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Plasma neuropeptide Y: a biomarker for symptom severity in chronic fatigue syndrome
BACKGROUND: Chronic fatigue syndrome (CFS) is a complex, multi-symptom illness with a multisystem pathogenesis involving alterations in the nervous, endocrine and immune systems. Abnormalities in stress responses have been identified as potential triggers or mediators of CFS symptoms. This study foc...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024290/ https://www.ncbi.nlm.nih.gov/pubmed/21190576 http://dx.doi.org/10.1186/1744-9081-6-76 |
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author | Fletcher, Mary A Rosenthal, Martin Antoni, Michael Ironson, Gail Zeng, Xiao R Barnes, Zachary Harvey, Jeanna M Hurwitz, Barry Levis, Silvina Broderick, Gordon Klimas, Nancy G |
author_facet | Fletcher, Mary A Rosenthal, Martin Antoni, Michael Ironson, Gail Zeng, Xiao R Barnes, Zachary Harvey, Jeanna M Hurwitz, Barry Levis, Silvina Broderick, Gordon Klimas, Nancy G |
author_sort | Fletcher, Mary A |
collection | PubMed |
description | BACKGROUND: Chronic fatigue syndrome (CFS) is a complex, multi-symptom illness with a multisystem pathogenesis involving alterations in the nervous, endocrine and immune systems. Abnormalities in stress responses have been identified as potential triggers or mediators of CFS symptoms. This study focused on the stress mediator neuropeptide Y (NPY). We hypothesized that NPY would be a useful biomarker for CFS. METHODS: The CFS patients (n = 93) were from the Chronic Fatigue and Related Disorders Clinic at the University of Miami and met the 1994 case definition of Fukuda and colleagues. Healthy sedentary controls (n = 100)) were from NIH or VA funded studies. Another fatiguing, multi-symptom illness, Gulf War Illness (GWI), was also compared to CFS. We measured NPY in plasma using a radioimmunoassay (RIA). Psychometric measures, available for a subset of CFS patients included: Perceived Stress Scale, Profile of Mood States, ATQ Positive & Negative Self-Talk Scores, the COPE, the Beck Depression Inventory, Fatigue Symptom Inventory, Cognitive Capacity Screening Examination, Medical Outcomes Survey Short Form-36, and the Quality of Life Scale. RESULTS: Plasma NPY was elevated in CFS subjects, compared to controls (p = .000) and to GWI cases (p = .000). Receiver operating characteristics (ROC) curve analyses indicated that the predictive ability of plasma NPY to distinguish CFS patients from healthy controls and from GWI was significantly better than chance alone. In 42 patients with CFS, plasma NPY had significant correlations (<0.05) with perceived stress, depression, anger/hostility, confusion, negative thoughts, positive thoughts, general health, and cognitive status. In each case the correlation (+ or -) was in the anticipated direction. CONCLUSIONS: This study is the first in the CFS literature to report that plasma NPY is elevated compared to healthy controls and to a fatigued comparison group, GWI patients. The significant correlations of NPY with stress, negative mood, general health, depression and cognitive function strongly suggest that this peptide be considered as a biomarker to distinguish subsets of CFS. |
format | Text |
id | pubmed-3024290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30242902011-01-21 Plasma neuropeptide Y: a biomarker for symptom severity in chronic fatigue syndrome Fletcher, Mary A Rosenthal, Martin Antoni, Michael Ironson, Gail Zeng, Xiao R Barnes, Zachary Harvey, Jeanna M Hurwitz, Barry Levis, Silvina Broderick, Gordon Klimas, Nancy G Behav Brain Funct Research BACKGROUND: Chronic fatigue syndrome (CFS) is a complex, multi-symptom illness with a multisystem pathogenesis involving alterations in the nervous, endocrine and immune systems. Abnormalities in stress responses have been identified as potential triggers or mediators of CFS symptoms. This study focused on the stress mediator neuropeptide Y (NPY). We hypothesized that NPY would be a useful biomarker for CFS. METHODS: The CFS patients (n = 93) were from the Chronic Fatigue and Related Disorders Clinic at the University of Miami and met the 1994 case definition of Fukuda and colleagues. Healthy sedentary controls (n = 100)) were from NIH or VA funded studies. Another fatiguing, multi-symptom illness, Gulf War Illness (GWI), was also compared to CFS. We measured NPY in plasma using a radioimmunoassay (RIA). Psychometric measures, available for a subset of CFS patients included: Perceived Stress Scale, Profile of Mood States, ATQ Positive & Negative Self-Talk Scores, the COPE, the Beck Depression Inventory, Fatigue Symptom Inventory, Cognitive Capacity Screening Examination, Medical Outcomes Survey Short Form-36, and the Quality of Life Scale. RESULTS: Plasma NPY was elevated in CFS subjects, compared to controls (p = .000) and to GWI cases (p = .000). Receiver operating characteristics (ROC) curve analyses indicated that the predictive ability of plasma NPY to distinguish CFS patients from healthy controls and from GWI was significantly better than chance alone. In 42 patients with CFS, plasma NPY had significant correlations (<0.05) with perceived stress, depression, anger/hostility, confusion, negative thoughts, positive thoughts, general health, and cognitive status. In each case the correlation (+ or -) was in the anticipated direction. CONCLUSIONS: This study is the first in the CFS literature to report that plasma NPY is elevated compared to healthy controls and to a fatigued comparison group, GWI patients. The significant correlations of NPY with stress, negative mood, general health, depression and cognitive function strongly suggest that this peptide be considered as a biomarker to distinguish subsets of CFS. BioMed Central 2010-12-29 /pmc/articles/PMC3024290/ /pubmed/21190576 http://dx.doi.org/10.1186/1744-9081-6-76 Text en Copyright ©2010 Fletcher et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Fletcher, Mary A Rosenthal, Martin Antoni, Michael Ironson, Gail Zeng, Xiao R Barnes, Zachary Harvey, Jeanna M Hurwitz, Barry Levis, Silvina Broderick, Gordon Klimas, Nancy G Plasma neuropeptide Y: a biomarker for symptom severity in chronic fatigue syndrome |
title | Plasma neuropeptide Y: a biomarker for symptom severity in chronic fatigue syndrome |
title_full | Plasma neuropeptide Y: a biomarker for symptom severity in chronic fatigue syndrome |
title_fullStr | Plasma neuropeptide Y: a biomarker for symptom severity in chronic fatigue syndrome |
title_full_unstemmed | Plasma neuropeptide Y: a biomarker for symptom severity in chronic fatigue syndrome |
title_short | Plasma neuropeptide Y: a biomarker for symptom severity in chronic fatigue syndrome |
title_sort | plasma neuropeptide y: a biomarker for symptom severity in chronic fatigue syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024290/ https://www.ncbi.nlm.nih.gov/pubmed/21190576 http://dx.doi.org/10.1186/1744-9081-6-76 |
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