Published online before print January 19, 2006, doi: 10.1161/01.STR.0000202655.64413.0c
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Stroke. 2006;37:906.)
© 2006 American Heart Association, Inc.
Research Reports |
SERPINA3 Polymorphism Is Not Associated With Primary Intracerebral Hemorrhage in a Polish Population
From the Department of Neurology, Jagiellonian University, Krakow, Poland.
Correspondence to Joanna Pera, MD, Department of Neurology, Jagiellonian University, Botaniczna 3, 31-503 Krakow, Poland. E-mail pera{at}su.krakow.pl
Background and Purpose— Genetic factors involved in the pathogenesis of primary intracerebral hemorrhage (PICH) remain unknown. One of the candidate genes is SERPINA3. Results of a Spanish study suggested that TT genotype of the A/T SERPINA3 polymorphism in the signal peptide sequence was a risk factor for PICH in normotensive subjects. The aim of the present study was to investigate whether SERPINA3 A/T polymorphism is associated with PICH in a Polish population.
Methods— We analyzed 95 PICH patients and 190 unrelated healthy controls matched for age and sex. A/T polymorphism of the SERPINA3 gene was investigated using polymerase chain reaction restriction fragment length polymorphism method.
Results— The distribution of SERPINA3 genotypes was similar among PICH patients (AA 27.4%; AT 46.3%; TT 26.3%) and controls (AA 23.7%; AT 50.5%; TT 25.8%; P=NS). There were also no significant differences in genotype distribution when analyzing separately hypertensive and normotensive PICH patients as well as patients with lobar and deeply located hemorrhage.
Conclusions— We failed to find an association between SERPINA3 A/T polymorphism and PICH in a Polish population.
Key Words: genetics • intracerebral hemorrhage