Dr Enlander: Mar 2010 Summary of XMRV research to date and good-science suggestions


Dr. Derek Enlander posted this to co-cure today

In October the Whittemore Peterson Institute in Nevada published a report on
the presence of XMRV virus in the ME/ CFS patients. This report, published
in Science, created much excitement in the medical world and in the media.
The report suggested the aetilogy of ME/CFS was indeed a physical disease,
tending to change public opinion.

However, we must temper this excitement with careful research that
replicates or denies the thesis. This new research must be careful to
replicate or deny the original research with a large cohort of patients and

There are numerous groups with their own agenda who wish to confirm or deny
the original research. Large government grants and insurance disability
interests are at stake. These groups have rushed to publish unsatisfactory
comparative research with anecdotal results, based on small number of
ill-defined patients, stale specimens and differing research methods.

It would be helpful if there was a collaborative effort to test a
significant number of the same specimens in different research centers.
Perhaps 200 Fukuda criteria and Canadian criteria patients and controls
could be divided and tested in multiple centers in a double-blind trial to
replicate or deny the original research. It is time for the psychological
and physical researchers to collaborate rather than cast aspersions on each
other's work. ESME would support such collaboration.

Dr. Derek Enlander

*The European Society for ME is a non-profit group, operated entirely by
volunteers. You can support ESME with a donation by visiting: **

*Your donation will go directly to our goals of educating doctors and helping scientists to solve the puzzle of ME/CFS: www.esme-eu.com*<http://www.esme-eu.com/>



Senior Member
Sheffield UK
Thanks for posting this Island Finn.

Seems Enlander is talking common sense.

Collaboration eh? Wow. Now that would be something.
Is he suggesting that if XMRV fails (or is proven a passanger virus/ only responsible for a small subset) -- that CFS/ME will somehow become a non-physical disease?

EDIT: Oh, I didn't see -- he's the one who's patients mostly tested negative. K, I give him a bit of a pass. Good for him for wanting to make sure there's 'good science' -- that's still a blah response though.


he stated very diplomatically that the european studies were rubbish!