R. Garnotel et al., CHANGES IN SERUM LIPOPROTEIN(A) LEVELS IN CHILDREN WITH CORTICOSENSITIVE NEPHROTIC SYNDROME, Pediatric nephrology, 10(6), 1996, pp. 699-701
Variations in lipoprotein(a) [Lp(a)] levels were evaluated during the
course of the nephrotic syndrome in 20 children (17 males, 3 females,
aged 2-16 years), to evaluate the use of this parameter in the prognos
is and monitoring of the disease. One patient was in relapse, 12 in re
mission, and 7 alternated between remission and relapse. Results were
compared with those obtained in a control population of 100 age-matche
d children. Lp(a) was measured by a previously described immunonephelo
metric technique. Serum Lp(a) levels were increased in children with r
elapsing nephrotic syndrome compared with controls (median value of 41
9 mg/l vs. 86 mg/l). The median Lp(a) level in patients with nephrotic
syndrome in remission was different from controls (270 mg/l under ste
roid therapy and 163 mg/l without steroid therapy), but remained withi
n the reference range. Of the patients in relapse, 66% had Lp(a) level
s above the generally accepted limit for cardiovascular risk of 300 mg
/l, compared with 16% of controls, 44% of patients with nephrotic synd
rome in remission under steroid therapy, and 18% of patients with neph
rotic syndrome in remission without steroid therapy. In 2 patients, Lp
(a) was measured repeatedly and was significantly higher during the ac
ute phase of the disease (up to sixfold basal level). Changes in Lp(a)
levels correlated with cholesterol levels, but the kinetics and the e
xtent of variations were different. These data suggest that measuremen
t of Lp(a) is useful for monitoring the nephrotic syndrome in children
, particularly for detecting complications.