Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Saturday, November 24, 2012

The novel role of epigenetics in primary prevention of cardiovascular diseases

I'm sure your doctor can tell you exactly how to prevent CV events.
http://scholar.google.com/scholar_url?hl=en&q=http://pagepressjournals.org/index.php/cardiogen/article/view/cardiogenetics.2012.e12/pdf&sa=X&scisig=AAGBfm2cd5v34ELJYFuTqQKH1JMGOAQQzA&oi=scholaralrt
Abstract
A great deal of evidences indicate that
impaired fetal growth and in utero exposure to
risk factors, especially maternal hypercholesterolemia,
may be relevant for human pathophysiological
signs of atherosclerosis and subsequent
development of cardiovascular disease
(CVD) during different life stages. Despite the
underlying mechanisms of fetal programming
are still unknown, epigenetics has been suggested
as one of the possible explanations for
the associations between intrauterine risk factors
and CVD development. Indeed, a lot of
translational studies support the hypothesis
that epigenetic changes are related to
increased CVD risk although it is still not possible
to establish a direct causality in humans.
Notably, epigenetic modifications can be
reversible through therapeutic approaches
employing histone deacetylase inhibitors, histone
acetyltransferase inhibitors and commonly
used drugs like statins. Thus, the whole
comprehension of these mechanisms will provide
in the next future the rationale for the
development of novel tools to be used in the
primary prevention and therapy of CVD.

No comments:

Post a Comment