Acute effects of low density lipoprotein apheresis on metabolic parametersof apolipoprotein B

Citation
Kg. Parhofer et al., Acute effects of low density lipoprotein apheresis on metabolic parametersof apolipoprotein B, J LIPID RES, 41(10), 2000, pp. 1596-1603
Citations number
28
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF LIPID RESEARCH
ISSN journal
00222275 → ACNP
Volume
41
Issue
10
Year of publication
2000
Pages
1596 - 1603
Database
ISI
SICI code
0022-2275(200010)41:10<1596:AEOLDL>2.0.ZU;2-7
Abstract
Apheresis is a treatment option for patients with severe hypercholesterolem ia and coronary artery disease. It is unknown whether such therapy changes kinetic parameters of lipoprotein metabolism, such as apolipoprotein B (apo B) secretion rates, conversion rates, and fractional catabolic rates (FCR), We studied the acute effect of apheresis on metabolic parameters of apoB i n five patients with drug resistant hyperlipoproteinemia, using endogenous labeling with D-3-leucine, mass spectrometry, and multicompartmental modeli ng. Patients were studied prior to and immediately after apheresis therapy, The two tracer studies were modeled simultaneously, taking into account th e nonsteady-state concentrations of apoB, The low density lipoprotein (LDL) -apoB concentration was 120 +/- 32 mg dl(-1) prior to and 52 +/- 18 mg dl(- 1) immediately after apheresis therapy, The metabolic studies indicate that no change in apoB secretion (13.9 +/- 4.9 mg kg(-1) day(-1)) is required t o fit the tracer and apoB mass data obtained before and after apheresis and that in four of the five patients the LDL-apoB FCR (0.21 +/- 0.02 day(-1)) was not altered after apheresis, In one subject the LDL-apoB FCR temporari ly increased from 0.22 day(-1) to 0.35 day(-1) after apheresis, The convers ion rate of very low density Lipoprotein (VLDL)-apoB to LDL-apoB is tempora rily decreased from 76 to 51% after apheresis and thus less LDL-apoB is pro duced after apheresis, We conclude that an acute reduction of LDL-apoB conc entration does not affect apoB secretion or LDL-apoB FCR, but that apoB con version to LDL is temporarily decreased. Thus, in most patients the decreas ed rate of delivery of neutral lipids or apoB to the liver does not result in an upregulation of LDL receptors or in decreased apoB secretion.