RT Journal Article
SR Electronic
T1 Fampridine and Acetazolamide in EA2 and Related Familial EA
JF Neurology: Clinical Practice
FD Lippincott Williams & Wilkins
SP e438
OP e446
DO 10.1212/CPJ.0000000000001017
VO 11
IS 4
A1 Carolin Muth
A1 Julian Teufel
A1 Ludger Schöls
A1 Matthis Synofzik
A1 Christiana Franke
A1 Dagmar Timmann
A1 Ulrich Mansmann
A1 Michael Strupp
YR 2021
UL http://cp.neurology.org/content/11/4/e438.abstract
AB Objective To determine the efficacy and safety of the treatment with prolonged-release 4-aminopyridine (fampridine) and acetazolamide for patients with episodic ataxia type 2 (EA2), patients with EA2 were treated with a random sequence of fampridine, acetazolamide, and placebo in a 3-period crossover trial.Methods A total of 30 patients with EA2 (8 female; aged 20–71 years; 18 genetically confirmed, 4 with a positive family history, 8 with the clinical diagnosis) were enrolled in this phase III, randomized, double-blind, placebo-controlled, 3-period crossover trial. Each period lasted 12 weeks with a 4-week washout period. Each patient received a random sequence of 20 mg/d fampridine, 750 mg/d acetazolamide, and placebo. The primary end point was the number of attacks during the last 30 days within the 12-week treatment period. Participants, caregivers, and those assessing the outcomes were blinded to the intervention.Results Compared with placebo, fampridine reduced the number of attacks to 63% (95% CI 54%–74%) and acetazolamide to 52% (95% CI 46%–60%). A total of 39 (26.5%) adverse events were observed under treatment with fampridine (mostly tingling paresthesia and fatigue), 66 (44.9%) happened under acetazolamide (mostly taste disturbance and gastrointestinal complaints), and 42 (28.6%) under placebo (mostly gastrointestinal complaints).Conclusion Both fampridine and acetazolamide significantly reduce the number of attacks in patients with EA2 and related EA in comparison to placebo. Fampridine 10 mg twice daily had fewer side effects than acetazolamide 250 mg 3 times daily. The trial was registered with DRKS.de (DRKS00005258) and EudraCT (2013-000107-17). This study was supported by the Federal Ministry of Education and Research (BMBF) (grant number 01EO0901). Fampridine (study medication) was provided by Biogen Idec.Classification of Evidence Class II evidence.