Lithium carbonate in Amyotrophic Lateral Sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A; protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial.

Author:

Willemse Sean William1ORCID,Roes Kit CB2,Damme Philip Van3,Hardiman Orla4,Ingre Caroline5,Povedano Monica6,Wray Naomi R7,Gijzen Marleen8,de Pagter Mirjam S8,Demaegd Koen C1,Janse Annemarie FC8,Vink Roel C8,Sleutjes Boudewijn THM1,Chiò Adriano9,Corcia Philippe10,Reviers Evy11,Al-Chalabi Ammar12,Kiernan Matthew C13,Berg Leonard H van den1,Es Michael A van1,Eijk Ruben PA van1

Affiliation:

1. UMC Utrecht Brain Center Rudolf Magnus

2. Radboud University Nijmegen: Radboud Universiteit

3. KU Leuven University Hospitals Leuven: Katholieke Universiteit Leuven Universitaire Ziekenhuizen Leuven

4. Beaumont Hospital

5. Karolinska Institutet

6. Bellvitge University Hospital: Hospital Universitari de Bellvitge

7. The University of Queensland

8. UMC Utrecht: Universitair Medisch Centrum Utrecht

9. University of Turin Department of Neurosciences Rita Levi Montalcini: Universita degli Studi di Torino Dipartimento di Neuroscienze Rita Levi Montalcini

10. CHRU Tours: Centre Hospitalier Regional Universitaire de Tours

11. The ALS Association

12. King's College Hospital

13. Royal Prince Alfred Hospital

Abstract

Abstract Background Given the large genetic heterogeneity in Amyotrophic Lateral Sclerosis (ALS), it seems likely that genetic subgroups may benefit differently from treatment. An exploratory meta-analysis identified that patients homozygous for the C-allele at SNP rs12608932, a single nucleotide polymorphism in the gene UNC13A, had a statistically significant survival benefit when treated with lithium carbonate. We aim to confirm the efficacy of lithium carbonate on the time to death or respiratory insufficiency in patients with ALS homozygous for the C-allele at SNP rs12608932 in UNC13A. Methods A randomised, group-sequential, event-driven, double-blind, placebo-controlled trial will be conducted in 15 sites across Europe and Australia. Patients will be genotyped for UNC13A; those homozygous for the C-allele at SNP rs12608932 will be eligible. Patients must have a diagnosis of ALS according to the revised El Escorial criteria, and a TRICALS risk-profile score between − 6.0 and − 2.0. An expected number of 1,200 patients will be screened in order to enrol a target sample size of 171 patients. Patients will be randomly allocated in a 2:1 ratio to lithium carbonate or matching placebo, and treated for a maximum duration of 24 months. The primary endpoint is the time to death or respiratory insufficiency, whichever occurs first. Key secondary endpoints include functional decline, respiratory function, quality of life, tolerability, and safety. An interim analysis for futility and efficacy will be conducted after the occurrence of 41 events. Discussion Lithium carbonate has been proven to be safe and well-tolerated in patients with ALS. Given the favorable safety profile, the potential benefits are considered to outweigh the burden and risks associated with study participation. This study may provide conclusive evidence about the life-prolonging potential of lithium carbonate in a genetic ALS subgroup. Trial registration EudraCT number 2020-000579-19, registered on 29-03-2021. https://www.clinicaltrialsregister.eu/ctr-search/trial/2020-000579-19/NL

Publisher

Research Square Platform LLC

Reference61 articles.

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. UNC13Ain amyotrophic lateral sclerosis: from genetic association to therapeutic target;Journal of Neurology, Neurosurgery & Psychiatry;2023-02-03

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