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
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
833-844Subventions
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