Associations between co-medications and survival in ALS-a cohort study from Austria

作者：Cetin Hakan^*; Klickovic Uros; Rath Jakob; Zulehner Gudrun; Fuezi Judith; Reichardt Berthold; Hagmann Michael; Wanschitz Julia; Loescher Wolfgang N; Auff Eduard; Zimprich Fritz

来源：Journal of Neurology, 2015, 262(7): 1698-1705.

DOI：10.1007/s00415-015-7767-7

• Amyotrophic lateral sclerosis
• Cohort study
• Co-medication
• Muscle relaxants, central
• Proton pump inhibitors

The aim of this study was to evaluate associations between co-medications and survival of patients with amyotrophic lateral sclerosis (ALS). Prescription databases of the Austrian sickness funds covering more than 5 million people formed the basis of this study. ALS cases were deduced from riluzole prescriptions during the study period from January 1, 2008, to June 30, 2012. After adjusting for potential confounding factors associations between co-medications and ALS survival were analyzed. A total of 522 ALS patients could be identified during the study period. Sixteen of the most frequently used drug classes were considered for the survival analyses of which two were nominally associated with ALS survival. Proton pump inhibitors (PPI) were negatively correlated with survival (HR 1.34, 95 % CI 1.04-1.73) and centrally acting muscle relaxants (CAMR) showed a positive association (HR 0.56, 95 % CI 0.39-0.81). After correcting for multiple testing, the association between CAMR and ALS survival remained significant (p = 0.03). In conclusion, this is the first study systematically evaluating potential associations between commonly used drugs and ALS disease course. We report a positive association between CAMR use and survival, which may have derived from an indication bias representing the better prognosis of the upper motor neuron predominant disease variant. However, this is still interesting since it demonstrates the sensitivity of our study design to pick up survival effects. The use of large prescription registries could thus provide a valuable basis to find clues to underlying pathophysiological mechanisms in ALS.

• 出版日期2015-7