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Research Article

Serum urate at trial entry and ALS progression in EMPOWER

, , , , , , & show all
Pages 120-125 | Received 29 Mar 2016, Accepted 21 Jun 2016, Published online: 28 Sep 2016
 

Abstract

Our objective was to determine whether serum urate predicts ALS progression. A study population comprised adult participants of EMPOWER (n = 942), a phase III clinical trial to evaluate the efficacy of dexpramipexole to treat ALS. Urate was measured in blood samples collected during enrollment as part of the routine block chemistry. We measured outcomes by combined assessment of function and survival rank (CAFs), and time to death, by 12 months.

Results showed that in females there was not a significant relation between urate and outcomes. In males, outcomes improved with increasing urate (comparing highest to lowest urate quartile: CAFS was 53 points better with p for trend = 0.04; and hazard ratio for death was 0.60 with p for trend = 0.07), but with adjustment for body mass index (BMI) at baseline, a predictor of both urate levels and prognosis, associations were attenuated and no longer statistically significant. Overall, participants with urate levels equal to or above the median (5.1 mg/dl) appeared to have a survival advantage compared to those below (hazard ratio adjusted for BMI: 0.67; 95% confidence interval 0.47–0.95). In conclusion, these findings suggest that while the association between urate at baseline and ALS progression is partially explained by BMI, there may be an independent beneficial effect of urate.

Acknowledgements

We thank the study participants and their families and caregivers, the study investigators and site staff (Citation14).

Declaration of interest

ML, DJ, DL, DRJ are employees of Biogen Idec. MEC has served as a consultant for AstraZenica, Biogen Idec, Cytokinetics, GlaxoSmithKline, Voyager, Denali, and Genentech. Merit E. Cudkowicz has served as a consultant for AstraZenica, Biogen Idec, Cytokinetics, GlaxoSmithKline, Voyager, Denali, and Genentech.

Funding for this study includes NIH grant awarded to AA [NS045893]. MAS is funded by Target ALS. SP is funded by an NIH Career Development Award [2K12HD001097-16]. The EMPOWER trial was designed by Biogen Idec and Knopp Biosciences and sponsored by Biogen Idec.

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