Apolipoprotein E genotypes and response of plasma lipids and progression-regression of coronary atherosclerosis to lipid-lowering drug therapy
- PMID: 11079660
- DOI: 10.1016/s0735-1097(00)00918-9
Apolipoprotein E genotypes and response of plasma lipids and progression-regression of coronary atherosclerosis to lipid-lowering drug therapy
Abstract
Objectives: We sought to examine the association of apolipoprotein (apo) E genotypes with baseline plasma lipid levels and severity of coronary artery disease (CAD), as well as the response to treatment with fluvastatin in the Lipoprotein and Coronary Atherosclerosis Study (LCAS).
Background: Apo E genotypes have been associated with plasma lipid levels and CAD. However, the influence of apo E genotypes on the response of plasma lipids and CAD progression or regression to statin treatment in patients with mildly to moderately elevated cholesterol remains unknown.
Methods: Apo E genotypes were determined by polymerase chain reaction and restriction mapping. Plasma lipids were measured at baseline and 12 weeks after therapy with fluvastatin or placebo in 320 subjects. In 287 subjects, quantitative coronary angiography was performed at baseline and after 2.5 years of treatment.
Results: Subjects with the 3/3 genotype had greater reductions in total cholesterol (20.4% vs. 15.4%, p = 0.01) and low density lipoprotein (LDL) cholesterol (28.8% vs. 22.7%, p = 0.03) than did the subjects with the 3/4 or 4/4 genotype. In contrast, subjects with the 2/3 genotype (n = 10) had a greater increase in high density lipoprotein cholesterol (19.1%) than did the subjects with the 3/3 genotype (4.3%, p = 0.002) and those with the 3/4 or 4/4 genotype (7.0%, p = 0.02). Subjects with the 3/4 or 4/4 genotype had an increased frequency of previous angioplasty, but other measures of baseline CAD severity and baseline lipids did not differ significantly among the genotypes, nor did CAD progression or clinical events.
Conclusions: Although subjects with the epsilon4 allele had less reduction in LDL cholesterol with fluvastatin, they had similar benefit in terms of CAD progression.
Similar articles
-
Interactions between angiotensin-I converting enzyme insertion/deletion polymorphism and response of plasma lipids and coronary atherosclerosis to treatment with fluvastatin: the lipoprotein and coronary atherosclerosis study.J Am Coll Cardiol. 2000 Jan;35(1):89-95. doi: 10.1016/s0735-1097(99)00535-5. J Am Coll Cardiol. 2000. PMID: 10636265 Clinical Trial.
-
Lipoprotein lipase gene mutations, plasma lipid levels, progression/regression of coronary atherosclerosis, response to therapy, and future clinical events. Lipoproteins and Coronary Atherosclerosis Study.Atherosclerosis. 1999 Jun;144(2):435-42. doi: 10.1016/s0021-9150(99)00004-0. Atherosclerosis. 1999. PMID: 10407505 Clinical Trial.
-
A prospective study of paraoxonase gene Q/R192 polymorphism and severity, progression and regression of coronary atherosclerosis, plasma lipid levels, clinical events and response to fluvastatin.Atherosclerosis. 2001 Feb 15;154(3):633-40. doi: 10.1016/s0021-9150(00)00495-0. Atherosclerosis. 2001. PMID: 11257264 Clinical Trial.
-
Managing dyslipidemia in the high-risk patient.Am J Cardiol. 2002 Mar 7;89(5A):50C-57C. doi: 10.1016/s0002-9149(02)02229-4. Am J Cardiol. 2002. PMID: 11900720 Review.
-
Fluvastatin in combination with other lipid-lowering agents.Br J Clin Pract Suppl. 1996 Jan;77A:28-32. Br J Clin Pract Suppl. 1996. PMID: 8729588 Review.
Cited by
-
Quantile-specific heritability of high-density lipoproteins with implications for precision medicine.J Clin Lipidol. 2020 Jul-Aug;14(4):448-458.e0. doi: 10.1016/j.jacl.2020.05.099. Epub 2020 May 29. J Clin Lipidol. 2020. PMID: 32600822 Free PMC article.
-
Pharmacogenomics: marshalling the human genome to individualise drug therapy.Gut. 2003 May;52 Suppl 2(Suppl 2):ii10-8. doi: 10.1136/gut.52.suppl_2.ii10. Gut. 2003. PMID: 12651877 Free PMC article. Review.
-
Pharmacogenetics of response to statins: where do we stand?Curr Atheroscler Rep. 2005 May;7(3):204-8. doi: 10.1007/s11883-005-0007-3. Curr Atheroscler Rep. 2005. PMID: 15811254 Review.
-
Endothelial lipase is a major genetic determinant for high-density lipoprotein concentration, structure, and metabolism.Proc Natl Acad Sci U S A. 2003 Mar 4;100(5):2748-53. doi: 10.1073/pnas.0438039100. Epub 2003 Feb 24. Proc Natl Acad Sci U S A. 2003. PMID: 12601178 Free PMC article.
-
A common PCSK9 haplotype, encompassing the E670G coding single nucleotide polymorphism, is a novel genetic marker for plasma low-density lipoprotein cholesterol levels and severity of coronary atherosclerosis.J Am Coll Cardiol. 2005 May 17;45(10):1611-9. doi: 10.1016/j.jacc.2005.01.051. Epub 2005 Apr 21. J Am Coll Cardiol. 2005. PMID: 15893176 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous