# Amyotrophic Lateral Sclerosis (ALS) Genetics and Microbiota: A Comprehensive Review

## TL;DR

This paper reviews the genetic and microbiota factors involved in ALS, highlighting new treatments like gene therapy and microbiome modulation.

## Contribution

The paper provides a comprehensive review of the genetic and microbiota connections in ALS and emerging personalized treatment strategies.

## Key findings

- Genetic mutations in C9orf72, SOD1, TARDBP, and FUS are key targets for novel treatments like Tofersen.
- Dysbiosis involving Akkermansia muciniphila and reduced neuroprotective metabolites may influence ALS progression.
- Personalized treatment strategies using gene therapy and microbiome modulation show promise but remain experimental.

## Abstract

Amyotrophic Lateral Sclerosis (ALS) is a severe, progressive neurodegenerative disorder characterized by the loss of upper and lower motor neurons, affecting 0.5 to 2.6 per 100,000 people, with a median survival of 2 to 5 years. It is increasingly seen as a multisystem disorder, sharing essential clinicopathological features with Frontotemporal Dementia (FTD). This convergence arises from overlapping molecular processes, including severe oxidative stress, glutamate-mediated excitotoxicity, mitochondrial dysfunction, and widespread aggregated TDP-43 proteinopathy in both sporadic and familial cases. Several key genetic factors have been identified, particularly mutations in C9orf72, SOD1, TARDBP, and FUS, which serve as important targets for novel treatments, such as Tofersen, a recently approved SOD1-specific antisense oligonucleotide (ASO) gene therapy. Additionally, there is increasing evidence of the gut–brain connection. Dysbiosis, involving species such as Akkermansia muciniphila, and lower levels of neuroprotective metabolites, such as nicotinamide, may affect the course of the disease. As a result, treatment strategies are shifting toward a personalized approach. This includes using gene therapy, ranging from ASOs and RNA interference (RNAi) to new CRISPR-based genome editing. It also involves exploring microbiome-modulating treatments, such as specific probiotics and Fecal Microbiota Transplantation (FMT). While microbiome and gene therapies remain largely experimental, their potential is promising, as highlighted by the recent approval of Tofersen. These novel approaches could be further enhanced and guided by more robust diagnostic criteria and by investigating early multimodal treatment strategies to slow the progression of this complex disease.