D. Willems et al., SERUM-LIPOPROTEIN (A) IN TYPE-1 DIABETIC CHILDREN AND ADOLESCENTS - RELATIONSHIPS WITH HBA1C AND SUBCLINICAL COMPLICATIONS, European journal of pediatrics, 155(3), 1996, pp. 175-178
In a population of 106 young type I diabetic patients, we evaluated wh
ether a relationship exists between lipoprotein (Lp)(a) or apolipoprot
eins and the degree of metabolic control (HbA1c, fructosamine) or the
subclinical complications. The patients were subdivided according to p
uberty and to the presence or not of subclinical complications (no com
plications [n = 32]; retinopathy at fluorescein angiography [n = 28];
neuropathy diagnosed by reduced peroneal motor nerve conduction veloci
ty [n = 30]; nephropathy determined by presence of micro-albuminuria [
n = 15]). Lp(a) concentrations were not significantly increased in the
whole group of diabetic patients. There was no difference between gir
ls and boys, nor between the prepubertal children and the others. Ther
e were no significant correlations between the markers of metabolic co
ntrol and Lp(a). Nevertheless, if the diabetic patients were divided i
nto two groups according to the levels of HbA1c (< 7.6 or greater than
or equal to 6% Hb), Lp(a) tends to be higher in the poorly controlled
, but not to any significant degree. On the other hand, significant in
creases of total cholesterol, triglycerides, low density lipoprotein c
holesterol and apolipoprotein B levels were observed in poorly control
led patients, Lp(a) concentrations were significantly lower in patient
s with subclinical neuropathy or nephropathy than in patients without
these complications, but not in patients with retinopathy versus no re
tinopathy. These results are confirmed by categorical analysis (i.e. L
p(a) less than or equal to 30 vs > 30 mg/dl). Conclusion Lp(a) levels
are not significantly increased in poorly controlled insulin-dependent
diabetes mellitus patients. High levels of Lp(a), in young diabetic p
atients, are not markers for subclinical complications (retinopathy, n
europathy and nephropathy). On the contrary, low Lp(a) levels were fou
nd in subjects with subclinical neuropathy or nephropathy.