Plasma amyloid-β levels, cerebral atrophy and risk of dementia: a population-based study

被引:45
作者
Hilal, Saima [1 ,2 ]
Wolters, Frank J. [2 ]
Verbeek, Marcel M. [3 ]
Vanderstichele, Hugo [4 ]
Ikram, M. Kamran [2 ,5 ]
Stoops, Erik [4 ]
Ikram, M. Arfan [1 ,2 ]
Vernooij, Meike W. [1 ,2 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Radiol & Nucl Med, Off 2505,Wytemaweg 80, NL-3015 CN Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Dept Epidemiol, Rotterdam, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Neurol & Lab Med, Donders Inst Brain Cognit & Behav,Radboud Alzheim, Nijmegen, Netherlands
[4] ADx NeuroSci, Ghent, Belgium
[5] Erasmus Univ, Dept Neurol, Med Ctr, Rotterdam, Netherlands
关键词
Plasma amyloid-beta levels; Magnetic resonance imaging; Atrophy; Dementia; Population-based; ALZHEIMERS-DISEASE; CEREBROSPINAL-FLUID; HYPOTHETICAL MODEL; DYNAMIC BIOMARKERS; COGNITIVE DECLINE; ELDERLY SUBJECTS; GAMMA-SECRETASE; ROTTERDAM SCAN; ASSOCIATION; PROTEIN;
D O I
10.1186/s13195-018-0395-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Plasma amyloid-beta (A beta) levels are increasingly studied as a potential accessible marker of cognitive impairment and dementia. However, it remains underexplored whether plasma A beta levels including the novel A beta peptide 1-38 (A beta(1-38)) relate to preclinical markers of neurodegeneration and risk of dementia. We investigated the association of plasma A beta(1-38), A beta(1-40), and A beta(1-42) levels with imaging markers of neurodegeneration and risk of dementia in a prospective population-based study. Methods: We analyzed plasma A beta levels in 458 individuals from the Rotterdam Study. Brain volumes, including gray matter, white matter, and hippocampus, were computed on the basis of 1.5-T magnetic resonance imaging (MRI). Dementia and its subtypes were defined on the basis of internationally accepted criteria. Results: A total of 458 individuals (mean age, 67.8 +/- 7.7 yr; 232 [50.7%] women) with baseline MRI scans and incident dementia were included. The mean +/- SD values of A beta(1-38), A beta(1-40), and A beta(1-42) (in pg/ml) were 19.4 +/- 4.3, 186.1 +/- 35.9, and 56.3 +/- 6.2, respectively, at baseline. Lower plasma A beta(1-42) levels were associated with smaller hippocampal volume (mean difference in hippocampal volume per SD decrease in A beta(1-42) levels, -0.13; 95% CI, -0.23 to -0.04; p = 0.007). After a mean follow-up of 14.8 years (SD, 4.9; range, 4.1-23.5 yr), 79 persons developed dementia, 64 of whom were diagnosed with Alzheimer's disease (AD). Lower levels of A beta(1-38) and A beta(1-42) were associated with increased risk of dementia, specifically AD (HR for AD per SD decrease in A beta(1-38) levels, 1.39; 95% CI, 1.00-2.16; HR for AD per SD decrease in A beta(1-42) levels, 1.35; 95% CI, 1.05-1.75) after adjustment for age, sex, education, cardiovascular risk factors, apolipoprotein E epsilon 4 allele carrier status, and other A beta isoforms. Conclusions: Our results show that lower plasma A beta levels were associated with risk of dementia and incident AD. Moreover, lower plasma A beta(1-42) levels were related to smaller hippocampal volume. These results suggest that plasma A beta(1-38) and A beta(1-42) maybe useful biomarkers for identification of individuals at risk of dementia.
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页数:8
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