Diagnosis, Prognosis, and Therapy of Transthyretin Amyloidosis

被引：339

作者：

Gertz, Morie A. ^{[1
]}

Benson, Merrill D. ^{[2
]}

Dyck, Peter J. ^{[3
]}

Grogan, Martha ^{[4
]}

Coelho, Terresa ^{[5
]}

Cruz, Marcia ^{[6
]}

Berk, John L. ^{[7
]}

Plante-Bordeneuve, Violaine ^{[8
]}

Schmidt, Hartmut H. J. ^{[9
]}

Merlini, Giampaolo ^{[10
]}

机构：

[1] Mayo Clin, Div Hematol, Rochester, MN 55905 USA

[2] Indiana Univ Sch Med, Indianapolis, IN 46202 USA

[3] Mayo Clin, Div Peripheral Nerve, Rochester, MN 55905 USA

[4] Mayo Clin, Div Cardiovasc Dis, Rochester, MN 55905 USA

[5] Hosp Santo Antonio, Oporto, Portugal

[6] Univ Fed Rio de Janeiro, Univ Hosp, Rio De Janeiro, Brazil

[7] Boston Univ, Sch Med, Amyloidosis Ctr, Boston, MA 02118 USA

[8] Univ Hosp, Creteil, France

[9] Univ Klinikum Munster, Munster, Germany

[10] Univ Pavia, Dept Mol Med, I-27100 Pavia, Italy

来源：

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY | 2015年 / 66卷 / 21期

关键词：

familial amyloid cardiomyopathy; familial amyloid polyneuropathy; genetics; liver transplantation; SENILE SYSTEMIC AMYLOIDOSIS; WILD-TYPE TRANSTHYRETIN; LATE GADOLINIUM ENHANCEMENT; SEVERE CARDIAC AMYLOIDOSIS; LIVER-TRANSPLANTATION; HEART-TRANSPLANTATION; MAGNETIC-RESONANCE; NATRIURETIC PEPTIDE; LONG-TERM; CARDIOVERTER-DEFIBRILLATOR;

D O I：

10.1016/j.jacc.2015.09.075

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Transthyretin amyloidosis is a fatal disorder that is characterized primarily by progressive neuropathy and cardiomyopathy. It occurs in both a mutant form (with autosomal dominant inheritance) and a wild-type form (with predominant cardiac involvement). This article guides clinicians as to when the disease should be suspected, describes the appropriate diagnostic evaluation for those with known or suspected amyloidosis, and reviews the interventions currently available for affected patients. (C) 2015 by the American College of Cardiology Foundation.

引用

页码：2451 / 2466

页数：16

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