Klotho gene polymorphism, brain structure and cognition in early-life development.

Variation in the klotho gene is linked to differences in health outcomes: klotho allele KL-VS heterozygosity is associated with longevity, better cognition and greater right frontal grey matter volume in late life. Contradicting reports, however, suggest that KL-VS's effect on health might be age-de...

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Publicado en:Brain Imaging & Behavior Vol. 14; no. 1; pp. 213 - 226
Autores principales: de Vries, Clarisse F., Staff, Roger T., Noble, Kimberly G., Muetzel, Ryan L., Vernooij, Meike W., White, Tonya, Waiter, Gordon D., Murray, Alison D.
Formato: Journal Article
Publicado: Springer Nature Feb2020
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Feb2020
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      pub: Springer Nature
      place: New York, New York
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        atl: Klotho gene polymorphism, brain structure and cognition in early-life development.
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          de Vries, Clarisse F.
          Staff, Roger T.
          Noble, Kimberly G.
          Muetzel, Ryan L.
          Vernooij, Meike W.
          White, Tonya
          Waiter, Gordon D.
          Murray, Alison D.
        affil: Aberdeen Biomedical Imaging Centre, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Foresterhill, AB25 2ZD, Aberdeen, UK
      sug:
        subj:
          Glycoside Hydrolases
          Glycoside Hydrolases Metabolism
          Cognition
          Heterozygote
          Child, Preschool
          Polymorphism, Genetic
          Brain Physiology
          Genotype
          Adolescence
          Child
          Female
          Alleles
          Male
          Young Adult
          Genes
          Prospective Studies
          Questionnaires
          Child, Preschool: 2-5 years
          Adolescent: 13-18 years
          Child: 6-12 years
          Female
          Male
      ab: Variation in the klotho gene is linked to differences in health outcomes: klotho allele KL-VS heterozygosity is associated with longevity, better cognition and greater right frontal grey matter volume in late life. Contradicting reports, however, suggest that KL-VS's effect on health might be age-dependent. Here we examine the relationship between KL-VS genotype, cognition and brain structure in childhood and adolescence. We hypothesized that KL-VS has early influences on cognitive and brain development. We investigated the associations of KL-VS carrier status with cognition and brain morphology in a cohort of 1387 children and adolescents aged 3-21 years, examining main effects and interactions between age, sex and socioeconomic circumstance. KL-VS had no main effect on either cognition or brain structure, though there was a significant KL-VS × age interaction for cognition (specifically executive function, attention, episodic memory, and general cognition), total grey matter and total brain volume. KL-VS heterozygotes had better cognition than non-carriers before age 11, but lower cognition after age 11. Heterozygotes had smaller brains than non-carriers did in early childhood. Sex moderated the association between KL-VS and white matter volume. Among girls, KL-VS heterozygotes had smaller white matter volumes than non-carriers. Among boys, heterozygotes had greater white matter volumes than non-carriers. However, a replication in a cohort of 2306 children aged 6-12 years showed no significant associations. In contrast to findings in late life, these results show that KL-VS does not have a main effect on cognition and brain structure. Furthermore, KL-VS's influence may depend on age and sex.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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