Association of cerebral small vessel disease burden with brain structure and cognitive and vascular risk trajectories in mid-to-late life

被引:12
|
作者
Jansen, Michelle G. [1 ,2 ]
Griffanti, Ludovica [3 ,4 ]
Mackay, Clare E. [3 ,4 ]
Anaturk, Melis [3 ,5 ]
Melazzini, Luca [4 ,6 ]
de Lange, Ann-Marie G. [3 ,7 ]
Filippini, Nicola [8 ]
Zsoldos, Eniko [3 ,4 ]
Wiegertjes, Kim [2 ]
de Leeuw, Frank-Erik [2 ]
Singh-Manoux, Archana [9 ,10 ]
Kivimaki, Mika [9 ]
Ebmeier, Klaus P. [3 ]
Suri, Sana [3 ,4 ]
机构
[1] Radboud Univ Nijmegen, Donders Ctr Cognit, Donders Inst Brain Cognit & Behav, POB 9104, NL-6500 HE Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Dept Neurol, Med Ctr, Nijmegen, Netherlands
[3] Univ Oxford, Dept Psychiat, Oxford, England
[4] Univ Oxford, Wellcome Ctr Integrat Neuroimaging, Oxford Ctr Funct MRI Brain & Human Brain Act, Oxford, England
[5] UCL, Ctr Med Image Comp, Dept Comp Sci, London, England
[6] Univ Milan, Dept Biomed Sci Hlth, Milan, Italy
[7] Univ Oslo, Dept Psychol, Oslo, Norway
[8] IRCCS San Camillo Hosp, Venice, Italy
[9] UCL, Dept Epidemiol & Publ Hlth, London, England
[10] Univ Paris, Epidemiol Ageing & Neurogenerat Dis, INSERM, Paris, France
来源
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM | 2022年 / 42卷 / 04期
基金
英国医学研究理事会; 英国惠康基金; 芬兰科学院; 欧盟地平线“2020”;
关键词
Ageing; cardiovascular risk; cognition; magnetic resonance imaging; small vessel disease; BLOOD-PRESSURE; PERIVASCULAR SPACES; STROKE; WHITEHALL; PROFILE; LEUKOARAIOSIS; INSIGHT; SCALE;
D O I
10.1177/0271678X211048411
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We characterize the associations of total cerebral small vessel disease (SVD) burden with brain structure, trajectories of vascular risk factors, and cognitive functions in mid-to-late life. Participants were 623 community-dwelling adults from the Whitehall II Imaging Sub-study with multi-modal MRI (mean age 69.96, SD = 5.18, 79% men). We used linear mixed-effects models to investigate associations of SVD burden with up to 25-year retrospective trajectories of vascular risk and cognitive performance. General linear modelling was used to investigate concurrent associations with grey matter (GM) density and white matter (WM) microstructure, and whether these associations were modified by cognitive status (Montreal Cognitive Asessment [MoCA] scores of < 26 vs. >= 26). Severe SVD burden in older age was associated with higher mean arterial pressure throughout midlife (beta = 3.36, 95% CI [0.42-6.30]), and faster cognitive decline in letter fluency (beta = -0.07, 95% CI [-0.13--0.01]), and verbal reasoning (beta = -0.05, 95% CI [-0.11--0.001]). Moreover, SVD burden was related to lower GM volumes in 9.7% of total GM, and widespread WM microstructural decline (FWE-corrected p < 0.05). The latter association was most pronounced in individuals who demonstrated cognitive impairments on MoCA (MoCA < 26; F-3,F-608 = 2.14, p = 0.007). These findings highlight the importance of managing midlife vascular health to preserve brain structure and cognitive function in old age.
引用
收藏
页码:600 / 612
页数:13
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