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Translational study demonstrates gastric mucosal denervation in hereditary transthyretin amyloidosis, indicating links between nerve loss, gut dysbiosis, and gastrointestinal symptoms.
Backgrounds Hereditary ATTR amyloidosis with polyneuropathy (ATTRv-PN) frequently presents with gastrointestinal autonomic dysfunction, but its underlying pathology remains unclear.Methods We examined gastric mucosal amyloid deposition and innervation using conventional endoscopic biopsies in ATTRv-PN patients and a human TTR (hTTR A117S) knock-in mouse model. Clinical assessments, gut microbiota, metabolomics, and neurite growth assays were integrated.Results Among 33 patients, 84.8% showed TTR(+) amyloid deposition in gastric mucosa. Gastric mucosal innervation density (GMID) was significantly reduced in all gastric regions compared with controls and was similarly decreased in hTTR(A117S) mice. Lower GMID correlated with gastroparesis and reflux symptom severity. Integrated analyses revealed positive associations between GMID, four microbial genera, and histidine levels. Both microbiota-derived principal components and histidine independently correlated with GMID. Histidine also promoted neurite growth in vitro.Conclusions Endoscopic biopsy enables assessment of both gastric amyloid pathology and mucosal innervation in ATTRv-PN. Reduced GMID is closely associated with gastrointestinal symptoms, microbiota alterations, and metabolomic changes, providing insights into disease mechanisms and potential biomarkers of autonomic gastrointestinal dysfunction.
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Hsueh et al. (2026) studied this question.
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