T. Adachi et al., QUANTITATIVE AND QUALITATIVE CHANGES OF EXTRACELLULAR-SUPEROXIDE DISMUTASE IN PATIENTS WITH VARIOUS DISEASES, Clinica chimica acta, 229(1-2), 1994, pp. 123-131
Extracellular-superoxide dismutase (EC-SOD) is a secretory glycoprotei
n that is the major SOD isozyme in extracellular fluids. It has previo
usly been shown that EC-SOD levels in sera from healthy persons are cl
early divided into two discontinuous groups: a lower group (named Grou
p I, below 120 ng/ml) and a higher group (Group II, above 400 ng/ml).
The family studies have shown that the high EC-SOD level in healthy pe
rsons is genetically transmitted. We report here on the EC-SOD levels
in the sera of patients with various diseases. The EC-SOD levels were
distinctly higher in patients with renal diseases and moderately highe
r in liver diseases and diabetes than those in normal healthy persons.
In cerebrovascular diseases, heart diseases and acute digestive disea
ses, significant differences of EC-SOD were not observed. In patients
with renal diseases, the increase of EC-SOD was accompanied by the lac
k of renal function. Serum EC-SOD in Group I healthy persons is known
to be heterogeneous with regard to heparin affinity and can be separat
ed into three fractions: A without affinity, B with weak affinity and
C with relatively strong heparin affinity, whereas the EC-SOD in Group
II is mainly one fraction of C-type. Also in the case of hemodialysis
patients, serum EC-SOD in Group I or Group I' (similar to 120-400 ng/
ml) was divided into three fractions. EC-SOD in Group II showed two di
fferent profiles on heparin-Sepharose column chromatographies: one con
sisted mainly of EC-SOD C and the other consisted of EC-SOD A and C. I
t is probable that the high serum EC-SOD level in hemodialysis patient
s was due to two possible factors: the genetic transmitted factor and
unknown pathophysiological factor(s).