Author(s)

M. D. V. Hernandez, T. Booth, C. Murray, A. J. Gow, L. Penke, Z. Morris, S. M. Maniega, N. A. Royle, B. S. Aribisala, M. E. Bastin, J. M. Starr, I. J. Deary, J. M. Wardlaw

ISBN

0197-4580

Publication year

2013

Periodical

Neurobiology of Aging

Periodical Number

12

Volume

34

Pages

2740-2747

Author Address

Wardlaw, JM Univ Edinburgh, Brain Res Imaging Ctr, Edinburgh EH4 2XU, Midlothian, Scotland Univ Edinburgh, Brain Res Imaging Ctr, Dept Clin Neurosci, Edinburgh EH4 2XU, Midlothian, Scotland Univ Edinburgh, Dept Psychol, Edinburgh EH4 2XU, Midlothian, Scotland Univ Edinburgh, Ctr Cognit Ageing & Cognit Epidemiol, Edinburgh EH4 2XU, Midlothian, Scotland Univ Edinburgh, Dept Geriatr Med, Edinburgh EH4 2XU, Midlothian, Scotland Heriot Watt Univ, Dept Psychol, Sch Life Sci, Edinburgh, Midlothian, Scotland Lagos State Univ, Dept Comp Sci, Lagos, Nigeria

Full version

Cerebral white matter hyperintensities (WMH) reflect accumulating white matter damage with aging and impair cognition. The role of childhood intelligence is rarely considered in associations between cognitive impairment and WMH. We studied community-dwelling older people all born in 1936, in whom IQ had been assessed at age 11 years. We assessed medical histories, current cognitive ability and quantified WMH on MR imaging. Among 634 participants, mean age 72.7 (SD 0.7), age 11 IQ was the strongest predictor of late life cognitive ability. After accounting for age 11 IQ, greater WMH load was significantly associated with lower late life general cognitive ability (beta = -0.14, p < 0.01) and processing speed (beta = -0.19, p < 0.001). WMH were also associated independently with lower age 11 IQ (beta = -0.08, p < 0.05) and hypertension. In conclusion, having more WMH is significantly associated with lower cognitive ability, after accounting for prior ability, age 11IQ. Early-life IQ also influenced WMH in later life. Determining how lower IQ in youth leads to increasing brain damage with aging is important for future successful cognitive aging. (C) 2013 The Authors. Published by Elsevier Inc. All rights reserved.