Evidence map›Paper›PMID 36471099›Full record

ArticleJournal of neurology2023

White matter hyperintensities are an independent predictor of cognitive decline 3 years following first-ever stroke-results from the PROSCIS-B study.

Huma Fatima Ali, Lea Fast, Ahmed Khalil, Eberhard Siebert, Thomas Liman, Matthias Endres, Kersten Villringer, Anna Kufner

Open access · hybridAbstract read
In one paragraph

Article in Journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

11 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

8 authors at 5 institutions in 1 country.

Huma Fatima AliBerlin School of Mind and Brain, Humboldt-Universität zu Berlin, Berlin, Germany.
Lea FastKlinik für Psychiatrie and Psychotherapie, Charité, Universitätsmedizin Berlin, Berlin, Germany.
Ahmed KhalilBerlin School of Mind and Brain, Humboldt-Universität zu Berlin, Berlin, Germany.
Eberhard SiebertDepartment of Neuroradiology, University Hospital of Berlin (Charité), Berlin, Germany.
Thomas LimanCenter for Stroke Research Berlin (CSB), Klinik Für Neurologie, Charité, Universitätsmedizin Berlin, Charitéplatz 1, 10117, Berlin, Germany.
Matthias EndresCenter for Stroke Research Berlin (CSB), Klinik Für Neurologie, Charité, Universitätsmedizin Berlin, Charitéplatz 1, 10117, Berlin, Germany.
Kersten Villringer *Center for Stroke Research Berlin (CSB), Klinik Für Neurologie, Charité, Universitätsmedizin Berlin, Charitéplatz 1, 10117, Berlin, Germany.
Anna Kufner *Center for Stroke Research Berlin (CSB), Klinik Für Neurologie, Charité, Universitätsmedizin Berlin, Charitéplatz 1, 10117, Berlin, Germany. anna.kufner@charite.de.ORCID http://orcid.org/0000-0001-7433-313X
Charité - Universitätsmedizin Berlin · DEHumboldt-Universität zu Berlin · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEGerman Center for Neurodegenerative Diseases · DEGerman Centre for Cardiovascular Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhite matter hyperintensities (WMH) are the result of cerebral small vessel disease and may increase the risk of cognitive impairment (CI), recurrent stroke, and depression. We aimed to explore the association between selected cerebrovascular risk factors (CVRF) and WMH load as well as the effect of increased WMH burden on recurrent vascular events, CI, and depression in first-ever ischemic stroke patients.

methods431 from the PROSpective Cohort with Incident Stroke (PROSCIS) were included; Age-Related White Matter Changes (ARWMC) score was used to assess WMH burden on FLAIR. The presence of CVRF (defined via blood pressure, body-mass-index, and serological markers of kidney dysfunction, diabetes mellitus, and hyperlipoproteinemia) was categorized into normal, borderline, and pathological profiles based on commonly used clinical definitions. The primary outcomes included recurrent vascular events (combined endpoint of recurrent stroke, myocardial infarction and/or death), CI 3 years post-stroke, and depression 1-year post-stroke.

resultsThere was no clear association between CVRF profiles and WMH burden. High WMH lesion load (ARWMC score ≥ 10) was found to be associated with CI (adjusted OR 1.05 [95% CI 1.00-1.11]; p < 0.02) in a mixed-model analysis. Kaplan-Meier survival analysis showed a visible increase in the risk of recurrent vascular events following stroke; however, after adjustment, the risk was non-significant (HR 1.5 [95% CI 0.76-3]; p = 0.18). WMH burden was not associated with depression 1-year post stroke (adjusted OR 0.72 [95% CI 0.31-1.64]; p = 0.44).

conclusionHigher WMH burden was associated with a significant decline in cognition 3 years post-stroke in this cohort of first-ever stroke patients.

Indexed as

Cognitive DysfunctionStrokeWhite MatterCognitionHumansMagnetic Resonance ImagingProspective StudiesCerebrovascular risk factorsCognitive impairmentDepressionFirst-ever ischemic strokeRecurrent cerebrovascular eventsWhite matter hyperintensities

Identifiers

PMID36471099
PMCPMC9971076
OpenAlexW4310772616

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Registered trials

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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.