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ALSUntangled #64: butyrates.

Yuyao SunRichard BedlackCarmel ArmonMorgan BeauchampTulio BertoriniRobert BowserMark BrombergJames CaressGregory CarterJesse CrayleMerit E CudkowiczJonathan D GlassCarlayne JacksonIsaac LundSarah MartinSabrina PaganoniGary PatteeDylan RatnerKristiana SalmonPaul Wicks
Published in: Amyotrophic lateral sclerosis & frontotemporal degeneration (2022)
ALSUntangled reviews alternative and off-label treatments for people living with amyotrophic lateral sclerosis (PALS). Here we review butyrate and its different chemical forms (butyrates). Butyrates have plausible mechanisms for slowing ALS progression and positive pre-clinical studies. One trial suggests that sodium phenylbutyrate (NaPB) in combination with Tauroursodeoxycholic acid (TUDCA) can slow ALS progression and prolong survival, but the specific contribution of NaPB toward this effect is unclear. Butyrates appear reasonably safe for use in humans. Based on the above information, we support a trial of a butyrate in PALS, but we cannot yet recommend one as a treatment.
Keyphrases
  • amyotrophic lateral sclerosis
  • phase iii
  • study protocol
  • phase ii
  • clinical trial
  • randomized controlled trial
  • open label
  • health information
  • free survival
  • social media
  • combination therapy