4.6 Article

Unique Phenotypes With Corresponding Pathology in Late-Onset Hereditary Transthyretin Amyloidosis of A97S vs. V30M

期刊

FRONTIERS IN AGING NEUROSCIENCE
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnagi.2021.786322

关键词

hereditary transthyretin amyloidosis (ATTRv); carpal tunnel syndrome; dysphagia; amyloid deposition; natural course

资金

  1. Ministry of Science and Technology, Taiwan [108-2321-B-002-068, 109-2320-B-002-025, 109-2320-B-002-024]
  2. National Taiwan University Hospital [UN110-014]
  3. Ministry of Education [107L9014-2]

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The study compares the clinical manifestations of A97S and V30M in hereditary transthyretin amyloidosis (ATTRv) and observes differences between the two genotypes. Dysphagia and carpal tunnel syndrome are common in A97S, and the onset age is younger. Autopsy findings in A97S reveal extensive amyloid deposits in the viscera and nerves of the tongue, larynx, and esophagus.
ObjectiveHereditary transthyretin amyloidosis (ATTRv) encompasses different phenotypes among various genotypes. The analysis of the natural history and risk factors of faster progression in different genotypes would refine the treatment strategy. MethodsThe clinical manifestations of ATTRv from A97S (p.A117S) of Taiwanese and late-onset V30M (p.V50M) of Japanese were compared. An autopsy study of A97S was performed. ResultsThere existed three unique features in the A97S cohort compared to the V30M cohort: (1) dysphagia, (2) carpal tunnel syndrome (CTS), and (3) onset age. First, dysphagia was common in A97S (53.4%) but not in V30M and served as a contributor to fast disease progression. All phases of swallowing were affected. In the autopsy pathology, there were extensive amyloid deposits in the viscera and nerves of the tongue, larynx, and esophagus. In A97S, 45 patients (43.3%) had a history of CTS before the onset of length-dependent symptoms by 3 years. The amyloid deposition was more prominent in the median nerve than that in the transverse carpal ligament. The onset age at different stages was younger in the A97S cohort than the V30M cohort by 4-5 years. ConclusionThese phenotypic characteristics together with autopsy pathology in A97S are distinct from V30M. Early dysphagia in A97S correlated with fast progression. In A97S, median neuropathy leading to CTS might be in a continuous spectrum of ATTRv course rather than an independent disease entity. Such observations may serve as a foundation to explore and analyze unique phenotypes among various genotypes.

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