Sodium oligomannate (GV-971) modulates gut microbiota, reduces amyloid pathology and enhances cognition in Alzheimer’s disease (AD) models; however, its clinical responses vary widely. Unravelling the mechanisms underlying this heterogeneity is thus essential for personalised treatment.
GV-971 drives reductive gut remodelling, which shifts tryptophan metabolic flux toward indole-3-propionic acid (IPA) production—unveiling a gut-brain axis signal that directly links microbial metabolism to host therapeutic outcomes.
This study complements the rational design of gut microbiome-targeted drugs and provides a framework for predicting responses to carbohydrate-based AD therapies.
Restoring bacterial reductive tryptophan-IPA metabolism offers a promising node for therapeutic intervention in Alzheimer’s disease.
Alzheimer’s disease (AD) remains incurable, with clinically meaningful therapeutic benefit being limited and highly variable across patients.