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For sickle cell anemia patients who are under age 20, stroke
is a major risk factor. In April's issue of the journal Nature
Genetics, a new research study proposed a model to predict stroke.
Compared to the model that is currently in use, this new model
can identify the risk of stroke for sickle cell anemia patients
more accurately and faster, and it can be a useful post-prediction
experiment.
In order to find the genes and clinical factors that are influential
of the risk of stroke, Dr Paola Sebastiani, Dr Marco Ramoni and
their colleagues have done analysis on 235 SNPs of 80 candidates
from 1,398 sickle cell anemia patients. They tested the validity
of this model on 114 independent individuals, and the accuracy
of this model for predicting stroke is 98.2%. The study also found
that the interaction of 25 SNPs in 11 genes with 4 clinical factors
greatly influenced the risk of stroke. These factors also contain
some factors that are previously identified as associated with
stroke in normal people, including three genes in the TGF-beta
pathway and SELP. The evidence provided by this new research shows
that the risk of stroke is a complex problem that involves multiple
genes and clinical factors.
Currently TCD is often used to predict the risk of stroke for
children and young adults with sickle cell anemia, but as a way
of predicting stroke, this method is very limited since only 10%
of the patients with abnormal TCD levels develop stroke, whereas
some patients with normal TCD levels also have stroke.
From Nature
Biotechnology Asia (April 2005). Translation: Ling Wang, Boston
University
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