H. Shigeta et al., SERUM AUTOANTIBODIES AGAINST SULFATIDE AND PHOSPHOLIPID IN NIDDM PATIENTS WITH DIABETIC NEUROPATHY, Diabetes care, 20(12), 1997, pp. 1896-1899
OBJECTIVE - We investigated the presence of antisulfatide and antiphos
pholipid antibodies and the relationship between these antibodies and
the results of quantitative tests of nerve function in NIDDM patients
with diabetic neuropathy. RESEARCH DESIGN AND METHODS - Antisulfatide
and antiphospholipid antibodies were measured in serum samples obtaine
d from 68 NIDDM patients with diabetic neuropathy by an enzyme-linked
immunosorbent assay (ELISA). Each patient was classified into one of t
hree groups based on the combined neuropathy score (determined by the
symptom score, the results of autonomic nerve function tests, and the
vibration perception test), as follows: mild in = 26), moderate in = 2
2), and severe (n = 20). Nerve conduction studies were performed in a
subgroup of 37 patients. RESULTS - The antisulfatide antibody was dete
cted in 1 (4%) of 26 patients in the mild group, 4 (18%) of 22 patient
s in the moderate group, and 8 (40%) of 20 patients in the severe grou
p (P < 0.01 vs. mild group). The antiphospholipid antibody was detecte
d in none of the patients in the mild group, 8 (36%) of 22 patients in
the moderate group (P < 0.001 vs. mild group), and 6 (30%) of 20 pati
ents in the severe group (P < 0.01 vs. mild group). The threshold ampl
itude, determined by the vibration perception test, was significantly
higher in antibody-positive patients than in antibody-negative patient
s: antisulfatide antibody, 55.9 +/- 46.8 mu m in = 13) vs. 22.9 +/- 13
.7 mu m (n = 55), P < 0.001; antiphospholipid antibody 47.2 +/- 32.5 m
u m in = 14) vs. 24.5 +/- 23.2 mu m (n = 54), P < 0.01. The conduction
velocity of the sural nerve was slower in the antisulfatide antibody-
positive group (37.9 +/- 11.1 m/s, n = 12) than in the antisulfatide a
ntibody-negative group (45.2 +/- 6.0 m/s, n = 19) (P < 0.05). CONCLUSI
ONS - These results suggest that autoimmune nerve destruction may be i
nvolved in diabetic neuropathy in NIDDM patients.