Epigenetic Alterations and an Increased Frequency of Micronuclei in Women with Fibromyalgia

Fibromyalgia (FM), characterized by chronic widespread pain, fatigue, and cognitive/mood disturbances, leads to reduced workplace productivity and increased healthcare expenses. To determine if acquired epigenetic/genetic changes are associated with FM, we compared the frequency of spontaneously occ...

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Main Authors: Victoria Menzies, Debra E. Lyon, Kellie J. Archer, Qing Zhou, Jenni Brumelle, Kimberly H. Jones, G. Gao, Timothy P. York, Colleen Jackson-Cook
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Nursing Research and Practice
Online Access:http://dx.doi.org/10.1155/2013/795784
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author Victoria Menzies
Debra E. Lyon
Kellie J. Archer
Qing Zhou
Jenni Brumelle
Kimberly H. Jones
G. Gao
Timothy P. York
Colleen Jackson-Cook
author_facet Victoria Menzies
Debra E. Lyon
Kellie J. Archer
Qing Zhou
Jenni Brumelle
Kimberly H. Jones
G. Gao
Timothy P. York
Colleen Jackson-Cook
author_sort Victoria Menzies
collection DOAJ
description Fibromyalgia (FM), characterized by chronic widespread pain, fatigue, and cognitive/mood disturbances, leads to reduced workplace productivity and increased healthcare expenses. To determine if acquired epigenetic/genetic changes are associated with FM, we compared the frequency of spontaneously occurring micronuclei (MN) and genome-wide methylation patterns in women with FM (n=10) to those seen in comparably aged healthy controls (n=42 (MN); n=8 (methylation)). The mean (sd) MN frequency of women with FM (51.4 (21.9)) was significantly higher than that of controls (15.8 (8.5)) (χ2=45.552; df = 1; P=1.49×10-11). Significant differences (n=69 sites) in methylation patterns were observed between cases and controls considering a 5% false discovery rate. The majority of differentially methylated (DM) sites (91%) were attributable to increased values in the women with FM. The DM sites included significant biological clusters involved in neuron differentiation/nervous system development, skeletal/organ system development, and chromatin compaction. Genes associated with DM sites whose function has particular relevance to FM included BDNF, NAT15, HDAC4, PRKCA, RTN1, and PRKG1. Results support the need for future research to further examine the potential role of epigenetic and acquired chromosomal alterations as a possible biological mechanism underlying FM.
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spelling doaj-art-d10a68fb724c4745ab6e6f4f1c8a31bb2025-02-03T06:07:27ZengWileyNursing Research and Practice2090-14292090-14372013-01-01201310.1155/2013/795784795784Epigenetic Alterations and an Increased Frequency of Micronuclei in Women with FibromyalgiaVictoria Menzies0Debra E. Lyon1Kellie J. Archer2Qing Zhou3Jenni Brumelle4Kimberly H. Jones5G. Gao6Timothy P. York7Colleen Jackson-Cook8Virginia Commonwealth University School of Nursing, 1100 East Leigh Street, Richmond, VA 23298-0567, USAVirginia Commonwealth University School of Nursing, 1100 East Leigh Street, Richmond, VA 23298-0567, USADepartment of Biostatistics, Virginia Commonwealth University, 830 East Main Street, Richmond, VA 23298, USADepartment of Biostatistics, Virginia Commonwealth University, 830 East Main Street, Richmond, VA 23298, USADepartment of Pathology, Virginia Commonwealth University, P.O. Box 980662, Richmond, VA 23298-0662, USADepartment of Pathology, Virginia Commonwealth University, P.O. Box 980662, Richmond, VA 23298-0662, USADepartment of Biostatistics, Virginia Commonwealth University, 830 East Main Street, Richmond, VA 23298, USADepartment of Human and Molecular Genetics, Virginia Commonwealth University, P.O. Box 980033, Richmond, VA 23298-0003, USAMassey Cancer Center, Virginia Commonwealth University, VA 23298-0037, USAFibromyalgia (FM), characterized by chronic widespread pain, fatigue, and cognitive/mood disturbances, leads to reduced workplace productivity and increased healthcare expenses. To determine if acquired epigenetic/genetic changes are associated with FM, we compared the frequency of spontaneously occurring micronuclei (MN) and genome-wide methylation patterns in women with FM (n=10) to those seen in comparably aged healthy controls (n=42 (MN); n=8 (methylation)). The mean (sd) MN frequency of women with FM (51.4 (21.9)) was significantly higher than that of controls (15.8 (8.5)) (χ2=45.552; df = 1; P=1.49×10-11). Significant differences (n=69 sites) in methylation patterns were observed between cases and controls considering a 5% false discovery rate. The majority of differentially methylated (DM) sites (91%) were attributable to increased values in the women with FM. The DM sites included significant biological clusters involved in neuron differentiation/nervous system development, skeletal/organ system development, and chromatin compaction. Genes associated with DM sites whose function has particular relevance to FM included BDNF, NAT15, HDAC4, PRKCA, RTN1, and PRKG1. Results support the need for future research to further examine the potential role of epigenetic and acquired chromosomal alterations as a possible biological mechanism underlying FM.http://dx.doi.org/10.1155/2013/795784
spellingShingle Victoria Menzies
Debra E. Lyon
Kellie J. Archer
Qing Zhou
Jenni Brumelle
Kimberly H. Jones
G. Gao
Timothy P. York
Colleen Jackson-Cook
Epigenetic Alterations and an Increased Frequency of Micronuclei in Women with Fibromyalgia
Nursing Research and Practice
title Epigenetic Alterations and an Increased Frequency of Micronuclei in Women with Fibromyalgia
title_full Epigenetic Alterations and an Increased Frequency of Micronuclei in Women with Fibromyalgia
title_fullStr Epigenetic Alterations and an Increased Frequency of Micronuclei in Women with Fibromyalgia
title_full_unstemmed Epigenetic Alterations and an Increased Frequency of Micronuclei in Women with Fibromyalgia
title_short Epigenetic Alterations and an Increased Frequency of Micronuclei in Women with Fibromyalgia
title_sort epigenetic alterations and an increased frequency of micronuclei in women with fibromyalgia
url http://dx.doi.org/10.1155/2013/795784
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