Cargando…

Topography and Determinants of Magnetic Resonance Imaging (MRI)‐Visible Perivascular Spaces in a Large Memory Clinic Cohort

BACKGROUND: Magnetic resonance imaging‐visible perivascular spaces (PVS) are related to interstitial fluid clearance pathways (including amyloid‐β) in the brain and are suggested to be a marker of cerebral small vessel disease. We investigated the role, topography, and possible implications of PVS i...

Descripción completa

Detalles Bibliográficos
Autores principales: Shams, Sara, Martola, Juha, Charidimou, Andreas, Larvie, Mykol, Granberg, Tobias, Shams, Mana, Kristoffersen‐Wiberg, Maria, Wahlund, Lars‐Olof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634282/
https://www.ncbi.nlm.nih.gov/pubmed/28939709
http://dx.doi.org/10.1161/JAHA.117.006279
_version_ 1783270057002926080
author Shams, Sara
Martola, Juha
Charidimou, Andreas
Larvie, Mykol
Granberg, Tobias
Shams, Mana
Kristoffersen‐Wiberg, Maria
Wahlund, Lars‐Olof
author_facet Shams, Sara
Martola, Juha
Charidimou, Andreas
Larvie, Mykol
Granberg, Tobias
Shams, Mana
Kristoffersen‐Wiberg, Maria
Wahlund, Lars‐Olof
author_sort Shams, Sara
collection PubMed
description BACKGROUND: Magnetic resonance imaging‐visible perivascular spaces (PVS) are related to interstitial fluid clearance pathways (including amyloid‐β) in the brain and are suggested to be a marker of cerebral small vessel disease. We investigated the role, topography, and possible implications of PVS in cognitive impairment. METHODS AND RESULTS: A total of 1504 patients undergoing memory clinic investigation and an associated brain magnetic resonance imaging scan were included in this cross‐sectional study. Magnetic resonance images were assessed for markers of small vessel disease. Additionally, 1039 patients had cerebrospinal fluid analysis of amyloid‐β 42, total tau (T‐tau), and phosphorylated tau (P‐tau); 520 patients had apoE genotyping done. Results were analyzed with generalized linear models. A total of 289 (19%; 95% confidence interval, 17–21) had a high‐grade PVS in the centrum semiovale (CSO) and 65 (4%; 95% confidence interval: 3%–5%) in the basal ganglia (BG). Centrum semiovale– and BG‐PVS were both associated with high age (P<0.001), hypertension (P<0.001), probable cerebral amyloid angiopathy (P<0.05), moderate‐to‐severe white matter hyperintensities (P<0.001), cortical superficial siderosis (P<0.001), cerebral microbleeds (P<0.001), and PVS. centrum semiovale–PVS was separately associated with strictly lobar cerebral microbleeds (P=0.057). BG‐PVS was associated with strictly deep cerebral microbleeds (P<0.001), lacunes (P<0.001), and vascular dementia (P=0.04). BG‐PVS showed a tendency to be associated with high cerebrospinal fluid tau (B=0.002, P=0.04) in the whole cohort and in Alzheimer's disease (B=0.005; P=0.02). No other associations with cerebrospinal fluid or the apoE e4 allele was observed. CONCLUSIONS: Centrum semiovale–PVS and BG‐PVS have different underlying etiology, being associated with cerebral amyloid angiopathy and hypertensive vasculopathy, respectively, although a significant overlap between these pathologies is likely to exist.
format Online
Article
Text
id pubmed-5634282
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-56342822017-10-18 Topography and Determinants of Magnetic Resonance Imaging (MRI)‐Visible Perivascular Spaces in a Large Memory Clinic Cohort Shams, Sara Martola, Juha Charidimou, Andreas Larvie, Mykol Granberg, Tobias Shams, Mana Kristoffersen‐Wiberg, Maria Wahlund, Lars‐Olof J Am Heart Assoc Original Research BACKGROUND: Magnetic resonance imaging‐visible perivascular spaces (PVS) are related to interstitial fluid clearance pathways (including amyloid‐β) in the brain and are suggested to be a marker of cerebral small vessel disease. We investigated the role, topography, and possible implications of PVS in cognitive impairment. METHODS AND RESULTS: A total of 1504 patients undergoing memory clinic investigation and an associated brain magnetic resonance imaging scan were included in this cross‐sectional study. Magnetic resonance images were assessed for markers of small vessel disease. Additionally, 1039 patients had cerebrospinal fluid analysis of amyloid‐β 42, total tau (T‐tau), and phosphorylated tau (P‐tau); 520 patients had apoE genotyping done. Results were analyzed with generalized linear models. A total of 289 (19%; 95% confidence interval, 17–21) had a high‐grade PVS in the centrum semiovale (CSO) and 65 (4%; 95% confidence interval: 3%–5%) in the basal ganglia (BG). Centrum semiovale– and BG‐PVS were both associated with high age (P<0.001), hypertension (P<0.001), probable cerebral amyloid angiopathy (P<0.05), moderate‐to‐severe white matter hyperintensities (P<0.001), cortical superficial siderosis (P<0.001), cerebral microbleeds (P<0.001), and PVS. centrum semiovale–PVS was separately associated with strictly lobar cerebral microbleeds (P=0.057). BG‐PVS was associated with strictly deep cerebral microbleeds (P<0.001), lacunes (P<0.001), and vascular dementia (P=0.04). BG‐PVS showed a tendency to be associated with high cerebrospinal fluid tau (B=0.002, P=0.04) in the whole cohort and in Alzheimer's disease (B=0.005; P=0.02). No other associations with cerebrospinal fluid or the apoE e4 allele was observed. CONCLUSIONS: Centrum semiovale–PVS and BG‐PVS have different underlying etiology, being associated with cerebral amyloid angiopathy and hypertensive vasculopathy, respectively, although a significant overlap between these pathologies is likely to exist. John Wiley and Sons Inc. 2017-09-22 /pmc/articles/PMC5634282/ /pubmed/28939709 http://dx.doi.org/10.1161/JAHA.117.006279 Text en © 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
Shams, Sara
Martola, Juha
Charidimou, Andreas
Larvie, Mykol
Granberg, Tobias
Shams, Mana
Kristoffersen‐Wiberg, Maria
Wahlund, Lars‐Olof
Topography and Determinants of Magnetic Resonance Imaging (MRI)‐Visible Perivascular Spaces in a Large Memory Clinic Cohort
title Topography and Determinants of Magnetic Resonance Imaging (MRI)‐Visible Perivascular Spaces in a Large Memory Clinic Cohort
title_full Topography and Determinants of Magnetic Resonance Imaging (MRI)‐Visible Perivascular Spaces in a Large Memory Clinic Cohort
title_fullStr Topography and Determinants of Magnetic Resonance Imaging (MRI)‐Visible Perivascular Spaces in a Large Memory Clinic Cohort
title_full_unstemmed Topography and Determinants of Magnetic Resonance Imaging (MRI)‐Visible Perivascular Spaces in a Large Memory Clinic Cohort
title_short Topography and Determinants of Magnetic Resonance Imaging (MRI)‐Visible Perivascular Spaces in a Large Memory Clinic Cohort
title_sort topography and determinants of magnetic resonance imaging (mri)‐visible perivascular spaces in a large memory clinic cohort
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634282/
https://www.ncbi.nlm.nih.gov/pubmed/28939709
http://dx.doi.org/10.1161/JAHA.117.006279
work_keys_str_mv AT shamssara topographyanddeterminantsofmagneticresonanceimagingmrivisibleperivascularspacesinalargememorycliniccohort
AT martolajuha topographyanddeterminantsofmagneticresonanceimagingmrivisibleperivascularspacesinalargememorycliniccohort
AT charidimouandreas topographyanddeterminantsofmagneticresonanceimagingmrivisibleperivascularspacesinalargememorycliniccohort
AT larviemykol topographyanddeterminantsofmagneticresonanceimagingmrivisibleperivascularspacesinalargememorycliniccohort
AT granbergtobias topographyanddeterminantsofmagneticresonanceimagingmrivisibleperivascularspacesinalargememorycliniccohort
AT shamsmana topographyanddeterminantsofmagneticresonanceimagingmrivisibleperivascularspacesinalargememorycliniccohort
AT kristoffersenwibergmaria topographyanddeterminantsofmagneticresonanceimagingmrivisibleperivascularspacesinalargememorycliniccohort
AT wahlundlarsolof topographyanddeterminantsofmagneticresonanceimagingmrivisibleperivascularspacesinalargememorycliniccohort