Evidence map›Paper›PMID 39271504›Full record

ArticleJournal of neurology2024

Genetic diagnosis of individuals at risk of CADASIL: prospect for future therapeutic development.

Madeleine Akrich, Vololona Rabeharisoa, Florence Paterson, Hugues Chabriat

Abstract read
In one paragraph

Article in Journal of neurology, 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. Novel Mutation ofBalkan journal of medical genetics : BJMG · 2025
    Article
  2. 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

4 authors.

Madeleine AkrichCSI-Centre de Sociologie de l'innovation, i3, UMR CNRS, Mines Paris, Paris Sciences & Lettres, Paris, France. madeleine.akrich@minesparis.psl.eu.
Vololona RabeharisoaCSI-Centre de Sociologie de l'innovation, i3, UMR CNRS, Mines Paris, Paris Sciences & Lettres, Paris, France.
Florence PatersonCSI-Centre de Sociologie de l'innovation, i3, UMR CNRS, Mines Paris, Paris Sciences & Lettres, Paris, France.
Hugues ChabriatCERVCO and INSERM U1134, Centre Neurovasculaire translationnel, FHU-NeuroVasc, Hôpital Lariboisière, Université Paris Cité et APHP, Paris, France. hugues.chabriat@aphp.fr.ORCID http://orcid.org/0000-0001-8436-6074

Funding

Agence Nationale de la Recherche RHU TRT_cSVD
6 · The paper itself

Abstract

CADASIL is the most frequent hereditary cerebral small vessel disease worldwide. The disease is responsible for a slow and progressive accumulation of cerebral ischemic insults that lead to disabling cognitive and motor symptoms at late age. Although there is currently no cure for this condition, future therapies may concern subjects only at early stage of the disease. This will raise the question of the participation of asymptomatic carriers of pathogenic NOTCH3 gene mutation in future clinical trials, which will presuppose acceptance of presymptomatic genetic diagnosis. In this study, we questioned the population at risk of CADASIL who had not undergone a diagnostic procedure yet. Based on a questionnaire survey carried out by an independent team of sociologists, we analyzed what underlies the choice of people at risk to undergo or not to undergo a genetic test, and what could constitute the tipping point that could lead people who were initially not interested in their diagnosis to have recourse to it. Our results suggest that, far from being a simple, unequivocal path, the decision-making process leading to the choice of diagnosis is initially slowed down by the need to distance oneself from the disease so that it doesn't take over one's life, and then evolves under the influence of a complex tangle between advancing age, the presence of early symptoms, and the personal relationship with uncertainty. It cannot be ruled out that the real and imminent prospect of therapy may also modify responses to this type of survey.

Indexed as

CADASILGenetic TestingReceptor, Notch3AdultAgedFemaleHumansMaleMiddle AgedSurveys and QuestionnairesNOTCH3 protein, humanReceptor, Notch3At-risk populationCADASILClinical TrialDecision makingFamily diseaseGenetic testingPresymptomatic diagnosis

Identifiers

PMID39271504
PMCPMC11447124

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.