Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
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
_version_ 1782196754185191424
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
work_keys_str_mv AT fletchermarya plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome
AT rosenthalmartin plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome
AT antonimichael plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome
AT ironsongail plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome
AT zengxiaor plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome
AT barneszachary plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome
AT harveyjeannam plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome
AT hurwitzbarry plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome
AT levissilvina plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome
AT broderickgordon plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome
AT klimasnancyg plasmaneuropeptideyabiomarkerforsymptomseverityinchronicfatiguesyndrome