Evidence map›Paper›PMID 42481725›Full record

ArticleJournal of neurology2026

Cerebellar cognitive affective syndrome (CCAS) and [18F]-FDG PET findings in spinocerebellar ataxia type SCA27B.

Laurine Cros, David Pellerin, Thomas Palpacuer, Salomé Puisieux, Solène Frismand, Armand Hocquel, Marion Wandzel, Virginie Roth, Carine Pourié, Bernard Brais and 8 more

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Article in Journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

18 authors.

Laurine CrosService de Neurologie, Centre Hospitalier Régional Universitaire de Nancy, Hôpital Central, Nancy, France.
David PellerinDr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.
Thomas PalpacuerService de Neurologie, Hôpitaux Civils de Colmar, Colmar, France.
Salomé PuisieuxService de Neurologie, Centre Hospitalier Régional Universitaire de Nancy, Hôpital Central, Nancy, France.
Solène FrismandService de Neurologie, Centre Hospitalier Régional Universitaire de Nancy, Hôpital Central, Nancy, France.
Armand HocquelService de Neurologie, Centre Hospitalier Régional Universitaire de Nancy, Hôpital Central, Nancy, France.
Marion WandzelLaboratoire de Génétique, CHRU de Nancy, Nancy, France.
Virginie RothLaboratoire de Génétique, CHRU de Nancy, Nancy, France.
Carine PouriéINSERM-U1256 NGERE, Université de Lorraine, Nancy, France.
Bernard BraisDepartment of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, QC, Canada.
Céline BonnetINSERM-U1256 NGERE, Université de Lorraine, Nancy, France.
Mylène MeyerService de Neurologie, Centre Hospitalier Régional Universitaire de Nancy, Hôpital Central, Nancy, France.
Céline DillierService de Neurologie, Centre Hospitalier Régional Universitaire de Nancy, Hôpital Central, Nancy, France.
Amory JardelService de Neurologie, Centre Hospitalier Régional Universitaire de Nancy, Hôpital Central, Nancy, France.
Lucie HopesService de Neurologie, Centre Hospitalier Régional Universitaire de Nancy, Hôpital Central, Nancy, France.
Antoine VergerService de Médecine Nucléaire, CHRU de Nancy, Nancy, France.
Mathilde Renaud *Service de Neurologie, Centre Hospitalier Régional Universitaire de Nancy, Hôpital Central, Nancy, France.
Guillemette Clément *Service de Neurologie, Centre Hospitalier Régional Universitaire de Nancy, Hôpital Central, Nancy, France. g.clement2@chru-nancy.fr.ORCID http://orcid.org/0000-0001-8412-2651

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpinocerebellar ataxia type 27B (SCA27B) is caused by ≥ 250 GAA repeat expansions in intron 1 of the FGF14 gene. While motor symptoms are well documented, cognitive manifestations remain insufficiently explored. The cerebellar cognitive affective syndrome scale (CCAS scale) provides a framework for assessing cognition.

methodsWe conducted a prospective study at Nancy University Hospital. The primary objective was to determine the prevalence of cerebellar cognitive affective syndrome. We subsequently characterized the cognitive profile using a standardized neuropsychological battery, evaluated quality of life, and examined the associations between CCAS score, GAA repeat length, motor severity, and age at onset. A [18F]-FDG PET metabolic analysis was performed, including individual visual analysis, followed by a whole-brain voxel-by-voxel comparison between SCA27B patients, healthy controls, and MSA patients.

resultsSeventeen patients with genetically confirmed SCA27B were included. Motor symptoms were moderate (mean SARA score: 7 ± 6.2/40). Definite cerebellar cognitive affective syndrome (≥ 3 failed subtests) was identified in 41% (7/17) of the patients. The comprehensive neuropsychological evaluation revealed mild-to-moderate cognitive impairment; across all cognitive functions tested, fewer than 12% of patients showed cognitive impairment, except for social cognition (23.6%). The PET scan showed preserved cerebellar metabolism in individual analyses (2 patients with hypometabolism). Whole-brain voxel-based analysis, when compared to healthy controls, identified 5 clusters of hypometabolism, with no hypermetabolism.

conclusionThis study is among the first to investigate cognitive impairment in patients with SCA27B using the CCAS scale and comprehensive neuropsychological testing. A substantial prevalence of cerebellar cognitive affective syndrome was observed, even if the decrease of cerebellar metabolic was modest. These findings highlight the need for systematic screening of cognitive and nonmotor symptoms to improve multidisciplinary management.

Indexed as

Cerebellar Cognitive Affective SyndromeSpinocerebellar AtaxiasAdultAgedFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedNeuropsychological TestsPositron-Emission TomographyProspective StudiesFluorodeoxyglucose F18[18F]-FDG PETCCASCerebellar cognitive affective syndromeSCA27BSpinocerebellar ataxia

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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.