Antigens of the major histocompatibility system in ischemic heart disease and idiopathic dilated cardiomyopathy

• Published in: Clinical cardiology (Mahwah, N.J.) Vol. 22; no. 4; pp. 292 - 296
• Main Authors: Osa, Ana, Almenar, Luis, Palencia, Miguel, Puig, Nieves, Montoro, Jose, Chirivella, Melitina
• Format: Journal Article
• Language: English
• Published: New York Wiley Periodicals, Inc 01-04-1999; Wiley
• Subjects: Adolescent; Adult; Biological and medical sciences; Biomarkers - analysis; Cardiology. Vascular system; Cardiomyopathy, Dilated - immunology; Chi-Square Distribution; dilated cardiomyopathy; Female; Heart; HLA Antigens - analysis; HLA Antigens - immunology; HLA-A Antigens - analysis; HLA-B Antigens - analysis; HLA-DQ Antigens - analysis; HLA-DR Antigens - analysis; human leukocyte antigens; Humans; ischemic heart disease; Male; Medical sciences; Middle Aged; Myocardial Ischemia - immunology; Myocarditis. Cardiomyopathies; Sensitivity and Specificity; Human; Heart failure; Congestive hypertrophic cardiomyopathy; Heart disease; Major histocompatibility system; Risk factor; Idiopathic; Cardiovascular disease; Complication; Exploration; Myocardial disease; Coronary heart disease
• ISSN: 0160-9289; 1932-8737
• DOI: 10.1002/clc.4960220408

Background: Although dilated cardiomyopathy (DCM) is a disease of unknown and probably multifactorial etiology, a change in immune mechanisms is presumably significant, with many abnormalities in humoral and cellular responses having been reported. The heart thus becomes the target organ for an initial episode of myocardial damage that triggers an autoimmune response.
Hypothesis: The purpose of this study was to analyze the frequency of different human leukocyte antigens in patients with a diagnosis of well‐advanced DCM and ischemic heart failure, comparing them with a control group of presumably healthy subjects.
Methods: The group with dilated cardiomyopathy consisted of 50 patients (7 women and 43 men), aged from 14 to 64 years. The group with ischemic heart disease included 76 patients (4 women and 72 men), with ages ranging from 34 to 64. The control group, consisting of 1,337 presumably healthy subjects from the Spanish Mediterranean area, was recruited based on paternity studies.
Results: Compared with the control group, we found in DCM a greater incidence of B15 (20 vs. 6%) and DQ 3 (83 vs. 50%) antigens. In ischemic heart disease we found a lower incidence of A1 (3 vs. 22%), B8 (5 vs. 12%), and DQ2 (16 vs. 50%) in comparison with the control group.
Conclusions: In the Spanish Mediterranean area, the presence of antigens B‐15 and DQ3 would be associated with advanced DCM. The absence of antigens A1, B8, and DQ2 would be associated with the occurrence of severe ischemic heart disease.