Literature DB >> 25096616

Visible Virchow-Robin spaces on magnetic resonance imaging of Alzheimer's disease patients and normal elderly from the Sunnybrook Dementia Study.

Joel Ramirez1, Courtney Berezuk1, Alicia A McNeely1, Christopher J M Scott1, Fuqiang Gao1, Sandra E Black2.   

Abstract

BACKGROUND: Visible Virchow-Robin spaces (VRS) are commonly used markers for small vessel disease in aging and dementia.
OBJECTIVE: However, as previous reports were based on subjective visual ratings, the goal of this project was to validate and apply an MRI-based quantitative measure of VRS as a potential neuroimaging biomarker.
METHODS: A modified version of Lesion Explorer was applied to MRIs from Alzheimer's disease patients (AD: n = 203) and normal elderly controls (NC: n = 94). Inter-rater reliability, technique validity, group/gender differences, and correlations with other small vessel disease markers were examined (lacunes and white matter hyperintensities, WMH).
RESULTS: Inter-rater reliability and spatial congruence was excellent (ICC = 0.99, SI = 0.96), and VRS volumes were highly correlated with established rating scales (CS: ρ = 0.84, p < 0.001; BG: ρ = 0.75, p < 0.001). Compared to NC, AD had significantly greater volumes of WMH (p < 0.01), lacunes (p < 0.001), and VRS in the white matter (p < 0.01), but not in the basal ganglia (n.s.). Compared to women, demented and non-demented men had greater VRS in the white matter (p < 0.001), but not in the basal ganglia (n.s.). Additionally, VRS were correlated with lacunes and WMH, but only in AD (r = 0.3, p < 0.01).
CONCLUSION: Compared to women, men may be more susceptible to greater volumes of VRS, particularly in the white matter. RESULTS support the hypothesis that VRS in the white matter may be more related to AD-related vascular pathology compared to VRS found in the basal ganglia. Future work using this novel VRS segmentation tool will examine its potential utility as an imaging biomarker of vascular rather than parenchymal amyloid.

Entities:  

Keywords:  Alzheimer's disease; Virchow-Robin; lacunes; perivascular spaces; small vessel disease; white matter hyperintensities

Mesh:

Year:  2015        PMID: 25096616     DOI: 10.3233/JAD-132528

Source DB:  PubMed          Journal:  J Alzheimers Dis        ISSN: 1387-2877            Impact factor:   4.472


  57 in total

1.  Large Perivascular Spaces Visible on Magnetic Resonance Imaging, Cerebral Small Vessel Disease Progression, and Risk of Dementia: The Age, Gene/Environment Susceptibility-Reykjavik Study.

Authors:  Jie Ding; Sigurður Sigurðsson; Pálmi V Jónsson; Gudny Eiriksdottir; Andreas Charidimou; Oscar L Lopez; Mark A van Buchem; Vilmundur Guðnason; Lenore J Launer
Journal:  JAMA Neurol       Date:  2017-09-01       Impact factor: 18.302

2.  Targeted Assessment of Enlargement of the Perivascular Space in Alzheimer's Disease and Vascular Dementia Subtypes Implicates Astroglial Involvement Specific to Alzheimer's Disease.

Authors:  Erin L Boespflug; Matthew J Simon; Emmalyn Leonard; Marjorie Grafe; Randall Woltjer; Lisa C Silbert; Jeffrey A Kaye; Jeffrey J Iliff
Journal:  J Alzheimers Dis       Date:  2018       Impact factor: 4.472

3.  Effects of traumatic brain injury on sleep and enlarged perivascular spaces.

Authors:  Ryan A Opel; Alison Christy; Erin L Boespflug; Kristianna B Weymann; Brendan Case; Jeffery M Pollock; Lisa C Silbert; Miranda M Lim
Journal:  J Cereb Blood Flow Metab       Date:  2018-08-10       Impact factor: 6.200

4.  Quantitative MRI of Perivascular Spaces at 3T for Early Diagnosis of Mild Cognitive Impairment.

Authors:  M Niazi; M Karaman; S Das; X J Zhou; P Yushkevich; K Cai
Journal:  AJNR Am J Neuroradiol       Date:  2018-08-09       Impact factor: 3.825

Review 5.  The Emerging Relationship Between Interstitial Fluid-Cerebrospinal Fluid Exchange, Amyloid-β, and Sleep.

Authors:  Erin L Boespflug; Jeffrey J Iliff
Journal:  Biol Psychiatry       Date:  2017-12-07       Impact factor: 13.382

Review 6.  Neuroimaging in Dementia.

Authors:  Adam M Staffaroni; Fanny M Elahi; Dana McDermott; Kacey Marton; Elissaios Karageorgiou; Simone Sacco; Matteo Paoletti; Eduardo Caverzasi; Christopher P Hess; Howard J Rosen; Michael D Geschwind
Journal:  Semin Neurol       Date:  2017-12-05       Impact factor: 3.420

7.  Characterization of MR Imaging-Visible Perivascular Spaces in the White Matter of Healthy Adolescents at 3T.

Authors:  J Piantino; E L Boespflug; D L Schwartz; M Luther; A M Morales; A Lin; R V Fossen; L Silbert; B J Nagel
Journal:  AJNR Am J Neuroradiol       Date:  2020-10-08       Impact factor: 3.825

Review 8.  Understanding the role of the perivascular space in cerebral small vessel disease.

Authors:  Rosalind Brown; Helene Benveniste; Sandra E Black; Serge Charpak; Martin Dichgans; Anne Joutel; Maiken Nedergaard; Kenneth J Smith; Berislav V Zlokovic; Joanna M Wardlaw
Journal:  Cardiovasc Res       Date:  2018-09-01       Impact factor: 10.787

9.  MR Imaging-based Multimodal Autoidentification of Perivascular Spaces (mMAPS): Automated Morphologic Segmentation of Enlarged Perivascular Spaces at Clinical Field Strength.

Authors:  Erin L Boespflug; Daniel L Schwartz; David Lahna; Jeffrey Pollock; Jeffrey J Iliff; Jeffrey A Kaye; William Rooney; Lisa C Silbert
Journal:  Radiology       Date:  2017-08-29       Impact factor: 11.105

Review 10.  [Importance of Virchow-Robin spaces].

Authors:  W Reith; A Haußmann
Journal:  Radiologe       Date:  2018-02       Impact factor: 0.635

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