TY - JOUR
T1 - Klotho, APOEε4, cognitive ability, brain size, atrophy, and survival
T2 - a study in the Aberdeen Birth Cohort of 1936
AU - de Vries, Clarisse F
AU - Staff, Roger T
AU - Harris, Sarah E
AU - Chapko, Dorota
AU - Williams, Daniel S
AU - Reichert, Polina
AU - Ahearn, Trevor
AU - McNeil, Christopher J
AU - Whalley, Lawrence J
AU - Murray, Alison D
N1 - Copyright © 2017 Elsevier Inc. All rights reserved.
PY - 2017/7
Y1 - 2017/7
N2 - A single copy of klotho allele KL-VS is associated with longevity, better health, increased cognition, and bigger regional brain volume. However, its longitudinal effects on cognition and brain volumes, both global and regional, in late life are unclear. In this study we show that, relative to noncarriers, KL-VS heterozygotes had (1) shorter survival; (2) smaller white matter volumes; (3) slower cognitive decline; and (4) greater right frontal lobe volumes. The KL-VS heterozygote survival and white matter volume disadvantages were unexpected. A possible explanation for these results in the context of the literature is a potential interaction between the environment and/or age of the participants, leading to a heterozygote disadvantage. The longitudinal cognitive trajectories indicate that heterozygotes would have an advantage in very late life. Collectively these results suggest that the genotype-survival advantage of the KL-VS allele is age-dependent and possibly mediated through differential cognition and brain volume.
AB - A single copy of klotho allele KL-VS is associated with longevity, better health, increased cognition, and bigger regional brain volume. However, its longitudinal effects on cognition and brain volumes, both global and regional, in late life are unclear. In this study we show that, relative to noncarriers, KL-VS heterozygotes had (1) shorter survival; (2) smaller white matter volumes; (3) slower cognitive decline; and (4) greater right frontal lobe volumes. The KL-VS heterozygote survival and white matter volume disadvantages were unexpected. A possible explanation for these results in the context of the literature is a potential interaction between the environment and/or age of the participants, leading to a heterozygote disadvantage. The longitudinal cognitive trajectories indicate that heterozygotes would have an advantage in very late life. Collectively these results suggest that the genotype-survival advantage of the KL-VS allele is age-dependent and possibly mediated through differential cognition and brain volume.
KW - Journal Article
U2 - 10.1016/j.neurobiolaging.2017.02.019
DO - 10.1016/j.neurobiolaging.2017.02.019
M3 - Article
C2 - 28431289
SN - 0197-4580
VL - 55
SP - 91
EP - 98
JO - Neurobiology of Aging
JF - Neurobiology of Aging
ER -