EFFECTS OF N-3 FATTY-ACIDS AND FENOFIBRATE ON LIPID AND HEMORRHEOLOGICAL PARAMETERS IN FAMILIAL DYSBETALIPOPROTEINEMIA AND FAMILIAL HYPERTRIGLYCERIDEMIA
C. Otto et al., EFFECTS OF N-3 FATTY-ACIDS AND FENOFIBRATE ON LIPID AND HEMORRHEOLOGICAL PARAMETERS IN FAMILIAL DYSBETALIPOPROTEINEMIA AND FAMILIAL HYPERTRIGLYCERIDEMIA, Metabolism, clinical and experimental, 45(10), 1996, pp. 1305-1311
There is increasing evidence that hemorrheological abnormalities are a
ssociated with an enhanced risk of atherosclerosis. The n-3 fatty acid
s (n-3-FA) have been shown to have beneficial effects on atheroscleros
is in patients with dyslipoproteinemias. We studied 23 patients with e
levated plasma triglycerides to evaluate the influence of fish oil and
fenofibrate therapy on hemorrheological parameters (15 patients with
familiar hypertriglyceridemia [FHTG] and eight with familial dysbetali
poproteinemia [FDL]). The patients (one woman and 22 men aged 45.7 +/-
2.0 years) were treated with increasing doses of n-3-FA (1.8 to 3.6 g
/d: 0.9 to 1.8 g eicosapentaenoic acid and 0.6 to 1.2 g docosahexaenoi
c acid) for 8 weeks. Lipid parameters, whole-blood viscosity at differ
ent shear rates, plasma viscosity, fibrinogen concentration, and red b
lood cell aggregation (RCA) were measured at baseline and at weeks 2,
4, 8 (end of n-3-FA therapy), and 12. Compliance was ensured by measur
ing plasma concentrations of eicosapentaenoic acid and docosahexaenoic
acid. After 12 weeks, patients began treatment with fenofibrate (250
mg daily); investigations were performed again at week 20. Total trigl
ycerides (from 6.90 +/- 1.70 to 3.61 +/- 0.78 mmol/L in FDL and 7.44 /- 1.50 to 4.15 +/- 0.55 in FHTG), very-low-density lipoprotein (VLDL)
triglycerides, and VLDL cholesterol were significantly decreased with
n-3-FA therapy in both groups (P < .05). In FHTG, low-density lipopro
tein (LDL) cholesterol increased significantly (from 2.75 +/- 0.28 to
3.97 +/- 0.35 mmol/L, P < .01); in FDL, total cholesterol decreased (f
rom 9.76 +/- 1.32 to 7.34 +/- 1.07 mmol/L, P < .05). No significant ch
anges were observed in hemorrheological parameters, except for reduced
RCA with 3.6 g n-3-FA in FHTG. However, with fenofibrate therapy, in
addition to comparable lipoprotein changes seen with fish oil, fibrino
gen levels and plasma and blood viscosity decreased in patients with F
DL. We conclude that n-3-FA and fenofibrate have comparable effects on
lipid parameters in patients with FDL and FHTG. Because of additional
beneficial effects on hemorrheological parameters, fenofibrate may be
preferred for the treatment of FDL. Copyright (C) 1996 by W.B. Saunde
rs Company