{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,3]],"date-time":"2026-03-03T04:10:50Z","timestamp":1772511050215,"version":"3.50.1"},"reference-count":25,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2024,12,12]],"date-time":"2024-12-12T00:00:00Z","timestamp":1733961600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Muscle and Nerve"],"published-print":{"date-parts":[[2025,2]]},"abstract":"<jats:title>ABSTRACT<\/jats:title><jats:sec><jats:title>Introduction\/Aims<\/jats:title><jats:p>It is imperative to screen asymptomatic carriers of transthyretin (TTR) mutations to initiate treatment early. The protocol for repeated electrodiagnostic (EDX) assessments over time lacks standardization. Our aim was to report the electrophysiological evolution of a cohort of asymptomatic carriers and to determine which biomarkers were most sensitive to change.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>We performed a retrospective review of medical records of asymptomatic carriers identified by screening families with amyloid neuropathy. Carriers who underwent two EDX assessments with a minimum 1\u2010year interval between studies were selected. EDX included analysis of median, ulnar, tibial, fibular and sural nerves, motor unit number index (MUNIX), electrochemical skin conductance, sympathetic skin response, and heart rate variability on deep breathing. Measurements were compared at first and second examinations.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Twenty\u2010three carriers were included with a median age of 49\u2009years (interquartile range 37\u201358). Median time between examinations was 3\u2009years (2\u20134). Compound muscle and sensory nerve action potential (CMAP and SNAP) amplitudes, nerve conduction velocities, autonomic small fiber testing and MUNIX remained stable except for motor distal latency of the median nerve (+0.07\u2009ms\/year) and CMAP duration of the ulnar (+0.10\u2009ms\/year) and fibular (+0.12\u2009ms\/year) nerves. The CMAP duration of the ulnar nerve was the most sensitive biomarker to change when performed within 10\u2009years preceding the age of the youngest case in the family, with a standardized response mean of 0.91.<\/jats:p><\/jats:sec><jats:sec><jats:title>Discussion<\/jats:title><jats:p>Nerve conduction parameters remain relatively stable in asymptomatic TTR carriers. Changes can only be detected using multimodal and extensive electrophysiological tests.<\/jats:p><\/jats:sec>","DOI":"10.1002\/mus.28318","type":"journal-article","created":{"date-parts":[[2024,12,13]],"date-time":"2024-12-13T07:30:27Z","timestamp":1734075027000},"page":"208-215","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Electrophysiological Monitoring of Asymptomatic Transthyretin Mutation Carriers"],"prefix":"10.1002","volume":"71","author":[{"given":"Nicolas","family":"Berard","sequence":"first","affiliation":[{"name":"Referral Centre for Neuromuscular Diseases and ALS, La Timone University Hospital Aix\u2010Marseille University, ERN Neuro\u2010NMD  Marseille France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Annie","family":"Verschueren","sequence":"additional","affiliation":[{"name":"Referral Centre for Neuromuscular Diseases and ALS, La Timone University Hospital Aix\u2010Marseille University, ERN Neuro\u2010NMD  Marseille France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Etienne","family":"Fortanier","sequence":"additional","affiliation":[{"name":"Referral Centre for Neuromuscular Diseases and ALS, La Timone University Hospital Aix\u2010Marseille University, ERN Neuro\u2010NMD  Marseille France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aude\u2010Marie","family":"Grapperon","sequence":"additional","affiliation":[{"name":"Referral Centre for Neuromuscular Diseases and ALS, La Timone University Hospital Aix\u2010Marseille University, ERN Neuro\u2010NMD  Marseille France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ludivine","family":"Kouton","sequence":"additional","affiliation":[{"name":"Referral Centre for Neuromuscular Diseases and ALS, La Timone University Hospital Aix\u2010Marseille University, ERN Neuro\u2010NMD  Marseille 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France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shahram","family":"Attarian","sequence":"additional","affiliation":[{"name":"Referral Centre for Neuromuscular Diseases and ALS, La Timone University Hospital Aix\u2010Marseille University, ERN Neuro\u2010NMD  Marseille France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5591-2774","authenticated-orcid":false,"given":"Emilien","family":"Delmont","sequence":"additional","affiliation":[{"name":"Referral Centre for Neuromuscular Diseases and ALS, La Timone University Hospital Aix\u2010Marseille University, ERN Neuro\u2010NMD  Marseille 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