Thrombotic thrombocytopenic
purpura (abbreviated TTP) is a rare disease that is caused by the
occurrence of blood clots (so-called blood platelet thrombi) in small
and the smallest blood vessels. Blockage of vessels leads to lesions in
the affected organs as a result of which stroke, kidney dysfunction,
etc. can arise. If left untreated, the disease leads to death in 90% of
cases.
For the most part we now distinguish between
two forms, acquired TTP and congenital (= hereditary or familial) TTP.
The congenital form is also called Upshaw-Schulman Syndrome, having been named after
those who first described it. Upshaw-Schulman Syndrome is caused by
genetic defects (mutations) in the ADAMTS13 (= Von Willebrand
factor-cleaving protease) gene. This results in functional ADAMTS13 no
longer being able to be formed. Hence, ADAMTS13 activity that can be
measured in plasma of Upshaw-Schulman Syndrome patients amounts to less
than 5% of normal levels.
Various case reports about
individual patients have been published since the Von Willebrand
factor-cleaving protease (ADAMTS13) and the connection between a serious
ADAMTS13 deficiency and TTP have been discovered. Based on this, we
estimate that there are currently approximately 150 families with known
Upshaw-Schulman in the world. Unfortunately, since too little is known
about Upshaw-Schulman Syndrome at this time, the disease is often
diagnosed too late or not at all and many patients or their siblings
have either died or suffered extremely serious, permanent organ damage
from it. This is all the more unfortunate since acute TTP episodes in
Upshaw-Schulman Syndrome patients can be successfully treated with
simple plasma infusions. Today, there are numerous patients receiving
plasma infusions every 2-3 weeks to prevent recurring episodes and
living normal lives. These days the question remains open as to whether
all patients should receive this type of preventative treatment, or
perhaps certain specific situations warrant the use of some other
therapy that may not be as effective in reducing the risk of an
episode’s occurring. (And what would these specific situations
be?)
Isabella Aebi, Research BMA
Coordinator TTP Registry University Hospital and University of Bern, Inselspital, Hemostasis Research Laboratory, Departement for BioMedical Research DBMR
Postal address:
Murtenstrasse 40 3008 Bern Switzerland
phone:
+41 31 632 77 16
fax:
+41 31 632 18 82
e-mail:
Isabella.Aebi-Huber@insel.ch
Dr. Anette van Dorland
Project Manager TTP Registry University Hospital and University of Bern, Inselspital, Hemostasis Research Laboratory, Departement for BioMedical Research DBMR