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Journal of Clinical Lipidology
Volume 2, Issue 4
, Pages 237-247
, August 2008
Clinical presentation, laboratory values, and coronary heart disease risk in marked high-density lipoprotein–deficiency states
References
- . Plasma-triglycerides in regulation of HDL-cholesterol levels. Lancet. 1978;2:391–393
- . Lipoprotein abnormalities in primary biliary cirrhosis: association with hepatic lipase inhibition as well as altered cholesterol esterification. Gastroenterology. 1985;89:1266–1278
- . Severe acquired (secondary) high-density lipoprotein deficiency. J Clin Lipidol. 2007;1:41–56
- . Apolipoprotein A-I(Milano) and apolipoprotein A-I(Paris) exhibit an antioxidant activity distinct from that of wild-type apolipoprotein A-I. Biochemistry. 2002;41:2089–2096
- . Executive summary of the third report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). JAMA. 2001;285:2486–2497
- . Prevalence of risk factors in men with premature coronary artery disease. Am J Cardiol. 1991;67:1185–1189
- Prevalence of familial lipoprotein disorders in patients with premature coronary artery disease. Circulation. 1992;85:2025–2033
- . Familial hypoalphalipoproteinemia in premature coronary artery disease. Arterioscler Thromb. 1993;13:1728–1737
- Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high-density lipoprotein cholesterol. N Engl J Med. 1999;341:410–418
- Relation of gemfibrozil treatment and lipid levels with major coronary events (VA-HIT: a randomized controlled trial). JAMA. 2001;285:1585–1591
- Diabetes, plasma insulin, and cardiovascular disease (Subgroup analysis from the Department of Veterans Affairs High-Density Lipoprotein Intervention Trial (VA-HIT)). Arch Intern Med. 2002;162:2597–2604
- . Plasma apolipoprotein A-I absence associated with marked reduction of high density lipoproteins and premature coronary artery disease. Arteriosclerosis. 1982;2:16–26
- . The clinical, biochemical, and genetic features in familial disorders of high density lipoprotein deficiency. Arteriosclerosis. 1984;4:303–322
- . Neuropathy in Tangier disease (Alpha-lipoprotein deficiency manifesting as familial recurrent neuropathy and intestinal lipid storage). Arch Neurol. 1967;17:1–9
- . The pathology of Tangier disease (A light and electron microscopic study). Am J Pathol. 1975;78:101–158
- . Isolation and characterization of an abnormal high density lipoprotein in Tangier Disease. J Clin Invest. 1977;60:242–252
- Apolipoprotein A-I and C-III deficiency, variant II. J Lipid Res. 1985;26:1089–1101
- . Familial apolipoprotein A-I, C-III, and A-IV deficiency with marked high density lipoprotein deficiency and premature atherosclerosis due to a deletion of the apolipoprotein A-I, C-III, and A-IV gene complex. J Biol Chem. 1989;264:16339–16342
- Familial deficiency of apolipoproteins A-I and C-III and precocious coronary artery disease. N Engl J Med. 1982;306:1513–1519
- . An inherited polymorphism in the human apolipoprotein A-I gene locus related to the development of atherosclerosis. Nature. 1983;301:718–720
- . DNA inversion within the apolipoprotein AI/CIII/AIV-encoding gene cluster of certain patients with premature atherosclerosis. Proc Natl Acad Sci U S A. 1987;84:7198–7202
- . Effect of blood high density lipoprotein cholesterol concentration on fecal steroid excretion in humans. Life Sci. 1983;32:2933–2937
- . Familial apolipoprotein AI and apolipoprotein CIII deficiency (Subclass distribution, composition, and morphology of lipoproteins in a disorder associated with premature atherosclerosis). J Clin Invest. 1984;74:1601–1613
- Apolipoprotein B metabolism in subjects with deficiency of apolipoproteins CIII and AI (Evidence that apoCIII inhibits catabolism of triglyceride-rich lipoproteins by lipoprotein lipase in vivo). J Clin Invest. 1986;78:1287–1295
- . Effect of apolipoprotein activators on the specificity lecithin:cholesterol acyltransferase: determination of cholesteryl esters formed in A-I/C-III deficiency. J Lipid Res. 1991;32:1601–1609
- . Characterization of apoA-I and apoB containing lipoprotein particles in a variant of familial apolipoprotein A-I deficiency with planar xanthomas: the metabolic significance of LP-A-II particles. J Lipid Res. 1991;32:1587–1599
- . Deficiency of apolipoproteins A-I and C-III and severe coronary artery disease. Clin Cardiol. 1986;9:349–352
- Apolipoprotein A-I deficiency due to a codon 84 nonsense mutation of the apolipoprotein A-I gene. Proc Natl Acad Sci U S A. 1991;88:2793–2797
- . Apolipoprotein A-I Q[-2]X causing isolated apolipoprotein deficiency in a family with analphalipoproteinemia. J Clin Invest. 1994;93:223–229
- . Case report: retinopathy and neuropathy associated with complete apolipoprotein A-I deficiency. Am J Med Sci. 1996;312:30–33
- Characterization of high density lipoprotein particles in familial apolipoprotein A-I deficiency. J Lipid Res. 2008;46:349–357
- Compound heterozygozity for an apolipoprotein AI gene promoter mutation and a structural nonsense mutation with apolipoprotein deficiency. Arterioscler Thromb Vasc Biol. 1999;19:348–355
- A novel two nucleotide deletion in the apolipoprotein A-I gene, apoA-I Shinbashi, associated with high density lipoprotein deficiency, corneal opacities, planar xanthomas, and premature coronary artery disease. Atherosclerosis. 2004;172:39–45
- A mutation in the apolipoprotein A-I gene. J Biol Chem. 1991;266:13654–13660
- Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency. Atherosclerosis. 2003;167:335–345
- . Tangier disease. Ann Intern Med. 1961;55:1016–1031
- . Coronary heart disease prevalence and other clinical features in familial high density lipoprotein deficiency (Tangier disease). Ann Intern Med. 1980;93:261–266
- Homozygous Tangier disease and cardiovascular disease. Atherosclerosis. 1994;107:85–98
- . Ocular manifestations of familial high density lipoprotein deficiency (Tangier disease). Arch Opthalmol. 1979;97:1926–1928
- . Subpopulations of high-density lipoproteins in homozygous and heterozygous Tangier disease. Atherosclerosis. 2001;156:217–225
- . HDL-mediated efflux of intracellular cholesterol is impaired in fibroblasts from Tangier disease patients. Arterioscler Thromb Vasc Biol. 1995;15:683–690
- . Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier disease. J Clin Invest. 1995;96:78–87
- Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nat Genet. 1999;22:352–355
- Molecular cloning of the human ATP-binding cassette transporter 1 (hABC1): evidence for sterol-dependent regulation in macrophages. Biochem Biophys Res Comm. 1999;257:29–33
- Mutation in ABC1 in Tangier disease and familial high density lipoprotein. Nature Gen. 1999;22:336–345
- The gene encoding ATP binding cassette transporter 1 is mutated in Tangier disease. Nature Gen. 1999;22:347–351
- Tangier disease is caused by mutations in the gene encoding ATP binding cassette transporter 1. Nature Gen. 1999;22:352–355
- Novel mutations in the gene encoding ATP-binding cassette 1 in four Tangier disease kindreds. J Lipid Res. 2000;41:433–441
- Cellular cholesterol efflux in heterozygotes for Tangier disease is markedly reduced and correlates with high density lipoprotein cholesterol concentration and particle size. J Lipid Res. 2000;41:1125–1135
- Cholesterol and apolipoprotein B metabolism in Tangier disease. Atherosclerosis. 2001;159:231–236
- . Familial plasma lecithin cholesterol acyl transferase deficient (Biochemical study if a new inborn error of metabolism). Scand J Clin Lab Invest. 1967;20:231–235
- The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families. Arterioscler Thromb Vasc Biol. 2005;25:1972–1978
- Role of LCAT in HDL remodeling: investigation of LCAT deficiency states. J Lipid Res. 2007;48:592–599
- . Differential effects of HDL subpopulations on cellular ABCA1 and SRB1-mediated cholesterol efflux. J Lipid Res. 2005;46:2246–2253
- High density lipoprotein subpopulation profile and coronary heart disease prevalence in male participants in the Framingham Offspring Study. Arterioscler Thromb Vasc Biol. 2004;24:2181–2187
- Value of high density lipoprotein (HDL) subpopulations in predicting recurrent cardiovascular events in the Veterans Affairs HDL Intervention Trial. Arterioscler Thromb Vasc Biol. 2005;25:2185–2191
- Change in alpha 1 HDL concentration predicts progression in coronary artery stenosis. Arterioscler Thromb Vasc Biol. 2003;23:847–852
PII: S1933-2874(08)00263-8
doi: 10.1016/j.jacl.2008.06.002
© 2008 National Lipid Association. Published by Elsevier Inc. All rights reserved.
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Journal of Clinical Lipidology
Volume 2, Issue 4
, Pages 237-247
, August 2008
