AUTONOMIC NERVOUS DYSFUNCTION IN SYSTEMIC LUPUS-ERYTHEMATOSUS (SLE) AND RHEUMATOID-ARTHRITIS (RA) - POSSIBLE PATHOGENIC ROLE OF AUTOANTIBODIES TO AUTONOMIC NERVOUS STRUCTURES
S. Maule et al., AUTONOMIC NERVOUS DYSFUNCTION IN SYSTEMIC LUPUS-ERYTHEMATOSUS (SLE) AND RHEUMATOID-ARTHRITIS (RA) - POSSIBLE PATHOGENIC ROLE OF AUTOANTIBODIES TO AUTONOMIC NERVOUS STRUCTURES, Clinical and experimental immunology, 110(3), 1997, pp. 423-427
Autonomic nervous dysfunction has been previously reported in SLE, RA
and systemic sclerosis, but the pathogenesis of such a complication is
poorly understood. In the present study, four standard cardiovascular
autonomic function tests were performed in 34 female patients with co
nnective tissue diseases and in 25 healthy control subjects, and resul
ts expressed as cardiovascular (CV) test scores. Moreover, in each sub
ject the presence of circulating complement-fixing autoantibodies dire
cted against sympathetic and parasympathetic nervous structures, repre
sented by superior cervical ganglia and vagus nerve, respectively, was
simultaneously assessed by an indirect immunofluorescent complement-f
ixation technique, using rabbit tissue as substrate. None of the patie
nts reported autonomic symptoms. However, an abnormal CV test score (g
reater than or equal to 5) was detected in 15% of the patients and in
none of the healthy control subjects, approaching statistical signific
ance (P = 0.07). No correlation was found between CV test results and
disease duration, type of therapy or presence of conventional autoanti
bodies. One or two autoantibodies to autonomic nervous structures were
detected in six patients (18%) and not in the control subjects (P < 0
.05). Values of deep breathing test were significantly lower in autoan
tibody-positive patients compared with those amongst the control subje
cts (P < 0.05), and an abnormal CV test score was significantly associ
ated with the presence of autoantibodies to autonomic nervous structur
es (P < 0.05). In conclusion, we confirm that autonomic nervous functi
on can be impaired in patients with connective tissue diseases, and su
ggest that autoantibodies directed against autonomic nervous system st
ructures may play a role in the pathogenesis of the autonomic dysfunct
ion.