Neuroendocrine and immune network re-modeling in chronic fatigue syndrome: An exploratory analysis

被引:46
作者
Fuite, Jim [1 ]
Vernon, Suzanne D. [2 ]
Broderick, Gordon [1 ]
机构
[1] Univ Alberta, Fac Med & Dent, Div Pulm, Dept Med,Walter Mackenzie Hlth Sci Ctr 2E4 41, Edmonton, AB, Canada
[2] Assoc Amer, CFIDS, Charlotte, NC USA
关键词
Endocrine; Chronic fatigue; Co-expression; Networks; Graph theory; Centrality; Connectivity; Immune function; Signaling;
D O I
10.1016/j.ygeno.2008.08.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This work investigates the significance of changes in association patterns linking indicators of neuroendocrine and immune activity in patients with chronic fatigue syndrome (CFS). Gene sets preferentially expressed in specific immune cell isolates were integrated with neuroendocrine data from a large population-based study. Co-expression patterns linking immune cell activity with hypothalamic-pituitary-adrenal (HPA), thyroidal (HPT) and gonadal (HPG) axis status were computed using mutual information criteria. Networks in control and CFS subjects were compared globally in terms of a weighted graph edit distance. Local re-modeling of node connectivity was quantified by node degree and eigenvector centrality measures. Results indicate statistically significant differences between CFS and control networks determined mainly by re-modeling around pituitary and thyroid nodes as well as an emergent immune sub-network. Findings align with known mechanisms of chronic inflammation and support possible immune-mediated loss of thyroid function in CFS exacerbated by blunted HPA axis responsiveness. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:393 / 399
页数:7
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