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. 1993 Jun;13(6):842-51.
doi: 10.1161/01.atv.13.6.842.

Increased production rates of LDL are common in individuals with low plasma levels of HDL cholesterol, independent of plasma triglyceride concentrations

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Increased production rates of LDL are common in individuals with low plasma levels of HDL cholesterol, independent of plasma triglyceride concentrations

H N Ginsberg et al. Arterioscler Thromb. 1993 Jun.

Abstract

Reduced plasma levels of high density lipoprotein (HDL) cholesterol are associated with increased risk for coronary heart disease. Although plasma HDL levels are, in general, inversely related to plasma triglyceride (TG) concentrations, a small proportion of individuals with low HDL cholesterol concentrations have normal plasma TG levels. We wished to determine whether subjects with low plasma levels of HDL cholesterol could be characterized by common abnormalities of lipoprotein metabolism independent of plasma TGs. Therefore, we studied the metabolism of low density lipoprotein (LDL) apolipoprotein B (apo B) and HDL apolipoprotein A-I (apo A-I) in subjects with low plasma HDL cholesterol concentrations with or without hypertriglyceridemia. Nine subjects with low plasma HDL cholesterol levels and normal levels of plasma TGs and LDL cholesterol were studied. Autologous 131I-LDL and 125I-HDL were injected intravenously, and blood samples were collected for 2 weeks. LDL apo B and HDL apo A-I levels were measured by specific radioimmunoassays. Fractional catabolic rates (FCRs, pools per day) and production rates (PRs, milligrams/kilogram.day) for each apolipoprotein were determined. The results were compared with those obtained previously in nine subjects with low plasma HDL cholesterol levels and hypertriglyceridemia and in seven normal subjects. The normal subjects had an HDL apo A-I FCR (mean +/- SD) of 0.21 +/- 0.04. Despite large differences in plasma TG levels, the HDL apo A-I FCRs were similar in the low-HDL, normal-TG group (0.30 +/- 0.09) and the low-HDL, high-TG group (0.33 +/- 0.10), although only the latter value was significantly increased versus control subjects (p < 0.03). Increased apo A-I FCRs were associated with reduced HDL apo A-I levels in both groups of patients. Apo A-I PRs were similar in all groups. In contrast, LDL apo B PR was increased approximately 50% in the low-HDL, normal-TG group (19.3 +/- 6.6; p < 0.01) compared with normal subjects (12.5 +/- 2.6). There was a strong trend toward a greater LDL apo B PR in the low-HDL, high-TG group (17.6 +/- 4.5; p = 0.06 versus normal subjects) as well. LDL apo B FCRs were similar in all three groups. LDL apo B concentrations were also increased in the group with low HDL cholesterol and normal TG levels. Both groups with low HDL cholesterol levels had cholesterol-depleted LDL and HDL particles.(ABSTRACT TRUNCATED AT 400 WORDS)

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Figures

Figure 1
Figure 1
Bar graphs showing high density lipoprotein (HDL) apolipoprotein A-I (apo A-I) fractional catabolic rates (FCR) (day−1) (left panel) and production rates (mg/kg · d) (right panel) in normal (N) (open bar), hypertrigfyceridemic (↑ TG)–low-HDL (open-hatched bar), and normal TG–low HDL (dark-shaded bar) groups. Apo A-I FCR was significantly greater in the hypertrigfyceridemic group vs. normal (*p<0.03). There was a trend (p=0.09) toward a greater apo A-I FCR in the group with isolated reductions in HDL. Production rates of apo A-I were similar in all three groups.
Figure 2
Figure 2
Bar graphs showing low density lipoprotein (LDL) apolipoprotein B (apo B) fractional catabolic rates (FCR) (day−1) (left panel) and production rates (PR) (mg/kg · day) (right panel) in normal (N) (open bar), hypertrigfyceridemic (↑ TG)–low high density lipoprotein (HDL) (open-hatched bar), and normal TG–low HDL (dark-shaded bar) groups. LDL apo B PR was significantfy greater in the normal TG–low HDL group vs. normal (*p<0.01). LDL apo B PR tended to be greater than normal in the hypertrigfyceridemic group as well (p=0.06). FCRs of apo B were similar in all three groups.
Figure 3
Figure 3
Bar graphs showing cholesterol/trigfyceride (TG) ratio in low density lipoprotein (LDL) (left panel) and high density lipoprotein (HDL) (right panel) in each group of subjects. The normal (N) subjects in whom we performed turnover studies did not have HDL and LDL TG concentrations measured. Therefore, we present ratio data for a separate group of normal subjects for whom we have compositional but not kinetic data. Both low-HDL groups had cholesterol-depleted LDL vs. normal (*p<0.003). Both low-HDL groups had cholesterol-depleted HDL vs. normal (*p<0.04 for normal TG–low HDL vs. normal and *p<0.001 for hypertrigfyceridemic [↑ TG] –low HDL vs. normal). In addition, HDL in the hypertrigfyceridemic group was more cholesterol depleted than the HDL in the normal TG–low HDL group (**p<0.03).
Figure 4
Figure 4
Graph showing relation between high density lipoprotein (HDL) apolipoprotein A-I (apo A-I) fractional catabolic rates (FCR) (y axis) and HDL cholesterol/trigfyceride (TG) ratio (x axis) for the hypertrigfyceridemic–low HDL (□;) and normal TG–low HDL (∆) subjects. The normal subjects who had onfy turnover studies had a mean FCR of 0.21; the normal subjects who had onfy cholesterol/trigfyceride ratios (Figure 3) had a mean ratio of 4. The combination of these two means (●) falls very close to the regression line.

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