Precision Dopaminergic Treatment in a Cohort of Parkinson's Disease Patients Carrying Autosomal Recessive Gene Variants: Clinical Cohort Data and a Mini Review.

Parkinson’s disease amantadine dopamine agonists genetic levodopa recessive treatment

Journal

Neurology international
ISSN: 2035-8385
Titre abrégé: Neurol Int
Pays: Switzerland
ID NLM: 101551564

Informations de publication

Date de publication:
30 Jul 2024
Historique:
received: 08 05 2024
revised: 24 07 2024
accepted: 27 07 2024
medline: 28 8 2024
pubmed: 28 8 2024
entrez: 28 8 2024
Statut: epublish

Résumé

Parkinson's disease (PD) patients harboring recessive gene variants exhibit a distinct clinical phenotype with an early disease onset and relatively mild symptoms. Data concerning individualized therapy for autosomal recessive PD forms are still scarce. Demographic and treatment data of a cohort of PD carriers of recessive genes (nine homozygous or compound heterozygous The average levodopa equivalent daily dose (LEDD) was 806.8 ± 453.5 (range 152-1810) in In the era of personalized treatment, the therapeutic approach in recessive PD gene carriers might differ as compared to idiopathic PD. Lower LEDD doses were efficient even in patients with a very long disease duration, while a few patients were doing well without any levodopa treatment decades after disease initiation. DAs or amantadine could be used as a first and main line treatment regimen if well tolerated. Literature data on therapeutic strategies in carriers of pathogenic mutations in recessive PD genes, including device-aided treatments, will be further discussed.

Identifiants

pubmed: 39195564
pii: neurolint16040062
doi: 10.3390/neurolint16040062
doi:

Types de publication

Journal Article

Langues

eng

Pagination

833-844

Subventions

Organisme : the National Network for Research of Neurodegenerative Diseases on the basis of Medical Precision, OF THE GENERAL SECRETARIAT OF RESEARCH AND TECHNOLOGY (GSRT).
ID : Grant 2018ΣΕ01300001

Auteurs

Christos Koros (C)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Athina-Maria Simitsi (AM)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Nikolaos Papagiannakis (N)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Anastasia Bougea (A)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Roubina Antonelou (R)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Ioanna Pachi (I)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Evangelos Sfikas (E)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Evangelia Stanitsa (E)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Efthalia Angelopoulou (E)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Vasilios C Constantinides (VC)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Sokratis G Papageorgiou (SG)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Constantin Potagas (C)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Maria Stamelou (M)

Hygeia Hospital, 15123 Athens, Greece.

Leonidas Stefanis (L)

1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Classifications MeSH