Neurovascular-glymphatic dysfunction and white matter lesions

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Neurovascular-glymphatic dysfunction and white matter lesions. / Sabayan, Behnam; Westendorp, Rudi G.J.

In: GeroScience, 2021.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Sabayan, B & Westendorp, RGJ 2021, 'Neurovascular-glymphatic dysfunction and white matter lesions', GeroScience. https://doi.org/10.1007/s11357-021-00361-x

APA

Sabayan, B., & Westendorp, R. G. J. (Accepted/In press). Neurovascular-glymphatic dysfunction and white matter lesions. GeroScience. https://doi.org/10.1007/s11357-021-00361-x

Vancouver

Sabayan B, Westendorp RGJ. Neurovascular-glymphatic dysfunction and white matter lesions. GeroScience. 2021. https://doi.org/10.1007/s11357-021-00361-x

Author

Sabayan, Behnam ; Westendorp, Rudi G.J. / Neurovascular-glymphatic dysfunction and white matter lesions. In: GeroScience. 2021.

Bibtex

@article{1b84f2fadfe941e2a3d514cf647068be,
title = "Neurovascular-glymphatic dysfunction and white matter lesions",
abstract = "Cerebral white matter lesions (WML) represent a spectrum of age-related structural changes that are identified as areas of white matter high signal intensity on brain magnetic resonance imaging (MRI). Preservation of white matter requires proper functioning of both the cerebrovascular and glymphatic systems. The cerebrovascular safeguards adequate cerebral blood flow to supply oxygen, energy, and nutrients through a dynamic process of cerebral autoregulation and neurovascular coupling to keep up with global and regional demands of the brain. The glymphatic system maintains white matter integrity by preserving flow of interstitial fluid, exchanging metabolic waste and eventually its clearance into the venous circulation. Here, we argue that these two systems should not be considered separate entities but as one single physiologically integrated unit to preserve brain health. Due to the process of aging, damage to the neurovascular-glymphatic system accumulates over the life course. It is an insidious process that ultimately leads to the disruption of cerebral autoregulation, to the neurovascular uncoupling, and to the accumulation of metabolic waste products. As cerebral white matter is particularly vulnerable to hypoxic, inflammatory, and metabolic insults, WML are the first recognized pathologies of neurovascular-glymphatic dysfunction. A better understanding of the underlying pathophysiology will provide starting points for developing effective strategies to prevent a wide range of clinical disorders among which there are gait disturbances, functional dependence, cognitive impairment, and dementia.",
keywords = "Aging, Glymphatic system, Neurovascular unit, Small vessel disease, White matter",
author = "Behnam Sabayan and Westendorp, {Rudi G.J.}",
year = "2021",
doi = "10.1007/s11357-021-00361-x",
language = "English",
journal = "GeroScience",
issn = "0161-9152",
publisher = "Springer Science+Business Media",

}

RIS

TY - JOUR

T1 - Neurovascular-glymphatic dysfunction and white matter lesions

AU - Sabayan, Behnam

AU - Westendorp, Rudi G.J.

PY - 2021

Y1 - 2021

N2 - Cerebral white matter lesions (WML) represent a spectrum of age-related structural changes that are identified as areas of white matter high signal intensity on brain magnetic resonance imaging (MRI). Preservation of white matter requires proper functioning of both the cerebrovascular and glymphatic systems. The cerebrovascular safeguards adequate cerebral blood flow to supply oxygen, energy, and nutrients through a dynamic process of cerebral autoregulation and neurovascular coupling to keep up with global and regional demands of the brain. The glymphatic system maintains white matter integrity by preserving flow of interstitial fluid, exchanging metabolic waste and eventually its clearance into the venous circulation. Here, we argue that these two systems should not be considered separate entities but as one single physiologically integrated unit to preserve brain health. Due to the process of aging, damage to the neurovascular-glymphatic system accumulates over the life course. It is an insidious process that ultimately leads to the disruption of cerebral autoregulation, to the neurovascular uncoupling, and to the accumulation of metabolic waste products. As cerebral white matter is particularly vulnerable to hypoxic, inflammatory, and metabolic insults, WML are the first recognized pathologies of neurovascular-glymphatic dysfunction. A better understanding of the underlying pathophysiology will provide starting points for developing effective strategies to prevent a wide range of clinical disorders among which there are gait disturbances, functional dependence, cognitive impairment, and dementia.

AB - Cerebral white matter lesions (WML) represent a spectrum of age-related structural changes that are identified as areas of white matter high signal intensity on brain magnetic resonance imaging (MRI). Preservation of white matter requires proper functioning of both the cerebrovascular and glymphatic systems. The cerebrovascular safeguards adequate cerebral blood flow to supply oxygen, energy, and nutrients through a dynamic process of cerebral autoregulation and neurovascular coupling to keep up with global and regional demands of the brain. The glymphatic system maintains white matter integrity by preserving flow of interstitial fluid, exchanging metabolic waste and eventually its clearance into the venous circulation. Here, we argue that these two systems should not be considered separate entities but as one single physiologically integrated unit to preserve brain health. Due to the process of aging, damage to the neurovascular-glymphatic system accumulates over the life course. It is an insidious process that ultimately leads to the disruption of cerebral autoregulation, to the neurovascular uncoupling, and to the accumulation of metabolic waste products. As cerebral white matter is particularly vulnerable to hypoxic, inflammatory, and metabolic insults, WML are the first recognized pathologies of neurovascular-glymphatic dysfunction. A better understanding of the underlying pathophysiology will provide starting points for developing effective strategies to prevent a wide range of clinical disorders among which there are gait disturbances, functional dependence, cognitive impairment, and dementia.

KW - Aging

KW - Glymphatic system

KW - Neurovascular unit

KW - Small vessel disease

KW - White matter

U2 - 10.1007/s11357-021-00361-x

DO - 10.1007/s11357-021-00361-x

M3 - Journal article

C2 - 33851307

AN - SCOPUS:85104549860

JO - GeroScience

JF - GeroScience

SN - 0161-9152

ER -

ID: 260946549