W. Herrmann et al., An increased serum level of free Apo(a) in renal patients is more strikingthan that of Lp(a) and is influenced by homocysteine, NEPHRON, 85(1), 2000, pp. 41-49
Lipoprotein(a) [Lp(a)] excess combined with hyperhomocysteinaemia and hyper
fibrinogenaemia may contribute to the high incidence of vascular diseases i
n dialysis patients. This study is aimed at investigating the role of free
apolipoprotein(a) [fapo(a)] in renal patients. We have been able to show th
at, as compared with controls (0.53 mg/l), the median serum concentrations
of fapo(a) in patients with nephrotic syndrome (2.58 mg/l) and with periton
eal dialysis (3.40 mg/l) were strongly elevated (5- to 7-fold), while the f
apo(a) levels in patients undergoing haemodialysis (1.02 mg/l) and after re
nal transplantation (0.90 mg/l) were about doubled. The observed difference
s in fapo(a) levels indicate that several mechanisms may increase the level
of fapo(a), i.e., reduced renal clearance, enhanced hepatic synthesis, or
homocysteine releasing apolipoprotein(a) from Lp(a). In the study collectiv
e, the median total homocysteine levels were significantly elevated in all
patient groups, stronger in patients on haemodialysis (31.4 mu mol/l) and p
eritoneal dialysis (31.2 mu mol/l) than in patients with nephrotic syndrome
(19.7 mu mol/l) and after renal transplantation (19.5 mu mol/l). In transp
lant patients with adequate renal function and without other apolipoprotein
(a)-increasing factors, fapo(a) was significantly increased when total homo
cysteine exceeded 22 mu mol/l. In conclusion, our findings let us presume t
hat an increased fapo(a) level in renal patients possibly could be one of t
he reasons contributing to the high incidence of vascular diseases in these
patients, because fapo(a) not covalently linked with Lp(a) is even more ea
sily able to inhibit the fibrinolytic system than the complete Lp(a). These
preliminary results have to be confirmed by further investigations. Copyri
ght (C) 2000 S. Karger AG, Basel.