Data di Pubblicazione:
2022
Abstract:
Axonal polyneuropathy is the main feature of hereditary transthyretin amyloidosis (ATTRv). Nerve morphological abnormalities have been reported, but longitudinal changes have never been assessed. We performed a prospective widespread nerve ultrasound evaluation and nerve cross-sectional area (CSA) was compared with baseline data in both ATTRv patients and pre-symptomatic carriers. Thirty-eight subjects were evaluated (mean follow-up 17.1 months), among them 21 had polyneuropathy while 17 were pre-symptomatic carriers. CSA significantly increased at brachial plexus in both groups (p = 0.008 and p = 0.012) pointing to progressive brachial plexus enlargement as a longitudinal biomarker of both disease progression and disease occurrence in pre-symptomatic carriers.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
*Amyloid Neuropathies, Familial/complications/diagnostic imaging
Elenco autori:
Salvalaggio, A.; Coraci, D.; Obici, L.; Cacciavillani, M.; Luigetti, M.; Mazzeo, A.; Pastorelli, F.; Grandis, M.; Cavallaro, T.; Bisogni, G.; Lozza, A.; Gemelli, C.; Gentile, L.; Russo, M.; Ermani, M.; Fabrizi, G. M.; Plasmati, R.; De Napoli, F.; Campagnolo, M.; Castellani, F.; Salvi, F.; Fenu, S.; Devigili, G.; Pareyson, D.; Gasparotti, R.; Rapezzi, C.; Martinoli, C.; Padua, L.; Briani, C.
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