Evidence map›Paper›PMID 38444323›Full record

ArticleInternational journal of stroke : official journal of the International Stroke Society2024

Sensitivity of the Boston criteria version 2.0 in Dutch-type hereditary cerebral amyloid angiopathy.

Rgj van der Zwet, E A Koemans, S Voigt, R van Dort, I Rasing, K Kaushik, T W van Harten, M R Schipper, G M Terwindt, Mjp van Osch and 3 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of stroke : official journal of the International Stroke Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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

13 authors at 2 institutions in 1 country.

Rgj van der ZwetDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0003-4578-1376
E A KoemansDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0003-0560-8077
S VoigtDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-5182-6676
R van DortDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-7777-3189
I RasingDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
K KaushikDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0003-1429-6853
T W van HartenDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-3408-9379
M R SchipperDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
G M TerwindtDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Mjp van OschDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
Maa van WalderveenDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
E S van EttenDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Mjh WermerDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Leiden University Medical Center · NLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimThe revised Boston criteria v2.0 for cerebral amyloid angiopathy (CAA) add two radiological markers to the existing criteria: severe visible perivascular spaces in the centrum semiovale and white matter hyperintensities (WMHs) in a multispot pattern. This study aims to determine the sensitivity of the updated criteria in mutation carriers with Dutch-type hereditary CAA (D-CAA) in an early and later disease stage.

methodsIn this cross-sectional study, we included presymptomatic and symptomatic D-CAA mutation carriers from our prospective natural history study (AURORA) at the Leiden University Medical Center between 2018 and 2021. 3-Tesla scans were assessed for CAA-related magnetic resonance imaging (MRI) markers. We compared the sensitivity of the Boston criteria v2.0 to the previously used modified Boston criteria v1.5.

resultsWe included 64 D-CAA mutation carriers (mean age 49 years, 55% women, 55% presymptomatic). At least one white matter (WM) feature was seen in 55/64 mutation carriers (86%: 74% presymptomatic, 100% symptomatic). Fifteen (23%) mutation carriers, all presymptomatic, showed only WM features and no hemorrhagic markers. The sensitivity for probable CAA was similar between the new and the previous criteria: 11/35 (31%) in presymptomatic mutation carriers and 29/29 (100%) in symptomatic mutation carriers. The sensitivity for possible CAA in presymptomatic mutation carriers increased from 0/35 (0%) to 15/35 (43%) with the new criteria.

conclusionThe Boston criteria v2.0 increase the sensitivity for detecting possible CAA in presymptomatic D-CAA mutation carriers and, therefore, improve the detection of the early phase of CAA.

Indexed as

Cerebral Amyloid Angiopathy, FamilialMagnetic Resonance ImagingAdultCross-Sectional StudiesFemaleHumansMaleMiddle AgedMutationNetherlandsProspective StudiesSensitivity and SpecificityWhite Mattercerebral amyloid angiopathyIntracerebral hemorrhagesmall vessel disease

Identifiers

PMID38444323
PMCPMC11408943
OpenAlexW4392516379

What OpenQuestion holds

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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.