Journal
AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION
Volume 23, Issue 7-8, Pages 638-643Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/21678421.2022.2045323
Keywords
ALS; butyrate; gut microbiome; neuroinflammation; alternative therapy
Categories
Funding
- Amyotrophic Lateral Sclerosis Association
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The article reviews the potential use of butyrates in the treatment of amyotrophic lateral sclerosis (ALS), with a focus on one trial involving sodium phenylbutyrate (NaPB) and Tauroursodeoxycholic acid (TUDCA). The results suggest that this combination can slow ALS progression and prolong survival, but the specific contribution of NaPB is unclear. However, more research is needed to determine the efficacy of butyrates as a treatment for ALS.
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.
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