Jg. Leu et al., LOW-MOLECULAR-WEIGHT HEPARIN IN DIABETIC AND NONDIABETIC HYPERCHOLESTEROLEMIC PATIENTS RECEIVING LONG-TERM HEMODIALYSIS, Journal of the Formosan Medical Association, 97(1), 1998, pp. 49-54
Dyslipidemia is a major factor associated with cardiovascular disease,
which is the leading cause of death in hemodialysis patients. Low mol
ecular weight heparin (LMWH) is superior to conventional unfractionate
d heparin in treating hyperlipidemia in nondiabetic long-term hemodial
ysis patients and has fewer side-effects. Only a few reports have addr
essed the influence of LMWH on serum lipids in diabetic patients, alth
ough dyslipidemia is common among this population. We investigated the
effect of LMWH on serum lipids in 12 nondiabetic and eight diabetic h
ypercholesterolemic patients receiving long-term hemodialysis. Patient
s had been receiving hemodialysis with unfractionated heparin for a mi
nimum of 6 months before beginning the study. Continuous LMWH infusion
during hemodialysis was administered to all patients for 2 months, fo
llowed by unfractionated heparin administration for 2 months. During L
MWH treatment, plasma anti-factor Xa activity increased from 0.06 +/-
0.04 IU/mL before dialysis to 0.49 +/- 0.25 IU/mL after 3 hours. Serum
total cholesterol (TC), low-density lipoprotein-cholesterol (LDL-C),
and apolipoprotein B (Apo B) in both nondiabetic and diabetic patient
groups and lipoprotein(a) (Lp(a)) in patients with higher initial valu
es (greater than or equal to 15 mg/mL) decreased significantly after L
MWH treatment (TC from 6.38 +/- 1.14 to 5.07 +/- 1.09 mmol/L, LDL-C fr
om 3.08 +/- 0.93 to 2.15 +/- 0.88 mmol/L, Apo B from 100 +/- 18 to 78
+/- 18 mg/dL, all p < 0.01; Lp(a) from 41.8 +/- 34.5 to 28.5 +/- 22.8,
p < 0.05). They rebounded to pre-LMWH levels after the 2 months on un
fractionated heparin (TC 5.72 +/- 1.11 mmol/L, LDL-C 2.97 +/- 1.01 mmo
l/L, Apo B 98 +/- 20 mg/dL, Lp(a) 38.1 +/- 29.0 mg/dL). We conclude th
at continuous infusion of LMWH during dialysis reduces serum total cho
lesterol, low-density lipoprotein-cholesterol, and apolipoprotein B co
ncentrations in both diabetic and nondiabetic hypercholesterolemic hem
odialysis patients, and does not increase the risk of bleeding compare
d with unfractionated heparin.