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...
Autores principales: | , , , , , , , |
---|---|
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 |