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The prion protein M129V polymorphism
Authors:Ewa Golanska  Monika Sieruta  Elizabeth Corder  Sylwia M. Gresner  Anna Pfeffer  Malgorzata Chodakowska-Zebrowska  Tomasz M. Sobow  Izabela Klich  Malgorzata Mossakowska  Aleksandra Szybinska  Maria Barcikowska  Pawel P. Liberski
Abstract:
The PRNP gene encodes the cellular isoform of prion protein (PrPc). The M129V polymorphism influences the risk of prion diseases and may modulate the rate of neurodegeneration with age. We present the first study of the polymorphism among Polish centenarians. In the control group (n = 165, ages 18 to 56 years) the observed M129V genotype frequencies agreed with those expected according to the Hardy-Weinberg equilibrium (MM, MV, VV): 43%, 44%, 13% (HWE p > 0.05). Among centenarians (n = 150, ages 100 to 107) both homozygotes were more common than expected and HWE was rejected: 46%, 37%, 17% (expected 42%, 46%, 13%; HWE p = 0.025). This finding is consistent with a higher mortality rate among heterozygotes. However, the observed allele and genotype frequencies did not differ significantly between the oldest-old and the young controls. The genotypic frequencies were not related to severe cognitive impairment among the centenarians.
Keywords:PRNP  longevity  codon 129 polymorphism  cognitive impairment  centenarians  M129V  selective mortality  genetic epidemiology
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