Evidence map›Paper›PMID 38886875›Full record

ArticleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2024

Microstructural white matter damage on MRI is associated with disease severity in Dutch-type cerebral amyloid angiopathy.

Ingeborg Rasing, Naomi Vlegels, Manon R Schipper, Sabine Voigt, Emma A Koemans, Kanishk Kaushik, Rosemarie van Dort, Thijs W van Harten, Alberto De Luca, Ellis S van Etten and 8 more

Abstract read
In one paragraph

Article in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

18 authors.

Ingeborg RasingDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Naomi VlegelsDepartment of Neurology and Neurosurgery, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Manon R SchipperDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0003-1463-0997
Sabine VoigtDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Emma A KoemansDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Kanishk KaushikDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0003-1429-6853
Rosemarie van DortDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Thijs W van HartenDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-3408-9379
Alberto De LucaDepartment of Neurology and Neurosurgery, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Ellis S van EttenDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Erik W van ZwetDepartment of Biostatistics, Leiden University Medical Center, Leiden, The Netherland.
Mark A van BuchemDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
Huub Am MiddelkoopDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Geert Jan BiesselsDepartment of Neurology and Neurosurgery, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Gisela M TerwindtDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Matthias Jp van OschDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-7034-8959
Marianne Aa van WalderveenDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
Marieke Jh WermerDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peak width of skeletonized mean diffusivity (PSMD) is an emerging diffusion-MRI based marker to study subtle early alterations to white matter microstructure. We assessed PSMD over the clinical continuum in Dutch-type hereditary CAA (D-CAA) and its association with other CAA-related MRI-markers and cognitive symptoms. We included (pre)symptomatic D-CAA mutation-carriers and calculated PSMD from diffusion-MRI data. Associations between PSMD-levels, cognitive performance and CAA-related MRI-markers were assessed with linear regression models. We included 59 participants (25/34 presymptomatic/symptomatic; mean age 39/58 y). PSMD-levels increased with disease severity and were higher in symptomatic D-CAA mutation-carriers (median [range] 4.90 [2.77-9.50]mm

Indexed as

White MatterAdultAgedCerebral Amyloid AngiopathyCerebral Amyloid Angiopathy, FamilialDiffusion Magnetic Resonance ImagingFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedMutationSeverity of Illness IndexCerebral amyloid angiopathycognitive impairmentdiffusion magnetic resonance imagingDutch-type hereditary cerebral amyloid angiopathyMRI CAA-small vessel disease burden

Identifiers

PMID38886875
PMCPMC11542140

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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.