Literature DB >> 24998826

[Senile systemic amyloidosis].

Masahide Yazaki1, Keiichi Higuchi.   

Abstract

Senile systemic amyloidosis (SSA) is a form of amyloidosis associated with aging, and is characterized by deposition of amyloid fibrils derived from wild-type transthyretin. Amyloid deposition is mainly seen in the myocardium, resulting in arrhythmia (atrial fibrillation) and/or heart failure. Previously, SSA was thought to represent a disease of aged patients over 80 years only; however, recent studies have indicated that SSA also affects much younger patients, with an onset around 50 years. In addition, a number of patients with SSA present with carpal tunnel syndrome (CTS), often several years prior to the onset of heart failure. Hence, CTS may be a key symptom suggestive of SSA, and amyloid deposits should always be confirmed in the operation specimens obtained during carpal tunnel release surgery in CTS patients aged over 50 years. Recently, effective drugs such as tafamidis and diflunisal, which stabilize the structure of the transthyretin tetramer, have been established in FAP patients, and therapeutic effectiveness of these drugs is also anticipated for SSA patients.

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Year:  2014        PMID: 24998826

Source DB:  PubMed          Journal:  Brain Nerve        ISSN: 1881-6096


  1 in total

1.  Echocardiographic and pathologic findings of wild-type transthyretin senile systemic amyloidosis developed in early 50s.

Authors:  Goro Yoshioka; Nozomi Watanabe; Hiroyuki Koita; Yujiro Asada; Keiichi Ashikaga; Nehiro Kuriyama; Yoshisato Shibata
Journal:  J Echocardiogr       Date:  2018-04-26
  1 in total

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