Register for email alerts and news feeds:
This journal | BMJ Group
rss
The most recent version of this article was published on 1 February 2007

J Clin Pathol. Published Online First: 25 August 2006. doi:10.1136/jcp.2006.042374
Copyright © 2006 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.

Inter-disciplinary

Current research priorities in Chronic Fatigue Syndrome / Myalgic Encephalomyelitis (CFS/ME): disease mechanisms, a diagnostic test and specific treatments

Jonathan R Kerr 1*, Peter Christian 2, Andrea Hodgetts 2, Paul R Langford 2, Lakshmi D Devanur 1, Robert Petty 1, Beverley Burke 1, Lindsey I Sinclair 3, Selwyn CM Richards 4, Jane Montgomery 4, Clare McDermott 4, Tim J Harrison 5, Paul Kellam 5, David J Nutt 3 and Stephen T Holgate 6

1 St George's University of London, United Kingdom
2 Imperial College London, United Kingdom
3 University of Bristol, United Kingdom
4 Dorset CFS Service, Poole Hospital, United Kingdom
5 University College London, United Kingdom
6 University of Southampton, United Kingdom

* To whom correspondence should be addressed. E-mail: jkerr{at}sgul.ac.uk.

Accepted 31 July 2006


Abstract

Chronic fatigue syndrome (CFS) is an illness characterised by disabling fatigue of at least 6 months duration which is accompanied by various rheumatological, infectious and neuropsychiatric symptoms. A collaborative study group has been formed in order to address the current areas for development in CFS research, namely, to develop an understanding of the molecular pathogenesis of CFS, to develop a diagnostic test, and to develop specific and curative treatments. Various groups have studied the gene expression in peripheral blood of CFS patients and of those studies which have been confirmed using polymerase chain reaction (PCR), it is clear that the most predominant functional theme is that of immunity and defense. However, we do not yet know the precise gene signature and metabolic pathways involved. Currently, this is being addressed using a microarray representing 47,000 human genes and variants, massive parallel signature sequencing (MPSS) and real-time PCR. It will be important to ensure that once a gene signature has been identified, that it is specific to CFS and does not occur in other diseases and infections. A diagnostic test is being developed using Surface-Enhanced, Laser-Desorption and Ionisation - Time of Flight (SELDI-TOF) mass spectrometry following a pilot study in which putative biomarkers were identified. And, finally, clinical trials are being planned; novel treatments which we believe are important to trial in CFS patients are interferon-â and one of the anti-tumour necrosis factor-á drugs.

Key Words: Chronic Fatigue Syndrome, Myalgic encephalomyelitis, biomarkers, gene expression, treatment


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

This Article

Services
Citing Articles
Google Scholar
PubMed
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Pathology jobs

Pathology jobs