A Randomized, Double Blind, Placebo-Controlled Trial of Pioglitazone in Combination with Riluzole in Amyotrophic Lateral Sclerosis

被引:108
作者
Dupuis, Luc [1 ,2 ,3 ]
Dengler, Reinhard [4 ]
Heneka, Michael T. [5 ]
Meyer, Thomas [6 ]
Zierz, Stephan [7 ]
Kassubek, Jan [1 ]
Fischer, Wilhelm [1 ]
Steiner, Franziska [1 ]
Lindauer, Eva [1 ]
Otto, Markus [1 ]
Dreyhaupt, Jens [8 ]
Grehl, Torsten [9 ]
Hermann, Andreas [10 ]
Winkler, Andrea S. [11 ]
Bogdahn, Ulrich [12 ]
Benecke, Reiner [13 ]
Schrank, Bertold [14 ]
Wessig, Carsten [15 ]
Grosskreutz, Julian [16 ]
Ludolph, Albert C. [1 ]
机构
[1] Univ Ulm, Dept Neurol, D-7900 Ulm, Germany
[2] INSERM, U692, Lab Signalisat Mol & Neurodegenerescence, Strasbourg, France
[3] Univ Strasbourg, UMRS692, Fac Med, Strasbourg, France
[4] Hannover Med Sch, Dept Neurol, D-3000 Hannover, Germany
[5] Univ Bonn, Dept Neurol, Bonn, Germany
[6] Charite, Dept Neurol, Berlin, Germany
[7] Univ Halle Wittenberg, Dept Neurol, Halle, Germany
[8] Univ Ulm, Inst Epidemiol & Med Biometry, Ulm, Germany
[9] Ruhr Univ Bochum, Dept Neurol, Bochum, Germany
[10] Tech Univ Dresden, Dept Neurol, Dresden, Germany
[11] Tech Univ Munich, Dept Neurol, Munich, Germany
[12] Univ Regensburg, Dept Neurol, Regensburg, Germany
[13] Univ Rostock, Neurol Clin, Rostock, Germany
[14] Deutsch Klin Diagnost, D-6200 Wiesbaden, Germany
[15] Univ Wurzburg, Dept Neurol, D-8700 Wurzburg, Germany
[16] Univ Hosp, Dept Neurol, Jena, Germany
关键词
TRANSGENIC MOUSE MODEL; CENTRAL-NERVOUS-SYSTEM; NONALCOHOLIC STEATOHEPATITIS; PPAR-GAMMA; HEXANUCLEOTIDE REPEAT; DISEASE PROGRESSION; DELAYS PROGRESSION; SOD1; MUTATIONS; ALS; MINOCYCLINE;
D O I
10.1371/journal.pone.0037885
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Pioglitazone, an oral anti-diabetic that stimulates the PPAR-gamma transcription factor, increased survival of mice with amyotrophic lateral sclerosis (ALS). Methods/Principal Findings: We performed a phase II, double blind, multicentre, placebo controlled trial of pioglitazone in ALS patients under riluzole. 219 patients were randomly assigned to receive 45 mg/day of pioglitazone or placebo (one: one allocation ratio). The primary endpoint was survival. Secondary endpoints included incidence of non-invasive ventilation and tracheotomy, and slopes of ALS-FRS, slow vital capacity, and quality of life as assessed using EUROQoL EQ-5D. The study was conducted under a two-stage group sequential test, allowing to stop for futility or superiority after interim analysis. Shortly after interim analysis, 30 patients under pioglitazone and 24 patients under placebo had died. The trial was stopped for futility; the hazard ratio for primary endpoint was 1.21 (95% CI: 0.71-2.07, p = 0.48). Secondary endpoints were not modified by pioglitazone treatment. Pioglitazone was well tolerated. Conclusion/Significance: Pioglitazone has no beneficial effects on the survival of ALS patients as add-on therapy to riluzole.
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页数:7
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