Literature DB >> 23864274

Incident lacunes preferentially localize to the edge of white matter hyperintensities: insights into the pathophysiology of cerebral small vessel disease.

Marco Duering1, Endy Csanadi, Benno Gesierich, Eric Jouvent, Dominique Hervé, Stephan Seiler, Boubakeur Belaroussi, Stefan Ropele, Reinhold Schmidt, Hugues Chabriat, Martin Dichgans.   

Abstract

White matter hyperintensities and lacunes are among the most frequent abnormalities on brain magnetic resonance imaging. They are commonly related to cerebral small vessel disease and associated with both stroke and dementia. We examined the spatial relationships between incident lacunes and white matter hyperintensities and related these findings to information on vascular anatomy to study possible mechanistic links between the two lesion types. Two hundred and seventy-six patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a genetically defined small vessel disease with mutations in the NOTCH3 gene were followed with magnetic resonance imaging over a total of 633 patient years. Using difference images and Jacobian maps from registered images we identified 104 incident lacunes. The majority (n = 95; 91.3%) of lacunes developed at the edge of a white matter hyperintensity whereas few lacunes were found to develop fully within (n = 6; 5.8%) or outside (n = 3; 2.9%) white matter hyperintensities. Adding information on vascular anatomy revealed that the majority of incident lacunes developed proximal to a white matter hyperintensity along the course of perforating vessels supplying the respective brain region. We further studied the spatial relationship between prevalent lacunes and white matter hyperintensities both in 365 patients with CADASIL and in 588 elderly subjects from the Austrian Stroke Prevention Study. The results were consistent with the results for incident lacunes. Lesion prevalence maps in different disease stages showed a spread of lesions towards subcortical regions in both cohorts. Our findings suggest that the mechanisms of lacunes and white matter hyperintensities are intimately connected and identify the edge of white matter hyperintensities as a predilection site for lacunes. Our observations further support and refine the concept of the white matter hyperintensity penumbra.

Entities:  

Keywords:  cerebral small vessel disease; lacunes; pathomechanisms; small vessel stroke; white matter hyperintensities

Mesh:

Substances:

Year:  2013        PMID: 23864274     DOI: 10.1093/brain/awt184

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  56 in total

Review 1.  Small vessel disease and memory loss: what the clinician needs to know to preserve patients' brain health.

Authors:  Christian Schenk; Timothy Wuerz; Alan J Lerner
Journal:  Curr Cardiol Rep       Date:  2013-12       Impact factor: 2.931

2.  Potassium channelopathy-like defect underlies early-stage cerebrovascular dysfunction in a genetic model of small vessel disease.

Authors:  Fabrice Dabertrand; Christel Krøigaard; Adrian D Bonev; Emmanuel Cognat; Thomas Dalsgaard; Valérie Domenga-Denier; David C Hill-Eubanks; Joseph E Brayden; Anne Joutel; Mark T Nelson
Journal:  Proc Natl Acad Sci U S A       Date:  2015-02-02       Impact factor: 11.205

3.  Different types of white matter hyperintensities in CADASIL: Insights from 7-Tesla MRI.

Authors:  François De Guio; Alexandre Vignaud; Hugues Chabriat; Eric Jouvent
Journal:  J Cereb Blood Flow Metab       Date:  2017-01-27       Impact factor: 6.200

Review 4.  Cerebral small vessel disease: neuroimaging markers and clinical implication.

Authors:  Xiaodong Chen; Jihui Wang; Yilong Shan; Wei Cai; Sanxin Liu; Mengyan Hu; Siyuan Liao; Xuehong Huang; Bingjun Zhang; Yuge Wang; Zhengqi Lu
Journal:  J Neurol       Date:  2018-10-05       Impact factor: 4.849

Review 5.  Cerebral small vessel disease: insights and opportunities from mouse models of collagen IV-related small vessel disease and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Authors:  Anne Joutel; Frank M Faraci
Journal:  Stroke       Date:  2014-02-06       Impact factor: 7.914

6.  Stroke outcomes are worse with larger leukoaraiosis volumes.

Authors:  Wi-Sun Ryu; Sung-Ho Woo; Dawid Schellingerhout; Min Uk Jang; Kyoung-Jong Park; Keun-Sik Hong; Sang-Wuk Jeong; Jeong-Yong Na; Ki-Hyun Cho; Joon-Tae Kim; Beom Joon Kim; Moon-Ku Han; Jun Lee; Jae-Kwan Cha; Dae-Hyun Kim; Soo Joo Lee; Youngchai Ko; Yong-Jin Cho; Byung-Chul Lee; Kyung-Ho Yu; Mi Sun Oh; Jong-Moo Park; Kyusik Kang; Kyung Bok Lee; Tai Hwan Park; Juneyoung Lee; Heung-Kook Choi; Kiwon Lee; Hee-Joon Bae; Dong-Eog Kim
Journal:  Brain       Date:  2016-12-22       Impact factor: 13.501

Review 7.  The current role of MRI in differentiating multiple sclerosis from its imaging mimics.

Authors:  Ruth Geraldes; Olga Ciccarelli; Frederik Barkhof; Nicola De Stefano; Christian Enzinger; Massimo Filippi; Monika Hofer; Friedemann Paul; Paolo Preziosa; Alex Rovira; Gabriele C DeLuca; Ludwig Kappos; Tarek Yousry; Franz Fazekas; Jette Frederiksen; Claudio Gasperini; Jaume Sastre-Garriga; Nikos Evangelou; Jacqueline Palace
Journal:  Nat Rev Neurol       Date:  2018-03-09       Impact factor: 42.937

Review 8.  Longitudinal change of small-vessel disease-related brain abnormalities.

Authors:  Reinhold Schmidt; Stephan Seiler; Marisa Loitfelder
Journal:  J Cereb Blood Flow Metab       Date:  2016-01       Impact factor: 6.200

9.  Periventricular hyperintensities are associated with elevated cerebral amyloid.

Authors:  Michael Marnane; Osama O Al-Jawadi; Shervin Mortazavi; Kathleen J Pogorzelec; Bing Wei Wang; Howard H Feldman; Ging-Yuek R Hsiung
Journal:  Neurology       Date:  2016-01-08       Impact factor: 9.910

Review 10.  Imaging Endophenotypes of Stroke as a Target for Genetic Studies.

Authors:  Xueqiu Jian; Myriam Fornage
Journal:  Stroke       Date:  2018-05-14       Impact factor: 7.914

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