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Familial Amyloid Polyneuropathy: Liver Transplantation as First-line Therapy Taro Yamashita 1,2 1Center of Intractable Neurological Diseases, National Hospital Organization, Kumamoto Minami Hospital 2Diagnostic Unit for Amyloidosis, Department of Neurology, Kumamoto University Hospital Keyword: アミロイドーシス , 肝移植 , エビデンス , 脳アミロイド血管症 , 熊本大学医学部アミロイドーシス診療体制構築事業 , amyloidosis , liver transplantation , evidence , cerebral amyloid angiopathy , Kumamoto University Diagnostic Unit for Amyloidosis pp.763-771
Published Date 2014/7/1
DOI https://doi.org/10.11477/mf.1416101836
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Abstract

Liver transplantation is the only potentially curative treatment currently available for transthyretin familial amyloid polyneuropathy (TTR-FAP) since transplantation results in the disappearance of amyloidogenic TTR, synthesized by the original liver, from plasma. An absolute risk reduction of 66.3%, class Ⅲ evidence, and grade B recommendation demonstrate that liver transplantation prolongs survival in patients with FAP Val30Met. Effect of new therapeutic drugs should be compared with that of liver transplantation, and outcome improvement of therapy for FAP is expected.


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電子版ISSN 1344-8129 印刷版ISSN 1881-6096 医学書院

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