Evidence map›Paper›PMID 40495913›Full record

ArticleClinical parkinsonism & related disorders2025

Prospective longitudinal cohort of Argentinean patients with progressive supranuclear palsy and corticobasal syndrome: A platform for epidemiological and translational research.

Maria Jose Angel, Gabril F Mizraji, Gonzalo Gomez-Arevalo, Garcia Silvia, Maria Eugenia Gonzalez-Toledo, Avale Elena, Paez-Paz Indiana, Falzone Tomas, Holubiec Mariana, C Peralta Maria and 10 more

Abstract read
In one paragraph

Article in Clinical parkinsonism & related disorders, 2025. 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
–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

1 citing paper in PubMed.

  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

20 authors.

Maria Jose AngelInstitute of Cognitive and Translational Neuroscience (INCyT) Favaloro-INECO-CONICET, Buenos Aires, Argentina.
Gabril F MizrajiUnidad de Movimientos Anormales, Instituto de Neurociencias de la Fundación Favaloro, Buenos Aires, Argentina.
Gonzalo Gomez-ArevaloUnidad de Movimientos Anormales, Instituto de Neurociencias de la Fundación Favaloro, Buenos Aires, Argentina.
Garcia SilviaUnidad de Movimientos Anormales, Instituto de Neurociencias de la Fundación Favaloro, Buenos Aires, Argentina.
Maria Eugenia Gonzalez-ToledoUnidad de Movimientos Anormales, Instituto de Neurociencias de la Fundación Favaloro, Buenos Aires, Argentina.
Avale ElenaINGEBI, Institute of Investigation in Genetic Engineering and Molecular Biology Dr Héctor N Torres, Argentina.
Paez-Paz IndianaINGEBI, Institute of Investigation in Genetic Engineering and Molecular Biology Dr Héctor N Torres, Argentina.
Falzone TomasInstituto de Biología Celular y Neurociencias (IBCN), Universidad de Buenos Aires, CONICET-UBA, Instituto de Investigación en Biomedicina de Buenos Aires (IBioBA), Partner Institute of the Max Planck Society, CONICET-MPSP, Buenos Aires, Argentina.
Holubiec MarianaInstituto de Biología Celular y Neurociencias (IBCN), Universidad de Buenos Aires, CONICET-UBA, Instituto de Investigación en Biomedicina de Buenos Aires (IBioBA), Partner Institute of the Max Planck Society, CONICET-MPSP, Buenos Aires, Argentina.
C Peralta MariaClínica de Enfermedad de Parkinson y Movimientos Anormales, Departamento de Neurociencias, Hospital Universitario CEMIC, Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno", Buenos Aires, Argentina.
Castano FedericoInstitute of Cognitive and Translational Neuroscience (INCyT) Favaloro-INECO-CONICET, Buenos Aires, Argentina.
Sevlever GustavoLaboratorio de Neuropatología y Biología Molecular, Banco de cerebros, Fleni, Argentina.
Mezmezian MonicaLaboratorio de Neuropatología y Biología Molecular, Banco de cerebros, Fleni, Argentina.
Marras ConnieEdmond J. Safra Program in Parkinson's Disease, Rossy Program for PSP Research and the Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, Toronto, ON, Canada.
Gershanik OscarInstitute of Cognitive and Translational Neuroscience (INCyT) Favaloro-INECO-CONICET, Buenos Aires, Argentina.
Chade AnabelUnidad de Movimientos Anormales, Instituto de Neurociencias de la Fundación Favaloro, Buenos Aires, Argentina.
Pardo CarolinaInstitute of Cognitive Neurology (INECO), Buenos Aires, Argentina.
Rellan FlorenciaInstitute of Cognitive Neurology (INECO), Buenos Aires, Argentina.
Campastri AnaInstitute of Cognitive Neurology (INECO), Buenos Aires, Argentina.
Couto BlasInstitute of Cognitive and Translational Neuroscience (INCyT) Favaloro-INECO-CONICET, Buenos Aires, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Progressive supranuclear palsy (PSP) and corticobasal syndrome (CBS) are neurodegenerative disorders with disabling postural instability, falls and cognitive impairment associated with 4-repeat tau protein neuropathology. The low prevalence (6/100,000 inhabitants) is estimated with data only from North American, European countries or Japan. Objective: A multicenter initiative for studying the epidemiology and tau biology of Argentinean patients with PSP and CBS and their ovelaps, Consorcio Argentino de Investigación Traslacional en Tauopatias Primarias (CAITauP). Methods: A prospective observational cohort of people with PSP (PwPSP), CBS and PSP/CBS overlaps will be longitudinally studied aiming at recruitment of 75 patients in 3 years. Deep clinical phenotyping, neurocognitive testing every 12 months, and biosamples collection at baseline are planned. Disease severity will be assessed every 6 months and history of environmental exposures will be assessed at baseline. Results: 33/75 expected patients with PSP (19) and CBS (14) have been enrolled. Female gender is 56%, mean age 76, with estimated disease duration of 4.73 years. More than 60% of enrolled patients have completed first visit and biosamples collection, one patient underwent brain donation, pathological diagnosis of PSP, clinical Richardson syndrome. Environmental exposures of a preliminary subsample are reported. Conclusions: The CAITauP enrolled a cohort of Argentinean PwPSP for deep clinical phenotyping and biobanking. Despite the rarity of PSP/CBS, we highlight the feasibility of establishing local cohorts in developing countries for translational research. The consortium aims to address underrepresented groups of Argentinean to improve diagnosis, treatment, and to create trial-ready cohorts.

Indexed as

BiobankCorticobasal syndromeEnvironmentalLongitudinal cohortProgressive supranuclear palsy

Identifiers

PMID40495913
PMCPMC12148815

What OpenQuestion holds

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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.