Evidence map›Paper›PMID 40198864›Full record

ArticleNeurology2025

One-Year Radiologic Progression in Sporadic and Hereditary Cerebral Amyloid Angiopathy.

Maaike C van der Plas, Emma A Koemans, Manon R Schipper, Sabine Voigt, Ingeborg Rasing, Reinier G J van der Zwet, Kanishk Kaushik, Rosemarie van Dort, Sanne Schriemer, Thijs W van Harten and 6 more

Abstract read
In one paragraph

Article in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

16 authors.

Maaike C van der PlasDepartment of Neurology, Leiden University Medical Center, the Netherlands.ORCID 0000-0002-1437-5482
Emma A KoemansDepartment of Neurology, Leiden University Medical Center, the Netherlands.
Manon R SchipperDepartment of Radiology, Leiden University Medical Center, the Netherlands.
Sabine VoigtDepartment of Neurology, Leiden University Medical Center, the Netherlands.
Ingeborg RasingDepartment of Neurology, Leiden University Medical Center, the Netherlands.ORCID 0000-0002-0953-7133
Reinier G J van der ZwetDepartment of Neurology, Leiden University Medical Center, the Netherlands.
Kanishk KaushikDepartment of Neurology, Leiden University Medical Center, the Netherlands.ORCID 0000-0003-1429-6853
Rosemarie van DortDepartment of Neurology, Leiden University Medical Center, the Netherlands.
Sanne SchriemerDepartment of Neurology, Leiden University Medical Center, the Netherlands.
Thijs W van HartenDepartment of Radiology, Leiden University Medical Center, the Netherlands.
Erik van ZwetDepartment of Biomedical Data Sciences, Leiden University Medical Center, the Netherlands; and.ORCID 0000-0001-5537-3179
Ellis S van EttenDepartment of Neurology, Leiden University Medical Center, the Netherlands.ORCID 0000-0002-8301-6846
Matthias J P van OschDepartment of Radiology, Leiden University Medical Center, the Netherlands.ORCID 0000-0001-7034-8959
Gisela M TerwindtDepartment of Neurology, Leiden University Medical Center, the Netherlands.ORCID 0000-0003-3140-6882
Marianne van WalderveenDepartment of Radiology, Leiden University Medical Center, the Netherlands.ORCID 0000-0003-4895-229X
Marieke J H WermerDepartment of Neurology, University Medical Center Groningen, the Netherlands.ORCID 0000-0002-6838-9521

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesKnowledge on the short-term progression of cerebral amyloid angiopathy (CAA) is important for clinical practice and the design of clinical treatment trials. We investigated the 1-year progression of CAA-related MRI markers in sporadic (sCAA) and Dutch-type hereditary (D-CAA).

methodsParticipants were included from 2 prospective cohort studies. 3T-MRI was performed at baseline and after 1 year. We assessed macrobleeds, cerebral microbleeds (CMBs), cortical superficial siderosis (cSS), convexity subarachnoid hemorrhages (cSAHs), white matter hyperintensities (WMH), enlarged centrum semiovale perivascular spaces (CSO-EPVS), and visually stimulated blood oxygenation level-dependent (BOLD) fMRI parameters. Progression was defined as increase in number of macrobleeds or CMBs, new focus or extension of cSS, increase in CSO-EPVS category, or volume increase of >10% of WMH. Multivariable regression analyses were performed to determine factors associated with progression and the association between events related to parenchymal injury (cSAH, macrobleeds) and radiologic progression.

resultsWe included 98 participants (47% women): 55 with sCAA (mean age 70 years), 28 with symptomatic D-CAA (mean age 59 years), and 15 with presymptomatic D-CAA (mean age 45 years). Progression of >1 MRI markers was seen in all 83 (100%) participants with sCAA and symptomatic D-CAA and in 9 (60%) with presymptomatic D-CAA. The number of CMBs showed the largest progression in sCAA (98%; median increase 24) and symptomatic D-CAA (100%; median increase 58). WMH volume (>10% increase in 70%; mean increase 1.2 mL) was most progressive in presymptomatic D-CAA. A decrease in the upslope of the visually evoked BOLD response was observed for most patients. Symptomatic D-CAA status was associated with more overall progression (adjusted odds ratio [aOR] 9.7; 95% CI 1.7-54.2), CMB (adjusted relative risk [aRR] 2.47; 95% CI 1.5-4.1), and WMH volume progression (β 2.52; 95% CI 0.3-4.8). Baseline CMB count (aRR 1.002; 95% CI 1.001-1.002) was associated with CMB progression and cSS presence at baseline (aOR 8.16; 95% CI 2.6-25.4) with cSS progression. cSS progression was also associated with cSAH and macrobleeds (aOR 21,029; 95% CI 2.042-216.537). DISCUSSION: CAA is a radiologically progressive disease even in the short-term. After 1 year, all symptomatic and most of the presymptomatic participants showed progression of at least 1 MRI-marker. CMBs and WMH volume (in symptomatic CAA) and WMH volume (in presymptomatic CAA) are the most promising markers to track short-term progression in future trials.

Indexed as

BrainCerebral Amyloid AngiopathyCerebral Amyloid Angiopathy, FamilialDisease ProgressionAgedCohort StudiesFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedProspective Studies

Identifiers

PMID40198864
PMCPMC11995281

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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.