Insulin dependent diabetes mellitus (IDDM) is an autoimmune
disease associated with the presence of different types of autoantibodies. The
presence of these antibodies and the corresponding antigens in the circulation
leads to the formation of circulating immune complexes (CIC). CIC are known to
persist in the blood for long periods of time. Such CIC following deposition in
the small blood vessels have the potential to lead to microangiopathy with
debilitating clinical consequences. The aim of our pilot study was to investigate
whether a correlation exists between CIC and the development of microvascular
complications in diabetic children. Isolation of a new glycoprotein complement
inhibition factor (CIF) from the parasitic plant Cuscuta europea seed, which appears
to bind specifically to complement component C3 has provided an unique tool
for the measurement of immune complexes by means of ELISA-type techniques
(CIF-ELISA). We studied the levels of CIC (IgG, IgM and IgA) in 58 diabetic
children (mean age 12.28±4.04 years, diabetes duration 5.3±3.7 years), 29 of
them had vascular complications (group 1) and the other 29 were without
vascular complications (group 2). As controls, we studied sera samples from
21 healthy children (mean age 13.54±4.03 years). Sera from the diabetic
patients showed statistically significant higher levels of CIC IgG ( p=0.03) than
sera from the control group. In sera from group 1 values of CIC IgG showed
statistically significant higher levels than controls (0.720±0.31 vs. 0.46±0.045;
p=0.011) Sera from 59% of the patients were positive for CIC IgG, 36% for CIC
IgM and 9% for CIC IgA. Among 26 patients with microalbuminuria, sera from
17/26 (65%) were positive for CIC IgG, 8/26 (31%) for CIC IgM and 2/26 (8%) for
CIC IgA. CIC IgG correlated with HbA1c (r=0.51; p=0.005) and microalbuminuria
(r=0.42, p=0.033). CIC IgA correlated with
age (r=0.44, p=0.03). CIC IgM
correlated with the duration of diabetes (r=0.63, p=0.02). These findings suggest
that elevated levels of CIC IgG are associated with the development of early diabetic nephropathy.