A polymorphic marker in the first intron of the Werner gene associates with cognitive function in aged Danish twins.

Abstract:

:Werner's syndrome is a premature aging syndrome with many features common to normal aging. The possible association between phenotypic markers for normal aging and SNP's in the WRN gene was investigated in 426 dizygotic, Danish twins age 70-90 years. All participants were scored every second year using a number of physical and cognitive tests. In addition their self-rated health was registered as well as self reported status with regards to nine diseases. Blood was drawn from all participants and purified DNA was typed for four SNP's in the WRN gene. The four SNP's were located in intron 1, exon 6, exon 9 and exon 34. In an unpaired analysis of this material a significant association between the intron 1 SNP and cognitive function was demonstrated. Our finding, which will need corroboration in independent samples, therefore may suggest that the t-allele of the intron 1 SNP is beneficial to cognitive function. However, since the t-allele of this SNP is very rare, we did not encounter any tt-homozygous individuals for this allele.

journal_name

Exp Gerontol

journal_title

Experimental gerontology

authors

Bendixen MH,Nexø BA,Bohr VA,Frederiksen H,McGue M,Kølvraa S,Christensen K

doi

10.1016/j.exger.2004.03.036

keywords:

subject

Has Abstract

pub_date

2004-07-01 00:00:00

pages

1101-7

issue

7

eissn

0531-5565

issn

1873-6815

pii

S0531556504001408

journal_volume

39

pub_type

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