, and many never receiving a clear diagnosis at all. In this study, a single‐cell Raman platform and artificial intelligence are utilized to analyze blood cells from 98 human subjects, including 61 ME/CFS patients of varying disease severity and 37 healthy and disease controls. These results demonstrate that Raman profiles of blood cells can distinguish between healthy individuals, disease controls, and ME/CFS patients with high accuracy (91%), and can further differentiate between mild, moderate, and severe ME/CFS patients (84%). Additionally, specific Raman peaks that correlate with ME/CFS phenotypes and have the potential to provide insights into biological changes and support the development of new therapeutics are identified. This study presents a promising approach for aiding in the diagnosis and management of ME/CFS and can be extended to other unexplained chronic diseases such as long COVID and post‐treatment Lyme disease syndrome, which share many of the same symptoms as ME/CFS. John Wiley and Sons Inc. 2023-08-31 /pmc/articles/PMC10602530/ /pubmed/37653608 http://dx.doi.org/10.1002/advs.202302146 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Xu, Jiabao
Lodge, Tiffany
Kingdon, Caroline
Strong, James W. L.
Maclennan, John
Lacerda, Eliana
Kujawski, Slawomir
Zalewski, Pawel
Huang, Wei E.
Morten, Karl J.
Developing a Blood Cell‐Based Diagnostic Test for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Using Peripheral Blood Mononuclear Cells
title Developing a Blood Cell‐Based Diagnostic Test for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Using Peripheral Blood Mononuclear Cells
title_full Developing a Blood Cell‐Based Diagnostic Test for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Using Peripheral Blood Mononuclear Cells
title_fullStr Developing a Blood Cell‐Based Diagnostic Test for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Using Peripheral Blood Mononuclear Cells
title_full_unstemmed Developing a Blood Cell‐Based Diagnostic Test for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Using Peripheral Blood Mononuclear Cells
title_short Developing a Blood Cell‐Based Diagnostic Test for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Using Peripheral Blood Mononuclear Cells
title_sort developing a blood cell‐based diagnostic test for myalgic encephalomyelitis/chronic fatigue syndrome using peripheral blood mononuclear cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602530/
https://www.ncbi.nlm.nih.gov/pubmed/37653608
http://dx.doi.org/10.1002/advs.202302146
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