Unknown

Dataset Information

0

CLEC3B p.S106G Mutant in a Caucasian Population of Successful Neurological Aging.


ABSTRACT: A number of efforts are underway to better understand the role of genetic variation in successful aging and longevity. However, to date, only two genes have been consistently associated with longevity in humans: APOE and FOXO3, with the APOE ?2 allele also protective against dementia. Recently, using an exome-wide SNP array approach, a missense variant CLEC3B c.316G>A (rs13963 p.S106G) was reported to associate with longevity in two independent cohorts of Japanese and Chinese participants. Interestingly, CLEC3B p.S106G is more frequent in Caucasian populations. Herein, we examined the frequency of CLEC3B p.S106G in a Caucasian series of 1,483 neurologically healthy individuals with a specific subset >80 years of age. Although our findings do not support an association between CLEC3B p.S106G and aging without neurological disease (p = .89), we confirmed the association between the APOE ?2 allele and better survival without neurological disease (p = .001). Further assessment of healthy aged cohorts that retain intact neurological function will be critical to understand the etiology of neurodegenerative disease and the role of age at risk.

SUBMITTER: Kolicheski A 

PROVIDER: S-EPMC7494029 | BioStudies | 2020-01-01

REPOSITORIES: biostudies

Similar Datasets

1000-01-01 | S-EPMC5861862 | BioStudies
2019-01-01 | S-EPMC6537750 | BioStudies
2014-01-01 | S-EPMC4149928 | BioStudies
2017-01-01 | S-EPMC6242152 | BioStudies
2018-01-01 | S-EPMC6286851 | BioStudies
2020-01-01 | S-EPMC7437271 | BioStudies
2020-01-01 | S-EPMC7822120 | BioStudies
2013-01-01 | S-EPMC3725963 | BioStudies
2012-01-01 | S-EPMC3326242 | BioStudies
2017-01-01 | S-EPMC5400530 | BioStudies