Microstructural white matter integrity in relation to vascular reactivity in Dutch-type hereditary cerebral amyloid angiopathy

Author:

Schipper Manon R1ORCID,Vlegels Naomi23,van Harten Thijs W1ORCID,Rasing Ingeborg4,Koemans Emma A4,Voigt Sabine14,Luca Alberto de25,Kaushik Kanishk4ORCID,van Etten Ellis S4,van Zwet Erik W6,Terwindt Gisela M4,Biessels Geert Jan2,van Osch Matthias JP1ORCID,van Walderveen Marianne AA1,Wermer Marieke JH47

Affiliation:

1. Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands

2. Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands

3. Institute for Stroke and Dementia Research, University Hospital, LMU Munich, Munich, Germany

4. Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands

5. Image Sciences Institute, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands

6. Department of Biostatistics, Leiden University Medical Center, Leiden, The Netherlands

7. Department of Neurology, University Medical Center Groningen, Groningen, The Netherlands

Abstract

Cerebral Amyloid Angiopathy (CAA) is characterized by cerebrovascular amyloid-β accumulation leading to hallmark cortical MRI markers, such as vascular reactivity, but white matter is also affected. By studying the relationship in different disease stages of Dutch-type CAA (D-CAA), we tested the relation between vascular reactivity and microstructural white matter integrity loss. In a cross-sectional study in D-CAA, 3 T MRI was performed with Blood-Oxygen-Level-Dependent (BOLD) fMRI upon visual activation to assess vascular reactivity and diffusion tensor imaging to assess microstructural white matter integrity through Peak Width of Skeletonized Mean Diffusivity (PSMD). We assessed the relationship between BOLD parameters – amplitude, time-to-peak (TTP), and time-to-baseline (TTB) – and PSMD, with linear and quadratic regression modeling. In total, 25 participants were included (15/10 pre-symptomatic/symptomatic; mean age 36/59 y). A lowered BOLD amplitude (unstandardized β = 0.64, 95%CI [0.10, 1.18], p = 0.02, Adjusted R2 = 0.48), was quadratically associated with increased PSMD levels. A delayed BOLD response, with prolonged TTP (β = 8.34 × 10−6, 95%CI [1.84 × 10−6, 1.48 × 10−5], p = 0.02, Adj. R2 = 0.25) and TTB (β = 6.57 × 10−6, 95%CI [1.92 × 10−6, 1.12 × 10−5], p = 0.008, Adj. R2 = 0.29), was linearly associated with increased PSMD. In D-CAA subjects, predominantly in the symptomatic stage, impaired cerebrovascular reactivity is related to microstructural white matter integrity loss. Future longitudinal studies are needed to investigate whether this relation is causal.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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