H. Yamaguchi et al., EFFECTIVENESS OF LDL-APHERESIS IN PREVENTING RESTENOSIS AFTER PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) - LDL-APHERESIS ANGIOPLASTY RESTENOSIS TRIAL (L-ART), Chemistry and physics of lipids, 67-8, 1994, pp. 399-403
To investigate the efficacy of reducing plasma lipoprotein(a) (Lp(a))
as well as low density lipoprotein cholesterol (LDL-C) levels on the p
revention of restenosis after PTCA, LDL-apheresis was attempted on a t
otal of 54 patients at six institutions. LDL-apheresis using a dextran
sulfate cellulose column has been proven to be an effective method fo
r reducing both plasma Lp(a) and LDL-C levels. As a subgroup (apheresi
s-drug combined group), 29 of the 54 patients were given Pravastatin (
HMG CoA reductase inhibitor) and Niceritrol (Nicotinic Acid) in additi
on to LDL-apheresis to maintain low plasma levels of both Lp(a) and LD
L-C through the follow-up period of 5 months after PTCA. Patients whos
e plasma Lp(a) levels were reduced by more than 50% showed a lower res
tenosis rate than those whose plasma Lp(a) levels were reduced by less
than 50% (21.2% vs. 52.4%, P = 0.0179), especially in patients with h
igh plasma Lp(a) levels above 30 mg/dl where a much lower restenosis r
ate (15.0%) was observed. Furthermore, in the apheresis-drug combined
group, the restenosis rate was 11.8% regardless of baseline plasma Lp(
a) levels, including even those below 30 mg/dl. In conclusion, in pati
ents with high plasma Lp(a) levels, a greater than 50% reduction in:Lp
(a) levels by LDL-apheresis is effective in preventing restenosis afte
r PTCA. If the plasma Lp(a) reduction rate is greater than 50%, LDL-ap
heresis combined with lipid-lowering drugs such as niceritrol and prav
astatin seems to be more effective, even in patients with low plasma L
p(a) levels.