Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke

Ischemic stroke in young adults is a well-known disease, but despite extensive clinical and laboratory investigations, its etiology remains unclear in approximately half of the cases. We examined the prevalence of factor V Leiden, the prothrombin G20210A genotype, and the C677T mutation in the methy...

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Published in:	Clinical and applied thrombosis/hemostasis Vol. 7; no. 4; p. 346
Main Authors:	Lopaciuk, S, Bykowska, K, Kwiecinski, H, Mickielewicz, A, Czlonkowska, A, Mendel, T, Kuczynska-Zardzewialy, A, Szelagowska, D, Windyga, J, Schröder, W, Herrmann, F H, Jedrzejowska, H
Format:	Journal Article
Language:	English
Published:	United States 01-10-2001
Subjects:	Adolescent Adult Brain Ischemia - blood Brain Ischemia - etiology Brain Ischemia - genetics Case-Control Studies Factor V - analysis Female Genetic Predisposition to Disease Genetic Variation Genotype Humans Male Methylenetetrahydrofolate Reductase (NADPH2) Middle Aged Oxidoreductases Acting on CH-NH Group Donors - blood Oxidoreductases Acting on CH-NH Group Donors - genetics Point Mutation Prevalence Prothrombin - analysis Prothrombin - genetics Risk Factors Stroke - blood Stroke - etiology Stroke - genetics
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Summary:	Ischemic stroke in young adults is a well-known disease, but despite extensive clinical and laboratory investigations, its etiology remains unclear in approximately half of the cases. We examined the prevalence of factor V Leiden, the prothrombin G20210A genotype, and the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in 100 patients (51 males and 49 females) who survived an ischemic stroke without a cardiac embolic source at an age < or = 45 years, and in 238 healthy control subjects from the same geographic area. The patients were selected for study only if the diagnosis of stroke was documented by computed tomography scan or nuclear magnetic resonance (NMR) of the brain, or both. Heterozygosity for the FV Leiden mutation was found in 3 patients (3.0%) and in 10 control subjects (4.2%). Two patients (2.0%) and five control subjects (2.1%) were heterozygous for the prothrombin G20210A mutation. The frequencies of the MTHFR 677TT, CT, and CC genotypes in the patient group were 12%, 37%, and 51%, respectively, and were not significantly different from those in control subjects (11%, 40%, and 49%, respectively). In conclusion, our results indicate that FV Leiden mutation, prothrombin G20210A genotype, and homozygosity for the C677T mutation in the MTHFR gene are not associated with an increased risk for ischemic stroke in young adults.
ISSN:	1076-0296
DOI:	10.1177/107602960100700418