Cargando…

Aromatic L‐Amino Acid Decarboxylase Gene Therapy Enhances Levodopa Response in Parkinson's Disease

BACKGROUND: As Parkinson's disease progresses, levodopa treatment loses efficacy, partly through the loss of the endogenous dopamine‐synthesizing enzyme L‐amino acid decarboxylase (AADC). In the phase I PD‐1101 study, putaminal administration of VY‐AADC01, an investigational adeno‐associated vi...

Descripción completa

Detalles Bibliográficos
Autores principales: Nutt, John G., Curtze, Carolin, Hiller, Amie, Anderson, Shannon, Larson, Paul S., Van Laar, Amber D., Richardson, R. Mark, Thompson, Marin E., Sedkov, Alexander, Leinonen, Mika, Ravina, Bernard, Bankiewicz, Krystof S., Christine, Chadwick W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318280/
https://www.ncbi.nlm.nih.gov/pubmed/32149427
http://dx.doi.org/10.1002/mds.27993
_version_ 1783550810459734016
author Nutt, John G.
Curtze, Carolin
Hiller, Amie
Anderson, Shannon
Larson, Paul S.
Van Laar, Amber D.
Richardson, R. Mark
Thompson, Marin E.
Sedkov, Alexander
Leinonen, Mika
Ravina, Bernard
Bankiewicz, Krystof S.
Christine, Chadwick W.
author_facet Nutt, John G.
Curtze, Carolin
Hiller, Amie
Anderson, Shannon
Larson, Paul S.
Van Laar, Amber D.
Richardson, R. Mark
Thompson, Marin E.
Sedkov, Alexander
Leinonen, Mika
Ravina, Bernard
Bankiewicz, Krystof S.
Christine, Chadwick W.
author_sort Nutt, John G.
collection PubMed
description BACKGROUND: As Parkinson's disease progresses, levodopa treatment loses efficacy, partly through the loss of the endogenous dopamine‐synthesizing enzyme L‐amino acid decarboxylase (AADC). In the phase I PD‐1101 study, putaminal administration of VY‐AADC01, an investigational adeno‐associated virus serotype‐2 vector for delivery of the AADC gene in patients with advanced Parkinson's disease, was well tolerated, improved motor function, and reduced antiparkinsonian medication requirements. OBJECTIVES: This substudy aimed to determine whether the timing and magnitude of motor response to intravenous levodopa changed in PD‐1101 patients after VY‐AADC01 administration. METHODS: Participants received 2‐hour threshold (0.6 mg/kg/h) and suprathreshold (1.2 mg/kg/h) levodopa infusions on each of 2 days, both before and approximately 6 months after VY‐AADC01. Infusion order was randomized and double blinded. Unified Parkinson's Disease Rating Scale motor scores, finger‐tapping speeds, and dyskinesia rating scores were assessed every 30 minutes for 1 hour before and ≥3 hours after start of levodopa infusion. RESULTS: Of 15 PD‐1101 patients, 13 participated in the substudy. Unified Parkinson's Disease Rating Scale motor score area under the curve responses to threshold and suprathreshold levodopa infusions increased by 168% and 67%, respectively, after VY‐AADC01; finger‐tapping speeds improved by 162% and 113%, and dyskinesia scores increased by 208% and 72%, respectively, after VY‐AADC01. Adverse events (mild/moderate severity) were reported in 5 participants during levodopa infusions pre–VY‐AADC01 and 2 participants post–VY‐AADC01 administration. CONCLUSIONS: VY‐AADC01 improved motor responses to intravenous levodopa given under controlled conditions. These data and findings from the parent study support further clinical development of AADC gene therapy for people with Parkinson's disease. © 2020 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
format Online
Article
Text
id pubmed-7318280
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-73182802020-06-29 Aromatic L‐Amino Acid Decarboxylase Gene Therapy Enhances Levodopa Response in Parkinson's Disease Nutt, John G. Curtze, Carolin Hiller, Amie Anderson, Shannon Larson, Paul S. Van Laar, Amber D. Richardson, R. Mark Thompson, Marin E. Sedkov, Alexander Leinonen, Mika Ravina, Bernard Bankiewicz, Krystof S. Christine, Chadwick W. Mov Disord Regular Issue Articles BACKGROUND: As Parkinson's disease progresses, levodopa treatment loses efficacy, partly through the loss of the endogenous dopamine‐synthesizing enzyme L‐amino acid decarboxylase (AADC). In the phase I PD‐1101 study, putaminal administration of VY‐AADC01, an investigational adeno‐associated virus serotype‐2 vector for delivery of the AADC gene in patients with advanced Parkinson's disease, was well tolerated, improved motor function, and reduced antiparkinsonian medication requirements. OBJECTIVES: This substudy aimed to determine whether the timing and magnitude of motor response to intravenous levodopa changed in PD‐1101 patients after VY‐AADC01 administration. METHODS: Participants received 2‐hour threshold (0.6 mg/kg/h) and suprathreshold (1.2 mg/kg/h) levodopa infusions on each of 2 days, both before and approximately 6 months after VY‐AADC01. Infusion order was randomized and double blinded. Unified Parkinson's Disease Rating Scale motor scores, finger‐tapping speeds, and dyskinesia rating scores were assessed every 30 minutes for 1 hour before and ≥3 hours after start of levodopa infusion. RESULTS: Of 15 PD‐1101 patients, 13 participated in the substudy. Unified Parkinson's Disease Rating Scale motor score area under the curve responses to threshold and suprathreshold levodopa infusions increased by 168% and 67%, respectively, after VY‐AADC01; finger‐tapping speeds improved by 162% and 113%, and dyskinesia scores increased by 208% and 72%, respectively, after VY‐AADC01. Adverse events (mild/moderate severity) were reported in 5 participants during levodopa infusions pre–VY‐AADC01 and 2 participants post–VY‐AADC01 administration. CONCLUSIONS: VY‐AADC01 improved motor responses to intravenous levodopa given under controlled conditions. These data and findings from the parent study support further clinical development of AADC gene therapy for people with Parkinson's disease. © 2020 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. John Wiley & Sons, Inc. 2020-03-09 2020-05 /pmc/articles/PMC7318280/ /pubmed/32149427 http://dx.doi.org/10.1002/mds.27993 Text en © 2020 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Issue Articles
Nutt, John G.
Curtze, Carolin
Hiller, Amie
Anderson, Shannon
Larson, Paul S.
Van Laar, Amber D.
Richardson, R. Mark
Thompson, Marin E.
Sedkov, Alexander
Leinonen, Mika
Ravina, Bernard
Bankiewicz, Krystof S.
Christine, Chadwick W.
Aromatic L‐Amino Acid Decarboxylase Gene Therapy Enhances Levodopa Response in Parkinson's Disease
title Aromatic L‐Amino Acid Decarboxylase Gene Therapy Enhances Levodopa Response in Parkinson's Disease
title_full Aromatic L‐Amino Acid Decarboxylase Gene Therapy Enhances Levodopa Response in Parkinson's Disease
title_fullStr Aromatic L‐Amino Acid Decarboxylase Gene Therapy Enhances Levodopa Response in Parkinson's Disease
title_full_unstemmed Aromatic L‐Amino Acid Decarboxylase Gene Therapy Enhances Levodopa Response in Parkinson's Disease
title_short Aromatic L‐Amino Acid Decarboxylase Gene Therapy Enhances Levodopa Response in Parkinson's Disease
title_sort aromatic l‐amino acid decarboxylase gene therapy enhances levodopa response in parkinson's disease
topic Regular Issue Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318280/
https://www.ncbi.nlm.nih.gov/pubmed/32149427
http://dx.doi.org/10.1002/mds.27993
work_keys_str_mv AT nuttjohng aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT curtzecarolin aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT hilleramie aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT andersonshannon aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT larsonpauls aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT vanlaaramberd aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT richardsonrmark aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT thompsonmarine aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT sedkovalexander aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT leinonenmika aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT ravinabernard aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT bankiewiczkrystofs aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease
AT christinechadwickw aromaticlaminoaciddecarboxylasegenetherapyenhanceslevodoparesponseinparkinsonsdisease