Plasma β-amyloid and MRI markers of cerebral small vessel disease
Three-City Dijon Study
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Abstract
Objective: We investigated the relation of circulating plasma β-amyloid (Aβ) with MRI markers of small vessel disease (SVD) in dementia-free community persons.
Methods: Participants were 1,690 individuals aged 65 to 80 years from the Three-City Dijon Study. Plasma Aβ measurement and MRI examination were performed at baseline and after a 4-year follow-up. MRI markers of SVD included white matter hyperintensities (WMH), lacunes, and enlarged perivascular spaces. We examined the relation of plasma Aβ levels with MRI markers of SVD at baseline and with progression of WMH over follow-up (n = 1,057). We also assessed whether these relations were modified by vascular risk factors, notably blood pressure.
Results: Low plasma Aβ1–40 levels were associated with increased progression of WMH, and low Aβ1–42 with higher odds of extensive WMH progression over the follow-up (odds ratio = 1.66, 95% confidence interval = 1.16–2.38). Consistently low Aβ1–40 and Aβ1–42 levels on both measurements were associated with accelerated progression of WMH. These associations were modified by blood pressure levels but not the APOE ε4 genotype.
Conclusions: Progression of WMH volume in dementia-free older persons is associated with levels of circulating plasma Aβ. These results reinforce the notion of an interrelation of vascular and neurodegenerative mechanisms in cerebral aging.
GLOSSARY
- Aβ=
- β-amyloid;
- AD=
- Alzheimer disease;
- BP=
- blood pressure;
- CAA=
- cerebral amyloid angiopathy;
- DBP=
- diastolic blood pressure;
- MMSE=
- Mini-Mental State Examination;
- PVS=
- perivascular space;
- SBP=
- systolic blood pressure;
- SVD=
- small vessel disease;
- 3C Dijon Study=
- Three-City Dijon Study;
- WM=
- white matter;
- WMH=
- white matter hyperintensity
Footnotes
Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
Supplemental data at Neurology.org
- Received July 3, 2014.
- Accepted in final form August 28, 2014.
- © 2014 American Academy of Neurology
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