Literature DB >> 30012821

Perivascular Spaces Volume in Sporadic and Hereditary (Dutch-Type) Cerebral Amyloid Angiopathy.

Sergi Martinez-Ramirez1, Sanneke van Rooden2, Andreas Charidimou1, Anna Maria van Opstal2, Marieke Wermer2, M Edip Gurol1, Gisela Terwindt3, Jeroen van der Grond2, Steven M Greenberg1, Mark van Buchem2, Anand Viswanathan1.   

Abstract

Background and Purpose- Magnetic resonance imaging visible perivascular spaces in the centrum semiovale (CSO-PVS) have been associated with cerebral amyloid angiopathy (CAA).We aimed to further confirm this link by evaluating CSO-PVS volume in pathologically-demonstrated sporadic and genetically-demonstrated hereditary forms of the disease. Methods- We studied a retrospective hospital-based cohort consisting of 63 individuals aged >55 having brain magnetic resonance imaging and pathological assessment of CAA (mean age, 73.6±8.5; 46% female), and a separate cohort consisting of 26 carriers, and 28 noncarriers of the hereditary cerebral hemorrhage with amyloidosis-Dutch type (mean age, 46.7±12.8; 61.1% female). CSO-PVS volume was quantified on a single magnetic resonance imaging slice using a computer-assisted segmentation method and expressed as the relative volume of the intracranial volume in that particular slice (CSO-PVS relative volume). We compared CSO-PVS relative volume (1) between subjects with and without the disease in both cohorts; (2) between non-CAA, CAA without hemorrhage, and CAA with hemorrhage cases in the sporadic CAA cohort. All variables reaching P<0.1 in bivariate analyses were entered in logistic regression models. Results- In both sporadic and Dutch cohorts, cases with CAA had significantly higher CSO-PVS relative volume than cases without (median [IQR]: 3.7% [2.5-5.3] versus 1.8% [1.2-2.4], P<0.0001; 3.8% [0.6-6.2] versus 0.7% [0.4-1.6], P=0.007; respectively). In linear regression models, sporadic CAA was associated with higher CSO-PVS relative volume ( P=0.008). In the sporadic CAA cohort, compared with non-CAA cases, CSO-PVS relative volume was higher in both CAA with hemorrhage and without hemorrhage (4.4% [2.6-6.1] and 3% [2.4-3.6] versus 1.8% [1.2-2.4], P<0.001 and P=0.005, respectively). Higher CSO-PVS relative volume was associated with CAA in regression models, both when hemorrhage was present (odds ratio, 2.63; [95% confidence interval, 1.33-5.18]; P=0.005) and absent (odds ratio, 4.55; [95% confidence interval, 0.98-21.04]; P=0.05). Conclusions- Increased CSO-PVS volume is a consistent magnetic resonance imaging marker of cerebrovascular amyloid deposition and a promising diagnostic tool for sporadic CAA without hemorrhagic manifestations.

Entities:  

Keywords:  cerebral amyloid angiopathy; cerebral hemorrhage; drainage; neuroimaging; white matter

Mesh:

Year:  2018        PMID: 30012821      PMCID: PMC6202219          DOI: 10.1161/STROKEAHA.118.021137

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  40 in total

1.  Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis-Dutch type share a decrease in cerebrospinal fluid levels of amyloid beta-protein precursor.

Authors:  W E Van Nostrand; S L Wagner; J Haan; E Bakker; R A Roos
Journal:  Ann Neurol       Date:  1992-08       Impact factor: 10.422

2.  Investigating how peptide length and a pathogenic mutation modify the structural ensemble of amyloid beta monomer.

Authors:  Yu-Shan Lin; Gregory R Bowman; Kyle A Beauchamp; Vijay S Pande
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3.  Large Virchow-Robin spaces: MR-clinical correlation.

Authors:  L A Heier; C J Bauer; L Schwartz; R D Zimmerman; S Morgello; M D Deck
Journal:  AJNR Am J Neuroradiol       Date:  1989 Sep-Oct       Impact factor: 3.825

4.  DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)

Authors:  E Bakker; C van Broeckhoven; J Haan; E Voorhoeve; W van Hul; E Levy; I Lieberburg; M D Carman; G J van Ommen; B Frangione
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025

5.  Plasma beta-amyloid and white matter lesions in AD, MCI, and cerebral amyloid angiopathy.

Authors:  M E Gurol; M C Irizarry; E E Smith; S Raju; R Diaz-Arrastia; T Bottiglieri; J Rosand; J H Growdon; S M Greenberg
Journal:  Neurology       Date:  2006-01-10       Impact factor: 9.910

6.  White matter perivascular spaces: an MRI marker in pathology-proven cerebral amyloid angiopathy?

Authors:  Andreas Charidimou; Zane Jaunmuktane; Jean-Claude Baron; Matthew Burnell; Pascale Varlet; Andre Peeters; John Xuereb; Rolf Jäger; Sebastian Brandner; David J Werring
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7.  Enlarged perivascular spaces are associated with cognitive function in healthy elderly men.

Authors:  A M J Maclullich; J M Wardlaw; K J Ferguson; J M Starr; J R Seckl; I J Deary
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-11       Impact factor: 10.154

8.  Cortical and leptomeningeal cerebrovascular amyloid and white matter pathology in Alzheimer's disease.

Authors:  Alex E Roher; Yu-Min Kuo; Chera Esh; Carmen Knebel; Nicole Weiss; Walter Kalback; Dean C Luehrs; Jennifer L Childress; Thomas G Beach; Roy O Weller; Tyler A Kokjohn
Journal:  Mol Med       Date:  2003 Mar-Apr       Impact factor: 6.354

9.  Hereditary cerebral haemorrhage caused by cortical amyloid angiopathy.

Authors:  W Luyendijk; G T Bots; M Vegter-van der Vlis; L N Went; B Frangione
Journal:  J Neurol Sci       Date:  1988-07       Impact factor: 3.181

Review 10.  Towards the automatic computational assessment of enlarged perivascular spaces on brain magnetic resonance images: a systematic review.

Authors:  Maria del C Valdés Hernández; Rory J Piper; Xin Wang; Ian J Deary; Joanna M Wardlaw
Journal:  J Magn Reson Imaging       Date:  2013-02-25       Impact factor: 4.813

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2.  Perivascular space dilation is associated with vascular amyloid-β accumulation in the overlying cortex.

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3.  MRI-Visible Perivascular Spaces in the Centrum Semiovale Are Associated with Brain Amyloid Deposition in Patients with Alzheimer Disease-Related Cognitive Impairment.

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4.  Centrum Semiovale Perivascular Space and Amyloid Deposition in Spontaneous Intracerebral Hemorrhage.

Authors:  Hsin-Hsi Tsai; Marco Pasi; Li-Kai Tsai; Chi-Ching Huang; Ya-Fang Chen; Bo-Ching Lee; Ruoh-Fang Yen; M Edip Gurol; Jiann-Shing Jeng
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5.  Longitudinal Progression of Magnetic Resonance Imaging Markers and Cognition in Dutch-Type Hereditary Cerebral Amyloid Angiopathy.

Authors:  Suzanne E van Dijk; Jeroen van der Grond; Jessie Lak; Annette van den Berg-Huysmans; Gerda Labadie; Gisela M Terwindt; Marieke J H Wermer; M Edip Gurol; Mark A van Buchem; Steven M Greenberg; Sanneke van Rooden
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6.  Topological relationships between perivascular spaces and progression of white matter hyperintensities: A pilot study in a sample of the Lothian Birth Cohort 1936.

Authors:  Abbie Barnes; Lucia Ballerini; Maria Del C Valdés Hernández; Francesca M Chappell; Susana Muñoz Maniega; Rozanna Meijboom; Ellen V Backhouse; Michael S Stringer; Roberto Duarte Coello; Rosalind Brown; Mark E Bastin; Simon R Cox; Ian J Deary; Joanna M Wardlaw
Journal:  Front Neurol       Date:  2022-08-24       Impact factor: 4.086

7.  Reduced Levels of Cerebrospinal Fluid/Plasma Aβ40 as an Early Biomarker for Cerebral Amyloid Angiopathy in RTg-DI Rats.

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Journal:  Int J Mol Sci       Date:  2020-01-01       Impact factor: 5.923

8.  Association between arterial stiffness and the presence of cerebral small vessel disease markers.

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Review 9.  Imaging for central nervous system (CNS) interstitial fluidopathy: disorders with impaired interstitial fluid dynamics.

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10.  Prevalence of cerebral amyloid angiopathy: A systematic review and meta-analysis.

Authors:  Lieke Jäkel; Anna M De Kort; Catharina J M Klijn; Floris H B M Schreuder; Marcel M Verbeek
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  10 in total

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