Evidence map›Paper›PMID 35137562›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Induced Cognitive Impairments Reversed by Grafts of Neural Precursors: A Longitudinal Study in a Macaque Model of Parkinson's Disease.

Florence Wianny, Kwamivi Dzahini, Karim Fifel, Charles Robert Eden Wilson, Agnieszka Bernat, Virginie Dolmazon, Pierre Misery, Camille Lamy, Pascale Giroud, Howard Michael Cooper and 6 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact, top 80% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 1 citations in OpenAlex.

  1. Pooled it
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  3. Disease-modifying, multidimensional efficacy of putaminal CaMolecular therapy : the journal of the American Society of Gene Therapy · 2025
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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 at 1 institution in 6 countries.

Florence WiannyUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Kwamivi DzahiniUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Karim FifelUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Charles Robert Eden WilsonUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Agnieszka BernatUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Virginie DolmazonUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Pierre MiseryUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Camille LamyUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Pascale GiroudUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Howard Michael CooperUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Kenneth KnoblauchUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Emmanuel ProcykUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Henry KennedyUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Pierre SavatierUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Colette DehayUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.
Julien VezoliUniv Lyon, Université Claude Bernard Lyon 1, Inserm U1208, Stem Cell and Brain Research Institute, Bron, 69500, France.ORCID 0000-0001-8319-5429
Université Claude Bernard Lyon 1 · FR

Funding

Agence Nationale de la Recherche ANR-11-BSV4-501Cluster Handicap Vieillissement Neurosciences Rhône-Alpes FP7-2007 ICT-216593Cluster Handicap Vieillissement Neurosciences Rhône-Alpes P6-2005 IST-1583Fédération pour la Recherche sur le Cerveau APE13 "Rotary - Espoir en Tête"Fondation Caisse d'Epargne Rhône-Alpes LyonFondation de FranceFondation NeurodisFondation pour la Recherche Médicale DEQ20160334943Fondation pour la Recherche Médicale DEQ20170336757IHU-B CESAME ANR-10-IBHU-003Infrastructure Nationale en Biologie et Santé, INGESTEM ANR-11-INBS-0009LabEX CORTEX ANR-11 LABX-0042LabEX DEVweCAN ANR-10-LABX-0061Région Rhône-AlpesRhône-Alpes cible 11-010869the program "Investissements d'Avenir"the Université de Lyon ANR-11-IDEX-0007
6 · The paper itself

Abstract

Parkinson's disease (PD) evolves over an extended and variable period in humans; years prior to the onset of classical motor symptoms, sleep and biological rhythm disorders develop, significantly impacting the quality-of-life of patients. Circadian-rhythm disorders are accompanied by mild cognitive deficits that progressively worsen with disease progression and can constitute a severe burden for patients at later stages. The gold-standard 6-methyl-1-methyl-4-phenyl-1,2,3,6-tetrahydropyridin (MPTP) macaque model of PD recapitulates the progression of motor and nonmotor symptoms over contracted periods of time. Here, this multidisciplinary/multiparametric study follows, in five animals, the steady progression of motor and nonmotor symptoms and describes their reversal following grafts of neural precursors in diverse functional domains of the basal ganglia. Results show unprecedented recovery from cognitive symptoms in addition to a strong clinical motor recuperation. Both motor and cognitive recovery and partial circadian rhythm recovery correlate with the degree of graft integration, and in a subset of animals, with in vivo levels of striatal dopaminergic innervation and function. The present study provides empirical evidence that integration of neural precursors following transplantation efficiently restores function at multiple levels in parkinsonian nonhuman primates and, given interindividuality of disease progression and recovery, underlines the importance of longitudinal multidisciplinary assessments in view of clinical translation.

Indexed as

Cognitive DysfunctionParkinson DiseaseAnimalsDopamineHumansLongitudinal StudiesMacacaDopaminecircadian rhythmscognition and motor controlembryonic stem cellsneural precursorsnonhuman primate low-dose MPTP

Identifiers

PMID35137562
PMCPMC8981458
OpenAlexW3111080513

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.