PRESENCE, EVOLVING CHANGES, AND PROGNOSTIC IMPLICATIONS OF MYOCARDIALDAMAGE DETECTED IN IDIOPATHIC AND ALCOHOLIC DILATED CARDIOMYOPATHY BYIN-111 MONOCLONAL ANTIMYOSIN ANTIBODIES

Citation
D. Obrador et al., PRESENCE, EVOLVING CHANGES, AND PROGNOSTIC IMPLICATIONS OF MYOCARDIALDAMAGE DETECTED IN IDIOPATHIC AND ALCOHOLIC DILATED CARDIOMYOPATHY BYIN-111 MONOCLONAL ANTIMYOSIN ANTIBODIES, Circulation, 89(5), 1994, pp. 2054-2061
Citations number
41
Categorie Soggetti
Cardiac & Cardiovascular System",Hematology
Journal title
ISSN journal
00097322
Volume
89
Issue
5
Year of publication
1994
Pages
2054 - 2061
Database
ISI
SICI code
0009-7322(1994)89:5<2054:PECAPI>2.0.ZU;2-K
Abstract
Background The clinical relevance of myocardial cell damage in dilated cardiomyopathy is uncertain. Myocardial uptake of In-111 monoclonal a ntimyosin antibodies (MAA) was used to study myocardial damage in pati ents with idiopathic (IDC) and alcoholic (ADC) dilated cardiomyopathy and to assess its prognostic implications. Methods and Results MAA and echocardiographic studies were performed in 117 patients. Intensity o f antibody uptake was measured by heart-to-lung ratio (HLR) (normal <1 .55). Studies were repeated in survivors and patients who did not rece ive a cardiac transplant. Follow-up extended up to 62 months (mean, 23 +/-16 months). Eighty-eight patients with IDC showed a 77% prevalence of abnormal MAA. After acute-onset IDC, reduction of HLR (1.81+/-0.2 t o 1.56+/-0.1) (P=.007) with improvement in ejection fraction (EF) (35/-10% to 46+/-14%) (P=.018) was observed. No changes in HLR or EF were detected in patients with chronic stable IDC. Twenty-nine patients wi th ADC showed a lower prevalence (48%) of abnormal MAA studies than th ose with IDC (P=.003). HLR was higher in 13 active (1.78+/-0.3) than i n 16 past consumers (1.49+/-0.2) (P=.019); in the former, HLR decrease d to 1.44+/-0.2 (P=.012), and EF improved (35+/-14% to 53+/-18%) (P=.0 5) after abstention. Intensities of uptake HLR of >1.87 were associate d with increased risk of death or transplantation. Conclusions In pati ents with IDC, variations of MAA uptake are detected in patients who p resent acutely but not in those with chronic stable disease. In patien ts with ADC, MAA uptake mainly depends on alcohol consumption. In both situations, reduction of uptake correlates with improvement of ventri cular function. Higher intensities of MAA uptake are associated with a worse outcome. The intensity of antibody uptake, along with other cli nical and functional variables, may be helpful in risk stratification of patients with dilated cardiomyopathy.