Serum Cardiac Troponins and N-Terminal Pro-Brain Natriuretic Peptide: A Staging System for Primary Systemic Amyloidosis
Top Cited Papers
- 15 September 2004
- journal article
- hematologic malignancies
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 22 (18) , 3751-3757
- https://doi.org/10.1200/jco.2004.03.029
Abstract
Purpose: Primary systemic amyloidosis (AL) is a multisystemic disorder resulting from an underlying plasma cell dyscrasia. There is no formal staging system for AL, making comparisons between studies and treatment centers difficult. Our group previously identified elevated serum cardiac troponin T (cTnT) as the most powerful predictor of overall survival. Others have reported that N-terminal pro-brain natriuretic peptide (NT-proBNP) is a valuable prognostic marker. We sought to develop a staging system for patients with AL. Patients and Methods: Two hundred forty-two patients with newly diagnosed AL who were seen at the Mayo Clinic between April 1979 and November 2000, and who had echocardiograms and stored serum samples at presentation were eligible for this retrospective review. NT-proBNP measurements were performed on 242 patients in whom cTnT and cardiac troponin I (cTnI) had been previously run. Two prognostic models were designed using threshold values of NT-proBNP and either cTnT or cTnI (NT-proBNP < 332 ng/L, cTnT < 0.035 μg/L, and cTnI < 0.1 μg/L). Depending on whether NT-proBNP and troponin levels were both low, were high for only one level, or were both high, patients were classified as stage I, II, or III, respectively. Results: Using the cTnT+NT-proBNP model 33%, 30%, and 37% of patients were stages I, II, and III, respectively, with median survivals of 26.4, 10.5, and 3.5 months, respectively. The alternate cTnI+NT-proBNP model predicted median survivals of 27.2, 11.1, and 4.1 months, respectively. Conclusion: Stratification of AL patients into three stages is possible with two readily available and reproducible tests setting the stage for more consistent and reliable cross comparisons of therapeutic outcomes.Keywords
This publication has 35 references indexed in Scilit:
- Stem cell transplantation for the management of primary systemic amyloidosisThe American Journal of Medicine, 2002
- Prognostic factors for survival and response after high‐dose therapy and autologous stem cell transplantation in systemic AL amyloidosis: a report on 21 patientsBritish Journal of Haematology, 1998
- The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvementQJM: An International Journal of Medicine, 1998
- Right Ventricular Dilation in Primary AmyloidosisThe American Journal of Cardiology, 1997
- Doppler index combining systolic and diastolic myocardial performance: Clinical value in cardiac amyloidisisJournal of the American College of Cardiology, 1996
- Amyloidosis: Prognosis and treatmentSeminars in Arthritis and Rheumatism, 1994
- Prognostic significance of Doppler measures of diastolic function in cardiac amyloidosis. A Doppler echocardiography study.Circulation, 1991
- Cardiac amyloidosisInternational Journal of Cardiology, 1990
- Primary systemic amyloidosis: multivariate analysis for prognostic factors in 168 casesBlood, 1986
- Echocardiographic findings in systemic amyloidosis: Spectrum of cardiac involvement and relation to survivalJournal of the American College of Cardiology, 1985