Evidence map›Paper›PMID 39616186›Full record

ArticleNPJ Parkinson's disease2024

Molecular and cellular determinants of L-Dopa-induced dyskinesia in Parkinson's Disease.

Federica Servillo, Maria De Carluccio, Giulia Di Lazzaro, Federica Campanelli, Gioia Marino, Giuseppina Natale, Ada Ledonne, Mariangela Massaro Cenere, Emanuela Paldino, Daniela Di Giuda and 13 more

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
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  7. Article
  8. Article
  9. Future Perspectives of NMDAR in CNS Disorders.Molecules (Basel, Switzerland) · 2025
    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

23 authors.

Federica Servillo *Neurologia, Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.
Maria De Carluccio *Neurologia, Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.
Giulia Di Lazzaro *Neurologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Federica CampanelliNeurologia, Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.
Gioia MarinoNeurologia, Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.
Giuseppina NataleNeurologia, Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.
Ada LedonneNeuroscienze Sperimentali, IRCCS Fondazione Santa Lucia, Rome, Italy.ORCID http://orcid.org/0000-0001-6302-207X
Mariangela Massaro CenereNeuroscienze Sperimentali, IRCCS Fondazione Santa Lucia, Rome, Italy.ORCID http://orcid.org/0000-0001-7758-8082
Emanuela PaldinoNeuroscienze Sperimentali, IRCCS Fondazione Santa Lucia, Rome, Italy.
Daniela Di GiudaMedicina Nucleare, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Anna PiccaNeurologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Francesco BoveNeurologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0002-2959-6659
Riccardo Di IorioNeurologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Benedetta AngeloniNeurologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Angelo Tiziano CimminoNeurologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0001-9298-565X
Giovanni BellomoLaboratorio di Neurochimica Clinica, Neurologia, Dipartimento di Medicina, Università degli Studi di Perugia, Perugia, Italy.ORCID http://orcid.org/0000-0003-0456-5650
Barbara PicconiDipartimento di Scienze Umane e Promozione della Qualità della Vita, Università Telematica San Raffaele, Rome, Italy.
Anna Rita BentivoglioNeurologia, Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.
Nicola Biagio MercuriNeuroscienze Sperimentali, IRCCS Fondazione Santa Lucia, Rome, Italy.ORCID http://orcid.org/0000-0001-6700-7491
Lucilla ParnettiLaboratorio di Neurochimica Clinica, Neurologia, Dipartimento di Medicina, Università degli Studi di Perugia, Perugia, Italy.ORCID http://orcid.org/0000-0001-5722-3967
Veronica Ghiglieri *Neurologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0003-2885-8298
Maria Teresa Viscomi *Neurologia, Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.
Paolo Calabresi *Neurologia, Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy. paolo.calabresi@policlinicogemelli.it.

Funding

Regulation of Motor Function in Parkinson's DiseaseR01NS045962 · NINDS · EMORY UNIVERSITY · PI PAPA, STELLA M, TRAYNELIS, STEPHEN F · 2004 to 2022
$5.2M
Regulation of Motor Function in Parkinson's DiseaseR56NS045962 · NINDS · EMORY UNIVERSITY · PI PAPA, STELLA M, TRAYNELIS, STEPHEN F · 2018 to 2018
$603k
NINDS NIH HHS R01 NS045962NINDS NIH HHS R56 NS045962
6 · The paper itself

Abstract

Treatment with L-3,4-dihydroxyphenylalanine (L-Dopa) compensates for decreased striatal dopamine (DA) levels and reduces Parkinson's disease (PD) symptoms. However, during disease progression, L-Dopa-induced dyskinesia (LID) develops virtually in all PD patients, making the control of PD symptoms difficult. Thus, understanding the mechanisms underlying LID and the control of these motor abnormalities is a major issue in the care of PD patients. From experimental and clinical studies, a complex cascade of molecular and cellular events emerges, but the primary determinants of LID are still unclear. Here, with a translational approach, including four animal models and a wide cohort of PD patients, we show that striatal DA denervation is the major causal factor for the emergence of LID, while α-synuclein aggregates do not seem to play a significant role. Our data also support the concept that maladaptive basal ganglia plasticity is the main pathophysiological mechanism underlying LID.

Identifiers

PMID39616186
PMCPMC11608318

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.