Noninvasive diagnosis of biopsy-proven cardiac amyloidosis

被引:265
作者
Rahman, JE
Helou, EF
Gelzer-Bell, R
Thompson, RE
Kuo, C
Rodriguez, ER
Hare, JM
Baughman, KL
Kasper, EK
机构
[1] Johns Hopkins Univ, Sch Publ Hlth & Hyg, Dept Biostat, Baltimore, MD USA
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Med, Div Cardiol, Baltimore, MD 21205 USA
关键词
D O I
10.1016/j.jacc.2003.08.043
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
OBJECTIVES This study analyzed the utility of electrocardiographic (ECG) and echocardiographic findings in the diagnosis of amyloidosis proven by endomyocardial biopsy. BACKGROUND Cardiac amyloidosis is associated with characteristic ECG and echocardiographic changes, yet each finding alone is relatively nonspecific. A combination of noninvasive prognostic parameters would be desirable for this tissue-based diagnosis. METHODS We performed an analysis of 196 consecutive patients referred for endomyocardial biopsy because of clinical suspicion of cardiac amyloidosis. The diagnosis was confirmed in 58 patients (29%). The ECGs, echocardiograms, and right heart hemodynamic data were reviewed to determine which findings strongly correlate with the diagnosis. These findings were then used to build multivariate logistic regression models that predict the log-odds of having cardiac amyloidosis. RESULTS The univariate analysis showed that low-voltage and pseudo-infarction patterns on the ECG and increased myocardial thickness and speckled-appearing myocardium on the echocardiogram were associated with biopsy-proven cardiac amyloidosis (each p < 0.01). In multivariate logistic regression models, a combination of a low voltage and measures of myocardial thickness produced the most statistically useful models. For instance, one model showed that if a low voltage was present and interventricular septal thickness is >1.98 cm, the diagnosis of cardiac amyloidosis could be made with a sensitivity of 72% and a specificity of 91%. In this model, the positive predictive and negative predictive values were 79% and 88%, respectively. CONCLUSIONS In patients with suspected cardiac amyloidosis, a combination of noninvasive parameters-namely, a low voltage and increased intraventricular septal thickness-is a useful diagnostic tool. (C) 2004 by the American College of Cardiology Foundation.
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收藏
页码:410 / 415
页数:6
相关论文
共 14 条
[1]
BACKMAN C, 1983, ACTA MED SCAND, V214, P273
[2]
Cacoub P, 2000, ANN MED INTERNE, V151, P611
[3]
AMYLOID CARDIOMYOPATHY - CHARACTERIZATION BY A DISTINCTIVE VOLTAGE MASS RELATION [J].
CARROLL, JD ;
GAASCH, WH ;
MCADAM, KPWJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1982, 49 (01) :9-13
[4]
ECHOCARDIOGRAPHIC FINDINGS IN SYSTEMIC AMYLOIDOSIS - SPECTRUM OF CARDIAC INVOLVEMENT AND RELATION TO SURVIVAL [J].
CUETOGARCIA, L ;
REEDER, GS ;
KYLE, RA ;
WOOD, DL ;
SEWARD, JB ;
NAESSENS, J ;
OFFORD, KP ;
GREIPP, PR ;
EDWARDS, WD ;
TAJIK, AJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1985, 6 (04) :737-743
[5]
Survival in patients with primary systemic amyloidosis and raised serum cardiac troponins [J].
Dispenzieri, A ;
Kyle, RA ;
Gertz, MA ;
Therneau, TM ;
Miller, WL ;
Chandrasekaran, K ;
McConnell, JP ;
Burritt, MF ;
Jaffe, AS .
LANCET, 2003, 361 (9371) :1787-1789
[6]
Familial and primary (AL) cardiac amyloidosis: Echocardiographically similar diseases with distinctly different clinical outcomes [J].
Dubrey, SW ;
Cha, K ;
Skinner, M ;
LaValley, M ;
Falk, RH .
HEART, 1997, 78 (01) :74-82
[7]
Medical progress - The systemic amyloidoses [J].
Falk, RH ;
Comenzo, RL ;
Skinner, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (13) :898-909
[8]
SENSITIVITY AND SPECIFICITY OF THE ECHOCARDIOGRAPHIC FEATURES OF CARDIAC AMYLOIDOSIS [J].
FALK, RH ;
PLEHN, JF ;
DEERING, T ;
SCHICK, EC ;
BOINAY, P ;
RUBINOW, A ;
SKINNER, M ;
COHEN, AS .
AMERICAN JOURNAL OF CARDIOLOGY, 1987, 59 (05) :418-422
[9]
AMYLOID CARDIOMYOPATHY IN SYSTEMIC NONHEREDITARY AMYLOIDOSIS - CLINICAL, ECHOCARDIOGRAPHIC AND ELECTROCARDIOGRAPHIC FINDINGS IN 30 PATIENTS WITH AA AND 24 PATIENTS WITH AL AMYLOIDOSIS [J].
HAMER, JPM ;
JANSSEN, S ;
VANRIJSWIJK, MH ;
LIE, KI .
EUROPEAN HEART JOURNAL, 1992, 13 (05) :623-627
[10]
McCarthy RE, 1998, CLIN CARDIOL, V21, P547