Natalie Busby PhD , Roger Newman-Norlund PhD , Janina Wilmskoetter PhD , Lisa Johnson PhD , Chris Rorden PhD , Makayla Gibson BS , Rebecca Roth BA , Sarah Wilson MA , Julius Fridriksson PhD , Leonardo Bonilha MD, PhD
{"title":"Longitudinal Progression of White Matter Hyperintensity Severity in Chronic Stroke Aphasia","authors":"Natalie Busby PhD , Roger Newman-Norlund PhD , Janina Wilmskoetter PhD , Lisa Johnson PhD , Chris Rorden PhD , Makayla Gibson BS , Rebecca Roth BA , Sarah Wilson MA , Julius Fridriksson PhD , Leonardo Bonilha MD, PhD","doi":"10.1016/j.arrct.2023.100302","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>To determine whether longitudinal progression of small vessel disease in chronic stroke survivors is associated with longitudinal worsening of chronic aphasia severity.</p></div><div><h3>Design</h3><p>A longitudinal retrospective study. Severity of white matter hyperintensities (WMHs) as a marker for small vessel disease was assessed on fluid-attenuated inversion recovery (FLAIR) scans using the Fazekas scale, with ratings for deep WMHs (DWMHs) and periventricular WMHs (PVHs).</p></div><div><h3>Setting</h3><p>University research laboratories.</p></div><div><h3>Participants</h3><p>This study includes data from 49 chronic stroke survivors with aphasia (N=49; 15 women, 34 men, age range=32-81 years, >6 months post-stroke, stroke type: [46 ischemic, 3 hemorrhagic], community dwelling). All participants completed the Western Aphasia Battery-Revised (WAB) and had FLAIR scans at 2 timepoints (average years between timepoints: 1.87 years, <em>SD</em>=3.21 years).</p></div><div><h3>Interventions</h3><p>Not applicable.</p></div><div><h3>Main Outcome Measures</h3><p>Change in white matter hyperintensity severity (calculated using the Fazekas scale) and change in aphasia severity (difference in Western Aphasia Battery scores) were calculated between timepoints. Separate stepwise regression models were used to identify predictors of WMH severity change, with lesion volume, age, time between timepoints, body mass index (BMI), and presence of diabetes as independent variables. Additional stepwise regression models investigated predictors of change in aphasia severity, with PVH change, DWMH change, lesion volume, time between timepoints, and age as independent predictors.</p></div><div><h3>Results</h3><p>22.5% of participants (11/49) had increased WMH severity. Increased BMI was associated with increases in PVH severity (<em>P</em>=.007), whereas the presence of diabetes was associated with increased DWMH severity (<em>P</em>=.002). Twenty-five percent of participants had increased aphasia severity which was significantly associated with increased severity of PVH (<em>P</em><.001, 16.8% variance explained).</p></div><div><h3>Conclusion</h3><p>Increased small vessel disease burden is associated with contributing to chronic changes in aphasia severity. These findings support the idea that good cardiovascular risk factor control may play an important role in the prevention of long-term worsening of aphasic symptoms.</p></div>","PeriodicalId":72291,"journal":{"name":"Archives of rehabilitation research and clinical translation","volume":"5 4","pages":"Article 100302"},"PeriodicalIF":1.9000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590109523000642/pdfft?md5=e84995db1d84243e449f07fc876cf13a&pid=1-s2.0-S2590109523000642-main.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of rehabilitation research and clinical translation","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590109523000642","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"REHABILITATION","Score":null,"Total":0}
引用次数: 1
Abstract
Objective
To determine whether longitudinal progression of small vessel disease in chronic stroke survivors is associated with longitudinal worsening of chronic aphasia severity.
Design
A longitudinal retrospective study. Severity of white matter hyperintensities (WMHs) as a marker for small vessel disease was assessed on fluid-attenuated inversion recovery (FLAIR) scans using the Fazekas scale, with ratings for deep WMHs (DWMHs) and periventricular WMHs (PVHs).
Setting
University research laboratories.
Participants
This study includes data from 49 chronic stroke survivors with aphasia (N=49; 15 women, 34 men, age range=32-81 years, >6 months post-stroke, stroke type: [46 ischemic, 3 hemorrhagic], community dwelling). All participants completed the Western Aphasia Battery-Revised (WAB) and had FLAIR scans at 2 timepoints (average years between timepoints: 1.87 years, SD=3.21 years).
Interventions
Not applicable.
Main Outcome Measures
Change in white matter hyperintensity severity (calculated using the Fazekas scale) and change in aphasia severity (difference in Western Aphasia Battery scores) were calculated between timepoints. Separate stepwise regression models were used to identify predictors of WMH severity change, with lesion volume, age, time between timepoints, body mass index (BMI), and presence of diabetes as independent variables. Additional stepwise regression models investigated predictors of change in aphasia severity, with PVH change, DWMH change, lesion volume, time between timepoints, and age as independent predictors.
Results
22.5% of participants (11/49) had increased WMH severity. Increased BMI was associated with increases in PVH severity (P=.007), whereas the presence of diabetes was associated with increased DWMH severity (P=.002). Twenty-five percent of participants had increased aphasia severity which was significantly associated with increased severity of PVH (P<.001, 16.8% variance explained).
Conclusion
Increased small vessel disease burden is associated with contributing to chronic changes in aphasia severity. These findings support the idea that good cardiovascular risk factor control may play an important role in the prevention of long-term worsening of aphasic symptoms.