Background and Purpose-A common G-to-T point mutation (Val 34 Leu) in
exon 2 of the alpha-subunit of the factor XIII is strongly negatively
associated with the development of myocardial infarction. This result
suggests that factor XIII Val 34 Leu is interfering with the formation
of cross-linked fibrin. The role of factor XIII Val 34 Leu in the pat
hogenesis of cerebral infarction and primary intracerebral hemorrhage
is unknown. Methods-Six hundred twelve patients with acute stroke, def
ined by World Health Organization criteria and cranial CT, and 436 age
-matched control subjects free of cerebrovascular disease were genotyp
ed for the factor XIII Val 34 Leu mutation. Venous blood was drawn for
the determination of hemostatic variables and lipids. Factor XIII gen
otype was determined through a single-stranded conformational polymorp
hism technique and plasminogen activator inhibitor (PAI)-1 4G/5G promo
ter genotype by allele-specific polymerase chain reaction. Results-The
mutation was more frequent in patients with primary intracerebral hem
orrhage (n=62) (54.8%; P=.05) than in control subjects (41.7%) or in p
atients with cerebral infarction (n=529) (46.5%; P=.22). There was no
relationship between PAI-1 levels and the PAI-1 4G/5G genotype. Conclu
sions-There was a slightly higher incidence of factor XIII Val 34 Leu
in patients with PICH. This may be related to impaired cross-linking o
f fibrin and/or coagulation proteins.