INCREASED FREQUENCY OF ORGAN-SPECIFIC CARDIAC ANTIBODIES IN HEALTHY RELATIVES OF PATIENTS WITH DILATED CARDIOMYOPATHY - EVIDENCE FOR AUTOIMMUNITY IN POLISH FAMILIES
Zt. Bilinska et al., INCREASED FREQUENCY OF ORGAN-SPECIFIC CARDIAC ANTIBODIES IN HEALTHY RELATIVES OF PATIENTS WITH DILATED CARDIOMYOPATHY - EVIDENCE FOR AUTOIMMUNITY IN POLISH FAMILIES, Clinical cardiology, 19(10), 1996, pp. 794-798
Background and hypothesis: Autoantibodies represent markers of autoimm
une involvement and are found with increased frequency in patients and
their symptom-free relatives al risk compared with normal controls. C
ardiac-specific autoantibodies, detected by immunofluorescence were fo
und in 20% of symptom-free relatives of patients with dilated cardiomy
opathy (DCM) from England and Italy. The role of autoimmunity may vary
in DCM patients from Poland due to ethnic differences in genetic susc
eptibility to autoimmune disease. Methods: We assessed the frequency o
f the organ-specific cardiac autoantibodies in 162 symptom-free relati
ves of DCM patients [85 male, mean (SD) age 27 (18 years] and 80 contr
ol subjects from Poland. Familial DCM (> 1 affected member) was presen
t in 1 families, nonfamilial DCM in the remaining 24 pedigrees. We per
formed antibody screening and noninvasive cardiological assessment in
the whole group. Results: The frequency of cardiac-specific autoantibo
dies was higher among patients with documented DCM (probands and relat
ives) (50%) and their symptom-free relatives (38%) than in unrelated n
ormal subjects (10%; p=0.0001). In 24 (86%) of the pedigrees studied,
autoantibodies were found in the proband and/or in at least one family
member and tended to be more common in familial than in nonfamilial D
CM (50 vs. 35%, p=NS). Echocardiographic indices of left ventricular s
ize and function were similar in relatives with and without detectable
antibodies. Conclusions: The presence of cardiac-specific autoantibod
ies in symptom-free relatives of DCM patients provides evidence for au
toimmunity in the majority (86%) of our pedigrees, including both fami
lial and nonfamilial forms of DCM.