CO2 cerebrovascular reactivity measured with CBF-MRI in older individuals: Association with cognition, physical function, amyloid and tau proteins

Author:

Sur Sandeepa1,Lin Zixuan12,Li Yang1,Yasar Sevil3,Rosenberg Paul B4,Moghekar Abhay5,Hou Xirui12,Jiang Dengrong1ORCID,Kalyani Rita R3,Hazel Kaisha1,Pottanat George1,Xu Cuimei1,Pillai Jay J16,Liu Peiying17,Albert Marilyn5,Lu Hanzhang128ORCID

Affiliation:

1. Department of Radiology, Johns Hopkins University, School of Medicine, Baltimore, MD, USA

2. Department of Biomedical Engineering, Johns Hopkins University, School of Medicine, Baltimore, MD, USA

3. Department of Medicine, Johns Hopkins University, School of Medicine, Baltimore, MD, USA

4. Department of Psychiatry and Behavioral Sciences, Johns Hopkins University, School of Medicine, Baltimore, MD, USA

5. Department of Neurology, Johns Hopkins University, School of Medicine, Baltimore, MD, USA

6. Division of Neuroradiology, Mayo Clinic College of Medicine and Science, Rochester, MN, USA

7. Department of Diagnostic Radiology & Nuclear Medicine, University of Maryland School of Medicine, Baltimore, MD, USA

8. F.M. Kirby Research Center, Kennedy Krieger Institute, Baltimore, MD, USA

Abstract

Vascular pathology is the second leading cause of cognitive impairment and represents a major contributing factor in mixed dementia. However, biomarkers for vascular cognitive impairment and dementia (VCID) are under-developed. Here we aimed to investigate the potential role of CO2 Cerebrovascular Reactivity (CVR) measured with phase-contrast quantitative flow MRI in cognitive impairment and dementia. Forty-five (69 ± 7 years) impaired (37 mild-cognitive-impairment and 8 mild-dementia by syndromic diagnosis) and 22 cognitively-healthy-control (HC) participants were recruited and scanned on a 3 T MRI. Biomarkers of AD pathology were measured in cerebrospinal fluid. We found that CBF-CVR was lower (p = 0.027) in the impaired (mean±SE, 3.70 ± 0.15%/mmHg) relative to HC (4.28 ± 0.21%/mmHg). After adjusting for AD pathological markers (Aβ42/40, total tau, and Aβ42/p-tau181), higher CBF-CVR was associated with better cognitive performance, including Montreal Cognitive Assessment, MoCA (p = 0.001), composite cognitive score (p = 0.047), and language (p = 0.004). Higher CBF-CVR was also associated with better physical function, including gait-speed (p = 0.006) and time for five chair-stands (p = 0.049). CBF-CVR was additionally related to the Clinical-Dementia-Rating, CDR, including global CDR (p = 0.026) and CDR Sum-of-Boxes (p = 0.015). CBF-CVR was inversely associated with hemoglobin A1C level (p = 0.017). In summary, CBF-CVR measured with phase-contrast MRI shows associations with cognitive performance, physical function, and disease-severity, independent of AD pathological markers.

Publisher

SAGE Publications

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