Postprandial hemorrheology and apolipoprotein B metabolism in patients with familial hypertriglyceridemia

Impaired postprandial lipoprotein metabolim has been found to be related to the extent of coronary artery disease. Moreover, since dyslipoproteinemias are associated with impaired hemorrheology, we investigated the effect of postprandial hypertriglyceridemia on hemorrheological parameters before and...

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Veröffentlicht in:Metabolism, clinical and experimental clinical and experimental, 1997-11, Vol.46 (11), p.1299-1304
Hauptverfasser: Otto, Carsten, Pschierer, Volkhard, Soennichsen, Andreas C., Schwandt, Peter, Richter, Werner O.
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container_end_page 1304
container_issue 11
container_start_page 1299
container_title Metabolism, clinical and experimental
container_volume 46
creator Otto, Carsten
Pschierer, Volkhard
Soennichsen, Andreas C.
Schwandt, Peter
Richter, Werner O.
description Impaired postprandial lipoprotein metabolim has been found to be related to the extent of coronary artery disease. Moreover, since dyslipoproteinemias are associated with impaired hemorrheology, we investigated the effect of postprandial hypertriglyceridemia on hemorrheological parameters before and after triglyceride-lowering therapy. Triglyceride-rich lipoproteins (TRLs) separated by ultracentrifugation (d < 1.006 g/dL) and chylomicron remnants (quantified by apolipoprotein [apo] B-48 determination) were determined after a fat load in 10 patients with familial hypertriglyceridemia before and after therapy with gemfibrozil (900 mg daily). Lipid and hemorrheological parameters (plasma and whole-blood viscosity (PV and BV], red cell aggregation [RCA], hematocrit, and fibrinogen) were determined at baseline and every hour up to 6 hours postprandially. Fasting total triglycerides and TRL triglycerides significantly decreased with gemfibrozil therapy ( P < .01). Total triglycerides postprandially increased from 9.53 ± 1.72 to 14.47 ± 2.07 mmol/L (TRL triglycerides by 61%) before therapy ( P < .05) and from 4.61 ± 1.28 to 7.17 ± 0.99 mmol/L (TRL triglycerides by 57%) after therapy ( P < .05). The postprandial TRL apo B increase was reduced with gemfibrozil (from 11.6 ± 2.8 to 20.7 ± 5.0 mg/dL with therapy v 19.0 ± 7.6 to 33.0 ± 12.5 mg/dL before therapy, P < .05, respectively) with proportionally greater increase in apo B-48 (119% and 169%, respectively) compared with apo B-100 (64% and 64%, respectively). Fasting RCA was improved with lipid-lowering therapy ( P < .05), but PV, BV, RCA, and fibrinogen did not show any statistically signifant postprandial changes either before or after lipid-lowering therapy. In summary, we did not find any statistically significant changes in hemorrheological parameters, despite a strong postprandial increase of triglycerides. In particular, these findings were independent of fasting triglyceride levels. We conclude that triglyceride-lowering therapy by gemfibrozil had no substantial beneficial effects with respect to hemorrheology in patients with familial hypertriglyceridemia.
doi_str_mv 10.1016/S0026-0495(97)90234-1
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Moreover, since dyslipoproteinemias are associated with impaired hemorrheology, we investigated the effect of postprandial hypertriglyceridemia on hemorrheological parameters before and after triglyceride-lowering therapy. Triglyceride-rich lipoproteins (TRLs) separated by ultracentrifugation (d < 1.006 g/dL) and chylomicron remnants (quantified by apolipoprotein [apo] B-48 determination) were determined after a fat load in 10 patients with familial hypertriglyceridemia before and after therapy with gemfibrozil (900 mg daily). Lipid and hemorrheological parameters (plasma and whole-blood viscosity (PV and BV], red cell aggregation [RCA], hematocrit, and fibrinogen) were determined at baseline and every hour up to 6 hours postprandially. Fasting total triglycerides and TRL triglycerides significantly decreased with gemfibrozil therapy ( P < .01). Total triglycerides postprandially increased from 9.53 ± 1.72 to 14.47 ± 2.07 mmol/L (TRL triglycerides by 61%) before therapy ( P < .05) and from 4.61 ± 1.28 to 7.17 ± 0.99 mmol/L (TRL triglycerides by 57%) after therapy ( P < .05). The postprandial TRL apo B increase was reduced with gemfibrozil (from 11.6 ± 2.8 to 20.7 ± 5.0 mg/dL with therapy v 19.0 ± 7.6 to 33.0 ± 12.5 mg/dL before therapy, P < .05, respectively) with proportionally greater increase in apo B-48 (119% and 169%, respectively) compared with apo B-100 (64% and 64%, respectively). Fasting RCA was improved with lipid-lowering therapy ( P < .05), but PV, BV, RCA, and fibrinogen did not show any statistically signifant postprandial changes either before or after lipid-lowering therapy. In summary, we did not find any statistically significant changes in hemorrheological parameters, despite a strong postprandial increase of triglycerides. In particular, these findings were independent of fasting triglyceride levels. 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Hyperlipoproteinemia ; Fasting - blood ; Female ; Gemfibrozil - administration &amp; dosage ; Hematocrit ; Humans ; Hyperlipoproteinemia Type IV - blood ; Hyperlipoproteinemia Type IV - drug therapy ; Hyperlipoproteinemia Type IV - metabolism ; Hypolipidemic Agents - administration &amp; dosage ; Lipid Metabolism ; Lipids - blood ; Male ; Medical sciences ; Metabolic diseases ; Postprandial Period ; Rheology ; Time Factors ; Triglycerides - blood ; Triglycerides - metabolism</subject><ispartof>Metabolism, clinical and experimental, 1997-11, Vol.46 (11), p.1299-1304</ispartof><rights>1997</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-e799f358e95a53151021238a81220583b3ecd2a0b2cb93d4bd814ebd4ffa8b243</citedby><cites>FETCH-LOGICAL-c389t-e799f358e95a53151021238a81220583b3ecd2a0b2cb93d4bd814ebd4ffa8b243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0026049597902341$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2057497$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9361689$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Otto, Carsten</creatorcontrib><creatorcontrib>Pschierer, Volkhard</creatorcontrib><creatorcontrib>Soennichsen, Andreas C.</creatorcontrib><creatorcontrib>Schwandt, Peter</creatorcontrib><creatorcontrib>Richter, Werner O.</creatorcontrib><title>Postprandial hemorrheology and apolipoprotein B metabolism in patients with familial hypertriglyceridemia</title><title>Metabolism, clinical and experimental</title><addtitle>Metabolism</addtitle><description><![CDATA[Impaired postprandial lipoprotein metabolim has been found to be related to the extent of coronary artery disease. Moreover, since dyslipoproteinemias are associated with impaired hemorrheology, we investigated the effect of postprandial hypertriglyceridemia on hemorrheological parameters before and after triglyceride-lowering therapy. Triglyceride-rich lipoproteins (TRLs) separated by ultracentrifugation (d < 1.006 g/dL) and chylomicron remnants (quantified by apolipoprotein [apo] B-48 determination) were determined after a fat load in 10 patients with familial hypertriglyceridemia before and after therapy with gemfibrozil (900 mg daily). Lipid and hemorrheological parameters (plasma and whole-blood viscosity (PV and BV], red cell aggregation [RCA], hematocrit, and fibrinogen) were determined at baseline and every hour up to 6 hours postprandially. Fasting total triglycerides and TRL triglycerides significantly decreased with gemfibrozil therapy ( P < .01). 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We conclude that triglyceride-lowering therapy by gemfibrozil had no substantial beneficial effects with respect to hemorrheology in patients with familial hypertriglyceridemia.]]></description><subject>Adult</subject><subject>Apolipoproteins B - blood</subject><subject>Apolipoproteins B - classification</subject><subject>Apolipoproteins B - drug effects</subject><subject>Apolipoproteins B - metabolism</subject><subject>Biological and medical sciences</subject><subject>Disorders of blood lipids. 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Moreover, since dyslipoproteinemias are associated with impaired hemorrheology, we investigated the effect of postprandial hypertriglyceridemia on hemorrheological parameters before and after triglyceride-lowering therapy. Triglyceride-rich lipoproteins (TRLs) separated by ultracentrifugation (d < 1.006 g/dL) and chylomicron remnants (quantified by apolipoprotein [apo] B-48 determination) were determined after a fat load in 10 patients with familial hypertriglyceridemia before and after therapy with gemfibrozil (900 mg daily). Lipid and hemorrheological parameters (plasma and whole-blood viscosity (PV and BV], red cell aggregation [RCA], hematocrit, and fibrinogen) were determined at baseline and every hour up to 6 hours postprandially. Fasting total triglycerides and TRL triglycerides significantly decreased with gemfibrozil therapy ( P < .01). Total triglycerides postprandially increased from 9.53 ± 1.72 to 14.47 ± 2.07 mmol/L (TRL triglycerides by 61%) before therapy ( P < .05) and from 4.61 ± 1.28 to 7.17 ± 0.99 mmol/L (TRL triglycerides by 57%) after therapy ( P < .05). The postprandial TRL apo B increase was reduced with gemfibrozil (from 11.6 ± 2.8 to 20.7 ± 5.0 mg/dL with therapy v 19.0 ± 7.6 to 33.0 ± 12.5 mg/dL before therapy, P < .05, respectively) with proportionally greater increase in apo B-48 (119% and 169%, respectively) compared with apo B-100 (64% and 64%, respectively). Fasting RCA was improved with lipid-lowering therapy ( P < .05), but PV, BV, RCA, and fibrinogen did not show any statistically signifant postprandial changes either before or after lipid-lowering therapy. In summary, we did not find any statistically significant changes in hemorrheological parameters, despite a strong postprandial increase of triglycerides. In particular, these findings were independent of fasting triglyceride levels. We conclude that triglyceride-lowering therapy by gemfibrozil had no substantial beneficial effects with respect to hemorrheology in patients with familial hypertriglyceridemia.]]></abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>9361689</pmid><doi>10.1016/S0026-0495(97)90234-1</doi><tpages>6</tpages></addata></record>
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subjects Adult
Apolipoproteins B - blood
Apolipoproteins B - classification
Apolipoproteins B - drug effects
Apolipoproteins B - metabolism
Biological and medical sciences
Disorders of blood lipids. Hyperlipoproteinemia
Fasting - blood
Female
Gemfibrozil - administration & dosage
Hematocrit
Humans
Hyperlipoproteinemia Type IV - blood
Hyperlipoproteinemia Type IV - drug therapy
Hyperlipoproteinemia Type IV - metabolism
Hypolipidemic Agents - administration & dosage
Lipid Metabolism
Lipids - blood
Male
Medical sciences
Metabolic diseases
Postprandial Period
Rheology
Time Factors
Triglycerides - blood
Triglycerides - metabolism
title Postprandial hemorrheology and apolipoprotein B metabolism in patients with familial hypertriglyceridemia
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