Association of Baseline Cerebrovascular Reactivity and Longitudinal Development of Enlarged Perivascular Spaces in the Basal Ganglia.


Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
Nov 2023
Historique:
pmc-release: 01 11 2024
medline: 1 11 2023
pubmed: 15 9 2023
entrez: 15 9 2023
Statut: ppublish

Résumé

Increasing evidence suggests that enlarged perivascular spaces (ePVS) are associated with cognitive dysfunction in aging. However, the pathogenesis of ePVS remains unknown. Here, we tested the possibility that baseline cerebrovascular dysfunction, as measured by a magnetic resonance imaging measure of cerebrovascular reactivity, contributes to the later development of ePVS. Fifty cognitively unimpaired, older adults (31 women; age range, 60-84 years) underwent magnetic resonance imaging scanning at baseline and follow-up separated by ≈2.5 years. ePVS were counted in the basal ganglia, centrum semiovale, midbrain, and hippocampus. Cerebrovascular reactivity, an index of the vasodilatory capacity of cerebral small vessels, was assessed using carbon dioxide inhalation while acquiring blood oxygen level-dependent magnetic resonance images. Low baseline cerebrovascular reactivity values in the basal ganglia were associated with increased follow-up ePVS counts in the basal ganglia after controlling for age, sex, and baseline ePVS values (estimate [SE]=-3.18 [0.96]; Our results demonstrate that low baseline cerebrovascular reactivity is a risk factor for later development of ePVS.

Sections du résumé

BACKGROUND BACKGROUND
Increasing evidence suggests that enlarged perivascular spaces (ePVS) are associated with cognitive dysfunction in aging. However, the pathogenesis of ePVS remains unknown. Here, we tested the possibility that baseline cerebrovascular dysfunction, as measured by a magnetic resonance imaging measure of cerebrovascular reactivity, contributes to the later development of ePVS.
METHODS METHODS
Fifty cognitively unimpaired, older adults (31 women; age range, 60-84 years) underwent magnetic resonance imaging scanning at baseline and follow-up separated by ≈2.5 years. ePVS were counted in the basal ganglia, centrum semiovale, midbrain, and hippocampus. Cerebrovascular reactivity, an index of the vasodilatory capacity of cerebral small vessels, was assessed using carbon dioxide inhalation while acquiring blood oxygen level-dependent magnetic resonance images.
RESULTS RESULTS
Low baseline cerebrovascular reactivity values in the basal ganglia were associated with increased follow-up ePVS counts in the basal ganglia after controlling for age, sex, and baseline ePVS values (estimate [SE]=-3.18 [0.96];
CONCLUSIONS CONCLUSIONS
Our results demonstrate that low baseline cerebrovascular reactivity is a risk factor for later development of ePVS.

Identifiants

pubmed: 37712232
doi: 10.1161/STROKEAHA.123.043882
pmc: PMC10615859
mid: NIHMS1927991
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2785-2793

Subventions

Organisme : NIBIB NIH HHS
ID : P41 EB031771
Pays : United States
Organisme : NINDS NIH HHS
ID : RF1 NS122028
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG072946
Pays : United States
Organisme : NIA NIH HHS
ID : F30 AG079506
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG068055
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG055449
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG028383
Pays : United States

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Auteurs

T J Libecap (TJ)

Department of Neuroscience (T.J.L., C.E.B., V.Z., C.A.P., B.T.G.), University of Kentucky College of Medicine, Lexington.

Christopher E Bauer (CE)

Department of Neuroscience (T.J.L., C.E.B., V.Z., C.A.P., B.T.G.), University of Kentucky College of Medicine, Lexington.

Valentinos Zachariou (V)

Department of Neuroscience (T.J.L., C.E.B., V.Z., C.A.P., B.T.G.), University of Kentucky College of Medicine, Lexington.

Colleen A Pappas (CA)

Department of Neuroscience (T.J.L., C.E.B., V.Z., C.A.P., B.T.G.), University of Kentucky College of Medicine, Lexington.

Flavius D Raslau (FD)

Department of Radiology (F.D.R., B.T.G.), University of Kentucky College of Medicine, Lexington.

Peiying Liu (P)

Department of Radiology, University of Maryland School of Medicine, Baltimore (P.L.).

Hanzhang Lu (H)

Department of Radiology, Johns Hopkins University School of Medicine, Baltimore, MD (H.L.).

Brian T Gold (BT)

Department of Neuroscience (T.J.L., C.E.B., V.Z., C.A.P., B.T.G.), University of Kentucky College of Medicine, Lexington.
Department of Radiology (F.D.R., B.T.G.), University of Kentucky College of Medicine, Lexington.
Magnetic Resonance Imaging and Spectroscopy Center, University of Kentucky, Lexington (B.T.G.).
Sanders-Brown Center on Aging University of Kentucky, Lexington (B.T.G.).

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Classifications MeSH