Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 Apr;65(4):1122-8.
doi: 10.1002/art.37842.

The fibromyalgia family study: a genome-wide linkage scan study

Affiliations

The fibromyalgia family study: a genome-wide linkage scan study

Lesley M Arnold et al. Arthritis Rheum. 2013 Apr.

Abstract

Objective: Familial aggregation of fibromyalgia has been increasingly recognized. The goal of this study was to conduct a genome-wide linkage scan to identify susceptibility loci for fibromyalgia.

Methods: We genotyped members of 116 families from the Fibromyalgia Family Study and performed a model-free genome-wide linkage analysis of fibromyalgia with 341 microsatellite markers, using the Haseman-Elston regression approach.

Results: The estimated sibling recurrence risk ratio (λs ) for fibromyalgia was 13.6 (95% confidence interval 10.0-18.5), based on a reported population prevalence of 2%. Genome-wide suggestive evidence of linkage was observed at markers D17S2196 (empirical P [Pe ]=0.00030) and D17S1294 (Pe=0.00035) on chromosome 17p11.2-q11.2.

Conclusion: The estimated sibling recurrence risk ratio (λs ) observed in this study suggests a strong genetic component of fibromyalgia. This is the first report of genome-wide suggestive linkage of fibromyalgia to the chromosome 17p11.2-q11.2 region. Further investigation of these multicase families from the Fibromyalgia Family Study is warranted to identify potential causal risk variants for fibromyalgia.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Results of genome-wide multipoint linkage scan for Fibromyalgia. For each chromosome (chr), genetic distance (cM) and −log10(P) are plotted on the X- and Y-axes, respectively. Horizontal line is drawn at P = 0.00074, the Lander and Kruglyak’s criterion for suggestive linkage.
Figure 2
Figure 2
Detailed multipoint linkage results for Fibromyalgia on Chromosome 17. Horizontal line is drawn at P = 0.00074, the Lander and Kruglyak’s criterion for suggestive linkage.

References

    1. Wolfe F, Smythe HA, Yunus MB, Bennett RM, Bombardier C, Goldenberg DL, et al. The American College of Rheumatology 1990 criteria for the classification of fibromyalgia: report of the multicenter criteria committee. Arthritis Rheum. 1990;33:160–72. - PubMed
    1. Wolfe F, Ross K, Anderson J, Russell IJ, Hebert L. The prevalence and characteristics of fibromyalgia in the general population. Arthritis Rheum. 1995;38:19–28. - PubMed
    1. Russell IJ, Larson AA. Neurophysiopathogenesis of fibromyalgia syndrome: a unified hypothesis. Rheum Dis Clin Norht Am. 2009;35:421–35. - PubMed
    1. Henriksson KG. Fibromyalgia--from syndrome to disease. Overview of pathogenetic mechanisms. J Rehabil Med. 2003;41(Suppl):89–94. - PubMed
    1. Ablin J, Neumann L, Buskila D. Pathogenesis of fibromyalgia - a review. Joint Bone Spine. 2008 May;75:273–9. - PubMed

Publication types