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ADRB2, brain white matter integrity and cognitive ageing in the Lothian Birth Cohort 1936
Authors:Donald M. Lyall  Lorna M. Lopez  Mark E. Bastin  Susana Muñoz Maniega  Lars Penke  Maria del C. Valdés Hernández  Natalie A. Royle  John M. Starr  David. J. Porteous  Joanna M. Wardlaw  Ian J. Deary
Affiliation:1. Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, EH8 9JZ, UK
2. Division of Neuroimaging Sciences, Brain Research Imaging Centre, University of Edinburgh, Edinburgh, EH4 2XU, UK
3. Department of Psychology, University of Edinburgh, Edinburgh, EH8 9JZ, UK
4. Medical Genetics Section, Molecular Medicine Centre, Western General Hospital, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XU, UK
5. Scottish Imaging Network, A Platform for Scientific Excellence (SINAPSE) Collaboration, Department of Neuroimaging Sciences, The University of Edinburgh, Edinburgh, EH4 2XU, UK
6. Geriatric Medicine Unit, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK
Abstract:
The non-synonymous mutations arg16gly (rs1042713) and gln27glu (rs1042714) in the adrenergic β-2 receptor gene (ADRB2) have been associated with cognitive function and brain white matter integrity. The current study aimed to replicate these findings and expand them to a broader range of cognitive and brain phenotypes. The sample used is a community-dwelling group of older people, the Lothian Birth Cohort 1936. They had been assessed cognitively at age 11 years, and undertook further cognitive assessments and brain diffusion MRI tractography in older age. The sample size range for cognitive function variables was N = 686–765, and for neuroimaging variables was N = 488–587. Previously-reported findings with these genetic variants did not replicate in this cohort. Novel, nominally significant associations were observed; notably, the integrity of the left arcuate fasciculus mediated the association between rs1042714 and the Digit Symbol Coding test of information processing speed. No significant associations of cognitive and brain phenotypes with ADRB2 variants survived correction for false discovery rate. Previous findings may therefore have been subject to type 1 error. Further study into links between ADRB2, cognitive function and brain white matter integrity is required.
Keywords:
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