White matter hyperintensities are common in midlife and already associated with cognitive decline

被引:52
|
作者
D'Arbeloff, Tracy [1 ]
Elliott, Maxwell L. [1 ]
Knodt, Annchen R. [1 ]
Melzer, Tracy R. [2 ,3 ]
Keenan, Ross [2 ,4 ]
Ireland, David [5 ]
Ramrakha, Sandhya [5 ]
Poulton, Richie [5 ]
Anderson, Tim [2 ,3 ]
Caspi, Avshalom [1 ,6 ,7 ,8 ]
Moffitt, Terrie E. [1 ,6 ,7 ,8 ]
Hariri, Ahmad R. [1 ]
机构
[1] Duke Univ, Dept Psychol & Neurosci, Durham, NC 27708 USA
[2] New Zealand Brain Res Inst, 66 Stewart St, Christchurch 8011, New Zealand
[3] Univ Otago, Dept Med, 2 Riccarton Ave, Christchurch 8011, New Zealand
[4] Christchurch Radiol Grp, 6-242 Ferry Rd, Christchurch 8011, New Zealand
[5] Univ Otago, Dept Psychol, Dunedin Multidisciplinary Hlth & Dev Res Unit, Dunedin 9016, New Zealand
[6] Kings Coll London, Social Genet & Dev Psychiat Res Ctr, Inst Psychiat Psychol & Neurosci, London SE5 8AF, England
[7] Duke Univ, Dept Psychiat & Behav Sci, Sch Med, Durham, NC 27708 USA
[8] Duke Univ, Ctr Genom & Computat Biol, Durham, NC 27708 USA
基金
英国医学研究理事会; 美国国家科学基金会;
关键词
white matter hyperintensity; cognition; cognitive decline; dementia risk;
D O I
10.1093/braincomms/fcz041
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
White matter hyperintensities proliferate as the brain ages and are associated with increased risk for cognitive decline as well as Alzheimer's disease and related dementias. As such, white matter hyperintensities have been targeted as a surrogate biomarker in intervention trials with older adults. However, it is unclear at what stage of aging white matter hyperintensities begin to relate to cognition and if they may be a viable target for early prevention. In the Dunedin Study, a population-representative cohort followed since birth, we measured white matter hyperintensities in 843 45-year-old participants using T-2-weighted magnetic resonance imaging and we assessed cognitive decline from childhood to midlife. We found that white matter hyperintensities were common at age 45 and that white matter hyperintensity volume was modestly associated with both lower childhood (beta=-0.08, P = 0.013) and adult IQ (beta=-0.15, P < 0.001). Moreover, white matter hyperintensity volume was associated with greater cognitive decline from childhood to midlife (beta=-0.09, P < 0.001). Our results demonstrate that a link between white matter hyperintensities and early signs of cognitive decline is detectable decades before clinical symptoms of dementia emerge. Thus, white matter hyperintensities may be a useful surrogate biomarker for identifying individuals in midlife at risk for future accelerated cognitive decline and selecting participants for dementia prevention trials.
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页数:7
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