4.5 Article

Sildenafil Improves Vascular and Metabolic Function in Patients with Alzheimer's Disease

Journal

JOURNAL OF ALZHEIMERS DISEASE
Volume 60, Issue 4, Pages 1351-1364

Publisher

IOS PRESS
DOI: 10.3233/JAD-161006

Keywords

Cerebral blood flow; cerebral metabolic rate of oxygen; cerebrovascular reactivity; magnetic resonance imaging; Montreal Cognitive Assessment; sildenafil

Categories

Funding

  1. NIH [P30 AG012300, R01 MH084021, R01 NS067015, R01 AG042753, R21 NS078656]

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Background: Alzheimer's disease (AD) is the leading cause of degenerative dementia in the aging population. Patients with AD have alterations in cerebral hemodynamic function including reduced cerebral blood flow (CBF) and cerebral metabolic rate. Therefore, improved cerebrovascular function may be an attractive goal for pharmaceutical intervention in AD. Objective: We wished to observe the acute effects of sildenafil on cerebrovascular function and brain metabolism in patients with AD. Methods: We used several novel non-invasive MRI techniques to investigate the alterations of CBF, cerebral metabolic rate of oxygen (CMRO2), and cerebrovascular reactivity (CVR) after a single dose of sildenafil administration in order to assess its physiological effects in patients with AD. CBF, CMRO2, and CVR measurements using MRI were performed before and one hour after the oral administration of 50 mg sildenafil. Baseline Montreal Cognitive Assessment score was also obtained. Results: Complete CBF and CMRO2 data were obtained in twelve patients. Complete CVR data were obtained in eight patients. Global CBF and CMRO2 significantly increased (p = 0.03, p = 0.05, respectively) following sildenafil administration. Voxel-wise analyses of CBF maps showed that increased CBF was most pronounced in the bilateral medial temporal lobes. CVR significantly decreased after administration of sildenafil. Conclusion: Our data suggest that a single dose of sildenafil improves cerebral hemodynamic function and increases cerebral oxygen metabolism in patients with AD.

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