Scientists at King's College London have identified a single blood protein
that may indicate the development of Mild Cognitive Impairment (MCI) years
before symptoms appear, a disorder that has been associated with an increased
risk of Alzheimer's disease or other dementias.
The new research, published today in Translational Psychiatry, used data
from over 100 sets of identical twins from TwinsUK, the biggest adult twin
cohort in the UK. The use of twins in the study indicated that the association
between the blood protein and a ten year decline in cognitive ability was
independent of age and genetics, both of which are already known to affect the
risk of developing Alzheimer's disease, the most common form of dementia.
The study, the largest of its kind, measured over 1,000 proteins in the
blood of over 200 healthy individuals, using a laboratory test called a
SOMAscan, a protein biomarker discovery tool which allows a high volume of
proteins to be measured simultaneously. Using a computerised test, the
researchers then assessed each individual's cognitive ability, and compared the
results with the measured level of each protein in the blood.
For the first time, they found that the blood level of a protein called
MAPKAPK5 was, on average, lower in individuals whose cognitive ability declined
over a ten year period.
There are currently no treatments available proven to prevent Alzheimer's
disease, and prevention trials for Alzheimer's disease can be problematic
because to be effective, they must involve individuals at risk of the disease,
who can be hard to identify. Studies using Magnetic Resonance Imaging (MRI) and
Positron Emission Tomography (PET) brain scans have been shown to display
visible signs of the disease before the onset of symptoms, but these types of
scans are both timely and costly.
To date, few other studies have looked at the blood of individuals with
very early stages of cognitive declineand therefore most appropriate for a
prevention study. Identifying blood markers such as MAPKAPK5, which may indicate
a person's future risk of Alzheimer's disease, could contribute towards the
better design of prevention trials.
Dr Steven Kiddle, lead author and Biostatistics Research Fellow at the MRC
Social, Genetic & Developmental Psychiatry Centre at King's College London,
said: 'Although we are still searching for an effective treatment for
Alzheimer's disease, what we do know is that prevention of the disease is likely
to be more effective than trying to reverse it.
'The next step will be to confirm whether or not our initial finding is
specific for Alzheimer's disease, as this could lead to the development of a
reliable blood test which would help clinicians identify suitable people
forprevention trials.'
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