Journal article
A new approach to find biomarkers in chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) by single-cell Raman micro-spectroscopy
- Abstract:
- Chronic fatigue syndrome (CFS), also called myalgic encephalomyelitis (ME), is a debilitating disorder characterized by physical and mental exhaustion. Mitochondrial and energetic dysfunction has been investigated in CFS patients due to a hallmark relationship with fatigue, however, no consistent conclusion has yet been achieved. Single-cell Raman spectra (SCRS) are label-free biochemical profiles, indicating phenotypic fingerprints of single cells. In this study, we applied a new approach using single-cell Raman microspectroscopy (SCRM) to examine 0 cells that lack mitochondrial DNA (mtDNA), and peripheral blood mononuclear cells (PBMCs) from CFS patients and healthy controls. The experimental results show that Raman bands associated with phenylalanine in 0 cells and CFS patient PBMCs were significantly higher than wild type model and healthy controls. Remarkably, an increase in intensities of Raman phenylalanine bands were also observed in CFS patients. As similar changes were observed in the 0 cell model with a known deficiency in the mitochondrial respiratory chain as well as in CFS patients, our results suggest that the increase in cellular phenylalanine may relate to mitochondrial/energetic dysfunction in both systems. Interestingly, phenylalanine can be used as a potential biomarker for diagnosis of CFS by SCRM. A machine learning classification model achieved an accuracy rate of 98% correctly assigning Raman spectra to either the CFS group or the control group. SCRM combined with machine learning algorithm therefore has the potential to become a diagnostic tool for CFS.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Accepted manuscript, pdf, 1.3MB, Terms of use)
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(Preview, Accepted manuscript, pdf, 125.7KB, Terms of use)
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(Preview, Accepted manuscript, pdf, 283.5KB, Terms of use)
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- Publisher copy:
- 10.1039/C8AN01437J
Authors
+ Natural Environment Research Council
More from this funder
- Funding agency for:
- Huang, W
- Grant:
- NE/M002934/1
+ Engineering and Physical Sciences Research Council
More from this funder
- Funding agency for:
- Huang, W
- Grant:
- NE/M002934/1
- Publisher:
- Royal Society of Chemistry
- Journal:
- Analyst More from this journal
- Volume:
- 144
- Issue:
- 3
- Pages:
- 913-920
- Publication date:
- 2018-08-22
- Acceptance date:
- 2018-08-21
- DOI:
- EISSN:
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1364-5528
- ISSN:
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0003-2654
- Keywords:
- Pubs id:
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pubs:909301
- UUID:
-
uuid:56069cef-320f-43ad-b970-20c1fdced6e4
- Local pid:
-
pubs:909301
- Source identifiers:
-
909301
- Deposit date:
-
2018-08-22
Terms of use
- Copyright holder:
- Xu et al
- Copyright date:
- 2018
- Notes:
-
This is the accepted manuscript version of the article. The final version is available online from the Royal Society of Chemistry at: https://doi.org/10.1039/C8AN01437J
Note: an erratum exists for this article, originally published and available at: http://dx.doi.org/10.1039/C9AN90055A
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