Evidence map›Paper›PMID 36215784›Full record

ArticleJournal of communication disorders

Aphasia severity is modulated by race and lesion size in chronic survivors: A retrospective study.

Davetrina S Gadson, Deliya B Wesley, Candace M van der Stelt, Elizabeth Lacey, Andrew T DeMarco, Sarah F Snider, Peter E Turkeltaub

Open access · greenAbstract read
In one paragraph

Article in Journal of communication disorders. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Davetrina S GadsonCenter for Brain Plasticity and Recovery, Georgetown University School of Medicine, Washington, (DC), USA; Georgetown University Medical Center, Washington, DC, USA. Electronic address: dg988@georgetown.edu.
Deliya B WesleyMedStar Health Research Institute, Hyattsville, MD, USA.
Candace M van der SteltCenter for Brain Plasticity and Recovery, Georgetown University School of Medicine, Washington, (DC), USA; Center for Aphasia Research and Rehabilitation, Georgetown University School of Medicine, Washington, (DC), USA.
Elizabeth LaceyCenter for Brain Plasticity and Recovery, Georgetown University School of Medicine, Washington, (DC), USA; Center for Aphasia Research and Rehabilitation, Georgetown University School of Medicine, Washington, (DC), USA; Research Division, MedStar National Rehabilitation Hospital, Washington, (DC), USA; Georgetown University Medical Center, Washington, DC, USA; Medstar National Rehabilitation Hospital, Washington, DC, USA.
Andrew T DeMarcoCenter for Brain Plasticity and Recovery, Georgetown University School of Medicine, Washington, (DC), USA; Center for Aphasia Research and Rehabilitation, Georgetown University School of Medicine, Washington, (DC), USA.
Sarah F SniderCenter for Aphasia Research and Rehabilitation, Georgetown University School of Medicine, Washington, (DC), USA.
Peter E TurkeltaubCenter for Brain Plasticity and Recovery, Georgetown University School of Medicine, Washington, (DC), USA; Center for Aphasia Research and Rehabilitation, Georgetown University School of Medicine, Washington, (DC), USA; Research Division, MedStar National Rehabilitation Hospital, Washington, (DC), USA; Georgetown University Medical Center, Washington, DC, USA; Medstar National Rehabilitation Hospital, Washington, DC, USA.
Georgetown University · USMedStar National Rehabilitation Hospital · USMedStar Health · US

Funding

Contributions of spared brain structures and connections to aphasia recoveryR01DC014960 · NIDCD · GEORGETOWN UNIVERSITY · PI TURKELTAUB, PETER ETHAN · 2017 to 2021
$4.0M
Neurorehabilitation and Restorative Neuroscience NetworkK12HD093427 · NICHD · GEORGETOWN UNIVERSITY · PI BREGMAN, BARBARA S, DROMERICK, ALEXANDER W · 2017 to 2021
$3.9M
Functional anomaly mapping of aphasia recoveryK99DC018828 · NIDCD · GEORGETOWN UNIVERSITY · PI DEMARCO, ANDREW T · 2021 to 2022
$242k
NICHD NIH HHS K12 HD093427NIDCD NIH HHS K99 DC018828NIDCD NIH HHS R01 DC014960
6 · The paper itself

Abstract

introductionIn stroke survivors with aphasia (SWA), differences in behavioral language performance have been observed between Black and White Americans. These racial differences in aphasia outcomes may reflect biological stroke severity, disparities in access to care, potential assessment bias, or interactions between these factors and race. Understanding the origin of disparities in aphasia outcomes is critical to any efforts to promote health equity among SWA. In this study, we explore aphasia outcomes by examining the relationship between race, socioeconomic status, and neurological factors in SWA.

methodEighty-five chronic left-hemisphere SWA (31 Black, 54 White) participated in the study. The primary aphasia outcome measure was the Western Aphasia Battery-Revised (WAB-R). Lesion size was measured based on manual lesion segmentations. FLAIR and T2 images were scored for severity of white matter disease. Independent sample t-tests were used to determine differences by race in education, age, income, aphasia severity, white matter disease, and lesion size. A linear regression model was used to explore factors that predicted aphasia severity on the WAB-R.

resultLevel of education and estimated income differed by race in our sample. For predictors of aphasia severity, the regression model revealed a significant effect of lesion size on WAB Aphasia Quotient and an interaction of race x lesion size, such that Black and White participants with small lesions had similar WAB scores, but in individuals with larger lesions, Black participants had lower WAB scores than White participants.

conclusionWe suggest two explanations for the difference between Black and White SWA in the relationship between lesion size and aphasia severity. First, the impact of disparities in access to rehabilitation after stroke may be more evident when a stroke is larger and causes significant aphasia. Additionally, an assessment bias in aphasia outcome measures may be more evident with increasing severity of aphasia. Future studies should further discern the drivers of observed disparities in aphasia outcomes in order to identify opportunities to improve equity in aphasia care.

Indexed as

AphasiaLeukoencephalopathiesStrokeHealth PromotionHumansRetrospective StudiesSurvivorsAfrican-American, LanguageAphasiaLanguageLesion symptom mappingStrokeWestern aphasia battery

Identifiers

PMID36215784
PMCPMC11744488
OpenAlexW4302009898

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.