4.4 Review

Assessment of age-related decline of neurovascular coupling responses by functional near-infrared spectroscopy (fNIRS) in humans

Journal

GEROSCIENCE
Volume 41, Issue 5, Pages 495-509

Publisher

SPRINGER
DOI: 10.1007/s11357-019-00122-x

Keywords

Aging; Neurovascular coupling; Functional near-infrared spectroscopy; fNIRS; Vascular cognitive impairment and dementia; VCI; VCID; Cognitive aging

Funding

  1. National Institute on Aging [R01-AG047879, R01-AG038747, R01-AG055395]
  2. National Institute of Neurological Disorders and Stroke (NINDS) [R01-NS056218, R01-NS100782, R01-NS085002]
  3. American Heart Association
  4. Oklahoma Center for the Advancement of Science and Technology
  5. Oklahoma Shared Clinical and Translational Resources (OSCTR) program - National Institute of General Medical Sciences [GM104938]
  6. Presbyterian Health Foundation
  7. NIA [T32AG052363]
  8. Oklahoma Nathan Shock Center [P30AG050911]
  9. Cellular and Molecular GeroScience CoBRE [1P20GM125528, 5337]

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Preclinical studies provide strong evidence that age-related impairment of neurovascular coupling (NVC) plays a causal role in the pathogenesis of vascular cognitive impairment (VCI). NVC is a critical homeostatic mechanism in the brain, responsible for adjustment of local cerebral blood flow to the energetic needs of the active neuronal tissue. Recent progress in geroscience has led to the identification of critical cellular and molecular mechanisms involved in neurovascular aging, identifying these pathways as targets for intervention. In order to translate the preclinical findings to humans, there is a need to assess NVC in geriatric patients as an endpoint in clinical studies. Functional near-infrared spectroscopy (fNIRS) is a non-invasive neuroimaging technique that enables the investigation of local changes in cerebral blood flow, quantifying task-related changes in oxygenated and deoxygenated hemoglobin concentrations. In the present overview, the basic principles of fNIRS are introduced and the application of this technique to assess NVC in older adults with implications for the design of studies on the mechanistic underpinnings of VCI is discussed.

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